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After LD sampling, plants were released into continuous light at constant 20°C (LL treatment).
Steps taken in growing the sampling plants were as follows: First, the seeds were sown on 10 Oct, 2012, and then were transplanted in the field outside after the seedlings with 5~6 pieces true leaves on 15 Nov, 2012.
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Further, preliminary dialysis membrane calibration issues for sampling plant-available N compounds are discussed.
At the time of the third soil sampling, plant sampling was also conducted including the above ground part of the plants.
Sampling number, sampling plant part and disease categories were different described as below.
After sampling, plant tissues were immediately frozen in liquid nitrogen and stored at -80°C.
By 7 every morning we were counting coffee beans on sample plants from one of 2,600 farms belonging to the Tarraz?operative.
After excavating, the sample plants were washed with tap water.
From each industry group, two sample plants were selected with five executives participating from each plant.
All traits were measured from 5 randomly sampled plants for each accession after harvest.
Adhered soil on the sampled plants were loosen by placing into plastic buckets filled with water.
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