Activity of bumble bees, Bombus impatiens Cresson, was examined in commercial tomato, Lycopersicon esculentum Mill. (Solanaceae), greenhouses in relation to greenhouse covering type, solar radiation, greenhouse temperature and humidity. Bumble bee activity was measured by photodiode monitors inserted into the entrance of the colonies. Colony sizes were monitored as an indicator of bee loss through gutter ventilation systems in relation to covering. Activity monitors were found to be a good predictor of actual bumble bee entrances and exits (r2 = 0.85). Bumble bee activity was 94.0% greater under the ultravioltet (UV)-transmitting covering than under ones that transmitted less UV light. No relationship was found between bee activity and the amount of solar radiation or internal greenhouse humidity. Bee activity was weakly positively correlated with internal greenhouse temperature (r2 = 0.18). Bee activity was not different during three periods of the day: morning, midday, and evening. The mean ± SE colony size under the UV-transmitting covering was 86.0 ± 2 bees per colony after 10 days within the greenhouses, compared with 36.4 ± 5.8 bees per colony under the other three types of covering. Our results suggest that bee activity is greatest and bee loss through gutter ventilation systems lowest in greenhouses made with coverings that transmit high levels of UV light.
In controlled environment plant production facilities, elevating either light or CO2 levels generally has led to increased biomass and yield due to enhanced canopy photosynthesis. Today, advancements in light-emitting diodes (LEDs) have made this technology a viable option for both supplementary lighting in greenhouses and a sole lighting source in controlled environment chambers. Our study used tomato plants grown under both ambient CO2 (AC) and elevated CO2 (EC) conditions then exposed them to various CO2 and lighting treatments during both whole plant and leaf level measurements. Plants grown under EC reached the first flower developmental stage 8 days sooner and were approximately 15cm taller than those grown under AC. However, under AC plants had more leaf area while their dry weights were similar. Of note, under EC chlorophyll a and b were lower, as were carotenoids per unit leaf area. Whole plant analyses, under all CO2 challenges, showed that plants exposed to high-pressure sodium (HPS), red-blue LED, and red-white LED had similar photosynthesis, respiration, and daily carbon gain. Under different light qualities, day-time transpiration rates were similar among CO2 conditions. Day-time water-use efficiency (WUE) was higher in plants grown and exposed to EC. Similarly, WUE of plants grown under AC but exposed to short-term elevated CO2 conditions was higher than those grown and tested under AC during all light treatments. Under all CO2 conditions, plants exposed to red-white and red-blue LEDs had lower WUE than those exposed to HPS lighting. Assessing alterations due to CO2 and light quality on a whole plant basis, not merely on an individual leaf basis, furthers our understanding of the interactions between these two parameters during controlled environment production. Principle component analyses of both whole plant and leaf data indicates that increasing CO2 supply has a more dramatic effect on photosynthesis and WUE than on transpiration.
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