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To calculate longer-term space use, three replications for each of three experimental GS were placed in nine 10 m2 enclosures for 1 week.
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Two abalone (2 years old; 4.8±0.69 cm; 14.1±6.04 g) were placed in each chamber.
Two samples each weighing 0.5 g were placed into different beakers.
Leave samples (0.2 g) were placed in test tubes containing 10 ml of double distilled water.
4.3 g were placed in a jar and then covered with an egg white.
CSD male rats (220 250 g) were placed in individual cages in a thermoregulated (22°C), 12 h night/12 h day room.
Sex-reversed male Nile tilapia Oreochromis niloticus (46.56 ± 2.53 g) were placed in 21 cages (6 m3 – 2 × 2 × 1.5 m each) with or without bamboo substrates for periphyton growth.
Soil samples (200 g) were placed in earthen pots (microcosm) and were artificially contaminated with SEO to a level of 10% w/w.
Fresh Vds (40 g) were placed inside glass containers (7 cm × 3.5 cm) and were orthonasally analysed as described earlier [20].
Aggregate larger than 0.4 mm was removed and oven-dried samples of approximately 0.5 g were placed in an Enslin Neff apparatus (Fig. 5).
The jute fibers, cut transversely in 5-cm segments and weighing approximately 2 g, were placed into 250-mL flasks to fill the bottom area.
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