Abstract

Brachiaria species are the most widely planted tropical forage grasses in the world (Miles et al., 2004). For example, in Brazil alone, about 80 million hectares are planted to Brachiaria pastures (Macedo, 2005). They increase animal productivity by 5 to 10 times with respect to native savanna vegetation in the tropical areas of Latin America, thus representing a significant contribution to farmer’s income (Rao et al., 1993). Although their origin is from the tropical areas of Africa, they are also used for livestock production in South-East Asia and Australia. Among them, Brachiaria decumbens cv. Basilisk, Brachiaria brizantha cv. Marandu, and Brachiaria ruziziensis cv. Kennedy have been more commonly utilized for livestock production in the tropics (Miles et al., 2004). Among the three grasses, B. decumbens is highly adapted to infertile acid soils, i. e., high level of tolerance to high aluminium (Al) saturation, low phosphorus (P) and low calcium (Ca) supply in soil (Louw-Gaume et al., 2010 a,b; Rao et al., 1995, 1996; Wenzl et al., 2001, 2003), but also highly sensitive to a major insect, spittlebugs (Miles et al., 2006) and produces mycotoxin after infection with Pithomyces chartarum (Andrade et al., 1978). B. brizantha cv. Marandu is highly resistant to spittlebugs, adapted to seasonal drought stress, highly responsive to fertilizer application but is not well adapted to low fertility acid soils (Miles et al., 2004, 2006). B. ruziziensis cv. Kennedy is sensitive to spittlebugs, performs better in well-drained fertile soils, has high forage quality but poorly adapted to low fertility acid soils (Ishigaki, 2010; Miles et al., 2004). B. decumbens and B. brizantha are generally tetraploid, apomicts while B. ruziziensis is diploid, sexual (Miles et al., 2004, 2006).

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