Figure 5. Control and brain blocked larvae movements.
Example of larva trajectories for each of 8 experimental treatments. Each treatment is signified by the Drosophila brain outlines and colour coding on the left of panels (A). BL/+ (light grey) and shits/+ (dark grey) treatments were conducted at normal (22°C) and restrictive temperatures (33°C) whereas MB247/+ and MB247 >shits (light blue), and BL >shits (pink) and BLsens > shits (red) were tested at 33°C. (B) For each treatment an example larva trajectory is given with paths showing complex patterns of movement. All trajectories showed similar complexity across scales but which are not possible to illustrate in a single panel as here, but which are evident from path tortuosity analysis. Scale of paths are denoted by the x,y coordinates in mm. (C) Tortuosity analysis shows complex alternations of long, straighter move steps (higher straightness index, S.I., values) with short, spatially intensive clusters of move steps of different size (lower values). Note the BL >shits larva with no function in the brain and a section of the suboesophageal ganglion (SOG), and BLsens > shits larva with blocked brain lobes, SOG and all somatosensation, both show complex exploration movements similar to controls. (D) MLE model fitting and selection demonstrates larvae move-step length rank frequency distributions best fit by truncated Lévy power laws for each experimental treatment (fitted red line) compared to a Brownian walk (exponential model; blue line). Move step length frequency distributions were well approximated by a truncated Lévy power law across all treatments, with exponents ranging from 1.3 to 2.0. It is striking that BLsens > shits larvae exponents were close to the theoretical optimum (µ ~2.0) indicating Lévy-like movements must be generated intrinsically within thoracic and abdominal neural circuitry.