Grass Genera of the World

L. Watson and M. J. Dallwitz


Microchloa R.Br.

From the Greek mikros (small) and chloe (a grass).

Including Micropogon Pfeiffer

Excluding Rendlia

Habit, vegetative morphology. Annual (rarely), or perennial; caespitose (low), or decumbent (mat-forming). Culms 5–60 cm high; herbaceous; unbranched above. Culm nodes glabrous. Culm internodes solid. Leaves mostly basal, or not basally aggregated; non-auriculate. Leaf blades narrow (stiff, often convolute); setaceous, or not setaceous; without abaxial multicellular glands; without cross venation; persistent; a fringed membrane (narrow), or a fringe of hairs.

Reproductive organization. Plants bisexual, with bisexual spikelets; with hermaphrodite florets; exposed-cleistogamous, or chasmogamous (?).

Inflorescence. Inflorescence a single spike (slender, often curved, the spikelets inclined to pectinate). Rachides hollowed (crescentic in section), or hollowed and winged. Inflorescence espatheate (but often embraced by the uppermost sheath); not comprising ‘partial inflorescences’ and foliar organs. Spikelet-bearing axes persistent (tough, narrow). Spikelets solitary; secund; biseriate; sessile; not in distinct ‘long-and-short’ combinations.

Female-fertile spikelets. Spikelets 1.7–5.5 mm long; adaxial (but twisted); not noticeably compressed to compressed dorsiventrally; disarticulating above the glumes. Rachilla terminated by a female-fertile floret. Hairy callus present. Callus short; pointed.

Glumes two; more or less equal; exceeding the spikelets; long relative to the adjacent lemmas; lateral to the rachis; hairless; glabrous; pointed (lanceolate-acute); awnless; very dissimilar (the lower asymmetric, cymbiform, keeled, twisted at the base, the upper flat). Lower glume 1 nerved. Upper glume 1 nerved. Spikelets with female-fertile florets only; without proximal incomplete florets.

Female-fertile florets 1. Lemmas not becoming indurated (membranous or hyaline); entire to incised; when entire pointed, or blunt; not deeply cleft (no more than emarginate); awnless, or mucronate; hairy (ciliate on the nerves); carinate to non-carinate; without a germination flap; 2 nerved. Palea present; entire to apically notched; awnless, without apical setae; textured like the lemma; not indurated; 2-nerved; 2-keeled. Palea keels hairy. Lodicules present; 2; free; fleshy; glabrous. Stamens 3. Anthers relatively long; not penicillate. Ovary glabrous. Styles free to their bases. Stigmas 2.

Fruit, embryo and seedling. Fruit free from both lemma and palea; small (0.9–1.5 mm long); ellipsoid; compressed dorsiventrally, or not noticeably compressed. Hilum short. Pericarp fused. Embryo large; not waisted. Endosperm hard; without lipid. Embryo with an epiblast; with a scutellar tail; with an elongated mesocotyl internode. Embryonic leaf margins meeting.

Abaxial leaf blade epidermis. Costal/intercostal zonation conspicuous. Papillae absent. Long-cells similar in shape costally and intercostally; of similar wall thickness costally and intercostally. Mid-intercostal long-cells rectangular; having markedly sinuous walls. Microhairs present; more or less spherical, or elongated; ostensibly one-celled, or clearly two-celled (?); chloridoid-type. Stomata common; 21.6–27 microns long. Subsidiaries triangular. Guard-cells overlapping to flush with the interstomatals. Intercostal short-cells common; in cork/silica-cell pairs (rarely), or not paired (usually solitary); silicified, or not silicified. Intercostal silica bodies absent. Costal short-cells conspicuously in long rows. Costal silica bodies present in alternate cell files of the costal zones; saddle shaped; not sharp-pointed.

Transverse section of leaf blade, physiology. Lamina mid-zone in transverse section open.

C4; XyMS+. PCR sheath outlines uneven, or even. PCR sheaths of the primary vascular bundles complete to interrupted; interrupted abaxially only. PCR sheath extensions absent. PCR cell chloroplasts centrifugal/peripheral (usually), or centripetal (in some individuals of M. caffra?). Mesophyll with radiate chlorenchyma; traversed by columns of colourless mesophyll cells (rarely), or not traversed by colourless columns. Leaf blade adaxially flat. Midrib not readily distinguishable; with one bundle only. Bulliforms present in discrete, regular adaxial groups; associated with colourless mesophyll cells to form deeply-penetrating fans (these sometimes linked with traversing columns of colourless cells). All the vascular bundles accompanied by sclerenchyma. Combined sclerenchyma girders present; forming ‘figures’. Sclerenchyma all associated with vascular bundles. The lamina margins without fibres.

Cytology. Chromosome base number, x = 10. 2n = 40.

Taxonomy. Chloridoideae; main chloridoid assemblage.

Distribution, ecology, phytogeography. 4 species; 3 in Africa, 1 pantropical. Mesophytic to xerophytic; species of open habitats; glycophytic. Savanna, in shallow hard soils.

Holarctic, Paleotropical, Neotropical, and Australian. Madrean. African, Madagascan, and Indomalesian. Saharo-Sindian, Sudano-Angolan, West African Rainforest, and Namib-Karoo. Indian, Indo-Chinese, and Malesian. Caribbean, Central Brazilian, Pampas, and Andean. North and East Australian. Sahelo-Sudanian, Somalo-Ethiopian, South Tropical African, and Kalaharian. Tropical North and East Australian.

Rusts and smuts. Rusts — Puccinia. Smuts from Ustilaginaceae. Ustilaginaceae — Ustilago.

References, etc. Leaf anatomical: Metcalfe 1960; this project.

Illustrations. • General aspect. • Inflorescence. • Inflorescence detail. • Abaxial epidermis of leaf blade. Microchloa indica.


Cite this publication as: Watson, L., and Dallwitz, M. J. (1992 onwards). ‘Grass Genera of the World: Descriptions, Illustrations, Identification, and Information Retrieval; including Synonyms, Morphology, Anatomy, Physiology, Phytochemistry, Cytology, Classification, Pathogens, World and Local Distribution, and References.’ http://biodiversity.uno.edu/delta/. Version: 18th August 1999. Dallwitz (1980), Dallwitz, Paine and Zurcher (1993 onwards, 1998), and Watson and Dallwitz (1994), and Watson, Dallwitz, and Johnston (1986) should also be cited (see References).

Index