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Leguminosae
Description
An erect, ascendent to decumbent, much-branched perennial.
Stems to 1 m high, woody toward the base, with short, dense, white hairs
and some scattered bristles, the pubescence generally more dense below
each node. Leaflets oblong to elliptic, to 30 mm long and 15 mm wide but
usually less, densely villous on both surfaces, seven to nine pairs of
conspicuous veins. Petioles 3 to 6 mm long, densely villous. Rachis 1.0
to 3.5 mm long. Sheath of stipules 7 to 9 mm long, densely villous, longer
than the subulate teeth, several nerved. Inflorescence a thick spike, capituliform,
about two thirds as wide as high, to 35 mm long, many flowered, on peduncles
usually 5 to 7 cm long. Bracts with a single, very reduced leaflet. Sheath
often purplish, 8 to 12 mm wide, conspicuously 11 to 17 nerved, copiously
softly pubescent. Axis rudiment 5 to 7 mm long in fruit, very long ciliate.
Outer bracteoles 1 to 3 mm long, ciliate. Inner bracteoles two, 2.0 to
2.5 mm long, much narrower than the outer, lobes mostly acute and sparsely
ciliate, about 2.5 mm long. Standard obovate, 5 to 7 mm long. Wings obovate,
4 to 5 mm long, auriculate at the base. Keel petals 3 to 4 mm long, falcate
and auriculate. Loment to 2.5 mm broad, reticulate nerved. Both articulations
usually fertile but either can sometimes be abortive, upper about 3.5 mm
long and glabrous, lower somewhat shorter and glabrous or sparsely pubescent.
Beak uncinate, about 1 mm long, glabrous or with a few short stiff hairs
on the inner face (Mohlenbrock, 1957).
Distribution
Native in a discontinuous pattern from south-eastern Brazil
to Venezuela. Restricted in distribution compared with S. humilis and S.
guianensis. CIAT collections range from 22°S in Brazil to 10°N
in Venezuela (Grof, Schultze-Kraft and Muller, 1979), and from lowlands
to 1 000 m in elevation.
Rainfall requirements
Grows from semi-arid tropical areas in Bahia, Brazil, to the
subtropical conditions of Mato Grosso and Minas Gerais, Brazil, to the
humid tropical coast of Pernambuco, Brazil. Rainfall range is from 500
to more than 1 500 mm annually.
Soil requirements
Often found in treeless and open woodland savanna habitats.
It thrives in the extremely acid (pH 4.5), infertile, sandy Cerrado soils,
often in association with S. scabra, but is absent from the savannas on
the western side of South America. On soils of medium acidity (pH 5.5 to
6.5), it fails to nodulate and dies.
Seed yield
Some accessions are extremely heavy seeders, producing yields
of up to 1 000 kg./ha.
Cultivars
There is wide variability and many natural ecotypes. One cultivar,
Capica, a mixture of five accessions, CIAT 1315, 1342, 1693, 1728 and 1943,
has recently been released by CIAT in Colombia. It is hoped that its wide
base will give it wide adaptation and some anthracnose control (Edye, Grof
and Walker, 1984).
General features
A very variable species in many morphological characters, including
size and shape of the inflorescence, habit of growth, hairiness of the
stems and leaves, and colour of the stems.
Its adaptation to the low phosphate, acid, sandy soils of the Cerrado
give it considerable promise in South America. Because of its many similarities
to S. scabra, it could also have considerable value in Australia, especially
in view of its high levels of anthracnose resistance. It appears well suited
to low-input, extensive grazing systems. To date, it has not received the
attention it deserves in Australia because of Rhizobium difficulties.
A prolific seed producer, with a high level of hard seed in inflorescences
that are readily grazed over the dry season, S. capitata can thus be spread
widely by livestock. It also regenerates readily from seed.
Rhizobium requirements
Highly specific.
Main references
Grof, Schultze-Kraft and Muller (1979); Edye, Grof and Walker
(1984).
Pests and diseases
Variation in reaction to anthracnose is present, with some
lines resistant to a wide range of races, and to stem borers and budworms
(Lenne and Calderon, 1984).
Breeding systems
Self-pollinates readily in isolation, but outcrossing of up
to 20 percent has been recorded in mixed populations (Miles, 1983).
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