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Treatment flowers were marked and bagged with finemesh (c. 0.3 mm) nylon net bags until the fruits were fully developed.
Samples were bagged and stored at the field station in a dry place at ambient temperature, until analysed within 3 d of collection.
Aphids were collected from the bagged plants by dipping and shaking the plants in a tub of hot water.
The trap heads were replaced on an annual basis, the old head being bagged and returned to the laboratory for processing.
Tubers are collected and bagged from the screen at which they stop.
Immediately, the bunches were bagged with blue plastic sleeves.
Eight of the collections came from bagged inflorescences.
Developing seeds were harvested from ears that had been bagged prior to presentation of the silks, control-pollinated and tagged with the pollination date.
Sticky traps were suspended above and placed below the bagged plants, and the plants remained in the field for one week.
Flowers (n = 40, from 10 plants) were bagged to estimate daily nectar volume and sugar concentration (using a pocket refractometer).
Examination of individuals collected from bagged female inflorescences indicate that they carry pollen.
Before the emergence of silk, ears at different developmental stages were bagged after surface sterilising the outer leaves with 70% ethanol.
Hand-pollinated flowers were bagged to exclude subsequent visitors.
Every bodily fluid was bagged and analyzed.
