“…In plants that precipitate Ca‐oxalate, the accumulation of oxalate is directly proportional to tissue Ca concentration and is, therefore, strongly dependent upon Ca phytoavailability and plant growth rate (Libert & Franceschi, 1987; Kinzel & Lechner, 1992; Franceschi & Nakata, 2005). Some within‐species genetic variation in oxalate concentrations has been observed in beet (Libert & Franceschi, 1987), spinach (Kitchen et al ., 1964; Libert & Franceschi, 1987; Kawazu et al ., 2003; Mou, 2008), rhubarb (Libert & Creed, 1985; Libert, 1987; Libert & Franceschi, 1987), carambola (Wilson et al ., 1982), oca (Ross et al ., 1999; Albihn & Savage, 2001; Sangketkit et al ., 2001), taro (Tanaka et al ., 2003) and soybean (Massey et al ., 2001; Horner et al ., 2005), and several mutants have been identified in the forage legume Medicago truncatula with reduced or altered accumulation of Ca‐oxalate in their leaves (Nakata & McConn, 2000; McConn & Nakata, 2002). For two of the M. truncatula calcium oxalate deficient mutants ( cod5 and cod6 ), reduced accumulation of Ca‐oxalate has been correlated with increased Ca bioavailability in herbage (Nakata & McConn, 2006, 2007; Morris et al ., 2007).…”