Heterocarpha Stapf & C.E. Hubb.
Sometimes referred to Drake-Brockmania
Habit, vegetative morphology. Perennial; stoloniferous and caespitose. Culms 1563 cm high; herbaceous; unbranched above. Culm nodes glabrous. Plants unarmed. Leaves not basally aggregated; non-auriculate; without auricular setae. Sheath margins free. Leaf blades lanceolate; narrow; (2)37(9.5) mm wide (and 318 cm long); flat; without abaxial multicellular glands; without cross venation; persistent; ligule present; a fringed membrane (a short rim, with a conspicuous fringe); 11.5 mm long. Contra-ligule absent.
Reproductive organization. Plants bisexual, with bisexual spikelets; with hermaphrodite florets.
Inflorescence. Inflorescence of spicate main branches (3.511 cm long, rather narrow, with short, dense racemes which are reflexed terminally). Primary inflorescence branches (5)812. Inflorescence espatheate; not comprising partial inflorescences and foliar organs. The racemes without spikelets towards the base. Spikelet-bearing axes persistent. Spikelets solitary; secund; biseriate (in two ranks on one side of rachis); subsessile; imbricate.
Female-fertile spikelets. Spikelets 610(14) mm long; adaxial; markedly compressed laterally; disarticulating above the glumes; disarticulating between the florets; with conventional internode spacings. Rachilla prolonged beyond the uppermost female-fertile floret; hairless (glabrous); the rachilla extension with incomplete florets. Hairy callus absent.
Glumes two; more or less equal; shorter than the spikelets; shorter than the adjacent lemmas; dorsiventral to the rachis to lateral to the rachis; hairless (scabrid on the keels); pointed (acute); awnless; carinate; similar (ovate, membranous). Lower glume 1 nerved, or 2 nerved. Upper glume 58 nerved. Spikelets with incomplete florets. The incomplete florets distal to the female-fertile florets. The distal incomplete florets merely underdeveloped. Spikelets without proximal incomplete florets.
Female-fertile florets (4)510. Lemmas similar in texture to the glumes (membranous); smooth; not becoming indurated; entire to incised; not deeply cleft (blunt to slightly notched); mucronate (minutely, from the slight apical sinus); hairy (villous on margins and keels), or hairless (?); glabrous; carinate; without a germination flap; 57 nerved (with 24 very thin nerves between the three heavy ones). Palea present (bent); relatively long; apically notched; awnless, without apical setae; not indurated (membranous); 2-nerved; 2-keeled (hairy between the keels, deeply furrowed). Lodicules present; 2; free; fleshy; glabrous; not or scarcely vascularized. Stamens 3. Anthers short; not penicillate; without an apically prolonged connective. Ovary glabrous. Styles free to their bases. Stigmas 2 (but sometimes with a vestigial third); red pigmented.
Fruit, embryo and seedling. Fruit free from both lemma and palea; small (1 mm long); somewhat compressed laterally. Hilum short. Pericarp free (thin). Embryo large.
Transverse section of leaf blade, physiology. Lamina mid-zone in transverse section open.
Taxonomy. Chloridoideae; main chloridoid assemblage.
Distribution, ecology, phytogeography. 1 species (H. haareri); tropical East Africa. Species of open habitats; halophytic. In maritime sands, in dry rather saline soils fringing Suaeda bush and in dry Acacia bush.
Paleotropical. African. Sudano-Angolan. Somalo-Ethiopian and South Tropical African.
References, etc. Morphological/taxonomic: Stapf and Hubbard 1929.
Special comments. Referred to Drake-Brockmania by Phillips (1974), but in view of the morphological differences, anatomical data are badly needed for H. haareri and B. fragilis. Fruit data wanting. Anatomical data wanting.
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).