​

Two non-destructive techniques, confocal laser scanning microscopy (CLSM) and planar optode (VisiSens imaging), were combined to relate the fine-scale spatial structure of biofilm components to real-time images of oxygen decay in aquatic biofilms. Both techniques were applied to biofilms grown for seven days at contrasting light and temperature (<math>10^oC/20^oC</math>) conditions. The geo-statistical analyses of CLSM images indicated that biofilm structures consisted of small (<math>~101 \mu m</math>) and middle sized (<math>~101 \mu m</math>) irregular aggregates. Cyanobacteria and EPS (extracellular polymeric substances) showed larger aggregate sizes in dark grown biofilms while, for algae, aggregates were larger in light<math>-20^oC</math> conditions. Light<math>-20^oC</math> biofilms were most dense while <math><math>10^oC</math> biofilms showed a sparser structure and lower respiration rates. There was a positive relationship between the number of pixels occupied and the oxygen decay rate. The combination of optodes and CLMS, taking advantage of geo-statistics, is a promising way to relate biofilm architecture and metabolism at the micrometric scale.

​

==Full Document==

​

<pdf>Media:Draft_Samper_789097209_4059_Biofouling+Rubol_et_al_2018.pdf</pdf>

​