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Fig. 2. for affects feeding rate and food acquisition. (A) Gut dissections
from larvae fed blue yeast paste for 15 min also indicated that
forR larvae ingested significantly less food than
fors or fors2 larvae
(F(2,26)=5.32, P<0.05). (B) The rate that the
gut filled with food was measured by feeding larvae on a yeast paste with
Brilliant Blue dye, extracting the gut, and comparing the length of the gut
with food to the length of the entire gut. Gut size did not differ
significantly between strains (F(2,67)=0.86,
P=0.43). Sitter (fors and
fors2) larvae filled their gut more quickly than rover
(forR) larvae (10–20 min feeding, two-way-ANOVA
F(8,36)=70.53 P=0.0008; effect of strain,
F(2,36)=5.82, P=0.007; effect of time,
F(2,36)=5.52, P=0.008; one-way ANOVAs: 5 min,
P=0.82; 10 min, P=0.10; 15 min, P=0.05; 20 min,
P=0.04). This difference stabilized after about 25–30 min of
feeding when the midguts of all larvae become saturated with the blue yeast
paste, resulting in no measurable difference in food intake (one-way ANOVAs:
25 min, P=0.85; 30 min, P=0.68). (C) Rovers showed
significantly less food intake on fructose–agarose
(F(2,87)=12.20, P<0.0001; forR
vs fors, P<0.0001; forR vs
fors2, P<0.0002; fors vs
fors2, P=0.92) and glucose–agarose
(F(2,87)=3.98, P=0.02; forR vs
fors, P=0.0078; forR vs
fors2, P=0.048; fors vs fors2,
P=0.47) when food intake was measured using Carmine dye. (D)
Drosophila larvae use their mouthhooks for both food ingestion and
locomotion. We found no significant correlation between mouthhook movements
and amount of dye ingested when larvae fed on a glucose–agarose
substrate (R2=0.18, P=0.11).