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. 2017 Oct 23;7:13800. doi: 10.1038/s41598-017-14231-0

Figure 1.

Figure 1

Panel (a) and (d) refer to Material & Method, panel (b), (c) and (e) to Results. (a) Visualization of the experimental setup. (b) Growth of inducer populations. The x-axis shows the densities of the inducer populations at the beginning of the experiment. The y-axis show log transformed growth rates of these inducer populations. The bigger the inducer populations were at the beginning the less they were growing. (c) Growth of tester (indicator) populations. The x-axis shows the densities of the inducer populations at the beginning of the experiment. The y-axis show log transformed growth rates of tester populations. The bigger the inducer populations were at the beginning the less the tester populations were growing. (d) Arrangement of units in a grid. All units – small cuvette standing in a big one, i.e. treatment group(s) – have been optically shielded from each other (by black cardboard of 0.33 mm thickness). In a typical experiment, the units are placed in a random design. Note, that volatiles – if existing – would affect the outcome by influencing all units across a microclimate. (e) Effect of graphite shielding. Shielded cells grow better than non-shielded tester populations when (both are) having neighbors.