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a USDA-ARS Dale Bumpers National Rice Research Center, P. O. Box, 1090 Stuttgart, AR 72160-0287
b Institute of Nuclear Agricultural Sciences, Zhejiang Univ., Hangzhou, P. R. China 310029
* Corresponding author (yjia{at}spa.ars.usda.gov)
In Volume 42, no. 6, pp. 21452149, Materials and methods "PCR amplification" reads "Each PCR reaction consisted of 10~20 ng of total DNA, 10 mL of Taq PCR Master Mix [(2x concentrated) containing 0.5 unit Taq DNA Polymerase, Qiagen PCR Buffer (with 3 mmol MgCl2)] and 400 mmol of each dNTP (Taq PCR Master Mix Kit, Qiagen), 2 µL of MgCl2 (25 mmol), 1 mL of primer 1 (10 mmol) and primer 2 (10 mmol) each in a final volume of 20 mL."
It should read "Each PCR reaction consisted of 10~20 ng of total DNA, 10 µL of Taq PCR Master Mix [(2x concentrated) containing 0.5 unit Taq DNA Polymerase, Qiagen PCR Buffer (with 3 mmol MgCl2)] and 400 µmol of each dNTP (Taq PCR Master Mix Kit, Qiagen), 2 µL of MgCl2 (25 mmol), 1 µL of primer 1 (10 µmol) and primer 2 (10 µmol) each in a final volume of 20 µL".
"Disease reactions" reads "Susceptible reaction was based on a lesion size greater than 3 cm in length, visible infection and conidia evident in affected tissue".
It should read "Susceptible reaction was based on a lesion size greater than 3 mm in length, visible infection and conidia evident in affected tissue".
Received for publication February 8, 2002.
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