Figure 1.
Intracellular Recordings of Voltage Responses and the Distribution of Information across Frequencies in R1–6 Photoreceptors of D. melanogaster and S. carnaria
(A) Quantum bumps (*) recorded from D. melanogaster in response to continuous illumination by the white-noise stimulus (lower trace, grey), which was attenuated by 5.5 log units to give a mean effective photon rate of 9 s−1.
(B) Average responses of a D. melanogaster R1–6 photoreceptor to 50 repetitions of a randomly modulated light of mean contrast 0.32.
(C) The corresponding average response of an R1–6 photoreceptor from S. carnaria. Note that the responses in (B) and (C) have dissimilar waveforms because they were generated by different random sequences of intensity modulation, shown in grey beneath each voltage record. In both (B) and (C) the mean stimulus intensity was set to approximately 5 × 106 effective photons s−1. Note that S. carnaria R1–6 responses (C) vary more rapidly than D. melanogaster (B).
(D) This faster response gave the S. carnaria R1–6 a wider bandwidth, as demonstrated in (D) by plotting the distribution of information across response frequency for the two cells.
Figure 2.
Comparison of Information Rates in R1–6 Photoreceptors from Four Dipteran Species
Information rates (mean ± standard error of the mean) are measured from the response to a randomly modulated light of mean contrast 0.32, presented at five background (average) light levels to: S. carnaria (blue), C. vicina (red), D. virilis (green), and D. melanogaster (black). Each adapting light background was converted to effective photons s−1 to allow the photoreceptors to be compared under equivalent conditions.
Figure 3.
Measurements of Photoreceptor Membrane Properties Allow the Calculation of Metabolic Cost
(A) The membrane potential (mean ± standard error of the mean) of R1–6 photoreceptors in the dark and at different effective photon rates, measured in four species S. carnaria (blue), C. vicina (red), D. virilis (green), and D. melanogaster (black).
(B) The corresponding resistances (mean ± standard error of the mean) of R1–6 photoreceptor in the dark and at different effective photon rates.
(C) The electrical model circuit of the photoreceptors. The model calculates from the measurements of membrane potential and resistance the rate at which the Na+/K+ pump, P, hydrolyses ATP molecules: gL = light-gated conductance; EL = reversal potential for light-gated current; iL = light-gated current; gK = potassium conductance; EK = potassium reversal potential; iK = potassium current.
(D) The rate of hydrolysis of ATP molecules calculated at each effective photon rate for R1–6 photoreceptor of the four species (mean).
Figure 4.
The Relationship between the Signalling Cost and the Fixed (Dark) Cost for R1–6 Photoreceptors from the Four Species S. carnaria, C. vicina, D.virilis, and D. melanogaster
(A) The rate of hydrolysis of ATP molecules during signalling at each effective photon rate.
(B) The maximum signalling cost versus the fixed cost for each of the four R1–6 photoreceptor types. The maximum is the signalling cost measured at the brightest light levels.
(C) The ratio of total cost to fixed cost of each photoreceptor type at each effective photon rate.
Figure 5.
The Metabolic Cost of Information Decreases with Increasing Light Intensity
(A) A double logarithmic plot of metabolic cost per bit at each effective photon rate and (B) a double logarithmic plot of the metabolic cost of signalling per bit at each effective photon rate are shown. Measurements are from R1–6 photoreceptors from four species, S. carnaria (blue), C. vicina (red), D. virilis (green), and D. melanogaster (black).
Figure 6.
The Metabolic Cost of Information in R1–6 Photoreceptors Decreases When the Information Rate Is Increased by Raising the Light Level
(A) The metabolic cost per bit plotted logarithmically versus the bit rate for R1–6 photoreceptors of the four species S. carnaria (blue), C. vicina (red), D. virilis (green), and D. melanogaster (black).
(B) The metabolic cost of signalling per bit plotted logarithmically versus the bit rate for R1–6 photoreceptors in the four species.
Figure 7.
The Scaling of Metabolic Cost with Performance in Dipteran R1–6 Photoreceptors
The logarithms of the total cost (open symbols) and the fixed cost (solid symbols) are plotted against the logarithm of maximum information rate. Costs are in ATP molecules hydrolysed per photoreceptor per second. Each data point represents the mean values from R1–6 photoreceptors in one of the four dipteran species used in this study. The linear fits suggest that the total cost of photoreceptor signalling (dashed line) increases as (information rate)1.7, and the fixed cost of maintaining the photoreceptor in the dark (solid line) increases as (information rate)1.47.