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Ecologia Mediterranea

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One chamber was left at the greenhouse CO 2<br />

conditions (referred to as ambient treatment –<br />

ACO 2 ) where the CO 2 concentration was<br />

around 500 ppm (Figure 1), and the other<br />

chamber was kept at high concentration of<br />

CO 2 (referred to as enriched treatment –<br />

ECO 2 ). CO 2 concentration was kept at around<br />

1000 ppm (Figure 1). The source of CO 2 was<br />

20-kg CO 2 canisters. The CO 2 levels were<br />

monitored using a carbon dioxide monitor and<br />

controller (TONGDY Ltd.). All other conditions<br />

were kept similar in both chambers (Figure<br />

1). Three groups of C. ciliaris plants, were<br />

grown in plastic pots (30 cm in diameter),<br />

exposed to enriched, ambient, or alternating<br />

CO 2 . The salinity stress sub-group contained<br />

four pots each with 20 planted seeds of C. ciliaris.<br />

Seeds were planted on 11 February. All<br />

plants were grown within pots from locally<br />

collected seeds.<br />

ecologia mediterranea – Vol. 38 (2) – 2012<br />

Salinity stress affects growth responses of Cenchrus ciliaris under CO 2 enrichment<br />

Figure 1 – Daily variations in A) Temperature, B) Humidity, C) light, and D) CO 2 concentration<br />

in the two growing chambers over the trial period.<br />

Plants that were grown under enriched CO2 conditions were exposed continually to<br />

enriched atmospheric CO2 during the whole<br />

trial between 7:00 to 18:00. A third group was<br />

referred to as alternating treatment (ALCO2 )<br />

where plants were grown under changing<br />

exposure between ambient and enriched<br />

atmospheric CO2 , every two weeks. Plant<br />

under salinity treatment were supplied with<br />

saline water (salinity=2.15 ppt), while the<br />

other plants in the other two treatments were<br />

irrigated with tap water (salinity=0.75 ppt).<br />

Shoot length, number of blades (green/dry),<br />

blade area and inflorescence production were<br />

measured every week throughout the trial<br />

period. The number of stomata was counted<br />

per square area using the epidermal peeling<br />

method. The peeling was done two to three<br />

times for each of three replicates.<br />

45

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