(A-B) Average rhabdomere numbers per ommatidia of (A) the scox mutant flies and (B) the porin mutant flies under the indicated conditions. Each data point was based on examination of >60 ommatidia from >3 flies. Error bars represent the SD. Asterisks indicate statistically-significant differences (one-way ANOVA and post-hoc Dunnett’s test, **p < 0.01). (C-K) Transmission electron microscopy sections of single ommatidia of fly compound eyes with the indicated genotype and conditions. (C) 10 day-old wild-type, (D) 1 day-old scox
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/hid (ey-flp Rh1::GFP; scox
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FRT40A/GMR-hid CL FRT40A), (E) 10 day-old scox
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/hid, (F) 10 day-old scox
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/hid under dark condition, (G) 10 day-old P-element excised scox
ex
/hid (ey-flp Rh1::GFP; scox
ex
FRT40A/GMR-hid CL FRT40A), (H) 1 day-old porin
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/hid (ey-flp Rh1::GFP; porin
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FRT40A/GMR-hid CL FRT40A), (I) 10 day-old porin
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/hid, (J) 10 day-old porin
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/hid under dark condition, (K) 10 day-old p-element excised porin
ex
/hid (ey-flp Rh1::GFP; porin
ex
FRT40A/GMR-hid CL FRT40A). Scale bar, 2 μm. With the exception of the dark-reared (F) scox
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/hid and (J) porin
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/hid flies, flies were maintained under a 12 hr light/12 hr dark cycle. (L) ERG responses of wild-type, scox
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/hid, scox
ex
/hid, porin
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/hid, and p-element excised porin
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/hid flies in response to a 10-s orange light stimulus as indicated. Flies used were less than 2 days old.