The grass genera of the world
Type species: Type: T. hispidum (Thunb.) Desv.
Including Brizopyrum Stapf, Lasiochloa Kunth, Plagiochloa Adamson and Sprague
Excluding Karrochloa, Urochlaena
Habit, vegetative morphology. Annual, or perennial; rhizomatous, or stoloniferous, or caespitose (mostly). Culms 2–60 cm high; herbaceous; branched above, or unbranched above. Culm nodes glabrous. Culm internodes hollow. Plants unarmed. Young shoots extravaginal (in T. uniolae), or intravaginal (the rest). Leaves mostly basal, or not basally aggregated; non-auriculate; without auricular setae (but sometimes hair-tufted at the mouth of the sheath). Leaf blades linear; narrow; 0.3–4 mm wide; setaceous, or not setaceous; flat, or rolled; without abaxial multicellular glands; not pseudopetiolate; without cross venation; persistent. Ligule a fringed membrane, or a fringed membrane to a fringe of hairs; 0.3–2 mm long (the fringe sometimes double, the row of short hairs interspersed with longer ones). Contra-ligule absent.
Reproductive organization. Plants bisexual, all with bisexual spikelets; with hermaphrodite florets. The spikelets of sexually distinct forms on the same plant (sometimes, in T. uniolae), or all alike in sexuality; hermaphrodite and sterile (T. uniolae), or hermaphrodite; homomorphic.
Inflorescence. Inflorescence few spikeleted to many spikeleted; a single spike (in T. uniolae, this distichous), or a single raceme (occasionally), or paniculate (generally, and compact, with short pedicels and branches); not deciduous; contracted; capitate, or more or less ovoid, or spicate (sometimes interrupted); espatheate; not comprising partial inflorescences and foliar organs. Spikelet-bearing axes persistent. Spikelets solitary; secund, or not secund; biseriate, or distichous (T. uniolae), or not two-ranked; very shortly pedicellate, or subsessile, or sessile; imbricate.
Female-fertile spikelets. Spikelets 2–10 mm long; broadly cuneate, or suborbicular; compressed laterally, or not noticeably compressed; disarticulating above the glumes; tardily disarticulating between the florets; with conventional internode spacings. Rachilla prolonged beyond the uppermost female-fertile floret; hairy, or hairless; the rachilla extension with incomplete florets. Hairy callus absent. Callus absent, or short (glabrous).
Glumes two; very unequal to more or less equal; shorter than the spikelets to exceeding the spikelets; shorter than the adjacent lemmas, or long relative to the adjacent lemmas; dorsiventral to the rachis (when orientation ascertainable); hairy (usually, with glandular, often tubercle-based hairs), or hairless; glabrous, or scabrous; pointed (acute, acuminate or subulate-caudate); awnless; carinate, or non-carinate; similar (naviculate, membranous to chartaceous). Lower glume shorter than the lowest lemma to much exceeding the lowest lemma; (3–)5(–7) nerved. Upper glume 5(–7) nerved. Spikelets with incomplete florets. The incomplete florets distal to the female-fertile florets. The distal incomplete florets merely underdeveloped; awned (Urochlaena), or awnless. Spikelets without proximal incomplete florets.
Female-fertile florets 2–9(–14). Lemmas less firm than the glumes to similar in texture to the glumes (membranous to chartaceous); not becoming indurated; entire (sometimes emarginate, scarcely incised); pointed to blunt (acute to emarginate); sometimes 2 lobed; not deeply cleft; awnless, or mucronate (rarely); hairy (usually with clavate hairs), or hairless; carinate (usually), or non-carinate (sometimes); without a germination flap; (5–)7 nerved, or 9 nerved; with the nerves confluent towards the tip. Palea present; relatively long; apically notched; awnless, without apical setae; thinner than the lemma; not indurated (membranous); 2-nerved; 2-keeled. Palea keels winged, or wingless; scabrous, or hairy. Lodicules present; 2; free; fleshy; ciliate, or glabrous; heavily vascularized, or not or scarcely vascularized. Stamens 3. Anthers 1–3 mm long; not penicillate; without an apically prolonged connective. Ovary apically glabrous. Styles free to their bases. Stigmas 2; white, or brown.
Fruit, embryo and seedling. Fruit free from both lemma and palea; small (1–2 mm long); yellow-brown; obovate; compressed dorsiventrally. Hilum short. Pericarp fairly loosely adherent. Embryo small; waisted; without an epiblast; with a scutellar tail; with an elongated mesocotyl internode. Embryonic leaf margins meeting.
Ovule, embryology. Micropyle not noticeably oblique. Outer integument more than two cells thick at the micropylar margin (T. obliterum). Inner integument discontinuous distally; not thickened around the micropyle. Synergids haustorial (strongly developed); exhibiting large, globular starch grains.
Abaxial leaf blade epidermis. Costal/intercostal zonation conspicuous. Papillae absent. Long-cells similar in shape costally and intercostally, or markedly different in shape costally and intercostally (when the costals are much narrower); of similar wall thickness costally and intercostally. Mid-intercostal long-cells rectangular to fusiform; having markedly sinuous walls. Microhairs present; elongated; clearly two-celled; panicoid-type. Microhair apical cell wall thinner than that of the basal cell and often collapsed. Microhairs (58.5–)64–84(–99) microns long. Microhair basal cells 30–36 microns long. Microhairs 9.6–16.5 microns wide at the septum. Microhair total length/width at septum 3.8–8.3. Microhair apical cells (30–)34–50(–60) microns long. Microhair apical cell/total length ratio 0.48–0.66. Stomata absent or very rare, or common; 21–33 microns long. Subsidiaries high dome-shaped, or dome-shaped and triangular. Guard-cells overlapped by the interstomatals (slightly), or overlapping to flush with the interstomatals. Intercostal short-cells common; in cork/silica-cell pairs (but often apparently solitary, through overlapping); silicified. Intercostal silica bodies present and perfectly developed. Costal zones with short-cells. Costal short-cells conspicuously in long rows. Costal silica bodies present throughout the costal zones; rounded (few), or panicoid-type; predominantly cross shaped and dumb-bell shaped (short), or dumb-bell shaped and nodular; not sharp-pointed.
Transverse section of leaf blade, physiology. Lamina mid-zone in transverse section open.
C3; XyMS+. Mesophyll with non-radiate chlorenchyma (the chlorenchyma closely packed); without adaxial palisade; tending to Isachne-type, or not Isachne-type. Leaf blade with distinct, prominent adaxial ribs to adaxially flat; with the ribs more or less constant in size. Midrib not readily distinguishable; with one bundle only. Bulliforms present in discrete, regular adaxial groups; in simple fans. Many of the smallest vascular bundles unaccompanied by sclerenchyma, or all the vascular bundles accompanied by sclerenchyma. Combined sclerenchyma girders present, or absent (but then with strong adaxial and abaxial strands); forming figures (most major bundles with narrow Is). Sclerenchyma all associated with vascular bundles, or not all bundle-associated. The extra sclerenchyma in abaxial groups. The lamina margins with fibres.
Phytochemistry. Tissues of the culm bases with abundant starch, or with little or no starch.
Special diagnostic feature. Not rush-like.
Cytology. Chromosome base number, x = 6. 2n = 12. 2–6 ploid.
Classification. Watson & Dallwitz (1994): Arundinoideae; Danthonieae. Soreng et al. (2015): Danthonioideae; Danthonieae. 10 species.
Distribution, phytogeography, ecology. South Africa.
Commonly adventive. Mesophytic to xerophytic (winter rainfall); species of open habitats; glycophytic. Fynbos and Karoo.
Rusts and smuts. Smuts from Ustilaginaceae. Ustilaginaceae Ustilago.
References, etc. Morphological/taxonomic: Renvoize 1985(c); Linder and Davidse 1997. Leaf anatomical: this project.
Special comments. Linder and Davidse (1997) included the very aberrant Urochlaena pusilla here on cladistic grounds; arguing that because its numerous characteristics are interpreted as unique autapomorphies, recognition of the monotypic genus Urochlaena renders Tribolium paraphyletic. Such rather startling applications of cladistic theory are at odds with the practical requirement that taxonomic systems should facilitate making generalisations; and in view of the well known difficulties regarding extent of sampling and interpretations of morphological characters and character states, and taxonomic sampling limitations (notably, lack of information on extinct forms), evidence from nucleic acid sequencing should be helpful. In this instance, however, subsequent classificatory implementation of the latter by Linder et al. (2010) has resulted in an unpractical version of Tribolium (incorporating Karroochloa, as well as Urochlaena) that cannot be diagnosed morphologically. Illustrations. • T. echinatum, as Lasiochloa ciliaris: Kunth (1835). • T. ciliare, as Brizopyrum: Hook. Ic. Pl. 27 (1901). • S. obliterum, as Brizopyrum glomeratum: Hook. Ic. Pl. 27 (1901). • General aspect (T. uniolae): Gibbs Russell et al., 1990. • T. acutiflora, abaxial epidermis of leaf blade: this project. • T. uniolae, TS leaf blade: this project
We advise against extracting comparative information from the descriptions. This is much more easily achieved using the DELTA data files or the interactive key, which allows access to the character list, illustrations, full and partial descriptions, diagnostic descriptions, differences and similarities between taxa, lists of taxa exhibiting or lacking specified attributes, distributions of character states within any set of taxa, geographical distribution, and classifications. See also Guidelines for using data taken from Web publications.
Cite this publication as: ‘Watson, L., Macfarlane, T.D., and Dallwitz, M.J. 1992 onwards. The 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. Version: 13th November 2017. delta-intkey.com/grass’.