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Root development was monitored over time.
Disease development was monitored for 14 days after Psl inoculation.
The compressive and flexural strength development was monitored for up to 180 days.
The bags were removed from the flowers only after the anthesis and the fruit development was monitored every week.
Disease development was monitored by randomly collecting 30 fruit and recording the percentage showing signs of fungal or bacterial infection.
Full-field strain development was monitored over time and fracture patterns were identified utilizing digital image correlation (DIC) technique.
Foam development was monitored in situ by means of X-ray radioscopy while foaming inside a closed mould.
Eggs were inseminated with fresh semen pooled from five males and embryo development was monitored until yolk sac resorption.
According to this chronological model, the normal process of flower development was monitored on plants assigned to the experimental control (EVP-treatment) group (Fig. 2a).
Tumour development was monitored using PET and BLI and in two subgroups, on days 3 and 4 or on days 6 and 7 after tumour cell inoculation.
Blast disease development was monitored over a period of 10-days post-inoculation (dpi) and the lesions were scored using standard procedures (Bonman and Mackill 1988).
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