文档库 最新最全的文档下载
当前位置:文档库 › Flacourtiaceae(Flora of china)大风子科

Flacourtiaceae(Flora of china)大风子科

Flacourtiaceae(Flora of china)大风子科
Flacourtiaceae(Flora of china)大风子科

FLACOURTIACEAE

大风子科 da feng zi ke

Yang Qiner (杨亲二)1; Sue Zmarzty2

Trees or shrubs, hermaphroditic, monoecious, dioecious, or polygamous, evergreen or deciduous; trunk, branches, and branch-lets sometimes spiny; hairs simple, rarely T-shaped or stellate. Leaves simple, usually alternate, rarely opposite or verticillate, some-times crowded at apices of branches; stipules usually small and caducous, sometimes larger, leaflike and persistent, rarely absent; petiole generally present, sometimes with apex 2-glandular and/or with additional glands along petiole length; leaf blade usually pinnate-veined, sometimes 3–5-veined from base or palmate-veined, with or without pellucid dots or lines, sometimes with a pair of glands at junction of blade and petiole, margin entire or toothed, teeth glandular or not. Inflorescences axillary, terminal, or cauliflor-ous, of various forms: racemose, spicate, cymose, corymbose, or paniculate, sometimes flowers fasciculate, or solitary; pedicels often articulate; bracts and bracteoles usually small to minute. Flowers radially symmetric, bisexual or unisexual, hypogynous, perigynous, or epigynous; perianth cyclic, rarely spiral, in unisexual flowers remnants of opposite sex present or absent. Sepals imbricate or valvate, rarely spathaceous, mostly (2 or)3–6, rarely more, usually free or connate at base only, sometimes partly united into a tube, caducous or persistent, rarely accrescent. Petals 3–8, rarely more, often isomerous and alternating with sepals, free, imbricate or val-vate, rarely contorted, similar to sepals or not, sometimes with a fleshy adaxial basal scale, or petals absent. Disk present, entire, lobed, or comprised of free or connate disk glands, these extrastaminal, interstaminal, or intrastaminal (bisexual or staminate flow-ers), or extragynoecial (pistillate flowers), or disk absent. Stamens 1 to many (ca. 100), 1- or many seriate, sometimes in epipetalous bundles, or on margin of cupular disk or rim of calyx tube; filaments free, rarely united into a column; anthers 2-thecate, usually longitudinally dehiscent, rarely opening by terminal pores, connective sometimes shortly projected or glandular. Ovary superior or semi-inferior, 1-loculed, with 2–9 parietal placentas, rarely incompletely 2–9(or more)-celled by placentas protruding deeply into locule; ovules 2 or more on each placenta, orthotropous, anatropous, or hemi-anatropous; styles isomerous with placentas, free or partly to completely united, rarely absent, stigmas small or large, capitate to flattened and branched. Fruit capsular or baccate, rarely a drupe, pericarp mostly smooth, sometimes winged or bristly. Seeds 1 to many, with or without a fleshy sometimes brightly colored sarcotesta and/or aril, sometimes with long hairs, or broadly winged; endosperm usually copious and fleshy; embryo straight or curved; cotyledons usually broad, often cordate.

About 87 genera and ca. 900 species: mostly in tropical and subtropical regions, some extending into the temperate zone; 12 genera (one endemic) and 39 species (nine endemic) in China; four additional species (all endemic) are poorly known (see Homalium).

Ahernia glandulosa Merrill (Philipp. J. Sci. 4: 295. 1909), described from the Philippines, reportedly occurs in Hainan, but the present authors have seen no specimens from the Flora area. Flacourtia cavaleriei H. Léveillé (Repert. Spec. Nov. Regni V eg. 9: 457. 1911) and Xylosma dunniana H. Léveillé (loc. cit.: 455) were both described from Guizhou. After studying specimens at K from the type gathering (Cavalerie 3327 and Cavalerie 1151, respectively), it is not clear where they belong, and for the time being they must be regarded as species incertae sedis. Erythrospermum hypoleucum Oliver is the basionym of Celastrus hypoleucus (Oliver) Warburg ex Loesener in the Celastraceae (see Fl. China 11). Oncoba spinosa Forsskal and Dovyalis hebecarpa (Gardner) Warburg are occasionally cultivated.

In some treatments, where the genera of Flacourtiaceae are completely transferred to other families, and Flacourtiaceae is treated as a synonym of Salicaceae sensu lato, Chinese genera have been reclassified as follows: two genera (Hydnocarpus and Gynocardia) moved to Achariaceae sensu lato, all others to Salicaceae sensu lato (Chase et al., Kew. Bull. 57: 141–181. 2002).

Lai Shushen. 1999. Flacourtiaceae. In: Ku Tsuechih, ed., Fl. Reipubl. Popularis Sin. 52(1): 1–80.

Key to genera based on material in flower

In flower, especially in staminate flower, Xylosma and Flacourtia are difficult to distinguish at genus level. In China, the two genera together include eight species. For identification, take material through keys to both genera; a combination of leaf size, leaf shape, sepal number and indumen-tum, and style/stigma form helps distinguish species in either genus.

1a. Petals present.

2a. Calyx tube present, obconic, adnate to ovary for lower 1/2–2/3 (i.e., flowers epigynous), with free sepal lobes and petals spreading from rim, ovary semi-inferior, lower 2/3 or more enclosed in adnate calyx tube ............... 11. Homalium 2b. Calyx tube absent, calyx not adnate to ovary (i.e., flowers hypogynous), sepals free or partly fused, sometimes completely fused in bud, ovary when present free.

3a. Flowers always bisexual; petals and sepals similar; petals ca. 4 mm or less, adaxial basal scale absent; disk glands present, small, in an extrastaminal row; stamens longer than sepals; style 1 ........................................... 3. Scolopia 3b. Flowers unisexual or bisexual; petals and sepals distinct; petals ca. 5 mm or more, with scale at least 1/4 as long as petal attached to inside at base; disk glands absent; stamens shorter than or equal to petals;

styles 3–6.

1 Institute of Botany, Chinese Academy of Sciences, 20 Nanxincun, Xiangshan, Beijing 100093, People’s Republic of China.

2 Herbarium, Royal Botanic Gardens, Kew, Richmond, Surrey TW9 3AE, United Kingdom.

FLACOURTIACEAE 113 4a. Sepals in bud completely fused, calyx closed or with a small circular opening at apex, later shortly

3–5-truncate lobed, sometimes splitting more regularly to 3–5 sepals; stamens ca. 100 (staminate

flowers); styles 5, stigmas small, cordate or peltate, erect or reflexed (pistillate flowers) ...................... 2. Gynocardia 4b. Sepals in bud imbricate, free or connate at base only; stamens 5–30 (staminate flowers); styles 3–6,

or nearly absent, stigmas conspicuous, broadly flattened, usually reflexed (pistillate flowers) ........... 1. Hydnocarpus 1b. Petals absent.

5a. Flowers bisexual, disk cuplike (cup sometimes very shallow), adnate to inside of calyx (but not adnate to ovary), with oblong to narrowly triangular hairy disk lobes in same row as stamens and alternating with them, lobes

ca. 1/2 as long as stamen filaments .......................................................................................................................... 12. Casearia 5b. Flowers unisexual, rarely bisexual, disk not cuplike nor with lobes alternating with stamens, nor adnate to inside calyx; instead disk a small fleshy annulus or comprising small, free or connate, fleshy glands, these in

an extrastaminal (staminate and bisexual flowers) or extra-gynoecial (pistillate flowers) row, or disk consisting

of free glands among stamen or staminode bases, or disk and disk glands completely absent.

6a. Sepals valvate, disk glands absent.

7a. Leaves pinnate-veined .......................................................................................................................................... 10. Itoa 7b. Leaves 3–5-veined from base.

8a. Inflorescence more than 30-flowered, very densely pale-grayish tomentose throughout,

indumentum obscuring rachis surface, bracts to 4 mm; sepals 4–5 mm, thickish in texture ............ 8. Poliothyrsis 8b. Inflorescence less than 20-flowered, pubescent to tomentose but indumentum not obscuring

rachis surface, bracts 5–30 mm; sepals more than 10 cm, papery ........................................................ 9. Carrierea 6b. Sepals imbricate; disk glands present, extrastaminal, extragynoecial, or among stamen or staminode bases.

9a. Leaves broadly ovate, base cordate or less often broadly rounded, petiole 6–12 cm or more, often with

1 or

2 large glands in lower half; sepals 5–6 mm, outside densely pubescent, hairs yellowish brown

when dry ............................................................................................................................................................. 7. Idesia 9b. Leaves not as above, petiole usually less than 4 cm, if longer then without glands in lower half;

sepals less than 4 mm, outside glabrous or only sparsely pubescent, hairs not yellowish when dry.

10a. Flowers usually in terminal panicles 6–12 cm (sometimes shorter); stamen or staminode

filaments with long hairs in lower half; disk glands free among filament bases .................. 6. Bennettiodendron 10b. Flowers in short racemes or cymes to 5 cm, these axillary or terminating short lateral

branches; stamen or staminode filaments glabrous, or with short hairs in lower half;

disk annular or comprised of connate or free glands, in an extragynoecial or

extrastaminal row, not dispersed among stamen or staminode bases ........................ 4. Flacourtia or 5. Xylosma

Key to genera based on material in fruit

Flacourtiaceae in fruit are neither easily nor practically accommodated in a dichotomous key. We have therefore used a combination of key couplets and spot characters, including characters that can be very useful but are not always present (e.g., style characters).

The single species of Poliothyrsis, P. sinensis, has capsules 2–3 cm and a seed completely encircled by a membranous wing. By these characters it can be distinguished easily from Carrierea calycina, which has larger capsules 3–7 cm and a seed with a wing at one end only. Poliothyrsis sinensis and the second species of Carrierea, C. dunniana, are more difficult to differentiate because both have similar capsules of about the same size. The dense, white rachis indumentum of P. sinensis can be a useful character. Leaves of P. sinensis and C. dunniana are quite similar, at least in dried material.

1a. Mature fruit enclosed for 2/3–3/4 of its length by persistent adnate perianth, sepals and petals persistent at calyx tube rim, fruit small, capsular (less than 12 mm) ......................................................................................................... 11. Homalium 1b. Mature fruit not at all enclosed by persistent perianth, fruit type and size various.

2a. Fruit a dehiscent ovoid or fusiform capsule, splitting from apex and base into narrow fusiform valves attached only by woody placental strands, outer tomentose layer sometimes dehiscent, locule filled with vertically

arranged winged seeds; disk characters, although often present and useful with experience, are not relied

upon heavily here as they are difficult to observe, and can be confused with perianth scars.

3a. Leaves pinnate-veined, lateral veins 10–26 pairs ....................................................................................................... 10. Itoa 3b. Leaves 3–5-veined from base, lateral veins 4–6 pairs.

4a. Seed completely encircled by wing ........................................................................................................... 8. Poliothyrsis 4b. Seed with wing at one end only ................................................................................................................... 9. Carrierea 2b. Fruit not as above.

5a. Mature fruit large, 4–12 cm in diam., seed embedded in pulp.

6a. Fruit arising from tubercles on stems, older branches, and trunks; pericarp glabrous, grayish; dried

mature leaves grayish green ...................................................................................................................... 2. Gynocardia 6b. Fruit not arising from tubercles on stems, older branches, and trunks; in H. annamensis and

H. hainanensis fruit tomentose or velutinous, distinguishable from Gynocardia on that basis; in

FLACOURTIACEAE

114

H. anthelminthicus fruit is finally glabrous, usually darkish brown in dried state, dried mature

leaves reddish brown .............................................................................................................................. 1. Hydnocarpus 5b. Mature fruit small to medium sized (3–30 mm in length or diam.).

7a. Fruit a drupe containing pyrenes; in dried state 10–30 mm, often longitudinally angled at maturity

and squarish or rectangular in longitudinal section, with a flattish apex; styles 4–7, persistent at

apex, free or partly to completely fused ...................................................................................................... 4. Flacourtia 7b. Fruit not as above: try using character combinations below:

3. Scolopia: spines sometimes present; fruiting racemes axillary or terminal, short, 0.5–6 cm, these

sometimes reduced almost to fascicles; fruit baccate, in dried state ca. 10 mm in diam. or less; sepal, petal, and

stamen remnants usually present at base of fruit (flowers bisexual, petalous), persistent style column 3–5 mm.

5. Xylosma: spines sometimes present; fruiting racemes, panicles, or fascicles axillary, to 5 cm; fruit

baccate, in dried state to ca. 7 mm in diam.; sepals persistent or not, petal remnants always absent, stamen

remnants usually absent (flowers apetalous, usually unisexual, very rarely bisexual), persistent style column 0–

1.5 mm.

6. Bennettiodendron: unarmed; panicles 6–12(–20) cm; fruit baccate, in dried state to 10 mm in diam.,

perianth caducous; stamens usually absent (flowers usually unisexual); pedicels to 1 cm, often conspicuously

warted by very prominent lenticels; leaves narrowly to broadly elliptic, elliptic-oblong, or obovate, bases acute or

obtuse cuneate, pinnate-veined; petioles never with glands in lower half.

7. Idesia: unarmed; fruiting panicles (sometimes racemelike) 20–30 cm; fruit baccate, in dried state to 10

mm in diam.; leaves broadly ovate, bases cordate or broadly rounded, 3–5-veined from base; petioles sometimes

with glands in lower half.

12. Casearia: unarmed; leaves sometimes pellucid-punctate; fruiting glomerules axillary (infructescence

axis absent); fruit capsular, though fleshy and berrylike before dehiscence, in dried state 8–30 mm, typically

longitudinally (2 or)3-angled, less often smooth, dehiscing finally by (2 or)3 valves, hairy disk lobes and stamens

often persistent at base.

1. HYDNOCARPUS Gaertner, Fruct. Sem. Pl. 1: 288. 1788.

大风子属 da feng zi shu

Taraktogenos Hasskarl.

Trees, rarely shrubs, dioecious, rarely monoecious or polygamous. Leaves alternate; stipules small, usually early caducous; petiole usually present, often thickened at apex; leaf blade leathery, pinnate-veined, margin entire or toothed. Flowers hypogynous, in axillary, ± branched cymes, these sometimes very short or reduced to fascicles or to a solitary flower, or rarely flowers in long racemelike panicles from trunk or older branches; bracts small to minute, sometimes persistent; pedicels articulate. Sepals (3 or)4 or 5(or 7–11), imbricate, free or slightly joined at base, concave, becoming reflexed, caducous. Petals 4 or 5(–14), free or slightly joined at base, each with a thick and usually hairy scale inside at base. Disk and disk glands absent. Staminate flowers: stamens 5 to many (more than 100); filaments free, sometimes very short; anthers oblong to ovate-cordate, longitudinally dehiscent, connective often di-lated; pistillode present or absent. Pistillate flowers: staminodes 5 to many, resembling stamens but anthers mostly reduced or absent; ovary superior, 1-loculed, placentas 3–6, each with several ovules; styles 3–6, short, or nearly absent; stigmas flattened, usually re-flexed. Fruit baccate, globose, or ovoid, rarely elongate; pericarp thick and hard, or thin and brittle, exocarp fibrous or not, mesocarp light yellow, usually very hard, endocarp soft. Seeds several to many, angular-ovoid, packed in pulp; testa hard, striate; aril mem-branous; endosperm oily; cotyledons large and broad, leaflike, compressed-flat or folded.

About 40 species: tropical Asia; three species in China.

In Chinese species: flowers to ca. 20 together in fascicles or cymes; stamens 5 to ca. 25; mature fruit globose.

Hydnocarpus kurzii (King) Warburg (in Engler & Prantl, Nat. Pflanzenfam. 3(6a): 21. 1893; Taraktogenos kurzii King, J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist. 59: 123. 1890), described from Myanmar, was recorded as native to S Y unnan by Lai (FRPS 52(1): 9. 1999), although the present authors have seen no material.

According to Fl. Y unnan. (6: 254. 1995), Hydnocarpus alpinus Wight is cultivated in S Y unnan.

Key to material in flower

1a. Sepals 5; petals 5, narrowly ovate-oblong, 12–15 mm; stamens 5 .................................................................. 3. H. anthelminthicus 1b. Sepals 4; petals 4 or (7 or)8, orbicular or reniform-ovate, less than 8 mm; stamens 15–30.

2a. Petals 4 or (7 or)8; inflorescence 2- or 3-flowered; leaves 17–35 × 7–12 cm, abaxially hairy ....................... 1. H. annamensis 2b. Petals 4; inflorescence 15–20-flowered; leaves 9–18 × 3–6 cm, abaxially glabrous ....................................... 2. H. hainanensis Key to (dried) material in fruit

1a. Leaves abaxially hairy; pericarp cross-section with radially striate layer ............................................................... 1. H. annamensis

FLACOURTIACEAE 115 1b. Leaves abaxially glabrous; pericarp cross-section without radially striate layer.

2a. Leaves typically 2–3 × as long as wide, usually greenish when dried; young and mature fruit pale to dark brown or yellowish tomentose, 4–5 cm in diam. .............................................................................................. 2. H. hainanensis 2b. Leaves typically 3–4(–5) × as long as wide, usually drying reddish brown; young fruit darkish brown velutinous, finally glabrous, 8–12 cm in diam. .......................................................................................... 3. H. anthelminthicus

1. Hydnocarpus annamensis (Gagnepain) Lescot & Sleumer, Fl. Cambodge Laos Vietnam 11: 10. 1970.

大叶龙角 da ye long jiao

Taraktog enos annamensis Gagnepain in Lecomte, Fl. Indo-Chine, Suppl. 1: 206. 1939; Hydnocarpus merrillianus H. L. Li (1943), not Sleumer (1938); T. merrilliana C. Y. Wu.

Trees, evergreen, 8–25 m tall; bark gray-brown; branchlets terete, gray-brown or reddish tomentose; winter buds ovoid-globose, scales brown tomentose outside. Petiole 1–2.5 cm, brown tomentose; leaf blade green abaxially, deep green adax-ially, obovate, elliptic-oblong, or oblong-lanceolate, 17–35 × 7–12 cm, thinly leathery, abaxially sparsely hairy or hairy only along veins, adaxially shiny and glabrous, midvein raised on both sides, lateral veins 5–10 pairs, reticulate veins conspic-uous, base broadly acute, cuneate, asymmetric, margin entire, apex obtuse, contracting abruptly to a short acumen. Inflores-cence axillary; flowers solitary, or 2 or 3 together in cymes 1–2 cm; rachis pubescent. Pedicels 3–5 mm, together with pedun-cles densely brown tomentose. Staminate flowers deep green; sepals 4 or 5, orbicular, 5–6 mm, outside yellowish tomentose, inside glabrous; petals 4 or 5, suborbicular, outer petals 4–5 mm, inner ones smaller, both sides (excl. scale) glabrous, mar-gin ± fimbriate; scale 3–3.5 mm, apex hairy and fimbriate; stamens many (ca. 25); filaments 4–5 mm, hairy; anthers glo-bose or subcordate, apex ± acute; pistillode absent. Pistillate flowers greenish, ca. 1.5 cm in diam.; sepals 4, oblong, 6–7 mm, outside densely rusty tomentose, inside glabrous, margin ciliate; petals 8, suborbicular, inner ones smaller, outer ones larger, both sides (excl. scale) glabrous, margin ± fimbriate; scales as for staminate flowers; staminodes 8; ovary ovoid-orbicular, slightly 8-angled, densely pubescent, styles nearly absent, stigmas 4 or 5. Berry subglobose, 4–6 cm in diam., reddish or brownish tomentose interspersed with longer stiffer bristles, stigmas persistent, pericarp cross-section with radially striate layer. Seeds numerous. Fl. Apr–May, fr. Jan–Dec.

Moist mountain slopes, thickets along streams; 200–600 m. S Guangxi, S Yunnan [Vietnam].

Li and Feng (in Fu & Jin, China Pl. Red Data Book 1: 308–309. 1992, as Taraktogenos annamensis) gave the conservation status of this species as rare, i.e., not in imminent danger of extinction but with very limited or scattered distribution. The 2006 IUCN Red List of Threatened Species (https://www.wendangku.net/doc/ca140526.html,, at 19 January 2007, as T. annamensis) gave the status as vulnerable (VU A1cd). In China the species has suffered catastrophic damage due to clearance for agriculture, and the fruits are often harvested for their medicinal value.

Treatments disagree with respect to petal number in the male flower. Wu (Acta Phytotax. Sin. 6: 226. 1957) recorded 4 or 5 petals, which agrees with material seen for the present treatment. Lescot (Fl. Cambodge Laos Vietnam 11: 10. 1970) recorded (7 or)8 petals.

2. Hydnocarpus hainanensis (Merrill) Sleumer, Bot. Jahrb. Syst. 69: 15. 1938. 海南大风子 hai nan da feng zi

Taraktogenos hainanensis Merrill, Philipp. J. Sci. 23: 255. 1923.

Trees, evergreen, 6–12 m tall; bark gray-brown; branchlets terete, glabrous. Petiole 1–1.5 cm, glabrous or initially sparsely appressed-pubescent,glabrescent;leaf blade usually oblong, less often elliptic, narrowly ovate, or slightly obovate, 9–18 × 3–6 cm, 2–3 × as long as wide, thinly leathery, both surfaces gla-brous, lateral veins 7 or 8 pairs, reticulate veins conspicuous, base acute to obtuse or rounded, cuneate, margin irregularly repand, serrulate or serrate, teeth sometimes sharply acute, leaf apex acute to obtuse, usually gradually or abruptly acuminate, acumen to ca. 2 cm. Inflorescence axillary or subterminal, 1.5–2.5 cm; flowers unisexual, 15–20 in much condensed (especi-ally staminate flowers) shortly pedunculate cymes. Pedicels 8–15 mm, initially with sparse, short, appressed hairs, soon gla-brous. Sepals 4, free, elliptic or orbicular, 5–6 × ca. 4 mm, both sides glabrous or outside sparsely appressed-hairy. Petals 4, free, reniform-ovate, 2–3 × 3–4 mm, both sides (excl. scale) glabrous, margin ciliate; scale ca. 1/2 as long as petal, irregu-larly 4–6-dentate, villous. Staminate flowers: stamens ca. 12; filaments ca. 1.5 mm, stout at base, sparsely hairy, hairs rather long, drying white; anthers sagittate, 1.5–2.5 mm; reduced ovary absent. Pistillate flowers: staminodes ca. 15, stamenlike but with anthers reduced, indumentum as for fertile stamens; ovary ovoid-ellipsoid, very densely yellowish brown pubescent, hairs closely appressed; placentas 5; ovules many; styles absent; stigmas 3 or 4, joined at base, flattened-deltoid, ca. 5 mm, bifid with each branch apex irregularly toothed or lobed, abaxially densely hairy at base, hairs as for ovary, adaxially glabrous. Berry globose, 4–5 cm in diam., densely pale to dark brown or yellowish tomentose, sometimes yellowish; pericarp leathery, exocarp not fibrous, stalk 6–7 mm, stout. Seeds ca. 20, ovoid, ca. 2.5 × 1.5–2 cm. Fl. Apr–May, fr. Jun–Aug.

Evergreen broad-leaved forests; 300–1800 m. Guangxi, Guizhou, Hainan, S Yunnan [Vietnam].

E (in Fu & Jin, China Pl. Red Data Book 1: 306–307. 1992) gave the conservation status of this species as vulnerable. The 2006 IUCN Red List of Threatened Species (https://www.wendangku.net/doc/ca140526.html,, at 19 J anuary 2007) also gave the status as vulnerable (VU A1cd). In China the spe-cies is under threat from habitat loss and harvesting of the timber (hard, heavy, compact, durable, and decay-resistant) and the fruit (the seeds have a relatively high component of chaulmoogric oil, locally important for the treatment of skin conditions). Natural regeneration is poor.

3. Hydnocarpus anthelminthicus Pierre in Lanessan, Pl. Util. Col. Fran?. 303. 1886 [“anthelminticus”].

泰国大风子 tai guo da feng zi

Trees,less often shrubs, evergreen, 7–20(–30) m tall; trunk strictly straight, bark gray-brown; branchlets stout, slightly en-larged at nodes. Petiole 5–15 mm, glabrous; leaf blade green

FLACOURTIACEAE 116

when fresh, often drying reddish brown, lanceolate, ovate-lan-ceolate or oblong, (7–)10–20(–30) × 3–8 cm, typically 3–4(–5) × as long as wide, thinly leathery, both surfaces glabrous, lat-eral veins 8–10 pairs, reticulate veins dense, conspicuous, base usually rounded, rarely obtuse-cuneate, oblique, margin en-tire, apex variable, acute to obtuse or rounded, often with a short acumen 3–10 mm. Inflorescences axillary, flowers 2 or 3 in often abbreviated false cymes or racemes to 1 cm, or flowers solitary (mostly pistillate flowers). Flowers mostly unisexual, yellowish or pinkish green, fragrant. Pedicels slender, to 2 cm, longer in fruit, yellowish stellate-tomentose. Sepals 5, united at base, ovate, narrowly oblong, or obovate, 8–9 mm, outside densely yellowish stellate-tomentose, inside appressed pubes-cent, apex obtuse. Petals 5, becoming reflexed, nearly free, yel-lowish pink, narrowly ovate-oblong, 12–15 mm, both sides (excl. scale) and margin glabrous or with a few scattered hairs; scales free except at extreme base, linear, subequaling petals, both sides glabrescent to glabrous, margin ciliate. Staminate flowers: stamens 5; filaments ca. 3 mm, dilated at base, taper-ing toward apex, glabrous; anthers sagittate, ca. 4 mm, connec-tive dilated; pistillode columnar, small, hairy. Pistillate flow-ers: pedicels tomentose; staminodes 5, similar to anthers but filaments ca. 1.5 mm, with or without anthers; ovary ovoid or obovoid, red-brown setaceous, drying yellowish; placentas 5; ovules 10–15; styles short, hairy; stigmas 5, reflexed, con-nate, forming a cap at apex of ovary, beneath setaceous like ovary, upper surface glabrous, margin crenate. Berry globose, 8–12 cm in diam.; stalk stout, pericarp orange-brown when fresh, when dried densely blackish hairy at first, gradually gla-brescent, finally dark brown with numerous minute white dots, verrucose, scaly; exocarp not fibrous, inner layers woody, thin, crisp when dry. Seeds many, 30–50(–100), 1.5–2.2 × 1–1.7 cm. Fl. Sep, fr. Nov–Jun of next year.

Rain forests or evergreen broad-leaved forests; 300–1300 m. Guangxi, Yunnan; cultivated in Guangxi, Hainan, and Taiwan [Cam-bodia, Thailand, Vietnam].

2. GYNOCARDIA R. Brown in Roxburgh, Pl. Coromandel 3: 95. 1820.

马蛋果属 ma dan guo shu

Chaulmoogra Roxburgh; Chilmoria Buchanan-Hamilton.

Trees, dioecious. Leaves alternate; stipules caducous, not seen; petiole present; leaf blade leathery, pinnate-veined, margin entire. Flowers hypogynous, solitary or few in axillary bracteate corymbs (staminate flowers), or in corymbose clusters arising from tubercles on stems and older branches (staminate or pistillate flowers), pedicellate; pedicels articulate, bracteolate; buds globose. Calyx closed in bud, later cupular, subtruncate, 5-dentate or shallowly 3–5-lobed, finally sometimes with 3–5 irregular or orbicular sepals. Petals 5, united at base, fleshy, each with a scale inside at base. Disk and disk glands absent. Staminate flowers: stamens many (ca. 100); filaments free, filiform; anthers basifixed, linear-sagittate, small; pistillode absent. Pistillate flowers: staminodes 10–15; ovary superior, 1-loculed, placentas 5, each with numerous ovules; styles 5, free, columnar; stigmas cordate or peltate, small. Fruit baccate, pericarp thick, woody. Seeds immersed in pulp, numerous, testa thick, crisp; endosperm oily, fleshy; cotyledons com-pressed-flat.

One species: Asia.

1. Gynocardia odorata R. Brown in Roxburgh, Pl. Coroman-del 3: 95. 1820.

马蛋果 ma dan guo

Chaulmoog ra odorata Roxburgh; Chilmoria dodecandra Buchanan-Hamilton.

Trees, evergreen, to 30 m tall; twig tips and branchlets gla-brous; bark brown, not flaking; branchlets terete; winter buds ovoid-orbicular. Petiole 1–3 cm, usually glabrous, sometimes sparsely appressed puberulous; leaf blade greenish abaxially, deep green adaxially, nearly concolored when dry, oblong-ellip-tic, rarely ovate-oblong or obovate-oblong, 13–20 × 5–10 cm, leathery, lateral veins 4–8 pairs, conspicuous abaxially, reticu-late veins parallel, margin entire, slightly uneven, base rounded or acute-cuneate, apex rounded, contracting abruptly to a short narrow acumen. Pedicels 2.5–5 cm, sparsely appressed hairy or glabrous. Staminate flowers 3–4 cm in diam., fragrant; calyx lobes ca. 7 mm, obtuse to rounded, outside glabrous or with short, sparse, appressed hairs; petals yellowish green, oblong or slightly obovate, 1.5–2 cm, glabrous, apex obtuse; epipetalous scale oblong or ovate, ca. 6 × 4 mm, densely ciliate, apex ob-tuse; stamens ca. 1 cm, filaments villous, anthers ca. 5 mm. Pistillate flowers larger than staminate flowers; petals ca. 2.5 cm; staminodes 10–15, villous; styles short, slender; stigmas peltate or cordate. Berry yellowish brown, globose, (5–)8–12 cm in diam.; pericarp grayish, ca. 5 mm thick, woody, rugose, glabrous. Seeds numerous, variable in shape and size, usually obovoid to ellipsoid, 2.5–3 cm, hilar region large, silvery gray. Fl. Jan–Feb, fr. Jun–Aug.

Moist sparse forests of mountain valleys; 800–1000 m. SE Xizang (Mêdog), SE Yunnan [Bangladesh, Bhutan, India, Myanmar, Nepal].

3. SCOLOPIA Schreber, Gen. Pl. 1: 335. 1789, nom. cons.

箣柊属 ce zhong shu

Aembilla Adanson; Phoberos Loureiro.

Shrubs or small trees, often spinose on trunk and branches. Leaves alternate; stipules small, caducous; usually petiolate; leaf blade leathery, pinnate-veined, sometimes 3-veined from base, with or without a pair of marginal glands at junction of petiole apex

FLACOURTIACEAE 117 and base of blade, margin entire or toothed, each tooth with a small marginal gland. Flowers bisexual (usually), hypogynous, small, arranged in terminal or axillary bracteate racemes, sometimes in axillary fascicles or solitary; pedicels articulate at base. Sepals 4–6, imbricate, slightly united at base; calyx often opening early in bud to reveal closely packed anther tips and slightly exserted style. Petals isomerous with and similar to sepals, alternating with them, free or joined at base only. Disk extrastaminal, composed of a single row of 8–10, orange, short, thick glands, or rarely disk absent. Stamens many, exserted; filaments free, filiform, inserted on receptacle; anthers small, versatile, longitudinally dehiscent, connective sometimes produced beyond thecae into a triangular or oblong (in dried material), glabrous or hairy appendage. Ovary superior, sessile, 1-loculed, with 2–4 placentas, each with few ovules; style 1, entire; stigma capitate, entire, or very shortly 2–4-lobed. Berry fleshy, drying blackish, with persistent perianth and stamens at base, and long slender persistent style conspicuous at apex. Seeds (1 or)2 or 3(–20).

About 40 species: tropical and subtropical regions of the E hemisphere; four species in China.

In Chinese species: leaf not conspicuously 3-veined from base, basal 1 or 2 pairs of lateral veins high ascending but weaker than midvein, both surfaces of leaf blade glabrous; stamens glabrous, anther connectives produced beyond thecae; disk glands present; receptacle hairy; ovary, style, and fruit glabrous; seeds 1–6.

Herbarium material of Scolopia can be difficult to identify to species; a study of fresh flowers and fruit might provide characters to improve the following key.

1a. Leaves with a pair of glands at junction of leaf base and petiole apex, these much larger than any elsewhere along leaf margin ..................................................................................................................................................................... 1. S. chinensis 1b. Leaves without a pair of glands at junction of leaf base and petiole apex, although sometimes with small glands on leaf margin some distance from petiole apex, these a similar size or only slightly larger than elsewhere along

leaf margin.

2a. Leaf blade 1.5–4 cm, abaxially vein reticulation often sparse or obscure (even at × 10 mag.), apex acute to rounded, never acuminate nor apiculate; petiole usually puberulous (view at × 20 mag.) .................................... 3. S. buxifolia 2b. Leaf blade 3–9 cm, both surfaces with vein reticulation clear, not sparse, apex various; petiole glabrous (view at × 20 mag.).

3a. Leaf apex acuminate, acumen 0.5–2 cm; mature berry reddish; plants of Fujian, Guangdong, Guangxi, Hainan, Yunnan [and Vietnam] ............................................................................................................................. 2. S. saeva 3b. Leaf apex acute to rounded, sometimes slightly acuminate, acumen ca. 0.5 cm or less; mature berry green or greenish black; plants of Fujian and Taiwan ................................................................................................ 4. S. oldhamii

1. Scolopia chinensis (Loureiro) Clos, Ann. Sci. Nat., Bot., sér. 4, 8: 249. 1857.

箣柊 ce zhong

Phoberos chinensis Loureiro, Fl. Cochinch. 1: 318. 1790; P. cochinchinensis Loureiro; Scolopia siamensis Warburg.

Shrubs or small trees, evergreen, 2–6 m tall; bark grayish; twig tips puberulous (viewed at × 20 mag.), branchlets gla-brous, branches and branchlets often spiny; spines simple, 1–5 cm. Petiole short, 3–5 mm, puberulous; leaf blade elliptic to oblong-elliptic, 4–7 × 2–4 cm, leathery, both surfaces glabrous, lateral veins 4–6 pairs, slender, basal 1 or 2 pairs high ascend-ing, reticulate veins clear on both surfaces (at × 10 mag. or less), not sparse, base broadly acute to subrounded, margin en-tire to serrulate, with a pair of glands at junction of blade and petiole, glands much larger than those elsewhere on margin, apex broadly acute to rounded, tip apiculate or with a very short blunt acumen 1–2 mm. Racemes axillary or terminal, 2–6 cm, puberulous. Pedicels 4–10 mm, puberulous. Flowers yellowish, ca. 4 mm in diam. Sepals 4 or 5(–7), ovate-triangular, 1–1.5 mm, abaxially pubescent, margin ciliate. Petals obovate-oblong, 1.5–2 mm, to 1.5 × as long as sepals, outside sparsely pubescent to subglabrous, margin ciliate. Disk glands 10, fleshy. Stamens ca. 5 mm; anthers globose, connective with conspicuous ap-pendage at apex, appendage ca. as long as connective, usually with 1 to few hairs at tip. Ovary ovoid; placentas 2 or 3, each with 2 pendulous ovules; style ca. 2 mm in young flowers, soon to 5 mm; stigma minutely lobed. Berry brownish red, dark purple, or black, orbicular-globose, (5–)8–10 mm in diam. Seeds (2–)4–6. Fl. Jun–Sep, fr. Oct–Apr of following year.

Sparse forests and thickets in hilly regions at low elevations, among rocks near coast; 50–400 m. Fujian, Guangdong, Guangxi, Hainan [Laos, Thailand, Vietnam; cultivated and/or naturalized in India, Malaysia, Sri Lanka].

Scolopia crenata (Wight) Clos was treated as a synonym of S. chinensis in FRPS (52(1): 16. 1999). However, S. crenata is, in fact, a different species that is distributed in India and the Andaman Islands.

2. Scolopia saeva (Hance) Hance, Ann. Sci. Nat., Bot., sér. 4, 18: 217. 1862.

广东箣柊 guang dong ce zhong

Phoberos saevus Hance, Ann. Sci. Nat., Bot., sér. 4, 3: 825. 1852; Scolopia cinnamomifolia Gagnepain; S. henryi Sleumer.

Shrubs or small trees, evergreen, 4–8(–10) m tall; bark grayish, not flaking; trunk spiny; spines simple or compound, to 11 cm; twig tips puberulous (view at × 20 mag.), early glabrescent, branchlets glabrous. Petiole 5–10 mm, glabrous; leaf blade ovate, elliptic, or elliptic-lanceolate, 5–8 × 2–5 cm, leathery, adaxially shiny, both surfaces glabrous, lateral veins 3–5 pairs, slender, basal 2 pairs high ascending, reticulate veins clear on both surfaces (at × 10 mag.), not sparse, base mostly acute, cuneate or sides concave, sometimes attenuate, margin subentire to remotely and shallowly repand-serrate, glands at

FLACOURTIACEAE 118

junction of blade and petiole absent, apex acuminate, acumen 0.5–2 cm. Racemes axillary or terminal, 2–5 cm, usually ca. 1/2 × to as long as leaves, puberulous. Pedicels 5–10 mm, puberu-lous though appearing glabrous (view at × 20 mag., even then hairs sometimes scarcely visible). Flowers whitish green. Se-pals 4 or 5, ovate, 1.2–1.5 mm, outside glabrous or sparsely hairy toward base, margin ciliate. Petals obovate-oblong, 1.5–2 mm, outside glabrous, margin ciliate. Disk glands 4 or 5(–?10). Stamens ca. 6 mm; anthers ovoid, connective with appendage at apex, glabrous or glabrescent. Ovary ovoid; placentas 2 or 3, each with 1 or 2 ovules; style 3–5 mm, stigma minutely lobed. Berry reddish, obovoid-orbicular, 6–8 mm. Seeds 1 or 2, ovoid-oblong, angled. Fl. May–Oct, fr. Aug–Apr of following year.

Dry plains, mixed forests in mountains; 400–1500 m. Fujian, Guangdong, Guangxi, Hainan, Yunnan [Vietnam].

3. Scolopia buxif olia Gagnepain, Bull. Soc. Bot. France 55: 52

4. 1908.

黄杨叶箣柊 huang yang ye ce zhong

Scolopia hainanensis Sleumer; S. nana Gagnepain.

Shrubs or small trees, evergreen, 2–8 m tall; twig tips pu-berulous (view at × 20 mag.); branchlets short, glabrous, spiny. Petiole short, ca. 3 mm, puberulous (view at × 20 mag.); leaf blade elliptic to obovate, 1.5–4 × 0.7–2 cm, leathery, both sur-faces glabrous, adaxially shiny, lateral veins 2–5 pairs, slightly raised on both surfaces, basal pair high ascending, reticulate veins sparse and/or obscure on both surfaces, especially abaxi-ally (at × 10 mag.), base acute-cuneate or more rarely rounded, extreme base usually slightly rounded, margin entire or incon-spicuously remotely serrulate, often slightly revolute, glands at junction of blade and petiole absent, apex broadly acute to rouned, never acuminate nor apiculate. Racemes usually axil-lary in upper part of branchlets, few flowered, to 3 cm, some-times extremely short, puberulous (view at × 20 mag.). Pedicels 5–11 mm, pubescent or glabrous. Flowers white. Sepals 4, rare-ly 5, ovate, 1–1.5 mm, outside glabrous, margin ciliate. Petals 1.5–2 mm, ovate-oblong, obovate-oblong, or nearly orbicular, outside glabrous, margin ciliate. Disk glands 8. Stamens 3–5 mm, glabrous or minutely and sparsely hairy; anthers small, connective with glabrous or glabrescent appendage. Ovary ovoid; placentas 3, each with 1 or 2(–?4) ovules; style 3–5 mm, stigma triangular-ovoid. Berry red at maturity, globose, 5–10 mm in diam. Seeds 3–6. Fl. Jun–Sep, fr. Jun–Oct.

Sandy places along seashores, dry sandy gentle slopes, thickets; low elevations. Guangxi, Hainan [Thailand, Vietnam].

4. Scolopia oldhamii Hance, Ann. Sci. Nat., Bot., sér. 5, 5: 206. 1866.

台湾箣柊 tai wan ce zhong

Shrubs or small trees, evergreen, 3–6 m tall; bark gray-brown,smooth,not flaking,spotted; twig tips and young branch-lets puberulous, older branchlets glabrous, branches spiny when young, unarmed when old. Petiole short, 2–6 mm, glabrous; leaf blade ovate, narrowly elliptic, ovate-lanceolate, or broadly obovate, 3–9 × 1.5–4 cm, subleathery to leathery, both surfaces glabrous, midvein raised abaxially, impressed adaxially, lateral veins 4–6 pairs, basal 1 or 2 pairs high ascending, reticulate veins raised on both sides, clear, not sparse, base usually acute-cuneate or with sides slightly concave, less often obtuse-cune-ate, margin entire or shallowly and remotely serrulate, glands at junction of blade and petiole absent, apex broadly acute to rounded, sometimes shortly acuminate, acumen ca. 5 mm or less, extreme tip blunt. Racemes axillary or terminal, few flow-ered, to 4 cm, sometimes very short, minutely puberulous (view at × 20 mag.). Pedicels 3–4 mm, to 1 cm in fruit, minutely puberulous or glabrous. Flowers yellowish to white, 6–8 mm in diam. Sepals 5–6, ovate or oblong, 1.5–2 mm, outside glabrous, margin ciliate.Petals obovate, 2.5–3 mm,outside glabrous, mar-gin ciliate. Disk glands 10–15. Stamens 4–5 mm, anther con-nective appendage glabrous or glabrescent. Ovary globose; style 3–5 mm; stigma minutely lobed. Berry green to blackish green when mature, globose, 7–9 mm in diam. Seeds 4 or 5. Fl. Aug–Sep, fr. Nov–May of following year.

Mountains, plains, sunny roadsides, roadside thickets, jungle mar-gins, seashores; below 400 m. Fujian, Taiwan [Japan (Ryukyu Islands)].

4. FLACOURTIA Commerson ex L’Héritier, Stirp. Nov. 3: 59. 1786.

刺篱木属 ci li mu shu

Stigmarota Loureiro.

Trees or shrubs, dioecious or hermaphroditic, rarely polygamous, usually spiny. Leaves alternate, petiolate; stipules small, early caducous; leaf blade pinnate-veined, sometimes 3–5-veined from base, margin glandular-toothed, rarely entire. Inflorescences axil-lary, or terminal on abbreviated lateral twigs, usually short, lax, racemose, or in form of small paniculate or umbel-like clusters. Flowers hypogynous, unisexual or bisexual, small; pedicels articulate. Sepals 4–7, imbricate, slightly connate at base, green, small. Petals absent. Disk fleshy, entire or comprised of distinct glands. Staminate flowers: stamens many, exserted, filaments free, filiform; anthers ellipsoid, small, versatile, longitudinally dehiscent, connective not projected beyond thecae; disk extrastaminal; abortive ovary much reduced or absent. Pistillate flowers: disk surrounding base of ovary; ovary superior, globose, ovoid, or bottle-shaped, incompletely 2–8-loculed by false septa; placentas 2-ovuled; styles isomerous with placentas, free or united, columnar; stigmas slightly dilated, flattened, reniform, recurved; staminodes usually absent. Fruit a berrylike indehiscent drupe with pyrenes 2 × as many as styles, globose, in dried material characteristically longitudinally angled, squarish or rectangular in longitudinal cross-section, with flattish apex and base, contracted or not at equator, disk persistent at base, style or stigma remnants persistent at apex. Seeds ellipsoid, compressed.

FLACOURTIACEAE 119

Between 15 and 17 species: tropical Africa and Asia; five species (one endemic) in China.

In Chinese species: plants usually dioecious; stamens (10–)15–30(–50), number apparently variable within each species.

Flacourtia species are often cultivated and harvested for fruit, medicinal use, or wood.

Male flowers of Flacourtia are easily confused with those of Xylosma; female flowers of the two genera are easily distinguished by style and stigma morphology, young fruits by style morphology and internal structure.

Key to material with female flowers or fruit

1a. Abaxial surface of leaf softly and densely pubescent throughout ..................................................................................... 5. F. mollis 1b. Abaxial surface of leaf glabrous or sparsely hairy.

2a. Styles completely united to form a distinct column with stigmas slightly spreading at apex .............................. 1. F. jangomas 2b. Styles free, or joined only at base.

3a. Styles free, arranged in a ring, becoming well-spaced as fruit develops; leaves ovate-oblong, elliptic-oblong, or oblong-lanceolate, 6–16 × 4–7 cm .................................................................................................................. 2. F. rukam 3b. Styles joined at base, remaining so in fruit; leaves obovate, oblong-obovate, elliptic, or elliptic-lanceolate, 2–10 × 1.5–6 cm.

4a. Leaves 2–4 × 1.5–3 cm, obovate or oblong-obovate; fruit 8–10 mm in diam. ............................................. 3. F. indica 4b. Leaves 4–10 × 2.5–6 cm, elliptic to elliptic-lanceolate; fruit 15–25 mm in diam. ................................ 4. F. ramontchi Identification of material with male flowers

Flacourtia mollis can be recognized by its leaf indumentum, and F. indica (as defined here) by its leaf size and shape. The remaining three species are much more difficult, at least from herbarium material, as staminate flowers seem to offer no useful characters; leaves on flowering specimens are often young, and therefore, generally small, and in all three species the leaf shape and size is variable, with character states overlapping between the species. Flacourtia jangomas usually has ovate to ovate-elliptic or more rarely ovate-lanceolate leaves, and F. ramontchi elliptic leaves, but all of these shapes seem to occur also in F. rukam. Most flora keys rely heavily on style characters to distinguish species. Staminate herbarium material might easily be misidentified. A molecular study based on fertile material could help resolve this problem.

1. Flacourtia jangomas (Loureiro) Raeuschel, Nomencl. Bot., ed. 3, 290. 1797.

云南刺篱木 yun nan ci li mu

Stig marota jang omas Loureiro, Fl. Cochinch. 2: 634. 1790; Flacourtia cataphracta Roxburgh ex Willdenow.

Large shrubs or small trees, 5–10 m tall, deciduous; trunk and older branches usually unarmed, young branches with sim-ple or divaricate spines; bark yellow-brown, reddish brown, or light brown, flaky; young branches smooth, glabrous or sparse-ly pubescent, lenticellate. Petiole 4–8 mm, pubescent or gla-brescent; leaf blade dark green abaxially, shiny adaxially, in fresh state pinkish to reddish or orange-brown when young, narrowly ovate, ovate-elliptic, or ovate-oblong, rarely oblong-lanceolate or (slightly) obovate-lanceolate, 7–14 × 2–5 cm, thinly leathery to papery, both surfaces practically glabrous, any hairs present very short, midvein slightly raised on both sur-faces, lateral veins 3–6 pairs, conspicuous adaxially, base acute, obtuse, or rounded, margin entire or serrate to crenate, apex ob-tuse or gradually tapering to narrowly acuminate, rarely more abruptly acuminate. Inflorescences axillary, racemose; rachis 0.5–2 cm, puberulous. Pedicels 5–10(–15) mm, very slender, minutely and sparsely puberulous or glabrous; bracts ovate, 0.5–1 mm, outside glabrous or sparsely hairy, inside pubescent, margin entire, ciliate. Flowers appearing with or before young leaves, white to greenish, honey-scented. Sepals 4 or 5, ca. 2 mm, ovate-triangular, apex obtuse, outside practically glabrous, inside pubescent, margin ciliate, hairs very short, often barely visible in female flowers.Staminate flowers:stamen filaments 2–3 mm, glabrous. Pistillate flowers: ovary bottle-shaped to globose, 2–3 mm; styles 4–6, united into a distinct column ca. 1 mm, not or slightly free at their apices; stigmas slightly reni-form, dilated, recurved. Fruit brownish red or purple, finally blackish, subglobose, fleshy, 1.5–2.5 cm in diam., in dried material sometimes constricted at equator, style column per-sistent. Seeds 4 or 5(–10). Fl. Apr–May, fr. May–Oct.

● Mountain rain forests, evergreen broad-leaved forests; 700–800 m. W Guangxi, S Hainan, S Yunnan.

According to Sleumer (Fl. Males., ser. 1, 5(1): 73. 1954), Flacour-tia jangomas is not known in the wild state. The species is cultivated around villages, and naturalized from them, throughout tropical regions, especially in E Africa and tropical Asia.

Morse 498 (K), from Guangxi, determined as “cf. Flacourtia jangomas” by Sleumer (determination slip dated 1954 on herbarium sheet), has pubescent stamen filaments. The leaves are small, ovate to narrowly elliptic, and possibly young. The specimen might represent immature F. ramontchi.

2. Flacourtia rukam Zollinger & Moritzi, Syst. Verz. 2: 3

3. 1846.

大叶刺篱木 da ye ci li mu

Trees, 5–15 m tall; bark gray-brown, not flaky; when young with simple or branched thorns to 10 cm on trunk and branches (thornless in cultivated forms); branchlets terete, gla-brous to densely pubescent when young. Petiole 4–8 mm, gla-brous or pubescent,hairs spreading;young leaves flaccid, droop-ing, rose-red to brown; mature leaves ovate-oblong, elliptic-oblong, or oblong-lanceolate, 6–16 × 4–7 cm, subleathery, both surfaces glabrous or minutely puberulous, in older leaves hairs mostly confined to midveins and lateral veins, midvein raised

FLACOURTIACEAE 120

and sometimes prominent abaxially, impressed adaxially, lat-eral veins 5–11 pairs, base obtuse to rounded, less often acute, margin serrulate, serrate, or dentate, teeth obtuse, apex gradu-ally to abruptly acuminate, acumen 0.5–2 cm, tip obtuse. In-florescences axillary, racemose, 0.5–1 cm, puberulous; bracts ovate, ca. 1 mm, pubescent. Pedicels 3–4 mm, puberulous to pubescent, hairs ± appressed, short. Flowers yellowish green, scentless. Sepals (3 or)4 or 5(or 6), ovate, 1–1.5 mm, both sur-faces pubescent, outside sparsely pubescent, inside more dense-ly so, margin ciliate, apex acute or obtuse. Staminate flowers: stamen filaments 3–4 mm, glabrous; disk orange-red to yellow-ish. Pistillate flowers: ovary bottle-shaped; placentas 4–6(–8); styles 4–6(–8), free, divergent, 0.7–1.5 mm; stigmas recurved, slightly dilated, reniform; staminodes (reduced stamens) or developed stamens (?functional) occasionally present. Fruit light green, pink, purplish, or dark red, globose, 2–2.5 cm in diam., 4–7-angled in dried state, persistent styles well-spaced, set in a circle at fruit apex. Seeds ca. 12. Fl. Apr–May, fr. Jun–Oct.

Evergreen broad-leaved forests; below 2000 m. Guangdong, Guangxi, Hainan, Taiwan, Yunnan [India, Indonesia, Malaysia, Thai-land, Vietnam, both wild and cultivated].

3. Flacourtia indica (N. L. Burman) Merrill, I nterpr. Herb. Amboin. 377. 1917.

刺篱木 ci li mu

Gmelina indica N. L. Burman, Fl. I ndica, 132. 1768; Flacourtia parvifolia Merrill.

Shrubs or small trees, 2–4 m tall, deciduous; bark gray-yellow, fissured, flaky; old branches usually not spiny; young branches with axillary, simple spines; branchlets puberulous or subglabrous. Petiole red, short, 3–5 mm, puberulous; leaf blade greenish abaxially, deep green adaxially, rose red when young, obovate to oblong-obovate, 2–4 × 1.5–3 cm, thickly papery, abaxially glabrous or sparsely pubescent, hairs spreading and short, adaxially glabrous, midvein raised abaxially, flat adaxi-ally, lateral veins 5–7 pairs, reticulate veins conspicuous, base mostly acute to obtuse, margin serrulate above middle, apex rounded, sometimes retuse. Inflorescences axillary or terminat-ing short lateral twigs, racemose, short; rachis 0.5–2 cm, puber-ulous. Pedicels 3–5 mm, puberulous, hairs spreading. Sepals 5 or 6, ovate, ca. 1.5 mm, outside glabrous or with a few scattered short hairs, inside sparsely to densely pubescent, margin white ciliate in dried material, apex obtuse. Staminate flowers: stamen filaments 2–2.5 mm, pubescent or less often glabrous. Pistillate flowers: ovary globose, placentas 5 or 6; styles 5 or 6, united only at base, radiating, 1–2 mm, slender. Fruit dull to blackish red, globose, 8–10 mm in diam., longitudinally 5- or 6-angled, styles persistent. Seeds 5 or 6. Fl. Jan–Mar, fr. Mar–Jul.

Broad-leaved forests; sea level to 1400 m. Fujian, Guangdong, Guangxi, Hainan [widespread and cultivated in tropical and subtropical regions of Africa, Asia, and the Pacific islands].

The taxonomy of Flacourtia indica is complex. Some authors have treated the species in a broad sense, and include in synonymy not only F. ramontchi (see below) but also several other entities found across tropical Asia and Africa. For an introduction to the problem, see Matthew (Fl. Tamilnadu Carnatic 3(1): 59–61. 1983), Mitra (in Sharma et al., Fl. India 2: 402–403. 1993), Sleumer (Fl. Males., ser. 1, 5(1): 76–77. 1954), and V erdcourt (in Dassanayake & Clayton, Rev. Handb. Fl. Ceylon 10: 222–224. 1996). Some of the taxonomic confusion might be due to a loss of significant field characters during the preparation of herbarium material (V erdcourt, loc. cit.). In the present account, F. ram-ontchi is treated as a separate species because, on the evidence of her-barium material at PE, it seems to be a distinct and recognizable entity within China. Descriptions of F. ramontchi vary; for example, compare that below with Matthew (loc. cit.).

4. Flacourtia ramontchi L’Héritier, Stirp. Nov. 3: 59. 1786.

大果刺篱木 da guo ci li mu

Trees, to 20 m tall; bark gray-brown; flowering and fruiting branches usually not spiny; branchlets puberulous or subglabrous. Petiole 4–8 mm, usually glabrous, rarely sparsely puberulous; leaf blade greenish abaxially, deep green and shiny adaxially, broadly elliptic, elliptic, or elliptic-lanceolate, 4–10 × 2.5–6 cm, papery, both surfaces glabrous, midvein raised abax-ially, lateral veins 4–6 pairs, reticulate veins conspicuous, base cuneate, margin serrate, apex obtuse or acute, rarely retuse. In-florescences terminal or axillary, racemose, 1–2 cm, puberu-lous. Sepals 5 or 6, ovate, ca. 1.5 mm, outside glabrous, inside puberulous, margin ciliate, apex obtuse. Staminate flowers: disk entire or shallowly lobed. Pistillate flowers: disk entire; ovary globose; placentas 5 or 6, each with 2 ovules; styles 5 or 6, free; stigmas 2-lobed. Fruit globose, 1.5–2.5 cm in diam., not longi-tudinally angled, with persistent styles. Seeds 4–6. Fl. Apr–May, fr. Jun–Oct. 2n = 22.

Evergreen broad-leaved forests; 200–1700 m. Guangxi, Guizhou, Yunnan [India, Malaysia, Philippines, Sri Lanka, Vietnam; Africa].

See taxonomic note under Flacourtia indica.

5. Flacourtia mollis J. D. Hooker & Thomson, Fl. Brit. India 1: 192. 1872.

毛叶刺篱木 mao ye ci li mu

Small trees or shrubs, 3–4 m (?or more) tall, apparently unarmed; branchlets ± rusty pubescent, hairs spreading, rather long. Petiole 5–10 mm, stoutish, densely hairy, hairs spreading, brownish, straight, long (0.5–1 mm); leaf blade ovate to ovate-elliptic, 11–18 × 4.5–7.5 cm, thickly papery, abaxially softly pubescent throughout, soft to the touch, hairs spreading and long (0.5–1 mm), adaxially glabrous except near petiole apex, midvein impressed above, lateral veins 4–6 pairs, prominent abaxially, base broadly acute to rounded, margin shallowly serrate to serrulate, entire toward base, apex obtuse, contracting to a narrow acumen 1–2 cm, extreme tip obtuse. Inflorescences mostly axillary, racemose with axis ca. 1 cm, or reduced to glomerules or fascicles; rachises densely hairy, appearing nearly bristly at × 10 mag., hairs spreading, ca. 0.5 mm; bracts ovate to lanceolate, 1–2 mm, both surfaces sparsely bristly. Pedicels ca. 1 mm in pistillate flowers, ca. 3 mm in staminate flowers (few specimens seen), bristly. Sepals 4–6, ovate, 1–1.5 mm, unequal in size, both sides and margin sparsely bristly, or adaxially nearly glabrous, apex acute. Staminate flowers: sta-men filaments 3–4 mm, glabrous. Pistillate flowers: ovary bottle-shaped, 1.5–2 mm, glabrous; styles connate into a short column ca. 0.5 mm; stigmas 4–6, radiating, recurved, flattened-

FLACOURTIACEAE 121

reniform. Dried fruit oblong-polygonal to obovoid-polygonal, to ca. 1 cm (?immature), longitudinally angled.

Mountain forests; 1000–1700 m. Yunnan [Myanmar].

Flacourtia mollis is sometimes misidentified as the Indian en-demic F. montana J. Graham. The two species can be distinguished by the abaxial indumentum of the leaf: in F. mollis, it is softly hairy throughout; in F. montana, it is sparsely hairy only along the midvein and lateral veins. Gatherings of F. mollis seem scarce; more material is required to confirm and improve the above description.

5. XYLOSMA G. Forster, Fl. Ins. Austr. 72. 1786, nom. cons.

柞木属 zuo mu shu

Apactis Thunberg; Hisingera Hellenius; Myroxylon J. R. Forster & G. Forster (1775), not Linnaeus f. (1782), nom. cons.

Shrubs or small trees, usually dioecious, rarely polygamous; trunk and branches usually spiny. Leaves alternate, stipulate, usually petiolate; leaf blade pinnate-veined, margin serrate, rarely entire, teeth glandular. Flowers hypogynous, small, in axillary fascicles, short racemes, or panicles, rudiments of opposite sex usually absent; bracts small, persistent or caducous; pedicels articulate at base. Sepals 4 or 5, imbricate, free or connate at base only. Petals absent. Disk extrastaminal, or in female flowers extragynoecial, comprised of several small closely set or connate glands (usually in staminate flowers) or annular (often in pistillate flowers). Staminate flowers: stamens ca. 10 to many, exserted; filaments free, filiform; anthers small, basifixed, sometimes apiculate by extension of connective. Pistillate flowers: ovary superior, 1-loculed; placentas 2(–6), each with 2 to many ovules; styles 2 or 3(or 4), often very short, joined in lower part only or completely joined to form a single style column, or styles absent; stigmas semilunate to U-shaped. Berry small, ca. 1 cm or less, pericarp thinly leathery, blackish when dried; disk and calyx often persistent at base; styles and/or stigmas persistent at apex. Seeds few.

About 100 species: tropical and subtropical regions, rarely extending to warm-temperate regions; three species in China.

The gender of the name Xylosma is feminine; see Art. 62.2(b) of the Vienna Code.

In Chinese species: stamens 10–20, filaments glabrous; ovary glabrous; berry red or black when fresh. See notes on identification under Fla-courtia.

Differentiation between fruiting material of Xylosma controversa and X. longifolia can be difficult when the calyx is absent (caducous) and the critical sepal indumentum character therefore unavailable. Ranges of other character states (e.g., leaf size, shape, lateral vein number) overlap, and lateral veins are difficult to count in dried material, especially toward the leaf apex. Characters used previously, for example dried leaf color, leaf shininess, leaf base shape, and style length, are not reliable. For some fruiting material examined for the Flora (at K), identification of X. controversa has been based solely on the absence of the calyx. Further study is required to test the strength of this character and, ideally, provide additional ones.

1a. Leaves broadly ovate or ovate to elliptic-ovate, 4–8 × 2.5–4 cm; lateral veins 3 or 4(or 5) pairs; seed sheath with dark striations ................................................................................................................................................................ 1. X. congesta 1b. Leaves oblong, oblong-lanceolate, lanceolate, or elliptic, 5–10(–18) × 2–7 cm; lateral veins more than 5 pairs;

seed sheath without dark striations.

2a. Leaves elliptic to oblong, lateral veins 5 or 6(or 7) pairs; inflorescence lax, 1.5–3(–5) cm, paniculate or racemose-paniculate, often yellow puberulous; sepals pubescent inside, margin entire, ciliate; calyx

deciduous in fruit ................................................................................................................................................ 2. X. controversa 2b. Leaves elliptic to oblong-lanceolate, lateral veins (6 or)7–11 pairs; inflorescence usually dense, often very short, 0.5–2 cm, racemose or condensed paniculate (as clusters of short racemes from a single axil), usually

glabrous or puberulous; sepals glabrous inside, margin entire to erose, glabrous; calyx persistent in fruit ........ 3. X. longifolia

1. Xylosma congesta (Loureiro) Merrill, Philipp. J. Sci. 15: 247. 1920 [“congestum,” “1919”].

柞木 zuo mu

Croton cong estus Loureiro, Fl. Cochinch. 2: 582. 1790 [“congestum”]; Apactis japonica Thunberg; Casearia sub-rhombea Hance; Flacourtia chinensis Clos; F. japonica Wal-pers; Hising era japonica Siebold & Zuccarini, nom. illeg. superfl.; H. racemosa Siebold & Zuccarini; Myroxylon japonicum (Thunberg) Makino; M. racemosum (Siebold & Zuccarini) Kuntze; Xylosma apactis Koidzumi, nom. illeg. superfl.; X. congesta var. caudata S. S. Lai; X. congesta var. pubescens (Rehder & E. H. Wilson) Chun; X. japonica A. Gray, nom. illeg. superfl.; X. japonica var. pubescens (Rehder & E. H. Wilson) C. Y. Chang; X. racemosa (Siebold & Zuc-carini) Miquel; X. racemosa var. caudata (S. S. Lai) S. S. Lai; X. racemosa var. glaucescens Franchet; X. racemosa var. pu-bescens Rehder & E. H. Wilson; X. senticosa Hance.

Shrubs or small trees, evergreen, 4–15 m tall; bark brown-gray; branches spiny when young, unarmed when old, glabrous or puberulous. Stipules subulate, minute, ca. 0.3 mm, glabrous, in dried material dark brown or blackish, caducous or persistent for some time; petiole short, 2–5 mm, glabrous to quite densely pubescent with spreading hairs; leaf blade broadly ovate to ovate-elliptic, 3–8 × 2.5–3.5 cm, leathery, often glaucous be-low, both surfaces glabrous, or scarcely pubescent along veins below, lateral veins 3 or 4(or 5) pairs, base usually obtuse to rounded, less often acute, margin serrate, apex acute, tip usually acuminate, acumen 5–10 mm. Inflorescence axillary, racemose,

FLACOURTIACEAE 122

short, 0.5–2 cm; rachis densely pubescent, hairs spreading, short; flowers yellowish. Pedicels very short, 1–3 mm in flower and fruit, pubescent. Bracts ovate to narrowly lanceolate, 1–2.5 mm, abaxially pubescent, ciliate, caducous or persistent. Sepals 4–6, broadly ovate with rounded apex, or orbicular, 1–2 mm, outside ± pubescent, inside glabrous, ciliate. Staminate flow-ers: stamen filaments long, eventually extending to ca. 3 mm; anthers ellipsoid, minute, ca. 0.2 mm, connective usually not projected beyond thecae; disk consisting of several, small, glabrous, closely set or connate glands. Pistillate flowers: disk annular, undulate; ovary ovoid, ca. 4.5 mm; placentas 2; styles 2, very short (to 0.5 mm) to nearly absent, joined in basal half. Berry dark red to black (black when dried), globose, 4–5 mm in diam.; calyx and disk persistent at least while fruit attached to plant; styles persistent. Seeds 2 or 3, reddish brown when dry, ovoid, flattened on one side by mutual pressure, 4–5 mm, completely covered in a thin membranous darkly streaked sheath. Fl. Jul–Nov, fr. Aug–Dec.

Forest margins, thickets on hills, plains, surrounding villages; 500–1100 m. Anhui, Fujian, Guangdong, Guangxi, Guizhou, Hubei, Hunan, Jiangsu, Jiangxi, Shaanxi, Sichuan, Taiwan, Xizang, Yunnan, Zhejiang [India (rare), Japan, Korea].

The varieties Xylosma racemosa var. glaucescens and X. race-mosa var. pubescens are not upheld here. The characters used to dis-tinguish them, glaucescence of the leaves, or hairiness of branchlets and petioles and venation of the abaxial leaf surface, were found to vary continuously throughout the species.

For Xylosma senticosa only three specimens (including the type) were available. Of these, Hance 7437 (type; K) and a specimen num-bered “9204” (collector illegible; K) were collected from Victoria Peak, Hong Kong. The third specimen, Ford 579 (K), possibly a cultivated specimen, is also annotated “Victoria Peak.” Between them, the speci-mens bear staminate or structurally bisexual flowers. All are similar to X. congesta but differ in the following combination of characteristics: leaves very small (1.5–3 cm), flowers sometimes structurally bisexual, sepals glabrous outside (margin ciliate), pedicel above the articulation glabrous, lower part of pedicel and inflorescence rachis glabrous or sparsely hairy, anther with connective projected as a fleshy, triangular appendage. After one of us (Yang) examined extensive gatherings of Xylosma from Hong Kong at PE, the inclusion of X. senticosa Hance within X. congesta was recommended.

2. Xylosma controversa Clos, Ann. Sci. Nat., Bot., sér. 4, 8: 231. 1857.

南岭柞木 nan ling zuo mu

Shrubs or small trees, evergreen, 4–10 m tall; young stems often spiny, bark gray-brown; branchlets terete, glabrous or puberulous. Stipules subulate or triangular, minute, ca. 0.2 mm, glabrous, in dried material dark brown or blackish, caducous or persistent for some time; petiole 5–10 mm, glabrous or pubes-cent; leaf blade elliptic to oblong-elliptic, 5–10(–18) × 3–7 cm, thickly papery to leathery, both surfaces glabrous, or abaxially spreading pubescent, midvein raised abaxially, impressed or flat adaxially, lateral veins 5 or 6(or 7) pairs, arched-ascending, especially basal pairs, conspicuous on both sides, base acute to slightly attenuate, margin serrate, apex acute or acuminate, acu-men 5–10 mm. I nflorescence axillary, paniculate, often with very short branches and then racemelike, lax; rachis 1.5–5 cm, puberulous to pubescent with spreading yellowish hairs, some-times glabrescent. Pedicels 2–3 mm, puberulous to pubescent; bracts ovate to lanceolate, 1–3 mm, both surfaces pubescent, persistent or caducous. Flowers numerous, greenish white, 3–4 mm in diam. Sepals 4, ovate-orbicular,(1–)2–2.5(–3) mm, often unequal in size, outside pubescent with short semispreading hairs, or nearly glabrous, inside densely hairy, hairs semi-spreading, white, long; sepal margin ciliate. Staminate flowers: stamens with filaments ca. 2 mm, anthers ellipsoid, ca. 0.5 mm; disk glands small, close set. Pistillate flowers: ovary ovoid-glo-bose, ca. 2 mm; disk annular or few lobed; placentas 2, each with 2 or 3 ovules; styles 2(or ?3), usually completely joined to form a single style column (0.5–)1(–1.5) mm. Fruit reported as red, drying black, globose, 3–5 mm in diam. Seeds 2–8, mid to darker brown when dried, ovoid, flattened at least on one side by mutual compression, 4–5 mm, completely enclosed in a thin sheath, sheath without dark streaks. Fl. Apr–May, fr. Aug–Sep.

Evergreen broad-leaved forests, forest margins; low elevations. Fujian, Guangdong, Guangxi, Guizhou, Hainan, Hunan, Jiangsu, Jiang-xi, Sichuan, Yunnan [India, Malaysia, Nepal, Vietnam].

1a. Leaf blades abaxially and branchlets

glabrous .............................................. 2a. var. controversa 1b. Leaf blades abaxially along veins and

branchlets puberulous ............................ 2b. var. pubescens 2a. Xylosma controversa var. controversa

南岭柞木(原变种) nan ling zuo mu (yuan bian zhong) Leaf blades abaxially and branchlets glabrous.

Evergreen broad-leaved forests, forest margins; low elevations. Fujian, Guangdong, Guangxi, Guizhou, Hainan, Hunan, Jiangsu, Jiang-xi, Sichuan, Yunnan [India, Malaysia, Nepal, Vietnam].

“Xylosma controversum var. glabrum” [sic] (S. S. Lai, Bull. Bot. Res., Harbin 14: 224. 1994) belongs here but was not validly published under Art. 37.2 of the Vienna Code because two gatherings were indicated as types: Q. H. Lu 324 (IBG) and L. Deng [L. Teng] 1492 (IBSC), the type status of the former being indicated by the text “Typus: in (IBG) et (INSC)” [sic].

2b. Xylosma controversa var. pubescens Q. E. Yang, var. nov.

毛叶南岭柞木 mao ye nan ling zuo mu

Type: China. Guangdong: Yangshan Xian, in rocky, shady places under dense forests, alt. 500 m, L. Teng 1675 (holotype, PE).

A var. controversa ramulis et foliis subtus ad venas puber-ulis differt.

Abaxial surfaces of leaf blades along veins and branchlets puberulous.

● Evergreen broad-leaved forests, forest margins; low elevations. Guangdong, Guangxi, Guizhou, Hunan, Jiangxi, Sichuan.

3. Xylosma longifolia Clos, Ann. Sci. Nat., Bot., sér. 4, 8: 231. 1857.

长叶柞木 chang ye zuo mu

Xylosma congesta (Loureiro) Merrill var. kwangtungensis

FLACOURTIACEAE 123

F. P. Metcalf; X. racemosa (Siebold & Zuccarini) Miquel var. kwangtungensis (F. P. Metcalf) Rehder.

Shrubs or small trees, evergreen, 4–7 m tall; bark gray-brown; branchlets spiny, glabrous. Stipules not seen; petiole 5–8 mm, glabrous; leaf blade narrowly elliptic, oblong-elliptic, oblong-lanceolate, or narrowly obovate, 4–15(–20) × (2–)2.5–5(–7 cm), leathery, both surfaces glabrous, lateral veins (6 or)7–11 pairs, raised on both surfaces, base acute, cuneate, very rarely obtuse, margin serrate, apex acuminate, acumen 1–2 cm. Inflorescence of short racemes or reduced panicles borne singly or in condensed clusters in leaf axils; rachis 0.5–2 cm, glabrous or puberulous; bracts ovate (staminate flowers) to lanceolate (pistillate flowers), small, 0.5–1 mm, glabrous or sparsely pu-berulous. Flowers greenish, 2.5–3.5 mm in diam. Pedicels 1–2 mm, slender, puberulous. Sepals 4 or 5, persistent, ovate or lanceolate, 1–2 mm, abaxially glabrous or sparsely puberulous with spreading hairs, adaxially glabrous, margin entire to erose (× 10 mag.), glabrous. Staminate flowers: stamen filaments eventually ca. 3 mm; anthers ellipsoid, minute, ca. 0.3 mm; disk glands small, ± connate. Pistillate flowers: disk annular or few lobed, ovary ovoid, ca. 2 mm; placentas 2 or 3, each with 2 or 3 ovules; styles 2 or 3, very short, 0.5–0.8 mm or less, partly or completely joined. Berry reported as red when ripe, drying black, globose, 4–6 mm in diam.; calyx, disk, and style per-sistent. Seeds 4 or 5, brown when dried, ca. 4 mm, ovoid, flat-tened on one or more sides by mutual compression, complete-ly enclosed in a thin sheath, sheath without dark streaks. Fl. Apr–May, fr. Jun–Oct.

Mountain forests; 1000–1600 m. Fujian, Guangdong, Guangxi, Guizhou, Hainan, Yunnan [India, Laos, Nepal, Thailand, Vietnam].

“Xylosma fascicuflorum” [sic] (S. S. Lai, Bull. Bot. Res., Harbin 14: 224. 1994) belongs here but was not validly published under Art.

37.2 of the Vienna Code because two gatherings were indicated as types

(B. Y. Qiu 50405 and M. G. Li [M. K. Li] 697).

6. BENNETTIODENDRON Merrill, J. Arnold Arbor. 8: 10. 192

7.

山桂花属 shan gui hua shu

Bennettia Miquel, Fl. Ned. Ind. 1(2): 105. 1858, not Gray (1821), nor R. Brown (1852), nor Bennetia Rafinesque (1830).

Shrubs or small trees, reportedly dioecious, young shoots with a perular bud, perular bracts persistent. Leaves alternate, upper-most often clustered at apices of branches; estipulate; petiole mostly elongate, shorter in upper leaves, with a pair of glands at apex only or glands completely absent; leaf blade pinnate-veined, sometimes 3–5-veined from base with lateral veins much weaker than midvein, margin ± coarsely glandular-serrate. Flowers hypogynous, small, unisexual, rarely at least structurally bisexual, in axillary or terminal, paniculate, rarely corymblike or racemelike inflorescences; bracts and bracteoles small, caducous; pedicels articulate. Sepals 3(–5), imbricate, free or joined at base only, small, ciliate, caducous, rarely persistent. Petals absent. Disk glands present, small, dispersed among stamen or staminode bases. Staminate flowers: stamens many; filaments free, filiform, pubescent with long hairs in lower half, rarely glabrous; anthers elliptic, small, dorsifixed, versatile; disk glands many, set between the stamen filament bases, small, short, fleshy, glabrous; abortive ovary small, with 3 short styles. Pistillate flowers: staminodes many, like the stamens but smaller and sterile, filaments less than 1/2 as long as those of staminate flowers, pubescent at base; disk glands many, small, trun-cate, set between staminode bases; ovary superior, incompletely 3-loculed; placentas 3, each with 2 or 3 ovules; styles 2–4, not or scarcely joined at base, divergent, slender, each dilated at apex into a flattened irregularly branched or lobed stigma, caducous. Berry globose, small, rather dry; style caducous or basal part persistent; pericarp thin, brittle when dried. Seeds 1(–4), yellowish when fresh, blackish when dry, shiny; testa slightly reticulate.

Two or three species: Asia; one species in China.

Fan (J. S. W. Forest. Coll. 15(3): 27. 1995) recorded Bennettiodendron cordatum Merrill from S Guangxi. The only specimen cited by him, X. R. Liang 69814, has leaves not obviously cordate at base, and can be safely referred to B. leprosipes. In B. cordatum, a species occurring in Vietnam, the leaves are obviously cordate at base.

1. Bennettiodendron leprosipes (Clos) Merrill, J. Arnold Arbor. 8: 11. 1927.

山桂花 shan gui hua

Xylosma leprosipes Clos, Ann. Sci. Nat., Bot., sér. 4, 8: 230. 1857; Bennettia leprosipes (Clos) Koorders; B. long ipes Oliver; Bennettiodendron brevipes Merrill; B. brevipes var. margopatens S. S. Lai [“margopatense”]; B. brevipes var. shangsiense (X. X. Chen & J. Y. Luo) S. S. Lai; B. lanceolatum H. L. Li; B. leprosipes var. ellipticum S. S. Lai; B. leprosipes var. pilosum G. S. Fan & Y. C. Hsu; B. leprosipes var. rugo-sifolium S. S. Lai; B. long ipes (Oliver) Merrill; B. macro-phyllum C. Y. Wu ex S. S. Lai; B. macrophyllum var. pilosum (G. S. Fan & Y. C. Hsu) S. S. Lai; B. shangsiense X. X. Chen & J. Y. Luo; B. simaoense G. S. Fan; B. subracemosum C. Y. Wu; Myroxylon leprosipes (Clos) Kuntze.

Shrubs or small trees, evergreen, 2–6(–15) m tall; bark gray-brown, fetid, not flaking; branchlets terete, densely gray-brown puberulous, later glabrescent or subglabrous. Petiole 0.3–6 cm, rarely to 10 cm, brown puberulous, grad-ually glabrescent, with or without 2 glands at apex; leaf blade mostly narrowly to broadly elliptic, elliptic-oblong, or obo-vate, usually (5–)10–23 × 4–7.5 cm, papery or thinly papery, both surfaces glabrous, or puberulous along veins abaxially, hairs spreading and very short, midvein raised on both sides, lateral veins 7–9 pairs including 1 or 2 pairs from base, base usually acute-cuneate, less often obtuse-cuneate, rarely round-ed, margin sparsely obtusely serrate, apex obtuse, contracting quite abruptly to an acumen to 2 cm. Inflorescence terminal, paniculate, 6–12(–20) × ca. 4.5 cm, many flowered (at least 20–30, usually more), initially densely brown puberulous, glabrescent, with age at least pistillate inflorescence rachises

FLACOURTIACEAE 124

becoming pale brown or grayish and conspicuously densely pustular-lenticellate; bracts and bracteoles narrowly triangu-lar, ca. 1 mm, pubescent. Flowers unisexual or apparently struc-turally bisexual, sordid-white or greenish yellow, scented. Pedi-cels 3–5 mm, to 1 cm in fruit. Staminate flowers: sepals broadly elliptic-ovate, 3–3.5 mm, texture thin, both surfaces sparsely pubescent to nearly glabrous, margin ciliate; stamens slightly exserted, light yellow, drying brown, filaments 3–4 mm, pubes-cent, hairs spreading, white when dried, long; anthers oblong; disk glands purplish when fresh. Pistillate flowers: sepals as in staminate flowers but ca. 1/2 as long; staminodes many, simi-lar to stamens but usually only 1/2 as long; disk glands small, truncate,among staminode bases; ovary yellowish green to orange in fresh state, ovoid, somewhat collapsed and coarsely wrinkled in dried material, ca. 4 mm, placentas 2–4-ovuled; styles 3 or 4, sordid-white when fresh, filiform, ca. 1 mm, gla-brous; stigmas ca. 0.3 mm. Berry red when mature, drying black, globose, 6–9 mm in diam., pericarp thin, brittle when dry. Seeds 1 or 2, globose, (semiglobose when 2 present), 3–4 mm in diam. Fl. Mar–Apr, fr. May–Nov.

Evergreen broad-leaved forests; 400–1800 m. Guangdong, Guangxi, Guizhou, Hainan, Hunan, J iangxi, Yunnan [Bangladesh, In-dia, Indonesia (Java, Sumatra), Myanmar, Thailand].

Bennettiodendron leprosipes is a highly polymorphic species in leaf shape, petiole length, inflorescence length, and fruit size.

“Bennettiodendron macrophyllum var. obovatum” (S. S. Lai, Bull. Bot. Res., Harbin 14: 227. 1994) belongs here but was not validly published under Art. 37.2 of the Vienna Code because two gatherings were indicated as types (Longgang Expedition 10755 and J. Y. Luo & Q. R. Lai 8014).

7. IDESIA Maximowicz, Bull. Acad. Imp. Sci. Saint-Pétersbourg 10: 485. 1866, nom. cons., not

Scopoli (1777).

山桐子属 shan tong zi shu

Cathayeia Ohwi; Polycarpa Linden ex Carrière (1868), not Linnaeus (1759), nor Polycarpaea Lamarck (1792).

Trees, deciduous, dioecious.Leaves alternate; stipules small, caducous; petiole elongate,with two sessile discoid or shortly cylindric glands at apex, sometimes with additional glands along petiole length; leaf blade palmately 3–5-veined from base, glandular-toothed. Flowers hypogynous, unisexual, many, in terminal and axillary pendulous panicles, these sometimes racemelike; bracts caducous; pedicels articulate. Sepals (3–)5(or 6), imbricate, free or joined only at base, caducous. Petals absent. Disk glands present. Staminate flowers: stamens many, inserted on disk, ca. as long as sepals; filaments free, slender, softly hairy; anthers elliptic, longitudinally dehiscent, basifixed; disk lobes many, small, set among stamen bases; reduced ovary present. Pistillate flowers: staminodes many, surrounding ovary base, resembling stamens but smaller and sterile; disk lobes many, small, set among staminode bases; ovary superior, 1-loculed, with (3–)5(or 6) placentas; ovules many; styles (3–)5(or 6), ± erect, cylindric, connate at base, apex dilated to form a nearly peltate, flattened, subcircular (actually U-shaped) stigma. Fruit a berry; pericarp thin. Seeds many.

One species: China, Japan, Korea.

“Idesia fargesii” and “I. polycarpa var. fargesii” are not treated here because no protologues could be traced and neither name is included in the International Plant Names Index (https://www.wendangku.net/doc/ca140526.html,). The taxon is represented at K by four sheets: Farges 76 (two sheets), Sichuan, annotated “Idesia polycarpa var. fargesii Franch.”; Farges s.n., same locality, annotated “Idesia fargesii Oliver”; and Cavalerie 2981, Guizhou, annotated “Idesia fargesii Franch.” All are duplicates from P. No significant differences were found between this material and I. polycarpa. Among the Farges specimens, all leaves are glued abaxial surface down; abaxial leaf surfaces of the Cavalerie sheet are more or less glabrous.

1. Idesia polycarpa Maximowicz, Bull. Acad. Imp. Sci. Saint-Pétersbourg 10: 485. 1866.

山桐子 shan tong zi

Trees, 8–21 m tall; bark grayish, not flaking; branchlets sparsely pubescent or glabrous. Petiole reddish, usually long, (4–)5–15 cm or more, glabrous, base slightly dilated; leaf blade deep green adaxially, broadly ovate, (6–)8–16(–20) × (4–)7–15(–20) cm, thinly leathery, abaxially pruinose, with a small dense patch of hairs at extreme base,elsewhere glabrous,sparse-ly hairy along veins or pubescent throughout, hairs (except in basal patch) mostly spreading, short, drying whitish or yellow-ish; adaxially usually glabrous, rarely sparsely hairy along mid-vein and main veins or throughout, lateral veins ca. 6 pairs, blade usually 5(–7)-veined from base,base cordate,often deeply so, less often rounded, margin serrate, usually coarsely so, apex gradually or more abruptly acuminate. Panicles (13–)20–30 cm; rachis sparsely to more densely pubescent. Flowers unisexual, yellowish green; pedicels 1–1.5 cm, densely pubescent, hairs appressed, yellowish brown, short; bracts lanceolate, 3–10 mm, reducing in size toward apex of rachis, papery, toothed or lobed. Staminate flowers: slightly larger than pistillate ones, 1.2–1.6 cm in diam.; sepals 5–6 × 2–3 mm, ovate to elliptic or slightly obovate,both surfaces densely pubescent,hairs yellowish brown, appressed, short; stamens 5–6 mm; filaments pubescent in lower half, hairs crisped, white when dry; disk glands globose to truncate, small, glabrous. Pistillate flowers: ca. 9 mm in diam.; sepals as in staminate flowers but slightly smaller, 4–5 × ca. 2.5 mm; disk glands globose to truncate, small; ovary superior, globose, glabrous; styles 5 or 6, 0.5–2 mm, joined at base; stigmas 0.5–1 mm in diam. Berry purple-red or orange-red when mature, drying blackish, globose, 8–10 mm in diam., apical scar left by styles pale, circular, flat, small, 0.5–1 mm in diam.; pericarp thin, brittle when dry; stalk 0.6–2 cm. Seeds drying reddish brown or purplish brown, broadly ovoid,2–3 mm, completely enclosed in a thin, translucent membrane. Fl. Apr–May, fr. Oct–Nov.

Deciduous broad-leaved forests, needle-leaved and broad-leaved mixed forests; 400–3000 m. Anhui, Fujian, Guangdong, Guangxi, Gui-zhou, Hubei, Hunan, J iangsu, J iangxi, Shaanxi, Shandong, Sichuan, Yunnan, Taiwan, Zhejiang [Japan, Korea].

FLACOURTIACEAE 125

Idesia polycarpa is grown as an ornamental.

1a. Leaf blade abaxially glabrous (except

at extreme base), or sparsely hairy only

along main veins .................................... 1a. var. polycarpa 1b. Leaf blade abaxially pubescent throughout.

2a. Petiole 2–3 cm, leaf blade 6–7 ×

4–5 cm .......................................... 1c. var. fujianensis 2b. Petiole ca. 4 cm or longer, leaf blade

ca. 8 cm or longer ............................... 1b. var. vestita 1a. Idesia polycarpa var. polycarpa

山桐子(原变种) shan tong zi (yuan bian zhong)

Cathayeia polycarpa (Maximowicz) Ohwi; Idesia poly-carpa var. intermedia Pampanini; I. polycarpa var. latifolia Diels; Polycarpa maximowiczii Linden ex Carrière.

Leaf blade abaxially glabrous (except at extreme base), or sparsely hairy only along main veins.

Deciduous broad-leaved forests, needle-leaved and broad-leaved mixed forests; 400–2500 m. Anhui, Fujian, Guangdong, Guangxi, Gui-zhou, Hubei, Hunan, Jiangsu, Jiangxi, Sichuan, Yunnan, Taiwan, Zhe-jiang [Japan, Korea].

1b. Idesia polycarpa var. vestita Diels, Bot. Jahrb. Syst. 39: 478. 1900. 毛叶山桐子 mao ye shan tong zi

Petiole ca. 4 cm or longer; leaf blade ca. 8 cm or longer, abaxially softly pubescent throughout.

Deciduous broad-leaved forests; 900–3000 m. Fujian, Guangxi, Guizhou, Hubei, Hunan, Jiangsu, Jiangxi, Shaanxi, Shandong, Sichuan, Yunnan, Zhejiang [Japan].

“Idesia polycarpa var. longicarpa” (S. S. Lai, Bull. Bot. Res., Harbin 14: 227. 1994) belongs here but was not validly published under Art. 37.2 of the Vienna Code because three gatherings were indicated as types (S. S. Lai et al. 20, S. C. Zhang 8, and P. X. Tan [P. C. Tam] 59730).

1c. Idesia polycarpa var. fujianensis (G. S. Fan) S. S. Lai, Fl. Reipubl. Popularis Sin. 52(1): 58. 1999.

福建山桐子 fu jian shan tong zi

Idesia fujianensis G. S. Fan, J. S. W. Forest. Coll. 5(3): 30. 1995.

Petiole 2–3 cm; leaf blade 6–7 × 4–5 cm. Infructescence 8–10 cm. Branchlets, petioles, leaf blades abaxially, peduncles, and fruiting pedicels densely yellowish pubescent.

● Forests; ca. 900 m. Fujian.

Idesia polycarpa var. fujianensis is possibly a small form of I. polycarpa var. vestita. Material was not seen by the present authors.

8. POLIOTHYRSIS Oliver, Hooker’s Icon. Pl. 19: t. 1885. 1889.

山拐枣属 shan guai zao shu

Trees, monoecious, deciduous. Leaves alternate; stipules not seen; petiole usually with a single or pair of small, rounded glands at apex on adaxial surface, sometimes with additional glands along distal half of petiole; leaf blade palmately 3–5-veined at base, margin glandular-serrate. Flowers hypogynous, unisexual, in terminal or rarely axillary many flowered panicles, pistillate flowers in upper part of inflorescence, staminate ones in lower part; bracts present; pedicels articulate. Sepals 5, valvate, nearly free, texture rather thick. Petals absent. Disk glands absent. Staminate flowers: stamens many, free, shorter than sepals; anthers ellipsoid or transverse-ellipsoid, connective much dilated, curved, bringing both locules to face in same direction (toward periphery of flower); abortive ovary very small. Pistillate flowers: staminodes many, surrounding ovary base, resembling small stamens; ovary superior, 1-loculed; placentas 3 or 4, filiform, finally woody, persistent; ovules numerous; styles 3, narrowly cylindric, joined in basal 1/3, with free distal parts strongly reflexed against ovary; stigmas flattened, triangular, lobed. Capsule narrowly ovoid, 3-valvate; outer layer of pericarp thin, dehiscent; inner layer thin, woody, persistent; valves characteristically splitting from apex and base and remaining attached by persistent woody placental strips; styles caducous. Seeds many, arranged vertically, compressed-flat, winged; wing flat, papery, completely encircling seed, seed proper less than 1/2 as long as wing.

● One species: China.

1. Poliothyrsis sinensis Oliver, Hooker’s Icon. Pl. 19: t. 1885. 1889.

山拐枣 shan guai zao

Trees, 7–15 m tall; bark gray-brown; branchlets gray, twig tips at first pubescent with short, spreading, crisped hairs, later glabrous. Petiole 2–6 cm, initially pubescent, glabrescent; leaf blade greenish abaxially, deep green and shiny adaxially, ovate or ovate-oblong, sometimes ovate-cordate, 8–18 × 4–10 cm, thickly papery, abaxially densely pubescent at first with hairs rather long (0.5–1 mm) and semiappressed, glabrescent, adaxi-ally pubescent along veins, midvein and lateral veins prominent abaxially, lateral veins 5 or 6 pairs, second basal pair high as-cending, base rounded or cordate, margin serrate, apex acute or obtuse and contracting gradually to a short acumen. Panicle 10–20 cm; rachis very densely pale grayish tomentose throughout, indumentum often completely obscuring rachis surface. Pedi-cels 2–3 mm in staminate flowers, 4–6 in pistillate flowers; bracts lanceolate, to 4 mm, very early caducous; bracteoles similar but much smaller, 1–1.5 mm. Sepals ovate, 4–5 mm, midvein prominent on outside, outside densely grayish tomen-tose, inside glabrous except for densely tomentose margin, mar-gin thickened, apex acute. Staminate flowers: stamens unequal in length, longest ca. 1 mm; filaments glabrous; anthers ca.

0.3 mm. Pistillate flowers: ovary ovoid, longitudinally ridged, densely tomentose; styles 1–3 mm, tomentose; stigmas large, 1–2 mm, ± bifurcate, branch tips dilated, flattened, lobed, adax-ially glabrous, drying blackish. Capsule ovoid, tomentose, in-

FLACOURTIACEAE 126

dividual valves acutely fusiform, 2–3 cm, ca. 1 cm in diam. Seeds compressed-flat, each surrounded and enclosed by a ± elliptic or oblong wing 5–10 mm, seed proper small, less than 1/2 as long as wing. Fl. Jun–Jul, fr. May–Sep.

● Evergreen and deciduous broad-leaved mixed forests, deciduous broad-leaved forests on mountain slopes or at foot of mountains; 400–1500 m. Anhui, Fujian, S Gansu, Guangdong, Guizhou, Henan, Hubei, Hunan, Jiangsu, Jiangxi, S Shaanxi, Sichuan, NE Yunnan, Zhejiang.

“Poliothyrsis sinensis f. subglabra” (S. S. Lai, Bull. Bot. Res., Harbin 14: 228. 1994) belongs here but was not validly published under Art. 37.2 of the Vienna Code because three gatherings were indicated as types (S. S. Lai 7001, H. L. Zhang & Y. R. Zeng 27133, and S. S. Lai 062).

9. CARRIEREA Franchet, Rev. Hort. (Paris) 68: 498. 1896.

山羊角树属 shan yang jiao shu shu

Trees, dioecious (?sometimes monoecious), deciduous; stipules minute, very early caducous. Leaves alternate; petiole elongate, sometimes with glands at apex or along length; leaf blade pinnate-veined, 3-veined from base, margin obtusely glandular-serrate. Flowers hypogynous, unisexual, in terminal or axillary, few flowered panicles or racemes; bracts present; pedicels articulate, with a pair of ± persistent bracteoles just below articulation. Sepals 5, nearly free, valvate, ovate, with base often appearing strongly cordate when sepals erect, papery, inside with glands at base near margin, margins conspicuously conduplicate. Petals absent. Disk glands absent. Staminate flowers: stamens many, free, inserted on slightly domed receptacle; filaments filiform; anthers oblong or ellipsoid, connective usually curved, bringing both locules to face in same direction (toward periphery of flower); abortive ovary very small. Pistillate flowers: smaller than staminate flowers; staminodes many, surrounding ovary base, resembling stamens but reduced; ovary 1-loculed; placentas 3 or 4, filiform, finally woody, persistent; ovules numerous; styles 3 or 4, very short; stigmas erect, spreading or strongly reflexed against ovary, flattened, irregularly 3-lobed. Capsule fusiform or narrowly ovoid, large, 3-valvate, outer layer of pericarp thin, dehiscent, inner layer thin, woody, persistent, valves characteristically splitting from apex and base and remaining attached by persistent woody placental strips; styles caducous. Seeds many, arranged vertically, compressed-flat, winged; wing flat, papery, not encircling seed, instead extending from one end only; seed proper small.

Two species: China, Vietnam; two species (one endemic) in China.

In fruit, forms of Carrierea calycina with smaller capsules can be difficult to distinguish from C. dunniana. The leaf length-to-width ratio can be helpful.

1a. Sepals 1.5–2 cm, base cordate; bracts 10–30 mm, bracteoles 4–8 mm; capsule 3–7 cm ............................................. 1. C. calycina 1b. Sepals 0.5–1 cm, base cuneate or only slightly cordate; bracts 5–7 mm, bracteoles 2.5–5 mm; capsule

2.5–4 cm ....................................................................................................................................................................... 2. C. dunniana

1. Carrierea calycina Franchet, Rev. Hort. (Paris) 68: 498. 1896.

山羊角树 shan yang jiao shu

Carrierea rehderiana Sleumer.

Trees, 12–16 m tall; bark black-brown; branchlets grayish, glabrous. Petiole (2.5–)3–7 cm, pubescent or glabrous; leaf blade greenish abaxially, deep green adaxially, variable in shape, ovate-oblong, oblong, or slightly obovate, less often elliptic, (8–)9–14 × 4–6 cm, mostly 1.7–2.2 × as long as broad, thinly leathery, both surfaces glabrous or abaxially sparsely tomentose along veins, 3-veined at base, lateral veins 4 or 5 pairs, base rounded to cordate, margin remotely serrate, often coarsely so, apex obtuse, contracting abruptly to a short acumen to 1(–2) cm, or more rarely leaf apex acute. Inflorescence ter-minal, to ca. 10-flowered, 5–10 cm including flowers, pubes-cent to tomentose; bracts lanceolate to narrowly ellipsoid, 1–3 cm, papery, both surfaces sparsely to densely appressed hairy; flowers sweetly scented. Pedicels 1.2–3 cm, 2-bracteolate near middle; bracteoles opposite, narrowly oblong, 4–8 mm, papery, pubescent, glandular along margin toward base, ± persistent. Sepals broadly ovate, 1.5–2 cm, in older flowers longer and narrower, both sides yellowish tomentose, inside more densely so, base cordate when sepal erect, apex obtuse. Staminate flow-ers: stamens with filaments unequal in length, longest 1–1.5 cm, glabrous; anthers narrowly ellipsoid, 1–1.2 mm. Pistillate flowers: staminodes like stamens but much reduced; ovary ob-long-ovoid, densely yellowish appressed-pubescent; placentas 3 or 4; styles 3 or 4, 0.5–1 mm, ± connate, densely pubescent as ovary, stigmas erect to reflexed, drying black, flattened, triangular, 2–3 mm, irregularly lobed, glabrous or abaxially pubescent. Capsule fusiform, slightly curved, 3–8 cm, tomen-tose; seed including wing 1–1.5 cm; wing oblong-obovate, asymmetric; seed proper ca. 5 mm. Fl. May–Jun, fr. Jul–Oct.

● Forests, forest margins; 1300–1600 m. Guangxi, Guizhou, Hu-bei, Hunan, Sichuan, Yunnan.

The type specimen of Carrierea calycina (Cavalerie 2925) at K includes both staminate and pistillate flowers. Carrierea rehderiana is here a new synonym of C. calycina.

2. Carrierea dunniana H. Léveillé, Repert. Spec. Nov. Regni Veg. 9: 458. 1911.

贵州嘉丽树 gui zhou jia li shu

Trees, 5–10 m tall; bark gray-brown; branchlets grayish, glabrous. Petiole 1–3 cm, slender, glabrous; leaf blade green-ish abaxially, deep green adaxially, ovate to oblong, 7–12 × 3–5.5 cm, 2.2–2.8 × as long as broad (based on a small sam-ple), thinly leathery, abaxially glabrous or sparsely tomentose along veins, adaxially glabrous, palmately 3-veined from base, lateral veins 4 or 5 pairs, base rounded, margin remotely

FLACOURTIACEAE 127

serrate, apex broadly acute, contracting gradually or more abruptly to an acumen 1–2 cm. Inflorescence terminal, to ca.

10 cm, 8–15-flowered; rachis pubescent to tomentose, hairs spreading to semiappressed, whitish, short; bracts ovate, 5–7 mm, papery, both surfaces sparsely appressed hairy, with one or two small glands on margin at base, apex rounded. Pedicels 1.5–1.8 cm, 2(or 4)-bracteolate near middle; bracteoles simi-lar to bracts, opposite or subopposite, broadly oblong, ovate, or elliptic, 2.5–5 mm, both surfaces sparsely appressed pubes-cent, scarcely or not glandular at margin near base. Sepals obovate to elliptic, 5–10 mm, both sides yellowish tomentose, base not or only slightly cordate when sepal erect, apex obtuse. Staminate flowers: stamens with filaments unequal, longest 3–5 mm, glabrous; anthers ca. 0.5 mm; pistillode very small. Pistillate flowers: staminodes like stamens but much reduced; ovary ovoid, ca. 4 mm, very densely yellowish pubescent, placentas 3; styles 3, very short (0.5–1 mm), connate at least at base to form a thick column, densely pubescent as ovary; stigmas strongly reflexed, drying black, 2–3 mm, flattened, narrowly triangular, bifurcate in distal half with branches irregularly lobed at apex, abaxially sparsely hairy, adaxially glabrous. Capsule fusiform, 2.5–4 cm. Fl. May–Jun, fr. Aug–Oct.

Broad-leaved forests, forest margins on mountain slopes; 1500–1700 m. Guangdong, Guangxi, Guizhou, Yunnan [N Vietnam].

The type specimen of Carrierea dunniana (Cavalerie 3001, Gui-zhou) at K includes both pistillate and staminate flowers.

10. ITOA Hemsley, Hooker’s Icon. Pl. 27: t. 2688. 1901.

栀子皮属 zhi zi pi shu

Mesaulosperma Slooten.

Trees, dioecious (or ?monoecious), evergreen. Leaves usually alternate, sometimes subopposite; stipules early caducous; petiole long, without glands at apex nor along length; leaf blade pinnate-veined, lateral veins closely set, mostly 1(–2) cm apart, margin glandular-serrate or glandular-crenate, sometimes minutely so. Flowers unisexual, hypogynous; staminate flowers in erect, terminal panicles; pistillate flowers 1 to few in short terminal or axillary racemes; bracts present; bracteoles 1 pair per pedicel, usually caducous. Pedicels not obviously articulate in dried material. Sepals appearing 3- or 4-merous in bud, in fact to 5-merous at anthesis, nearly free, valvate, ovate, with base appearing ± cordate when sepal erect, texture rather thick, margins slightly conduplicate. Petals absent. Disk glands absent. Staminate flowers: stamens many; filaments free, filiform; anthers ellipsoid to oblong, basifixed, con-nective usually curved, bringing both locules to face in same direction (toward periphery of flower); abortive ovary present. Pistillate flowers: ovary superior, 1-loculed; placentas 6–8, rarely 5, filiform, finally woody, persistent; ovules numerous; styles 6–8, very short, connate, forming a short longitudinally ribbed column; stigmatic branches (4–)6–8, spreading or strongly reflexed against ovary, irregularly palmately lobed; staminodes many, extragynoecial, like stamens but very much reduced. Capsule ovoid or ellipsoid, large, woody, tomentose, outer layer probably finally dehiscent; valves (5 or)6–8, fusiform, splitting from apex and base and remaining attached by woody persistent placental strips; styles caducous. Seeds many, arranged vertically in capsule, winged; wing broad, flat, thin, triangular, squarish or rectangular, completely surrounding seed; seed proper small.

Two species: Asia; one species in China.

Itoa has been reported as dioecious (e.g., Sleumer, Flora Males., ser. 1, 5(1): 12. 1954) but might also be monoecious. Hoogland 5079, a specimen of I. stapfii (Koorders) Sleumer from New Guinea, has a short raceme bearing a pistillate flower with young fruit developing, and a stam-inate flower with pollen-bearing anthers. In dried specimens of Itoa seen for the present account, the majority of flowers were in bud; those dissected contained stamenlike structures that may be stamens or staminodes.

1. Itoa orientalis Hemsley, Hooker’s I con. Pl. 27: t. 2688. 1901.

栀子皮 zhi zi pi

Trees, 8–12 m tall; bark gray; twig tips densely pubescent, branchlets finally glabrous. Leaves usually alternate, sometimes subopposite or clustered at apices of branches; petiole 2–6 cm, pubescent with short spreading hairs or glabrous; leaf blade greenish abaxially, deep green adaxially, narrowly to broadly elliptic, oblong-elliptic, or ovate, large, 13–40 × 6–18 cm, thinly leathery, abaxially densely pubescent with hairs rather long (ca. 0.5 mm) and spreading, or glabrous, adaxially initially pubescent, especially along midvein and main veins, finally gla-brous, midvein raised abaxially, slightly impressed adaxially, lateral veins 10–26 pairs, base obtuse to rounded, margin ser-rate to serrulate, teeth obtuse, leaf apex usually obtuse to round-ed, contracting abruptly to a short acumen, or apiculate, rarely acute. Inflorescences paniculate or racemose; rachises, pedicels, and abaxial surfaces of bracts densely pubescent to tomentose, hairs spreading, brownish when dry, short; bracts lanceolate, 5–6 mm. Flowers unisexual. Sepals 3 or 4, triangular-ovate, 0.6–1.5 cm, outside tomentose, hairs yellowish when dry. Staminate flowers: arranged in erect terminal pubescent panicles 4–8(–15) cm; stamens 120–160, 3–6 mm, glabrous; filaments ca. 5 mm; anthers oblong, ca. 1 mm. Pistillate flowers: solitary at apices of branches; ovary globose; styles (4–)6–8, very short; stigmas (4–)6–8, ca. 1 cm, palmately branched; branches irregularly lobed, flattened, tortuous, shortly pubescent beneath, glabrous above. Capsule ovoid, to 9 × 6 cm, densely orange-yellow or reddish tomentose (drying brown), glabrescent, (5–)6–8-val-vate. Seeds including wing ca. 2 cm, dark to light brown when dry, seed proper small. Fl. May–Jun, fr. Sep–Oct.

Evergreen broad-leaved forests; 500–1700 m. Guangxi, Guizhou, Hainan, Sichuan, Yunnan [Vietnam].

FLACOURTIACEAE 128

1a. Branchlets, petioles, and leaf blades

abaxially puberulous ............................... 1a. var. orientalis 1b. Branchlets, petioles, and leaf blades

abaxially glabrous ............................... 1b. var. glabrescens 1a. Itoa orientalis var. orientalis

栀子皮(原变种) zhi zi pi (yuan bian zhong)

Carrierea vieillardii Gagnepain; Mesaulosperma vieil-lardii (Gagnepain) Slooten.

Branchlets, petioles, and leaf blades abaxially puberulous.

Evergreen broad-leaved forests; 500–1400 m. Guangxi, Guizhou, Hainan, Sichuan, Yunnan [Vietnam].

1b. Itoa orientalis var. glabrescens C. Y. Wu ex G. S. Fan, J. Wuhan Bot. Res. 8(2): 133. 1990.

光叶栀子皮 guang ye zhi zi pi

Branchlets, petioles, and leaf blades abaxially glabrous. Fl. Mar–Jun, fr. Jul–Dec.

● Evergreen broad-leaved forests in mountains; 500–1700 m. Guangxi, Guizhou, Yunnan.

11. HOMALIUM Jacquin, Enum. Syst. Pl. 5, 24. 1760.

天料木属 tian liao mu shu

Astranthus Loureiro; Blakwellia Commerson ex Jussieu (1789), not Scopoli (1777), nor Lamarck (1785); Pierrea Hance (1877), not F. Heim (1891), nom. cons.

Trees or shrubs. Leaves alternate, rarely opposite or verticillate; stipules caducous; usually petiolate; leaf blade pinnate-veined, margin with glandular teeth, rarely entire. Flowers bisexual, epigynous, small, in terminal or axillary, many flowered racemes or panicles, inserted singly along rachis, or in sessile to shortly pedunculate fascicles; bracts small, caducous or persistent; pedicels slender in flower, articulate at or above middle. Sepals and/or petals often accrescent after anthesis. Calyx tube obconic, adnate to lower 2/3 of ovary and later to lower 2/3 of capsule; sepals (4 or)5–8(–12), spreading, linear, oblong, or obovate-spatulate, persistent. Petals inserted at rim of calyx tube, usually isomerous with and similar to sepals, alternating with them. Disk glands 1 opposite each sepal, rarely more or fewer, small, fleshy, ± globose and hairy. Stamens inserted singly or in groups before each petal, alternating with disk glands and inserted between them, usually finally overtopping perianth; filaments free, filiform; anthers subglobose, small, dorsifixed. Ovary semi-inferior, only upper conic part free above adnate calyx tube, 1-loculed; placentas 2–6(–8), with (1–)3–7 ovules near apex of each placenta; styles 2–5(–7), filiform, free or united in lower 1/3 or less, free parts divergent, usually finally overtopping perianth; stigmas capitate to punctiform, small. Capsule obconic, small, for most of its length enclosed in adnate calyx tube and persistent perianth segments, leathery, apex 2–8-valvate; styles ± persistent. Seeds 1 to few.

Between 180 and 200 species: tropical regions of both hemispheres; ten species (six endemic) in China; four additional species (all endemic) are poorly known.

In Chinese species: disk glands 1 or 2 opposite each sepal; stamens 1 opposite each petal; capsules to 7 mm.

Much uncertainty remains in the taxonomy of Chinese Homalium. Further gatherings and detailed study are recommended to establish reliable diagnostic characters (especially comparing the perianth in flower and fruit) and a stronger taxonomic framework. Where possible, descriptions of taxa in this account have been extended to include detail of perianth indumentum, which can be a useful character at species level. Sepal and petal lengths (both absolute and relative) are sometimes less useful, because of their accrescent nature. Inflorescence type (panicle vs. raceme) needs to be used with caution: apparent racemes sometimes have lateral branches although these are very short (to ca. 5 mm); false panicles occur when the leaves subtending all axillary racemes on a lateral branch are lost.

See also the four inadequately known species briefly described at the end of Homalium.

1a. I nflorescence paniculate.

2a. Leaves 17–19 × 5–7 cm, hairs on calyx tube spreading .................................................................................. 2. H. kwangsiense 2b. Leaves 3–14 × 1–6 cm, hairs on calyx tube spreading or appressed.

3a. Leaf acumen more than 10 mm, usually much longer(–30 mm), adaxial surface of leaf drying

blackish brown, shiny; hairs on calyx tube appressed ..................................................................... 10. H. phanerophlebium 3b. Leaf acumen less than 8 mm, or absent, adaxial surface of leaf not drying blackish brown,

nor shiny; hairs on calyx tube spreading or appressed.

4a. Leaf blade narrowly elliptic, narrowly oblong-elliptic, or slightly oblanceolate, 1–3 cm wide,

usually 3–4 × as long as wide, petiole 2–5 mm, lateral veins 4–6 pairs ........................................... 1. H. stenophyllum 4b. Leaf blade elliptic or obovate, sometimes broadly so, 3–6 cm wide, usually ca. 2 × as long as

wide, petiole 4–15 mm, lateral veins 5–8 pairs .............................................................................. 3. H. paniculiflorum 1b. I nflorescence racemelike.

5a. Flowers small, to 3.5 mm from base of calyx tube to tip of longest perianth segment ..................................... 5. H. ceylanicum 5b. Flowers ca. 4 mm or more from base of calyx tube to tip of longest perianth segment.

6a. Abaxial surface of leaf sparsely to densely hairy throughout, hairs long (ca. 0.5 mm), spreading,

yellowish, especially dense in young leaves, abaxial surface of older leaves soft and velutinous to

touch ........................................................................................................................................................... 7. H. mollissimum 6b. Abaxial surface of leaf with hairs on midvein and lateral veins only, or completely glabrous, or soon becoming so.

FLACOURTIACEAE 129 7a. Petioles 8–15 mm, leaves with acumen ca. 10 mm or more, blade drying blackish brown;

hairs on calyx tube appressed .................................................................................................... 10. H. phanerophlebium 7b. Character combination not as above; petioles ca. 6 mm or less; hairs on calyx tube appressed or spreading.

8a. Leaves narrowly elliptic or narrowly elliptic-oblong, 2–3 cm wide, 3–4 × as long as wide ........ 9. H. sabiifolium 8b. Leaves elliptic, oblong-elliptic, or obovate-elliptic, 3–7 cm wide, ca. 2 × as long as wide.

9a. Petals broadly spatulate, 2–3 mm wide across broadest part, apex broadly obtuse .............. 4. H. kainantense 9b. Petals oblanceolate linear to narrowly spatulate, 1–1.5 mm wide across broadest part,

apex acute to narrowly obtuse.

10a. Twig tips and petioles hairy ..................................................................................... 6. H. cochinchinense

10b. Twig tips and petioles glabrous ............................................................................. 8. H. breviracemosum

1. Homalium stenophyllum Merrill & Chun, Sunyatsenia 2: 287. 1935.

海南天料木 hai nan tian liao mu

Trees, rarely shrubs, to 18 m tall; bark grayish or brownish gray, not flaking; young branchlets hairy; old branches terete, glabrous. Stipules minute, subulate, glabrous, early caducous; petiole 2–5 mm, hairy when young, gradually glabrescent; leaf blade narrowly elliptic, narrowly oblong-elliptic, or slightly ob-lanceolate, usually 3–4 × as long as wide, 4–10 × 1–3 cm, thinly leathery, both surfaces glabrous, sometimes abaxially fasciculate-hairy in vein axils, lateral veins 4–6 pairs, reticulate veins slightly conspicuous, base narrowly to broadly cuneate, margin shallowly serrate to subentire, slightly revolute, apex acute to shortly acuminate, rarely obtuse, acumen to 6 mm, usually shorter, extreme tip blunt. I nflorescence terminal or axillary, paniculate, 4–8(–12) cm; rachis pubescent, hairs spreading; lower bracts resembling small leaves, upper bracts linear, lanceolate, or narrowly oblanceolate, 2–3 mm, glabrous except for ciliate margin. Pedicels 1.5–2 mm, articulate near middle, pubescent, hairs spreading. Flowers numerous, inserted along rachis singly or in fascicles, white, 8- or 9-merous, ca. 5 mm in diam., to 8 mm in diam. at fruiting stage. Calyx tube (1–)1.5–2 mm, smooth or longitudinally ribbed, outside pubes-cent, hairs spreading, long; sepals drying white, 2.5–3 mm, linear to linear-spatulate, both sides glabrous, margin densely ciliate, cilia longer than 1/2 width of sepal, apex acute to ob-tuse, often mucronate. Petals narrowly elliptic or linear-oblan-ceolate, 3–4 mm, slightly longer and wider than sepals, both sides glabrous, margin densely ciliate, cilia as for sepals, apex slightly obtuse. Disk glands ca. 0.5 mm in diam., pubescent. Stamens 8 or 9(or 10); filaments 3–4.5 mm, finally overtopping perianth, hairy, hairs spreading, white, long. Free part of ovary sparsely hairy, hairs spreading, white, long; styles 3 or 4, ca. 2.5 mm, joined in basal part to form a thick column, sparsely hairy in lower part; placentas 3 or 4, each with 2–4 ovules. Capsule ca. 3.5 mm. Fl. May–Dec, fr. Dec–Jan of following year.

● Mountain forests, also on rocks along streams; 500–1000 m. Hainan.

Lau 3225 (A), collected from Hainan, is not referable to Homa-lium stenophyllum; see inadequately known “species A” below. Also from Hainan, A. Chun & Tso 43732 (A, K) looks rather different from most other specimens; perhaps the inflorescences are at a younger stage.

2. Homalium kwangsiense How & Ko, Acta Bot. Sin. 8: 35. 1959.

广西天料木 guang xi tian liao mu

Trees, to 15 m tall; bark not flaking; branchlets terete, striate, dull-yellowish pubescent. Petiole 2–3 mm, stout, densely dark brown pubescent; leaf blade black-brown when dry, ovate-elliptic or ovate-oblong, 17–19 × 5–6 cm, thinly leathery, abaxially sparsely crisped-pubescent, more densely so along midvein and lateral veins, adaxially papillose-pubescent, midvein prominent abaxially, flat adaxially, lateral veins 9–11 pairs, conspicuously anastomosing near margin, base broadly cuneate to slightly obtuse, margin crenulate-serrate, teeth apices fasciculate-hairy, leaf apex long acuminate, acumen 8–12 mm, straight or falcate. Inflorescence axillary, paniculate, 10–13 cm; rachis densely pubescent, hairs spreading, dull yellowish. Pedi-cels 2–4 mm, articulate at middle, sparsely pubescent, hairs spreading, dull-yellowish. Flowers numerous, inserted singly on rachis or less often 2–4-fasciculate, creamy-white, 8- or 9-merous, 6–7 mm in diam. Calyx tube ca. 2 mm, conspicuously longitudinally canaliculate, sparsely pubescent, hairs spreading, dull-yellowish, long; sepals linear-lanceolate, 3.5–4 mm, mar-gin long ciliate, apex mucronate. Petals linear-oblanceolate, ca. as long as sepals but broader, apex mucronate. Disk glands squarish, pubescent. Stamen filaments 4–5 mm, soon over-topping perianth, sparsely hairy in lower part, hairs spreading, long. Free part of ovary densely pubescent, hairs spreading, yel-lowish, long; styles 3 or 4, 4–7 mm, indumentum as for ovary; placentas 3(or 4), each with 3–5 pendulous ovules. Capsule ca.

4 mm. Fl. Aug–Sep, fr. Sep–Dec.

● Shaded places in forests; low elevations. Guangxi.

3. Homalium paniculiflorum How & Ko, Acta Bot. Sin. 8: 36. 1959.

广南天料木 guang nan tian liao mu

Trees or shrubs, 8–12 m tall; bark gray or black-gray, not flaking;branchlets black-brown, terete, densely pubescent when young, soon glabrescent, irregularly angled. Stipules not seen, possibly early caducous; petiole 4–15 mm, pubescent; leaf blade elliptic or obovate, sometimes broadly so, excluding acu-men usually ca. 2 × as long as wide, 6–10 × 3–6 cm, papery, both surfaces glabrous, or abaxially barbate in vein axils, mid-vein and lateral veins raised on both surfaces, lateral veins 5–8 pairs, base generally broadly acute to rounded, margin serrate, teeth obtuse, leaf apex obtuse to rounded, contracting abruptly to a short acumen to ca. 5 mm. Inflorescence terminal or axil-lary, paniculate, 9–11 cm; rachis densely pubescent, hairs ap-pressed, short; bracts ovate, 1–3 mm, pubescent, early cadu-cous. Pedicels 2–3.5 mm, articulate above middle, densely pu-bescent, hairs appressed, short. Flowers numerous, inserted

FLACOURTIACEAE 130

along rachises singly or in fascicles of 2–4, yellowish, fragrant, 8-merous, 4–6 mm in diam. Calyx tube 2–2.5 mm, ca. 1 mm in diam., pubescent, hairs appressed, mostly much shorter than those of sepal and petal margins; sepals linear-oblong, 2–3 × ca.

0.5 mm, apex acute, both surfaces hairy, sparsely so on outside, hairs white, long (ca. 0.5 mm), appressed, especially on outside, less so on inside; sepal margin densely ciliate, hairs spreading, white, longer than 1/2 width of sepal. Petals narrowly oblong, 2.5–3.5 × ca. 0.5 mm, slightly longer and broader than sepals, indumentum of both surfaces and margin similar to sepals, apex obtuse. Disk glands ca. 0.5 mm in diam., hairy. Stamens 4–5 mm, finally overtopping perianth, glabrous or with a few long hairs in lower part. Free part of ovary hairy, hairs spreading, white, long; styles (2 or)3, 2.5–3 mm, free nearly to base, sparsely hairy in lower half, hairs spreading; placentas 3, each with 4 or 5 ovules. Capsule 6–7 mm, 1.5–2 mm in diam. Fl. Jun–Dec, fr. Dec–Feb of following year.

● Dense or thin forests, thickets along streams, dry or moist gentle slopes, sandy or clay soil, seashores; (sea level to)100–400 m. Guang-dong, Hainan.

4. Homalium kainantense Masamune, Trans. Nat. Hist. Soc. Taiwan 33: 169. 1943.

阔瓣天料木 kuo ban tian liao mu

Homalium brevisepalum How & Ko.

Trees, 10–12 m tall; branchlets purple-brown or black-brown, terete, twig tips at first minutely whitish puberulous (view at × 10 mag.), glabrescent. Stipules linear-oblong, to ca. 4 mm, papery, minutely puberulous, early caducous; petiole very short, ca. 1.5 mm, rarely to 3 mm, stout, very sparsely puber-ulous; leaf blade elliptic, oblong-elliptic, or obovate-elliptic, 7–13 × 4–6 cm, papery or subleathery, both surfaces initially densely and minutely puberulous (almost imperceptibly, view at × 20 mag.) with spreading hairs, becoming glabrous or with a few minute hairs remaining along veins (view at × 20 mag.), midvein and lateral veins raised abaxially, flat adaxially, lateral veins 6 or 7 pairs, reticulate veins inconspicuous, base acute, cuneate, margin serrate, teeth obtuse, apex broadly acute to obtuse, contracting to an acumen 5–10 mm. Inflorescence axil-lary, racemelike, 7–12 cm, sometimes with very short branches less than 5 mm; rachis pubescent, hairs spreading, whitish, short; bracts not seen. Pedicels ca. 3 mm, articulate near apex, pubescent, hairs spreading, short. Flowers numerous, 2–4-fas-ciculate along rachis, white, 5–7-merous, ca. 1.2 cm in diam., fragrant. Calyx tube narrowly obconic, 3–4 mm, sparsely pu-berulous, hairs whitish, semiappressed, short; sepals linear-lan-ceolate, 1.5–2 mm, outside sparsely pubescent, hairs appressed and short, margin ciliate with short (0.1–0.2 mm) appressed hairs, apex acute or obtuse. Petals ca. 5 × 2–3 mm, broadly spatulate, conspicuously veined, outside glabrous, inside with a few semispreading short hairs toward base, margin ciliate, hairs spreading and short (ca. 0.2 mm), apex obtuse. Disk glands ca.

1 mm wide, sides sparsely hairy, apex flat, glabrous. Stamen filaments ca. 6 mm, longer than or equal to petals, with a few hairs scattered in lower part. Free part of ovary sparsely hairy, hairs spreading, whitish, short (ca. 0.

2 mm); styles 3, free nearly to base, ca. 4 mm, hairy in lower part, hairs as for ovary; pla-centas 3, each with 2 or

3 ovules. Capsules (not seen) probably 6–8 mm. Fl. Aug–Dec, fr. Sep–Mar of following year.

● Mixed forests and thickets; low elevations. Guangdong, Guang-xi, Hainan.

5. Homalium ceylanicum (Gardner) Bentham, J. Linn. Soc., Bot. 4: 35. 1859 [“zeylanicum”].

斯里兰卡天料木 si li lan ka tian liao mu

Blackwellia ceylanica Gardner, Calcutta J. Nat. Hist. 7: 452. 1847; Homalium balansae Gagnepain; H. bhamoense Cubitt & W. W. Smith; H. ceylanicum var. laoticum (Gagne-pain) G. S. Fan; H. hainanense Gagnepain; H. laoticum Gagne-pain; H. laoticum var. glabratum C. Y. Wu.

Trees, 6–30(–40) m tall, buttressed; bark smooth to coarse; branchlets brown, angular to terete, puberulous to glabrous. Stipules linear-lanceolate, 1.5–3 mm, glabrous or glabrescent, early caducous; petiole 5–12 mm, glabrous or finely hairy; leaf blade variable in shape and size, elliptic to oblong, rarely ob-ovate, excluding acumen 1.5–2.5(–3) × as long as broad, 6–18(–20) × 2.5–8(–9) cm, thinly leathery to thickly papery, ab-axially pubescent with appressed short hairs or glabrous, ad-axially glabrous or ± glabrescent, midvein raised abaxially, flat or impressed adaxially, lateral veins 7–10 pairs, raised abax-ially,base acute with concave sides,acute-cuneate,or subround-ed, margin serrate-crenate to practically entire, teeth apices obtuse, leaf apex acute to rounded, contracting (sometimes very abruptly) to an acumen to 1 cm. Inflorescence axillary, racem-ose, pendulous, 5–20(–30) cm; rachis sparsely to very densely, pale grayish brown shortly pubescent; bracts narrowly trian-gular, minute, to ca. 2 mm, papery, sparsely hairy, caducous. Pedicels 1–3 mm, articulate at or above middle, densely pu-berulous to appressed shortly pubescent. Flowers numerous, in fascicles of 3 to ca. 20, sometimes very crowded along rachis, reddish or whitish, 4–6-merous, 2.5–3 mm in diam. at anthesis, fragrant. Calyx tube 0.5–1.5 mm, sparsely to densely pubescent, hairs whitish, appressed, short (0.1–0.2 mm); sepals linear-oblong or spatulate, 0.5–2 × 0.3–0.5 mm, apex acute, in-dumentum outside as for calyx tube, inside slightly denser, mar-gin densely ciliate, hairs spreading, whitish, length less than 1/2 to 1 × sepal width. Petals whitish or pinkish, ovate-oblong or spatulate, 0.8–2 × ca. 0.6 mm, both surfaces densely appressed whitish pubescent, sometimes more so than sepals, margin densely white-ciliate, apex obtuse. Disk glands truncate at apex, hairy. Stamens 4–6; filaments 2–3 mm, glabrous; anthers ca.

0.4 mm. Free part of ovary gray pubescent; placentas 4–6, each with 3–6 ovules;styles4–6,free nearly to base,1–2 mm,sparse-ly hairy at base; stigmas capitate to slightly peltate. Mature fruit not seen. Fl. Jan–Nov, fr. Feb–Dec.

Sparse or dense forests of mountain valleys, forest margins, rain forests, evergreen broad-leaved forests, along streams, in forested ra-vines,on gentle slopes;400–1200m.Guangdong,Guangxi, Hainan, Hu-nan, J iangxi, SE Xizang, S Yunnan [Bangladesh, India, Laos, Myan-mar, Nepal, Sri Lanka, Thailand, Vietnam].

Homalium ceylanicum is cultivated for ornament, and its wood is used commercially. Y u (in Fu & Jin, China Pl. Red Data Book 1: 304–

FLACOURTIACEAE 131

305. 1992) gave H. laoticum var. glabratum as an accepted taxon and categorized it as vulnerable. They noted it as a rare and valuable timber tree, with small, scattered populations under threat from felling and bush fires. Natural regeneration is poor and seed set is low (despite pro-lific flowering).

Homalium ceylanicum is treated here in a wide sense as a highly polymorphic species within which various elements show intergrading variation in indumentum, leaf size, and raceme length. Indian floras recognize also H. ceylanicum subsp. minutiflorum (Kurz) Mitra, with H. ciliatum N. Mukherjee in synonymy. Wu Zhengyi (pers. comm., 2005) recommended recognition of H. bhamoense at species level, with a new species to accommodate plants from Xizang. Resolution of the H. ceylanicum complex requires a study across its entire range. Material with mature fruit is apparently scarce. V erdcourt (in Dassanayake & Clayton, Rev. Handb. Fl. Ceylon 10: 219. 1996) recommended a field study to investigate fruit production.

6. Homalium cochinchinense (Loureiro) Druce, Rep. Bot. Exch. Club. Brit. Isles 4: 628. 191

7.

天料木 tian liao mu

Astranthus cochinchinensis Loureiro, Fl. Cochinch. 1: 222. 1790; Blackwellia fagifolia Lindley; B. padiflora Lindley; Homalium cochinchinense var. pseudopaniculatum (Yama-moto) Li; H. digynum Gagnepain; H. fagifolium (Lindley) Ben-tham; H. fagifolium var. pseudopaniculatum Yamamoto.

Shrubs or small trees, 2–10 m tall; bark gray-brown or purple-brown; branchlets terete, densely yellowish pubescent when young, gradually glabrescent. Stipules linear to narrowly obovate, to 8 mm, papery, hairy; petiole 2–3 mm (rarely to 6 mm), yellowish pubescent; leaf blade broadly elliptic, elliptic-oblong, or obovate, ca. 2 × as long as wide, 6–15 × 3–8 cm, thickly papery, both surfaces pubescent along midvein and lat-eral veins, midvein raised abaxially, impressed adaxially, lateral veins 7–9 pairs, anastomosing near margin, conspicuous on both surfaces, margin obtusely serrate, serrate-crenate, or den-tate, sometimes minutely so, remotely toothed to entire toward leaf base, base acute,sometimes broadly so,usually cuneate, ex-treme base sometimes rounded, apex variable, acute to shortly acuminate (acumen to ca. 10 mm) or not. Inflorescence ra-cemelike, (5–)8–15 cm, sometimes with very short branches less than 5 mm; rachis pubescent, hairs spreading; bracts linear to lanceolate,1–4 mm, papery,pubescent,early caducous. Pedi-cels 2–3 mm, articulate above middle, densely pubescent, hairs spreading, yellowish. Flowers numerous, inserted along rachis singly or few together in sessile to very shortly pedunculate fascicles, whitish, 7- or 8-merous, 6–9 mm in diam., fragrance-free (once recorded). Calyx tube 2–3 mm, longitudinally ribbed, sparsely pubescent, hairs spreading or semispreading, white, mostly shorter than hairs of sepal and petal apex margins; sepals linear to narrowly oblanceolate, 2–4 × 0.3–0.5 mm, membranous, with conspicuous midvein, outside subglabrous to sparsely hairy, inside sparsely hairy, hairs on both surfaces appressed or spreading, white, shorter and generally weaker than those on margins; sepal margin ciliate, hairs spreading, white, ca. as long as 1/2 sepal width; sepal apex acute, often apiculate. Petals 2–4.5 mm × 1–1.5 mm, narrowly oblanceolate-linear to narrowly spatulate, midvein and lateral veins conspicu-ous, indumentum on both surfaces and margin as for sepals, hairs at petal apex 0.5–0.7 mm, ca. 1/2 as long as petal width. Disk glands pubescent, hairs white, straight, long. Stamens 6–9; filaments 3–4 mm, sparsely hairy in lower half, hairs spreading, white, long. Free part of ovary densely hairy, hairs spreading, white, straight, long; styles usually 3, ca. 3 mm, hairy in lower 1/3, hairs as for ovary; placentas 3, each with 2–4 ovules. Cap-sule 5–6 mm, subglabrous. Fl. Feb–Nov, fr. Sep–Dec.

Broad-leaved forests in mountains; 400–1200 m. Fujian, Guang-dong, Guangxi, Hainan, Hunan, Jiangxi, Taiwan [Vietnam].

See also inadequately known “species D” (Liang 63511 (K) and Liang 63788 (K), from Hainan), below.

7. Homalium mollissimum Merrill, Lingnan Sci. J. 14: 39. 1935.

毛天料木 mao tian liao mu

Shrubs or small trees, 6–7 m tall; bark gray or gray-brown; branchlets terete, densely pubescent, hairs spreading, yellowish. Stipules sometimes persistent, 5–10 mm, linear, narrowly ellip-tic, or obovate, pubescent with long white hairs, margin toothed or erose; petiole 2–5 mm, densely pubescent; leaf blade elliptic or oblong-elliptic, rarely oblong or obovate, ca. 2 × as long as wide, 5–11 × 2.5–5 cm, leathery, both surfaces sparsely to densely yellow pubescent throughout, midvein and lateral veins raised abaxially, flat adaxially, lateral veins 6–8 pairs, base acute to rounded, margin remotely shallowly serrate, apex acute to shortly acuminate, acumen to ca. 7 mm. I nflorescence ter-minal or axillary, racemose, 4–8 cm; rachis densely pubescent, hairs spreading, yellowish white, long; bracts narrowly lanceo-late to linear, 1–4 mm, papery, margin entire, toothed, or erose, pubescent, hairs spreading, white, long. Pedicels 2–3 mm, articulate above middle, densely pubescent, hairs spreading, yellowish, long. Flowers numerous, inserted along rachis singly or in pairs, white, 7- or 8-merous, 4–6 mm in diam. Calyx tube ca. 2 mm, conspicuously longitudinally ribbed, outside dense-ly pubescent, hairs mostly as long as those on sepal and petal margins, spreading, yellowish; sepals linear or oblanceolate-linear, 3–5 × 1–1.5 mm, apex usually acute, both surfaces sparsely pubescent, hairs spreading, white, long; sepal margin densely ciliate, hairs spreading, white, long. Petals oblanceo-late, slightly longer than sepals, apex acute or obtuse, both sur-faces sparsely pubescent, hairs spreading, white, long; margin densely ciliate, hairs spreading, long, to 1.5–2 mm at petal apex. Disk glands minute. Stamens 7 or 8; filaments ca. equal to or overtopping petals, with long spreading hairs in lower part. Free part of ovary pubescent, hairs spreading, white, straight, ca. 1 mm or more; styles 3 or 4, ca. 3 mm, ca. 2 × longer at fruiting stage, hairy except for distal 1/4, hairs as for ovary; placentas 3 or 4, each with 3 or 4 ovules. Capsule 5–7 mm. Fl. Jun–Dec, fr. Jul–Jan of following year.

Mountain forests, thickets, on dry, rocky, clay or sandy soil, gentle slopes; low elevations. Hainan [N Vietnam].

Taam 286 (A, K), collected from Guangdong, might not be refer-able to Homalium mollissimum; see inadequately known “species B” below.

中国梦我的梦演讲稿范文5篇

中国梦我的梦演讲稿范文5篇 篇一 亲爱的老师、同学们:一个人梦想的追寻和实现,成就了中国的腾飞和光荣,这就是“中国梦”。 比如:神州五号载人飞船的发射成功,嫦娥三号圆满发射,都是中国富强的表现。曾经,邓小平说过:”我要让中国富起来!“还有周恩来总理:”我要让中国强大起来!“后来他们都实现了自己的中国梦。然而,我的中国梦就是——让中国变成绿色。 现在,因为伐木工过度砍伐树木,水泥厂越来越多,沙漠化越来越厉害,还有农业污水越来越多,把蓝色的小溪都变成了灰色和黑色。中国的环境越来越差,全是灰色和黄色。我实在是太心疼了,不忍心看下去,所以我逐渐的开始保护环境。在过年的时候,我会对爸爸妈妈亲戚朋友分别说:”今年不要放烟花爆竹了,您看那灰色的天空,还有电视上说的雾霾天气,环境多差呀!“有空的时候,我还会出去打扫卫生,甚至植几株草和花。植树节,我还会去植树。我还会有空的时候去贴几张”告示“,让大家不要破坏花草树木等。每个普通中国人的普通中国梦,都可以汇聚成一个伟大的中国梦!如果每个人都实现了自己的中国梦,那么我们的中国会越来越强大。如果每个人都嘴上说说,却不去实现,口是心非,那又有什么用呢? 篇二 亲爱的老师、同学们:每个人都有梦想,老师有希望学生成绩出色的梦,军人有希望国家繁荣富强的梦,医生有希望病人早日康复的梦,宇航员有希望发星球更

多秘密的梦…… 同样,我也有一个美好的梦。我梦想长大以后当一位能歌善舞的舞蹈家,代表国家四处比赛,为祖国争光。为了实现这个梦想,每周,我都要去文化馆上舞蹈课,上课前,我们都会自己拉拉腰、压压腿,做好课前准备,以免上课时把身体拉伤。虽然做了课前准备,可在练习时,总会清晰地听到自己骨头咔咔响的音。有时把一只腿放在厚厚的毯子上,另一只腿放在地上,摆成竖叉,大腿贴地,然后用手拉住后面那只脚,倒数二十秒,就可以了。可是,在这过程中,总会感到疼痛难忍,有时,我会疼得哭起来,有时,会疼得坐不稳,每当这时候,只要心里一想到那个美丽又美的梦,我就不觉得那么痛了,也轻松多了。有时在排练舞时,有的动作很难,练了很多次,可还是没做好。每当我相放弃不练了的时侯,只要一闭上眼睛,脑海里就会浮现出我在台上表演,台下的观众个个鼓掌叫好的场景。这些景象让我一次又一次地从摔倒的地方重新站了起来,完成了一个又一个困难却好看的舞姿。每当我们表演完节目,崔老师总不忘鼓励我们一句‘你们今天表现得真棒!’虽然这话在别人听起来十分平淡,可我听起这话总能让我紧张不以的心平静下来,感受到温暖。通过自己的努力,我参加了许多比赛,每次拿到奖时,我都十分激动,心里像吃了蜜一样甜甜的,希望自己更上一层楼。 也许,在不久的将来,我的梦想会成为现实,我一定要好好学习,天天向上,努力实现我美好的理想。 篇三 亲爱的老师、同学们:梦想是什么?相信每个人都有自己的理解,是卖火柴的小女孩渴望点燃一根火柴来取得温暖,还是丑小鸭幻想自己有一天可以脱去丑陋的

最新版中国梦我的梦演讲稿10篇

最新版中国梦我的梦演讲稿10篇 忆往昔峥嵘岁月,看今朝锦绣河山。回味改革开放的三十年,华夏神洲留下了太多的梦想奇迹。1997年7月1日,香港正式回归祖国,举国欢庆,“统一梦”迈出了坚定的第一步;2001年12月11日,中国正式成为世界贸易组织成员,从此,国家经济快速、平稳、健康的发展,“小康梦”已不再是一个遥不可及的目标;2013年6月12日,神十问天,璀璨的星河中留下了炎黄子孙的身影,编织了千年的“飞天梦”也终于迎风远航……一个个梦想的实现,一份份成就的辉煌无不昭示着“中国梦”——“复兴之梦”必将在党的领航下乘风破浪、直挂风帆。 走过历史的长廊,回顾百年的沧桑,“中国梦”一词在岁月的书卷中熠熠生辉。作为一种最为朴素、浓烈的民族情感,它的萌发、形成之于耻深痛极的近代百年,有着深刻的时代烙印。无论是谭嗣同“四万万人齐天下泪,天涯何处是神洲”的哀恸,还是秋瑾“拼将十万头颅血,誓把乾坤力挽回”的决绝,所体现的都是对国家前途命运的关切与焦虑。而今,随着时代的变迁,“中国梦”也从“救亡图存”变为了“强国富民”。然而我坚信有一点却始终不会改变,那就是坚定的民族自信,国人始终坚信有着五千年优秀历史文化的中华民族,无论面临怎样严峻的考验,终将转危为安、再

造辉煌,实现百年的“复兴之梦”。 俗话说:“聚沙成塔,集腋成裘”。“中国梦”既承载着国家的强国之梦、民族的复兴之梦,也包涵着亿万国人同胞千千万万个小小的梦想。有“富裕梦”,有“健康梦”、有“求学梦”……正是由于这些如涓涓细流般的梦想汇聚成河,才会让“中国梦”愈发的凝实。大学毕业之初,怀揣着对未来的憧憬,我选择了公务员考试。最终,经过重重选拔、层层考验我来到了隆化这个美丽的小城。抛弃了国企的高薪,远离了父母的怀抱,背离了自己的故乡,踏上一个陌生城市的土地,在这里去拼搏、去奋斗,这样的生活真的是我想要的吗我也曾无数次的扪心自问。时至今日,月余的法庭生活给了我一个满意的答复。这里也许没有车水马龙的的喧闹,却有着一份乡村独有的宁静;这里也许没有灯火通明的高楼,却能映照出一张张质朴的面容;这里也许没有频繁的人际交往,却有着一句句真诚的关怀。在这片广袤无垠的大地上,我找到了追寻梦想的原动力。 选择了到基层工作就意味着选择着艰苦;选择了公务员这个职业就意味着肩负着责任;选择了到法院任职就意味着守护着公正。在过去的一个月里,我体验到了从一个懵懂的书生向一名法院工作者转变的酸甜苦辣。现实和理想尽管错位不断,但热情和动力却与日俱增。基层法庭是法院工作的前沿阵地,直接面向农村,密切联系群众,受理的案件虽不

为实现中国梦做贡献 小学生征文

向着中国梦,前进! 绥芬河市北寒小学四年级李鸣 梦,通常指人们的理想。每个人都会做梦,每个人都会有自己的梦想。美羊羊的梦想是能够在青青草原上尽情地玩耍,光头强的梦想是把大森林里的树木都砍光。我的梦想,可以是一个漂亮的发卡,一盒可口的点心,是考试后的100分,妈妈对我夸奖的笑容……可今天,老师说,我们每个人不但要有自己的梦,还要有中国梦。 那么,什么是中国梦呢?中国梦是建立在祖国发展基础上的,是对祖国有利的梦,每个人的中国梦都不相同,有大有小,但它们又都有相同之处,那就是都怀着一颗为祖国作出贡献的心,对人民有功利的心。我想中国梦还应该是国家富强,小朋友们都有新衣服穿,有变形金刚、芭比娃娃;民族团结,不会有战争与饥饿;大人们高高兴兴地上班,孩子们能够一块儿在草地上做游戏。但我觉得,最重要的是要建设一个美丽、洁净的家园,那就是天蓝、地绿、水清、气爽的美丽中国。没有地沟油,没有沙尘暴,没有禽流感…… 建设美丽中国,就要从小事做起。在学校,看到地上有纸屑,我会主动弯腰捡起;看到水龙头滴水,我要主动上前把它关紧;看到有人说脏话,我会及时上前制止。春天来了,我拉着爸爸妈妈买树苗,到附近山坡上植树,因为我知道,绿化造林是防治大气污染的一种有效方法。我还要宣传环保知识,动员更多的人加入环保队伍,让天变得更蓝,水变得更绿。我还会在村里钉上一块“爱护环境、人人有责”的警示牌,让全村的人跟我一起行动起来,保护我们的环境、净化我们的环境。我知道我一个人,一家人的力量很微薄,但是如果全中国的孩子都能行动起来,每个中国家庭都行动起来,那就会汇成强大的环保能量,才能建设好美丽中国。 每个中国人都有着自己的中国梦,只要每个人能为这伟大的梦想贡献出自己的力量,哪怕是微不足道,但当所有的贡献汇集到一起,将会是一股多么强大的力量,这股力量会把中国推向更美好的明天,只要人人行动起来,我相信建设美丽祖国这个中国梦将会很快实现。

中国梦-我的梦演讲稿

中国梦我的梦 有一种东西,它承载着人们的希望,虽然他看不见,摸不着,却能在人们心中产生巨大的力量。它,就叫梦想。上帝没有赐予我们翅膀,却赐予了我们会飞的心灵和能够梦想的大脑,使我们有了一双“隐形的翅膀”,带着我们在人生辽阔的天空里自由地翱翔。 今年三月,全国人大和全国政协会议在北京召开,关于“中国梦”的话题也进行过热烈的讨论。每个人或多或少也在思考“中国梦”的问题。 那么,中国梦是什么呢?习近平总书记说“每个人都有理想和追求,都有自己的梦想。实现中华民族的伟大复兴,就是中华民族近代以来最伟大的梦想。这个梦想,凝聚了几代中国人的夙愿,体现了中华民族和中国人民的整体利益,是每一个中华儿女的共同期盼。”是的,每个人都有自己的梦,梦想能够照亮生活,亦能成就未来。而有一个梦,它既是你的梦,也是我的梦,它是万千中华儿女共同的心愿,那就是实现中华民族伟大复兴的中国梦。 每个人的梦都是中国梦的组成部分,我的梦亦如此。都说学生的主业是学习,的确如此,我的梦来自学习。我喜欢在午休时一个人独自读书的静谧;喜欢在难题前不停运用各种公式演算的执着;也喜欢与同学一起为一道题目争执不休的吵吵闹闹。这样所诠释的梦是理想之梦。 梦也来自家庭,对于我的成长,它最有发言权。平日里与父母相处的时间虽然不多,但是一起吃饭时,父亲在饭桌上的高谈阔论;

坐在同一书桌前各自忙碌时,偶尔抬头与母亲随意交谈的闲话,都在影响着我对生活的态度。 有了梦,便要去追寻。三年前,在懵懂的状态下,在家长的引导下选好了脚下的路—上高中、考大学。渐渐地,考大学也真正成为了我的梦。清晰地记得,老师在中考前说“我们将做出人生第一次重大选择”,面对众多的学校,我固执地选择了朝中,心中似乎在坚守着什么。后来,随着一个个目标的制定,无数次为“自己的事”的奋斗,我逐渐明白,我是在坚守着自己的梦,并且开始懂得为了理想和追求而努力拼搏。其实走到现在,蓦然回首,才发现人生是一个条件从句,梦的方向并无过多区别,而我们最终选择的那个梦,正是因为被自己选择,被自己填充,才显得与众不同,才显得适合自己。 我相信,只要坚持不懈,努力拼搏,梦想就一定能够成真。我的梦,我们的梦,铸就了实现国富民强的中国梦。可以想想,如果中国民族实现了伟大复兴,那么世界梦一定会更加流光溢彩。

中国梦我的梦演讲稿

演讲稿一 尊敬的各位领导、敬爱的老师、亲爱的同学们: 大家好!今天我演讲的题目是《中国梦,我的梦》。 在发言前我想问同学们一个问题就是:你们有梦吗?假如有梦的同学请大声的回答我。很好!我想你们的梦一定是绚烂的、美丽的、丰富的、美好的。生命因责任而美丽,人生因梦想而精彩。假如还在犹豫自己真正的的梦是什么?请认真听我们中国所共同的梦——中国梦 人生如梦,梦想是帆,每个人都有一个只属于自己的梦,但我们同属一个国家,所以每个人的梦又与国家的兴衰荣辱紧密相连。先哲顾炎武曾说:“天下兴亡,匹夫有责。”只有国家好,大家才能好。 有梦才能使中国富强! 我依然清楚的记得: 当甲午战争战败,日寇无礼踏破中国的门户;当八国联军侵入北京,无情掠夺中国的财产;当七七事变发生,中国的老人、妇孺被残忍杀害的时候,我在想那时中国的梦是怎样的! 我虽不曾亲眼看到,但那却是铁一般的事实。因为从老人们那深邃的眼神中可以感到无尽的愤懑;从他们干瘪的脸颊可以看到深情的泪水,从他们嘹亮的军歌中可以想到那奋勇杀敌时的豪迈;从他们激昂话语中听到那誓要捍卫家园振兴中华的誓言。作为新一代青年的我们难道不应该树立远大的理想,付之以踏实的行动,去继承先辈们的使命。去实现中华民族的伟大崛起和复兴吗? 有梦才能使中国繁荣! 在改革开放以来中国取得了一系列的可以载入中国史册的成就。香港、澳门的回归,经济特区的建立,使中国成为发展国家中的经济大国,科技先进国和军事强国。当中国成功举办奥运的时候,当神九飞天的时候,当蛟龙入海的时候,当航母下水的时候,当莫言荣获诺贝尔文学奖的时候。我相信每个人都感觉到了无比的自豪。但是现在的中国与其他发达国家还有很大差距。作为新一代的我们,难道不应该志存高远吗? 我想有的人会说,我们的力量是有限的。的确个人的力量很渺小,但是中国梦就是因一个个微不足道的个人的梦一直汇集、汇集,然后凝聚成的一个巨大的梦。冯至在《十四行诗》中写道,我们准备着,深深领受,那些意想不到的奇迹,在漫长的岁月里,忽然有彗星的出现,狂风乍起。 梦想是美丽的,它是最美的期望;梦想是阳光的,它使人由浮躁走向踏实;梦想是充满力量的,它可以激发人身体里无限的潜能。我们期盼的是国泰民安、经济发展、政治清明、文化繁荣、社会和谐、生态良好、公平正义。这才是中国人最伟大的梦。

2018年工信财务处我为实现中国梦做贡献演讲稿

2018年工信财务处我为实现中国梦做贡献演讲稿 梦想在前路在脚下 梦想,是每个人希望的开始。中华民族五千年历史传承着一个长长的梦,几经辗转,几经沉浮。时至今日,汇聚成了一个梦,中国梦。 一个人不能没有梦想。因为有梦想,我们才经历坎坷依然前行,因为有梦想,我们才经历沧桑信心不改。有梦想才会有希望;有希望才会有激情;有激情才会有事业;有事业才会有未来。中华民族是一个命运共同体,只有民族、国家全面科学发展,个人才能实现梦想。同样,只有每个人都充满激情和梦想,“中国梦”才够美丽,才够坚实。 工信人同样承担着实现中国梦的使命,一代一代在工业和电子、信息产业的人们前仆后继,奋勇拼搏,为了这个梦想奉献着自己的青春。 “疾风知劲草,岁寒见后凋”在财务处工作这段时间以来,我有过艰辛的汗水、也有过收获时的喜悦;有过扬帆起航时的热忱与豪情、也有过风雨骤来时的动摇与退却;有过风平浪静时的欢喜与惬意、也有过漫漫征途的寂寞与煎熬!财务工作赋予我人生新的意义和追求,它为我带来了淳朴的友谊,让我品尝到工作的无限快乐。在梦开始的这片热土上,我们平凡的财务人员在平凡的岗位上,默默无闻,奉献青春;我们用坚定的信念,用点滴的小事,书写着一幕幕爱岗敬业的篇章。 我们财务处就是这样一个群体,整日跟毫无生气的数字凭证、账簿打交道,整理核算杂乱的原始票据和凭证,日复一日,与数字相伴,与票据为友,但这一切都磨灭不了我们对财务工作的饱满热情,我们无怨无悔。既然扎根于工信财务工作,那么确保数字核算的准确无误,各项财务制度执行的缜密就是我们的责任,按时、顺利、高效地完成会计核算工作,为领导及时提供准确数据,为各部门提供最好服务,为厅机关及厅系统各项工作的顺利开展提供有力的保障是我们每个财务人员最大的心愿和使命! 梦想不是说说而已……我有一个大大的梦想,那么这个大大的梦想要从现在小小

关于我的梦中国梦主题演讲稿800字

关于我的梦中国梦主题演讲稿800字 尊敬的各位老师: 你们好!今天我演讲的题目是《我的梦中国梦》。 我有一个梦想,深深扎根于我的心中。那就是长大后,我要成为一个科学家。 尽管我没有过人的才智,没有严密的思维,也没有特别准确的判断力,但是我仍不会放弃努力。尽管这个梦想距我很遥远,但我仍 不会停止追求。尽管在实现梦想的过程中,会有很多挫折和无数的 磨难,但我仍不会灰心丧气。因为我相信,只有经历地狱般的磨练,才能练出创造天堂的力量;只有流过血的手指,才能弹出世间的绝唱;只有经历困难和挫折,才能实现自己的梦想。 以前,每当我看到科学家们令人瞩目的成就时,总会感到羡慕和敬佩。是他们,推动了社会的发展;是他们,使人民生活水平得到提高;更是他们,为祖国的发展赢来了一个崭新的明天。 因此,我想成为一个科学家,成为一个对国家有贡献的人,成为这个国家的栋梁。每当我看到浪费时间的人时,我会为他们感到惋惜;每当我看到灰心丧气的人时,会为他们感到悲哀;每当我看到不 务正业的人时,我会感到愤恨。因为他们没有看到自己的价值,没 有属于自己的梦想。这样的人生,是没有意义的人生。 而我,至少有一个梦想,一个目标。有了这个梦想,我就会一直努力下去,永不放弃。有了这个梦想,就等于把握了自己的人生航向,不会再迷失方向。有了这个梦想,就好象一盏明灯,照亮了我 前进的道路。一直通往胜利的顶峰。 我有梦,中国也有梦。我的梦想,用自己的智慧站在时代的顶峰,中国的梦,用自己的勤劳,自立于世界之上!为了这个梦想,他发奋,他图强,他忍受无法言语的苦难,只为自己可以挺起胸膛!地震来了,

不怕,他有的是铁一般的脊骨,洪水来了,不怕,他有的是山一般 的胸膛!奥运会来了,不怕,他有的是腾飞的翅膀!有梦的人,才是 真正的人,有梦的国,才是真正的国!我的梦就是国的梦,我的梦, 成为科学家,为国家尽力,国的梦,繁荣富强,让我们幸福! 我的中国梦演讲到此结束,谢谢大家! 中国梦也是我的梦。我生在中国,长在中国,读过中华几千年的历史,曾为之激动,忧伤,悲愤,骄傲,曾为之食不能安,夜不能寐,,中国已与我紧密的联系在了一起,我为中国伤心,为中国欢乐。我还记忆犹新那句话:犯我大汉天威者,虽远必诛。它深刻的 体现出我中华民族,我大汉的骄傲与荣耀,或许很狂妄,或许很嚣张,但它却让我深深为之感动,为了中华的荣耀,我可以吃苦,可 以受累,甚至我可以献上我微不足道的生命,可就是这份愿意,让 我为中国喝彩,让我对中华民族更加钦佩,对中华历史更加热衷。 或许,我说的对;或许,我说的不对,但是我想认同我的人总是有的,我想这么做的人总是有的! 中国梦,到底是什么,我仔细地思考过一番,我想中国梦应该是振兴中华的梦想。虽说我们消沉过几百年,但是我们也荣耀过几千年,所以我们中华民族最不缺少的便是一种资质,一种让我们曾经 荣耀过几千年的资质,所以我不认为我们与其他民族相比有任何的 不如之处,所以我相信认清现实之后的我们必将会取得成功,必将 会实现我们近年来振兴中华的梦想。 霍去病将军匈奴未灭,何以为家。诸葛亮鞠躬尽瘁,死而后已。周恩来为中华崛起而读书...... 这些历史上让人怀念的伟人们,都有一个和中国梦一样的梦。霍去病将军将自己的一切都献给了中华民族的安危与荣耀,虽说他并 不完美,但瑕不掩瑜,他守护大汉,永不后悔,留下了封狼居胥的 佳话。至于诸葛亮很多资料认为罗贯中是亲蜀派将蜀国的人物进行 了美化,比如历史上根本没有他三气周瑜的事情。但是罗贯中为什 么这么写,我个人认为除了刘备得民心之外,还有一点,那就是蜀 汉一称,正因为蜀国在后面加上了一个“汉”,赢得了更多人的偏

为实现中国梦做贡献_小学生征文

向着中国梦,前进! 学校:南召中心校务滋小学班级:五年级 学生:李斯言 指导教师:屈海川

向着中国梦,前进! 梦,通常指人们的理想。每个人都会做梦,每个人都会有自己的梦想。美羊羊的梦想是能够在青青草原上尽情地玩耍,光头强的梦想是把大森林里的树木都砍光。我的梦想,可以是一个漂亮的发卡,一盒可口的点心,是考试后的100分,妈妈对我夸奖的笑容……可今天,老师说,我们每个人不但要有自己的梦,还要有中国梦。 那么,什么是中国梦呢?中国梦是建立在祖国发展基础上的,是对祖国有利的梦,每个人的中国梦都不相同,有大有小,但它们又都有相同之处,那就是都怀着一颗为祖国作出贡献的心,对人民有功利的心。我想中国梦还应该是国家富强,小朋友们都有新衣服穿,有变形金刚、芭比娃娃;民族团结,不会有战争与饥饿;大人们高高兴兴地上班,孩子们能够一块儿在草地上做游戏。但我觉得,最重要的是要建设一个美丽、洁净的家园,那就是天蓝、地绿、水清、气爽的美丽中国。没有地沟油,没有沙尘暴,没有禽流感…… 建设美丽中国,就要从小事做起。在学校,看到地上有纸屑,我会主动弯腰捡起;看到水龙头滴水,我要主动上前把它关紧;看到有人说脏话,我会及时上前制止。春天来了,我拉着爸爸妈妈买树苗,到附近山坡上植树,因为我知道,绿化造林是防治大气污染的一种有效方法。我还要宣传环保知识,动员更多的人加入环保队伍,让天变得更蓝,水变得更绿。我还会在村里钉上一块“爱护环境、人人有责”的警示牌,让全村的人跟我一起行动起来,保护我们的环境、净化我们的环境。我知道我一个人,一家人的力量很微薄,但是如果全中国的孩子都能行动起来,每个中国家庭都行动起来,那就会汇成强大的环保能量,才能建设好美丽中国。 每个中国人都有着自己的中国梦,只要每个人能为这伟大的梦想贡献出自己的力量,哪怕是微不足道,但当所有的贡献汇集到一起,将会是一股多么强大的力量,这股力量会把中国推向更美好的明天,只要人人行动起来,我相信建设美丽祖国这个中国梦将会很快实现。 建设美丽祖国——这个伟大而又现实的中国梦,我会行动起来的,爱护环境、节约用水……,我要向着中国梦,前进!

中国梦我的梦主题演讲稿

中国梦我的梦 每当听着国歌,看着鲜艳的五星红旗冉冉升起,我总是热血沸腾,梦想着为国家的富强贡献自己微薄的力量,纵然力量微薄,但只要大家一起为我们美丽的祖国做贡献,就可以使她变得更强更美。梁启超先生说过:“少年富则国富,少年强则国强”,我们年轻人的命运与国家的命运息息相关,同样,强国梦与我们的梦想荣辱与共,实现中国梦,就是我的梦。 实现中国梦就需要我们紧握梦想的缰绳。 实现中国梦需要有正确的方向,找到了方向,勤加努力就会成功;找不到梦想的希望,或者妄自堕落,或者碌碌无为,都会抱憾终生。如果说梦想是马,那么我们就需要抓住梦想的缰绳,找到方向,加速驰骋。爱国和报国的信念就是我们梦想的缰绳,古往今来,多少仁人志士为了爱国报国前仆后继,他们用生命铸成了中华民族的不倒长城,他们用热血染成了中华民族的鲜红旗帜。想起爱国报国,我们仿佛看到岳飞在战场上高举精忠,文天祥在狱中延续丹青,仿佛看到张自忠横刀立马,杨靖宇挥斥峥嵘;先烈们为我们指明了中国梦的方向,我们更应该延续我们的梦想,紧握梦想的缰绳,让爱国之心长存,让报国之心长青,才能让梦想之门长开。 实现中国梦就需要我们握紧梦想的双桨。 实现我们的梦想就需要坚强的意志和毅力,任何道路都会有坎坷和挫折,实现理想的道路更不是一帆风顺,无数的困难和险阻会阻挠

我们的梦想,无数的选择和诱惑会改变我们的梦想,而无数的打击和失败会气馁我们的梦想。要想成功实现梦想,就需要我们紧握梦想的双桨,齐心协力,奔向成功。如果说梦想是船,那么意志和毅力就是船的双桨,握桨快行,可以接近梦想;搁桨不走,只能望洋兴叹。邓小平为了改革开放历经经三上三下,仍然矢志不渝地坚定梦想,终于取得了改革的成功;邓稼先为了强国之梦历经艰苦卓绝,仍然矢志不渝地坚定梦想,终于实现了我国自有核技术的成就。所以说梦想需要坚强的意志和毅力,“不弛于空想,不鹜于虚声”,一切尽在行动中。 实现中国梦就需要我们补充文化的能量。 邓小平同志说:“科学技术是第一生产力”,当今世界,任何事业没有先进的科学技术做支撑都很难取得进步,我们年轻人的梦想更是如此,如果没有始终不断地吸收先进的科学知识,在实现成功的道路上,我们就显得力不从心;而有了知识储备,就可以如借东风。如果说梦想是车,那么科学和文化就是能量,有了能量,梦想之车全速前行,失去能量,梦想之车不再启动。历史上我中华民族闭关锁国,导致科学技术得不到学习和推广,在同列强的斗争中,屡战屡败深受凌辱;后来我们站起来了,尊重知识尊重科学,有了自己的火箭卫星和自己的导弹核弹,我们才站直腰板,成了自己的主人。可见,梦想需要知识,需要我们不断地学习和创新。 每个年轻人的梦想就是报效国家,所有年轻人的梦想合起来就是我们民族复兴的中国梦,不知不觉中我发现我的梦想早已同国家的梦想联系起来,而且紧密不可分离。我们经历了辉煌的古代文明,屈辱

中国梦我的梦演讲稿400字

中国梦我的梦演讲稿400字 篇一 尊敬的各位评委,亲爱的同学们: 大家上午好!我是来自祁县中学校高一年级的参赛选手李沁,今天我演讲的题目是《中国梦,我的梦》。 梦想,是一个人生活的动力,梦想,是一个人前进的方向。梦想,周而复始;梦想,锲而不舍。中华民族五千年的历史传承着一个长梦,几经沉浮,时至今日汇聚成了一个梦——中国梦。 翻看中国的历史,我们无一不对古老的中华民族感到骄傲,那一串串的科技之光在世界的各个角落熠熠发光;我们无一不对先贤青少年时期的中国梦去仰望:*"指点江山,激扬文字,粪土当年万户侯",*"面壁十年图破壁,难酬蹈海亦英雄",周树人"寄意寒星荃不察,我以我血荐轩辕";我们无一不对革命先烈的精神所打动,他们抛头颅,洒热血,不畏强敌,保家卫国,绝不容他人染指。

中国梦,我的梦。"墙角数枝梅,凌寒独自开",我想做一朵梅花,傲立雪中,不屈不挠,自强不息。曾经为了中考,操场上的挥汗如雨,考场上跃动的笔杆。今日站在这里,成为祁县中学实验班的一员,继续追逐我的大学梦。古人云:"行胜于言"。月已高悬,夜已人静,仍有挑灯苦读,思想之花穿行于夜空,几何图案填充星宿,梦的翅膀到我飞行。认真,勤奋,坚持,顽强,把握高中生活,珍惜一点一滴,是我的梦,也是我们的梦。我们用汗水浇灌梦想之花,让它开放,散发芳香。是的,我们正在一步一步的绘着中国梦。试问:少年无梦,国哪有梦?少年无志,国哪有志?少年不强,国哪能强? 地平线上冉冉升起的太阳,如我们;海上掀起的层层浪花,如我们;那愈燃愈旺的火焰,如我们,我们肩负着中华民族伟大复兴的历史重任。让梦如黑夜中的星星,指引我们前行;让梦如火,照亮前方的路;让梦如光,绽放无限魅力。 当今世界,经济全球化,科技高速发展,竞争力不断加强。中国梦,让中国强大,让中国发展,让中国雄鸡挺起胸膛,让亚洲雄风吹遍世界。为此,让我的梦,让我们的梦,共同点燃中国梦,让我们用知识开启圆梦引擎,用品格筑牢圆梦基石。

中国梦我的梦国旗下演讲稿范文

中国梦我的梦国旗下演讲稿800字范文篇一 亲爱的老师、同学们: 人类不能没有梦想,自古至今,从女娲造人到人类飞天。 梦想,是生活的航标;梦想,是美好的憧憬;梦想,是理想的翅膀。拥有梦想,才会拥有未来。我的梦想是——三尺讲台写春秋。 一根教鞭,指点江山,上下几千年,纵横几万里。一只粉笔,绘出大千世界,五彩纷呈,写不尽苦辣酸甜。一块黑板,倒映着历史的叱咤风云,显露着文字艺术的魅力。 是谁,用自己的汗水浇灌着祖国的花朵? 是谁,用自己的光芒指引少年前行的道路?是谁,用自己的言行引导我们,走向同样的一方讲台?是那辛勤的园丁,是那化为灰烬的蜡烛,是那人类灵魂的工程师,他们都有一个响亮而光辉名字:老师! 每每看到丁老师在讲台挥舞着教鞭,娓娓动听地讲着一篇篇美文,我的心都充满着一股莫名的激动。正是由于班主任丁老师的言传身教,我爱上了老师这个职业,爱上了这个“春蚕到死丝方尽,蜡炬成灰泪始干”的职业,爱上了这个

“化作春泥更护花”的职业。 假如有一天我的梦想实现,站在了讲台上,真正的成为一名老师。我会和同学们成为知心的朋友,走进他们的内心,倾听他们的喜怒哀乐,关注他们学习和心理健康。我会给同学们少布置一些作业,让他们有一定的休息和玩耍时间,第二天能够精神抖擞地听讲。 我会把全部的爱献给学生。我国古代教育学家孔子主张对学生施以“仁爱”,要做到“诲人不倦”,做到“随风潜入夜,润物细无声”。 我也要让同学们与书为伴,以书为侣,多读些对生活和学习有帮助的书,像名著、散文小说这类的。在书中认识斗酒诗百篇的李白,认识有感铁般意志的保尔.柯察金以及坚贞不屈、视死如归的革命先烈,体会我们幸福生活的来之不易,更加珍惜今天的美好生活。 写作离不开素材,我会带领同学们走出教室,去广阔的天地中寻找素材。春天,我会和同学们到野外踏青、放风筝。夏天,我会带同学们去欣赏出淤泥而不染的荷花,向荷花学习它们坚贞不屈的品质。秋天,我会带同学们去田野里,看雪白雪白的棉花,看高举红火把的高梁,看裂开嘴笑、露出

中国梦我的梦演讲稿范文3篇

中国梦我的梦演讲稿范文3篇 篇一:中国梦我的梦演讲稿 展翅高飞,是鸟儿的梦;自由奔放,是骏马的梦:百花盛开,是春 日的梦;教书育人,是我的梦。 梦伴随着我们每一个人。梦是美丽的,是我们每个心中最真实的 写照;梦是我们每个人前行的动力。中国梦,我的梦—教师梦。 清晨,当第一缕阳光照射着我的时候,我迎来了崭新的一天,在 这个天中,我和我的学生们一起经历吃饭、睡觉、学习。日复一日, 不知不觉我已和他们一起走过了365个日日夜夜。在这期间,我抱怨、埋怨过,试图想要放弃、逃脱过;可就在我真正想要放弃的那一霎那, 我才发现我不能,不能这样做。在心底的一个声音告诉我:要坚持, 为了梦想,再坚持一天、一个星期、一个月。逐步地,我意识到了我 已经放不下了,我深深的爱上了他们,爱上了这个职业。[莲山课件 ] 我所带的班级就是一个剧组,我就是导演。我想要导出充满时代 气息的连续剧:团结、紧张、严肃、活泼是它的主调;理解、友爱、开拓、创新是它的主色,爱这个集体和被爱这个集体是它的主要故事。 作为导演,我精心设计着生动的情节、典型的角色,动人的故事奉献 给63位演员。 想到自己培育的是祖国的花朵,祖国的未来,我怎么能够放弃, 应该引以为豪。想到自己要把知识的种子传播给孩子们,让他们学习 到知识,长大后去实现自己的梦想;想到将是用自己的知识灌溉祖国的 未来;将是用自己的心血去呵护明天的希望,使他们健康快乐地成长。 心中不免泛起幸福的涟漪。 老师就是奉献的代名词。作了老师的我才深深体会到了奉献的快乐。看到孩子们脸上洋溢着幸福的笑脸,听到家长们满意的答案,我 顿时感到自己身上所肩负的责任,任重而道远。为了祖国的未来,为

如何为实现中国梦做出自己的贡献

论青年大学生如何为实现中国梦做出自己的贡献 首先,作为一名青年学生,中国梦归根结底是全体中国人的梦,也是我们每一名青年学子的梦,要实现中华民族的伟大复兴这一中国梦,需要广大青年的接力奋斗。作为新时代的青年,不但心中要有梦,更要坚定这个梦,怀着坚定不移的信念,紧跟党的步伐,不断提高自身素质,勇于创新,艰苦奋斗,锤炼出高尚的品格,成为祖国栋梁。青年学生一定要坚定理想信念,勤奋学习练好本领,提升道德品格和人文素养,在实现中国梦的伟大实践中贡献青春和力量。吾辈青年应时刻铭记“少年强则国强”的警言,培养社会责任感、创新精神、实践能力,为实现中国梦而努力。 其次,明确个人目标,成就自身价值。作为年轻人,在基层工作,要满怀激情,敢于担当,敢于创造,用‘两个百年’的目标激励自己顽强奋斗、艰苦奋斗、不懈奋斗,奋勇投身中国特色社会主义事业伟大实践,才能为实现“中国梦”发挥生力军作用,用“青年梦”托起“中国梦”。 再有,努力学习,掌握本领,为实现中国梦而贡献青春,这是我们当代青年的历史使命 .我们这一代大学生是祖国的未来与民族 的希望,是社会上富有朝气、富有创造性、富有生命力的群体。实现建党建国“双百”目标的宏伟蓝图,进而实现中华民族的伟大复兴成为时代赋予当代青年的历史使命。 最后,勇于创新,在创新中发展。时代在变迁,社会在进步,陈旧的思想已经适应不了只要广大青年胸怀理想,只有创新才能实现我们的梦想,最终实现民族复兴。“天行健,君子以自强不息”, 每个人都有一个只属于自己的梦,中华民族是一个充满着朝气的民族,新时期的中国是我们实现梦想的时代,所以年轻人的梦想与国家民族兴衰荣辱紧密相连,要勇敢追求自己心中的梦想,并付诸行动,为实现“中国梦“增添新的活力。 忧患增人慧,艰难玉汝成。当代大学生要积极响应党的号召,把个人的前途命运与国家和民族的前途命运紧密联系起来,努力学习,掌握本领,艰苦奋斗,自觉磨练自己,积极投身中国特色社会主义伟大事业中,让我们的青春在为实现“中国梦”的过程中焕发出更加绚丽的光彩! 我们可以自信地说,在不久的将来,更多的人会实现他们的“中国梦”!在实现民族复兴的中国梦的征程上,只要我们坚定信心,一步一个脚印,实实在在做实事、做好事,我们的中国梦也终将会实现!

小学生我的梦中国梦演讲稿10篇

小学生我的梦中国梦演讲稿10篇 亲爱的老师、同学们: 大家好! “林花谢了春红。太匆匆,无奈朝来寒雨晚来风。胭脂泪,留人醉,几时重,自是人生长恨水长东。”感叹的是时光的流逝。岁月 的翩然轻檫,无可奈何。“人生若只如初见,何事秋风悲画扇。等 闲变却故人心,却道故人心易变。”是对人事沧桑的感概:“苟利 国家生死以,岂因祸福避趋之。”驾长车踏破。贺兰山缺。壮志饥 餐胡虏肉,笑谈渴饮奴血。这是林则徐和岳飞的爱国宣言,不算激 昂也不算壮阔,却表达了他们深深的爱国之情,在我心里。这些文 化的结晶代表了中国一代人的思想,有的是相思情,有的是人生叹。而有时。却是中国梦。 90后的我们奋发图强,乐以忘忧,青灯黄卷,宵衣肝食,是的,生应无所息。王维曾经在人间词话中说过三重境界;一是“衣带渐宽 终不悔,为伊消得人憔悴”;二是“昨夜西风凋碧树,独上高楼,望 尽天涯路;三是”众里寻他千百度,蓦然回首,那人却在,灯火阑珊处。’在我看来,我们的求学道路,我们的爱国道路,都需要经过 这三重境界,方能上善若水,泽万物而无言。一叶绽放一追寻,一 花盛开一世界。我们的中国梦,是和平,是暖,是希望。是燕在梁 间的呢喃,是人间的四月天。 亲爱的老师、同学们: 大家好! 很高兴能站在这里演讲,今天我演讲的题目是《我的中国梦》。 当浦江的浪花摇落满天繁星,点亮我们身后中国馆敞开的门窗,我们在流光异彩的世博园里,我的梦在长城上生长,这梦想的长城,正在延伸祖先的荣光,长城的脚下,是五千年文明的土壤,长城的

天界,是一个名叫未来的地方,下一个百年,我的梦,中国梦,花开何方,来吧!同学们!请打开心中最美丽的翅膀,这一刻让我们一起飞向北京,在那万里长城之上对话星空,和世界一起分享, 今夜当世博园的灯光相逢长城的目光,我们要在这里集合起所有属于未来的梦想,哪怕只是一道稍纵即逝的流星,也请关注它,也许哪一天就能触发出新世界的曙光,请未来登上长城吧!一起收获中国少年永无止尽的梦想,少年智则中国智,少年强则中国强,我的梦是中国梦,中国的梦是我们的梦,要实现梦想,不单单要靠自己的努力,更重要的需要同伴多给我鼓励,给我帮助,理解,支持,也就是这份理解,支持,最终会实现我们的梦想。坚持成就梦想。 人可有很多梦想,但是可能实现一个就足够了,只不过是刚刚才第一步跌到了,为什麽就不愿爬起来?明天总要面对,明天太阳还要升起,我们如果还想继续走下去的话,那只能换一条路。天空不留鸟飞的痕迹,但我已经飞过,如果我们尽力了,却依然抵达不了梦的彼岸,我们无悔,因为我们至少奋斗过,如果我们付出了,得到的却不成正比的收获,我们无悔,以为至少我们付出过,此刻,唯有向前,唯有向前 小时候,其实变换梦想没有关系,你需要的是不断的去想,不断地去想快乐的事情,其实梦想不必要很大,只需要觉得这很现实,这你能做得到,但第二个是梦想跟眼泪和汗水,是在一起的,假如梦想离开了汗水的眼泪,那就变成乱想,空想。 亲爱的老师、同学们: 大家好! 今天我演讲的题目是《中国梦,我的梦》。 什么是梦?什么是中国梦?历史的点点滴滴如散落在偌大沙滩上的沙石贝壳,我悄悄走过,贪婪地看着这些晶莹宝贵的财富,时而拾起一两颗打动心灵的贝壳,寄出一份梦想,蹲下投放。中国梦,流淌在岁月。

大学生为实现中国梦做出自己的贡献

论大学生为实现中国梦做贡献 随着社会主义经济体制的逐步建立和改革开放的不断深入,我国社会各个领域发生了巨大的变化,对当代大学生的人生价值取向也直接产生了影响。如何进一步加强对当代大学生的思想政治教育,营造积极向上的校园文化,为实现中国梦做出贡献,这成为当前高校思想政治工作的一项重要任务。 中共十七大报告中指出,要建设社会主义核心价值体系,增强社会主义意识形态的吸引力和凝聚力;要切实把社会主义核心价值体系融入国民教育和精神建设全过程,转化为人民的自觉追求。社会主义核心价值体系的提出,为大学生思想政治教育注入了新的血液。大学生作为充满理想、活力和激情的优秀群体,理应成为社会主义核心价值观学习和践行的“先行军”。 一、大学生应培养社会主义核心价值观 核心价值观是一个社会中居统治地位、起支配作用的核心理念,也是一个社会必须长期普遍遵循的基本价值准则,具有相对稳定的特点。社会主义价值观是对社会主义价值的总的看法和最根本观点。在党的十七大召开之前的十六届六中全会上,党第一次提出了社会主义核心价值体系这一科学命题,并对社会主义核心价值体系的科学内涵作了界定。社会主义核心价值体系包括四个方面的基本内容,即马克思主义指导思想、中国特色社会主义共同理想、以爱国主义为核心的民族精神和以改革创新为核心的时代精神、以“八荣八耻”为主要内容的社会主义荣辱观。 青年大学生正处于人生观、价值观形成的关键时期,他们思想观念逐渐趋于成型,但仍具有较大的可塑性;他们接受新鲜事物的能力很强,但鉴别力明显欠缺。赢得青年就赢得未来,我们以社会主义核心价值观加强大学生思想教育,具有鲜明的时代意义和现实意义。应从以下几个方面进行社会主义核心价值观教育: 1.夯实思想政治理论课教学基础。高校思想政治理论课是大学生思想政治教育的主渠道,加强大学生思想政治理论课教育教学,首先科学的课程设置是其基本环节。应充分体现当代中国马克思主义发展的最新成果,全面反映党领导人民建设中国特色社会主义的生动实践和基本经验,全面反映在毛泽东思想、邓小平理论和“三个代表”重要思想、科学发展观指导下哲学社会科学研究的最新进展。 2.提高教师素养,通过教师的言传身教感化学生 教师承担着培育社会主义事业的建设者和接班人的历史重任,对大学生进行社会主义核心价值观教育,高校教师不论是思想政治课教师还是专业课教师要在提高专业知识素质的同时,还要加强政治学习提高政治素质。专业素质是“才”,政治素质是“德”,是教师职业道德中的思想品德。这两个方面是相辅相成,相互促进的。教师加强和提高自身“德”方面的修养,不仅使自己成为一个道德高尚的人和合格的教育者,重要的是通过自己的教育活动和良好的思想、道德、品质、人格把学生培育和感化成德才兼备的人才。 3.树立优秀大学生典型,通过学生感化学生 心理学家认为,人的行为往往被其内在动机和需要所驱动。树立典型,塑造榜样就是为了提供行为参照,确立行为目标。学习者有了目标参照,进而努力使自己的行为与榜样的行为一致。大学生身边的优秀典型,他们的精神比较容易为大学生们所接受。对校园中在思想品德方面涌现的优秀大学生典型要及时大力宣传,使良好的风气在大学校园中弘扬,成为大学校园中主导地位的风尚,使大学生们的行为有可仿效的行为作参照,从而见贤思齐。 二、营造积极向上的校园文化 党的十七大在关于党的建设的部署中,明确提出在党的基层组织和党员中深入开展创先争优活动。探索如何加强校园文化建设以推动创先争优显得尤为重要。校园文化建设是学校稳步发展的保证。校园文化建设的出发点和落脚点是学生。学生是校园文化建设的主体,加强

中国梦我的梦(大学生中国梦演讲稿)

中国梦我的梦(大学生中国梦演讲稿)中国梦我的梦(大学生中国梦演讲稿) 时玉婷 梦是什么? 从心理学的角度回答,弗洛伊德认为,梦是有意识看无意识的一扇窗子。从医学的角度回答,梦是脑在作资讯处理与巩固长期记忆时所释放出的一些神经脉冲,它是被意识脑解读成光怪陆离的视、听觉所造成的。从梦学的角度回答,梦是人睡眠时的一种心理活动,梦中离奇的梦境是因人睡眠大脑意识不清时对客观事物的刺激产生的错觉引起的。总之,梦是一种主体经验,是人在睡眠时产生的影像、声音、思考或感觉,通常是非自愿的。 那么梦想是什么? 有人说,梦想等于理想;有人说,梦想就是空想、幻想;还有人说,梦想是期望达到的一种高度。而我说,梦想是心灵的思想,是对美好事物的憧憬和渴望。因此,梦想不是梦。 陈信宏曾说:“如果我不在梦想里,就是在通往梦想的路上。”是啊,谁不是这样呢?每个人都有理想和追求,有人向往自由自在的日子,也有人喜欢平平淡淡的幸福,还有人追求富贵奢华的生活。这些不都是美好的理想吗?或许有一天,他们过上了曾经梦想的生活,那么在通往梦想的这条路上,他们已经到达了终点。一路上,有阳光的照耀,亦有风雨的陪伴,他们该是不孤单的吧?或许有的人还在路上艰难的行走着,他们该是充满力量的吧?又或许这条路根本没有尽

头,但路上的风景确实是美丽的吧? 我也有梦想,而且我有很多梦想。 小时候我喜欢看电视,每当看到英雄侠客的出现,顿时肃然起敬,好想成为他们那样的人,可以无拘无束,浪迹天涯,该是多么自在啊!每当看到那些英姿飒爽的士兵在战场上冲锋陷阵的身影,就好渴望将来能够像他们一样保家卫国,做国家的坚强捍卫者。每当看到那些威武严肃的警察,又会以他们为榜样,憧憬未来如他们一般一身正气,为社会惩恶扬善,向人们弘扬正义。那时的想法真的好单纯,只是想想,就会觉得幸福。 后来我上小学了,认识了很多小朋友,我们一起玩耍,一起做作业,他们陪伴我度过了快乐的童年。但唯一令我遗憾的是,父母没能看着我一点点长大。因为农村人唯一的生活来源就是那点微薄的耕地收入,然而家里开销大,经常入不敷出,所以父母只好去外地打工挣钱来填补家用。至此,父母踏上了漫漫的打工之旅。那时的我还不明白父母背着包裹要干嘛,直到思念的滋味冒上心头,我才开始慌张,才哭着着急寻找他们。为此,爷爷奶奶花了好多时间来哄我,他们对我说,爸妈是出去挣钱了,只要你乖乖的,他们就会很快回来,并且会给你买好多礼物。我渐渐接受他们的说法,不嚷嚷着找他们了,但心里却更渴望见到他们,想着他们回来时带的礼物是什么。就这样盼着盼着,终于要过年了,父母该回来了,那段时间的我就会特别高兴。而每次爸妈归来时,都给我买了好多吃的和玩的礼物,有时还有漂亮的衣裳,看着爸妈脸上的笑容,我也幸福地笑了。所以,在小学的时

大学生为中国梦可以做什么

青年大学生如何为实现中国梦作出贡献 大学生是“中国梦”的寄托者,“中国梦”的本质内涵是实现国家富强、民族复兴、人民幸福,而青年学生是祖国的未来、民族的希望,是党和人民事业发展朝气蓬勃的推动力量。我们中 国人,几千年来,做了三个梦:天下梦,国家梦,个人梦。天下梦就是大同梦,国家梦就是强 国梦,个人梦就是幸福梦。这些梦是互为前提,彼此成全的。中国的道路,不是理论问题,是 实践问题。这是易中天教授在北大的演讲中所提到的中国梦!现在大家都在讨论中国梦。我 认为,实现中华民族伟大复兴,就是中华民族近代以来最伟大的梦想。这个梦想凝聚了几代 中国人的夙愿,体现了中华民族和中国人民的整体利益,是每一个中华儿女的共同期盼。当 代大学生承担历史的重任,是社会上富有朝气、充满生命力的群体。良好的形象不仅是大学生 成才的一个重要方面,也是社会对大学生的要求。同学们要适应时代要求,自觉地塑造积极健 康向上的崭新形象。所以,必须要做到以下几点:第一,大学生应培养社会主义核心价值观。核心价值观是一个社会中居统治地位、起支配作用的核心理念,也是一个社会必须长期普遍 遵循的基本价值准则,具有相对稳定的特点。社会主义价值观是对社会主义价值的总的看法 和最根本观点。在党的十七大召开之前的十六届六中全会上,党第一次提出了社会主义核心 价值体系这一科学命题,并对社会主义核心价值体系的科学内涵作了界定。社会主义核心价值 体系包括四个方面的基本内容,即马克思主义指导思想、中国特色社会主义共同理想、以爱 国主义为核心的民族精神和以改革创新为核心的时代精神、以“八荣八耻”为主要内容的社会主 义荣辱观。大学生正处于人生观、价值观形成的关键时期,他们思想观念逐渐趋于成型,但仍 具有较大的可塑性;他们接受新鲜事物的能力很强,但鉴别力明显欠缺。赢得青年就赢得未来,我们以社会主义核心价值观加强大学生思想教育,具有鲜明的时代意义和现实意义。第二, 当代大学生应该努力学习勤奋刻苦,善于合理利用学习时间,在学习中起表率作用。这是我 作为一名学生党员首先应该做到的,在努力让自己做到优秀的同时,和大家共同进步,经常 交流学习经验,不保留,乐于帮助后进的同学。另外,提高自己在知识的摄取方面的宽度和 深度,在学好专业知识的同时还要注意个人文化修养的培养,增加自己的知识面,丰富自己 的文化底蕴。与此同时,也应该学好理论,提高素质,在政治上带动同学进步。第三,增强 党性修养,增强党性修养。要有坚定的马克思主义信仰,要讲政治道德,要自觉提高政治道 德修养。要讲大局,在认真学习和积极宣传党的先进思想、政治理论的基础上,要从实际出发、发挥带头作用,勇于实践“三个代表”重要思想,积极参加社会实践,在实践中检验所学 的理论知识,并不断提高自己的思想修养和理论水平。 第四,追求真理、善于创新。当代大学生应当发挥朝气蓬勃、思维敏捷、敢为人先、最少 陈旧观念、最多创造活力的诸多优势,坚持追求真理的精神,不断夯实科学文化知识基础,掌 握善于创新的技能,努力提高持续创新能力,使自己成为祖国和人民需要的、富有创新精神 的高素质人才。要善于从马克思主义理论中汲取营养,树立科学的世界观,把握正确的方法论,努力做科学探索和创新的先锋。第五、德才兼备、全面发展。当代大学生要掌握扎实的专业 基础知识和最前沿的科学文化知识,以造福国家人民。没有坚实的科学知识,就不能发展经济,更谈不上建设社会主义现代化。同时,要坚持以德为先,德才兼备。中目前社会上出现的社会 腐败和高科技犯罪等现象,为人们敲响了正确把握德才关系的警钟。对当代大学生来说,“德” 绝不是可有可无的。德才兼备是衡量大学生全面发展的一个重要标准。第六、知行统一、脚 踏实地。当代大学生要努力将书本知识和实际行动密切联系起来,塑造“知行统一、脚踏实地” 的良好形象。“知行统一”式和道德人格紧密结合在一起的。一个人能否做到言行一致,是他能否在立身处世等方面取得成功的重要条件。我们在日常的学习和生活中,要时时提醒自己,比 如应该做的事情,认识到了,但是是否做到了;应该改正的错误,认识到了,但是否改正了。一个大学生如果能够从身边的事情做起,做到言行一致,老老实实做人,踏踏实实做事,他的 道德人格必然会不断完善。我们应该从现在做起,从我作起,在平时生活中严格按照共产党 员的标准要求自己,多关注国家大事,刻苦学习,努力奋斗,争取成为国家的有用之才,将 来为祖国的社会主义现代化建设作出自己应有的贡献,为全面建成小康社会,实现中华民族的 伟大复兴贡献积极力量。

相关文档