Centrolepis Labill.

Genus

Angiosperms > Poales > Restionaceae

Characteristics

Plants annual or perennial. Leaves radical or distichous, eligular. Inflorescences a head consisting of 2 opposite, inequilateral, 1-11-flowered bracts. Flowers hermaphrodite, sessile, if several, alternate and inserted in 1 or 2 rows, flowering in a centrifugal sequence; each flower consisting of 1-3 glumes, 1 stamen and 2-20 carpels. Glumes 1 to 3, hyaline, unequal in length, erose at the apex, monostichous and dorsal, very rarely opposite (ventral and dorsal). Stamens 1, dorsal (in the median) between the carpels and the glumes; anther 1-celled, dorsifixed near the base. Carpels 2 to 20 to a carpophore, sac-like, superposed in 1 or 2 rows, free or connate, the pairs transversal; style one to each carpel, terminal, free or united at the base, twisted or curled at the tips, adaxial, apical part papillose, stigmatic. Fruiting carpels dehiscing with a lengthwise, lateral (outward) slit.
More
Fls ∞, in a complex "spike" within 2 ± opp., unequal, glume-like bracts. Partial infls (pseudanthia) 1–8–(20) within each bract, each with 1–3, or 0 hyaline scales. ♂, 1 or 0 per pseudanthium with 1-celled anther. ♀, (1)–2–20 in each pseudanthium, ± connate and superposed in 1–2 rows, all styles free or ± connate at the base. Fr. dehiscing longitudinally. Small herbs, tufted and annual, or perennial and cushion-forming. Lvs linear-filiform and crowded at base of stem, or, in perennial cushion plants, densely imbricate up the stem, with stiff, terete, compressed or channelled lamina. Flowering stems slender, terminated by the 2 floral bracts and "spike". About 25 spp. chiefly in Australia, extending through Malaysia to Southeast Asia. Three N.Z. spp. are endemic and C. strigosa occurs also in Australia.
Small herbs, tufted annuals, or cushion-forming perennials. Leaves linear-filiform and crowded at base of stem, or, in perennial cushion plants, densely imbricate up stem, with stiff, terete, compressed or channelled laminae. Flowers numerous, in a terminal complex "spike" within 2 ± opposite, unequal glume-like bracts. Pseudanthia (partial inflorescences) within each bract 1-8-(20), each with 1-3, or 0 hyaline bracteoles. Male flowers 1 or 0 per pseudanthium with 1-celled anther. Female flowers (1)-2-20 in each pseudanthium, ± connate and superposed in 1-2 rows, all styles free or ± connate at base. Fruit dehiscing longitudinally. Spp. c. 25 of Australia, N.Z., Malaysia and S.E. Asia. C. strigosa of Australia is now regarded as adventive in N.Z., the other 3 N.Z. spp. are endemic.
Herbs, small, annual or perennial. Hairs unbranched or absent. Leaves basal with dilated membranous sheathing bases and linear to subulate 1-veined laminae; ligule absent. Inflorescence a terminal cymose head, often scapose on a single erect internode, enclosed by 2 primary bracts on a very short rachis. Secondary bracts 2 or 3 per pseudanthium or absent. Flowers arranged in 1–many sessile pseudanthia each comprising 0 or 1 male and 1–30 female flowers. Male flower with capillary filament. Ovaries within each pseudanthium superficially connate, alternating in 2 rows on a false axis (gynophore); styles at least partially free. Fruit compound, of connate 1-seeded follicles dehiscing abaxially. Seed ovoid to fusiform.
Herbs annual or perennial. Leaves radical or distichous; leaf blade linear to filiform. Inflorescence a head subtended by 2 opposite, inequilateral bracts, flowering in a centrifugal sequence. Flowers usually bisexual, 1--13, in 1 or 2 rows when several, sessile. Bracteoles 1--3 per flower, unequal, hyaline, apex erose. Carpels 3--20 per carpophore, in 1 or 2 rows, free or connate. Style 1 per carpel, free or connate at base; stigma papillose. Mature carpels dehiscing longitudinally.
Life form perennial
Growth form herb
Growth support -
Foliage retention evergreen
Sexuality hermaphrodite
Pollination -
Spread -
Mature width (meter) -
Mature height (meter) -
Root system -
Rooting depth (meter) -
Root diameter (meter) -
Flower color -
Blooming months -
Fruit color -
Fruiting months -
Nitrogen fixer -
Photosynthetic pathway -

Environment

Lowland up to c. 4000 m, in marshy places, humid sandy grounds, open heaths, and on rocks, in Malaysia exclusively above 2100 m.I have examined and photographed the two mountain species in North Sumatra and Central Celebes in the field and have observed that both start as small pin-cushions which may occur scattered, but in other cases fuse together in a cushion or turf, which may be later invaded by seedlings of other plants (Fig. 3Fig. 4). Isolated tufts will grow and increase in size but in reaching a diameter over c. 10-20 cm, the central part of the cushion will decay (or mummify) into a bare hole, thus bringing about the remarkable ring-shaped cushion of which a specimen is shown in Fig. 5. I have observed the same phenomenon in several other high mountain plants in Malaysia, notably Oreobolns and Monostachya, with which Centrolepis is often associated in Malaysia. It occurs also in other caespitose plants in Europe and is obviously due to the polarity of the stems causing centrifugal growth with natural decay of the older, central (distal) parts. This puts the cause of the formation of the rings on the same level with those popularly known as 'fairy circles' in toadstools, rather than assuming that the central part of the plant decays because in this portion either necessary trace minerals are exhausted or the decayed matter contains self-poisoning substances. Field experiments should be made to ascertain the non-poisonous nature of the bare central part in the rings. — Van Steenis.
Light -
Soil humidity -
Soil texture -
Soil acidity -
Soil nutriment -
Hardiness (USDA) 8-12

Usage

Uses -
Edible -
Therapeutic use -
Human toxicity -
Animal toxicity -

Cultivation

Mode -
Germination duration (days) -
Germination temperacture (C°) -
Germination luminosity -
Germination treatment -
Minimum temperature (C°) -
Optimum temperature (C°) -
Size -
Vigor -
Productivity -