The grass genera of the world
~ Schismus, Tribolium, Danthonia sensu lato
Type species: Type: K. curva (Nees) Conert & Túrpe.
Habit, vegetative morphology. Annual, or perennial; stoloniferous, or caespitose. Culms 4–40 cm high; herbaceous; unbranched above. Culm nodes glabrous. Culm internodes solid. Plants unarmed. Young shoots extravaginal (rarely), or intravaginal. Leaves mostly basal to not basally aggregated; non-auriculate. Hair-tufted at the mouth of the sheath. Leaf blades linear; narrow; to 2 mm wide; flat, or folded, or rolled; not pseudopetiolate; without cross venation; persistent. Ligule present; a fringe of hairs. Contra-ligule present (as a line of hairs).
Reproductive organization. Plants bisexual, all with bisexual spikelets; with hermaphrodite florets.
Inflorescence. Inflorescence paniculate; contracted (1–6 cm long); more or less ovoid; espatheate; not comprising partial inflorescences and foliar organs. Spikelet-bearing axes persistent. Spikelets solitary; not secund; pedicellate.
Female-fertile spikelets. Spikelets 4–6(–7) mm long; compressed laterally; disarticulating above the glumes; disarticulating between the florets; with conventional internode spacings. Rachilla prolonged beyond the uppermost female-fertile floret; hairy; the rachilla extension with incomplete florets. Hairy callus present. Callus short, or long; blunt.
Glumes two; more or less equal (subequal); about equalling the spikelets; long relative to the adjacent lemmas; hairless; glabrous; pointed; awnless; carinate; similar (membranous, the margins and apices hyaline). Lower glume much exceeding the lowest lemma; 3–5 nerved. Upper glume 3–5(–7) nerved. Spikelets with incomplete florets. The incomplete florets distal to the female-fertile florets. The distal incomplete florets merely underdeveloped; awned. Spikelets without proximal incomplete florets.
Female-fertile florets 3–7. Lemmas with fringes or tufts of white hairs, except in K. curva; similar in texture to the glumes (membranous); not becoming indurated; incised; 2 lobed; deeply cleft; awned. Awns 1, or 3; median, or median and lateral (by small extensions from the lobes); the median different in form from the laterals (when laterals present); from a sinus; geniculate; hairless; about as long as the body of the lemma to much longer than the body of the lemma. The lateral awns shorter than the median (and straight). Lemmas hairy. The hairs in tufts, or not in tufts; in transverse rows, or not in transverse rows. Lemmas non-carinate; without a germination flap; 9 nerved; with the nerves non-confluent. Palea present; relatively long (almost equalling the lemma); entire to apically notched; awnless, without apical setae (glabrous or pilose); textured like the lemma; not indurated (membranous, the margins hyaline); 2-nerved; 2-keeled. Palea keels wingless; glabrous, or scabrous. Lodicules present; 2; free; fleshy; ciliate. Stamens 3. Anthers 1.4–2.2 mm long; not penicillate; without an apically prolonged connective. Ovary apically glabrous. Styles free to their bases. Stigmas 2.
Fruit, embryo and seedling. Fruit free from both lemma and palea (but enclosed); small (0.8–1 mm long). Hilum short. Embryo small.
Ovule, embryology. Micropyle not noticeably oblique. Outer integument covering no more than the chalazal half of the ovule; more than two cells thick at the micropylar margin, or two cells thick at the micropylar margin. Inner integument not thickened around the micropyle. Synergids haustorial (strongly developed); exhibiting large, globular starch grains.
Abaxial leaf blade epidermis. Costal/intercostal zonation conspicuous. Papillae absent. Mid-intercostal long-cells rectangular, or rectangular and fusiform; having markedly sinuous walls. Microhairs present; panicoid-type. Stomata common, or absent or very rare. Subsidiaries dome-shaped. Intercostal short-cells common; in cork/silica-cell pairs, or not paired; silicified. Costal short-cells usually conspicuously in long rows, or neither distinctly grouped into long rows nor predominantly paired (in K. purpurea). Costal silica bodies tall-and-narrow to crescentic (K. purpurea), or panicoid-type (usually); usually cross shaped, or dumb-bell shaped.
Transverse section of leaf blade, physiology. C3; XyMS+. Mesophyll with non-radiate chlorenchyma; Isachne-type (or at least tending to this), or not Isachne-type. Leaf blade with distinct, prominent adaxial ribs to nodular in section, or adaxially flat; when ribbed with the ribs more or less constant in size. Midrib not readily distinguishable (apart from position); with one bundle only. Bulliforms present in discrete, regular adaxial groups, or not present in discrete, regular adaxial groups; sometimes in simple fans. All the vascular bundles accompanied by sclerenchyma. Combined sclerenchyma girders absent. Sclerenchyma all associated with vascular bundles.
Special diagnostic feature. Female-fertile lemmas with a bent awn, the awn twisted below. Spikelets 46(7) mm long, inflorescence 1060 mm long.
Cytology. Chromosome base number, x = 6. 2n = 12 and 24. 2 and 4 ploid.
Classification. Watson & Dallwitz (1994): Arundinoideae; Danthonieae. Soreng et al. (2015): Danthonioideae; Danthonieae. 4 species.
Distribution, phytogeography, ecology. Southern Africa.
Mesophytic; species of open habitats; glycophytic. Grassland and among rocks.
References, etc. Morphological/taxonomic: Conert 1969. Leaf anatomical: Conert and Türpe 1969; photos of K. purpurea provided by R.P. Ellis.
Illustrations. • General aspect (K. curva): Gibbs Russell et al., 1990
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: 11th December 2017. delta-intkey.com/grass’.