Using Insect Electroantennogram Sensors on Autonomous Robots for Olfactory Searches

Summary

We describe a protocol for using insect antennae in the form of electroantennograms (EAGs) on autonomous robots. Our experimental design allows stable recordings within a day and resolves individual odor patches up to 10 Hz. The efficiency of EAG sensors for olfactory searches is demonstrated in driving a robot toward an odor source.

Abstract

Robots designed to track chemical leaks in hazardous industrial facilities¹ or explosive traces in landmine fields² face the same problem as insects foraging for food or searching for mates³: the olfactory search is constrained by the physics of turbulent transport⁴. The concentration landscape of wind borne odors is discontinuous and consists of sporadically located patches. A pre-requisite to olfactory search is that intermittent odor patches are detected. Because of its high speed and sensitivity^5-6, the olfactory organ of insects provides a unique opportunity for detection. Insect antennae have been used in the past to detect not only sex pheromones⁷ but also chemicals that are relevant to humans, e.g., volatile compounds emanating from cancer cells⁸ or toxic and illicit substances^9-11. We describe here a protocol for using insect antennae on autonomous robots and present a proof of concept for tracking odor plumes to their source. The global response of olfactory neurons is recorded in situ in the form of electroantennograms (EAGs). Our experimental design, based on a whole insect preparation, allows stable recordings within a working day. In comparison, EAGs on excised antennae have a lifetime of 2 hr. A custom hardware/software interface was developed between the EAG electrodes and a robot. The measurement system resolves individual odor patches up to 10 Hz, which exceeds the time scale of artificial chemical sensors¹². The efficiency of EAG sensors for olfactory searches is further demonstrated in driving the robot toward a source of pheromone. By using identical olfactory stimuli and sensors as in real animals, our robotic platform provides a direct means for testing biological hypotheses about olfactory coding and search strategies¹³. It may also prove beneficial for detecting other odorants of interests by combining EAGs from different insect species in a bioelectronic nose configuration¹⁴ or using nanostructured gas sensors that mimic insect antennae¹⁵.

Introduction

Nowadays, animals like dogs are frequently used in safety and security applications that involve the localization of chemical leaks, drugs and explosives because of their excellent smell detection capabilities¹⁶. Yet, they show behavioral variations, get tired after extensive work, and require frequent retraining as their performance decreases over time¹⁷. One way to circumvent these limitations is to replace trained dogs by olfactory robots.

Nonetheless, tracking scents and odor sources is a major challenge in robotics. In turbulent environments, the landscape of an odor plume is very heterogeneous and unsteady, and consists of sporadically located patches⁴. Even at moderate distances from the source, as short as few meters, detections become sporadic and only provide cues intermittently. Furthermore, local concentration gradients during detections do not generally point towards the source. Given discontinuous flow of information and limited local information when detections are made how to navigate a robot toward the source?

It is well known that insects such as male moths use chemical communication to successfully locate their mates over long distances (hundreds of meters). To do so, they adopt a stereotypical behavior^18-20: they surge upwind upon sensing an odor patch and perform an extended search called casting when odor information vanishes. This surge-casting strategy is purely reactive, i.e. actions are completely determined by current perceptions (detection and non-detection events). Yet, its implementation on olfactory robots had limited success in the past because the detection of odor patches is hampered by the slowness of artificial gas sensors.

Metal-oxide sensors used in most of the olfactory robots have response and recovery times of several tens of seconds so that they generally filter out the concentration fluctuations encountered in turbulent plumes²¹. In contrast, the response time of insect chemoreceptors is much shorter, e.g., the rise time of insect electroantennograms (EAGs) is less than 50 msec²². Consequently, by using insect EAGs, odor pulses are resolved at frequencies of several Hertz²³. This property makes EAG sensors well suited for the detection of odor filaments in natural plumes. We describe here a protocol for embedding insect EAGs on robots allowing for efficient olfactory searches using surge and casting strategies.

Protocol

The protocol is based on a commercially available robot (see Materials table) and male moths (Agrotis ipsilon) with their sex pheromone. Yet, it can be adapted with minor modifications to other insect species, odorants, and robots.

1. Insects

1. Rear larvae of Agrotis ipsilon Hufnagel (Lepidoptera: Noctuidae) on an artificial diet and maintain them in individual plastic cups until pupation at 23±1 °C and 50±5% relative humidity as described previously²⁴.
2. Sex pupae and keep adult males separately from females in plastic boxes. Give them free access to a 20% sucrose solution.
3. Perform experiments with males. Male moths are highly sensitive to the sex pheromone emitted by their conspecific females. In A. ipsilon, the major pheromone component, cis-7-dodecenyl acetate (Z7-12:OAc) is the most active compound on the antenna.

2. Electrophysiology

1. Record the EAG from a whole-insect preparation, as described below (Figure 1A). Intact antennae are preferred over excised antennae because they exhibit a longer lifetime (see representative results).
2. Chlorinate two silver wires by immersion in concentrated bleach solution for 10-20 min and rinse afterwards. This process prevents electrodes from polarizing. It has to be repeated whenever the baseline drifts during experiments or when the offset voltage between the electrodes becomes too large to be compensated by the amplifier.
3. Make glass electrodes from fire polished capillaries with an electrode puller. Fire polishing prevents scratching the chlorinated silver wire with electrodes.
4. Anesthetize a male moth with CO₂ and place it inside a Styrofoam block with the head protruding from the top.
5. Tether the insect’s head with painter’s tape around the neck.
6. Insert a silver wire serving as reference electrode into the neck.
7. Under a stereomicroscope, immobilize one of the antennae with thin strips of painter’s tape on the tip and the base.
8. Cut out the distal 2-3 segments of the antenna with surgical scissors.
9. Position the glass electrode near the cut tip of the antenna with a micro-manipulator.
10. Cut out the extremity of the glass capillary with forceps to obtain a diameter slightly larger than the cut tip of the antenna.
11. Fill the glass pipette with (in mM) 6.4 KCl, 340 glucose, 10 Hepes, 12 MgCl₂, 1 CaCl₂, 12 NaCl, pH 6.5.
12. Insert the cut tip of the antenna into the glass capillary with the micromanipulator.
13. Slip the silver wire serving as the recording electrode into the largest extremity of the glass capillary.

3. Hardware Interface

1. Mount the whole preparation, i.e. insect-electrodes-micromanipulator, on a metal plate screwed on the top of the robot (Figure 1B). Connect the electrodes to the robot, as described below.
2. Based on previous works^25-26, design a hardware interface to adapt the EAG output voltage (order 1 mV at several MΩ) to the range appropriate for the extension board of the robot. The board accepts 0-5 V analog inputs and a negative voltage below -200 mV may cause severe damage. Follow the steps 3.2.1 to 3.2.4 to design the interface with Eagle.
   1. Design a ±5V power supply from a +12V battery using voltage regulator 78L10 (① in Figures 2A-2C).
   2. Design a headstage preamplifier (10X) based on instrumentation amplifier INA121 (③ in Figures 2A-2C).
   3. Design a second-stage amplifier (25X) with noise filtering (first order high-pass 0.1 Hz filter, second order low-pass 500 Hz filter, notch 50 Hz filter) based on quad op-amps LT1079 (④ in Figures 2A-2C).
   4. Design a signal conditioning stage that computes with op-amp LT1079 and diode 1N4148 (⑤ in Figures 2A-2C). The total gain is 250 and the EAG output is in the range 0-5 V with zero being at 2.5 V.
3. Connect the electrodes to the differential EAG inputs (② in Figures 2A-2C). Connect the recording electrode to the inverting input of the INA121 to obtain positive EAGs.
4. Connect the EAG output (⑥ in Figures 2A-2C) to the 12 analog inputs of the extension board of the robot. As each input is read sequentially every millisecond, the sampling frequency is 1 KHz.

4. Software Interface

The main threads contain a graphical user interface (GUI), methods for signal detection and various functions for controlling the robot.

1. Write a GUI (Figure 2D) in Qt-C++ for data visualization, digital filtering (20 Hz 5^th order Butterworth low pass filter) and odor detection from the EAG. The latter can be performed in two ways: either by deconvolving the EAG with an appropriate filter (engineering approach, section 4.2), or by modeling the neural mechanisms that allow fast and reliable pheromone detection in A. ipsilon moths (bioinspired approach, section 4.3).
2. Deconvolution filter. The EAG is well described by a nonlinear cascade²⁷ that consists of a static nonlinearity and a 1^st order low-pass filter with exponential impulse function for , see Figure 3A. In response to fluctuating odor concentration , the EAG output is given by the convolution integral . Deconvolution is simply obtained by the inverse of the system; that is in the frequency domain. Then, as the Fourier transform of the impulse response is . For signal detection, follow the steps 4.2.1 to 4.2.3.
   1. Perform the deconvolution process in the time domain as and , Figure 3B.
   2. Approximate the nonlinearity by a polynomial function. Fit the polynomial parameters and the time constant on input-output data pairs to minimize the mean square error between real and reconstructedodor concentration.
   3. Detect the pheromone hits whenever exceeds a predefined threshold.
3. Neuromorphic detector. An alternative approach to detection consists in mimicking biology. In A. ipsilon moths, central neurons receiving input from the antenna respond to the pheromone with a stereotypical firing pattern of excitation-inhibition¹³. A Hodgkin–Huxley type neuron model with four ionic currents (a delayed rectifier K⁺ current, voltage-gated Na⁺ and Ca²⁺ currents, a small conductance Ca²⁺-dependent K⁺ current) was previously developed to reproduce the observed physiological responses¹³. For signal detection, follow the steps 4.3.1 to 4.3.3.
   1. Implement the neuron model as differential equations. Use the EAG signal as input current in the evolution of the membrane potential . Use a membrane capacitance C = 22.9 pF and a leak current given by with conductance g_L = 0.011161 µS and reversal potential E_L = -61.4 mV. The ionic currents are described by with by where are nonlinear functions of V. See previous work¹³ for the details.
   2. Simulate the neuron model in real time with Sirene by integrating the differential equations with a 4^th order Runge-Kutta method and a time step = 0.01 msec. Run the spike test V(t^f) >0 mV and V(t^f - ) <0 mV online to obtain spike times and interspike intervals.
   3. Detect the pheromone hits whenever a burst of excitation (3 consecutive interspike intervals <70 msec) is followed by inhibition (interspike interval ≥350 msec), see Figure 3C.

Representative Results

The protocol described above was first tested with short 20 msec pulses of pheromone (dose 1 μg and 10 μg) directly puffed on the antenna. Figure 4A shows the EAGs in response to pheromone pulses. They are positive because the recording electrode was connected to the inverting input of the amplifier, as described in step 3.3. As indicated by the power spectrum, the measurement system is able to resolve pheromone pulses up to 10 Hz. For comparison, we also tested a commercially available gas sensor. The TGS2620 is a metal oxide sensor manufactured for the detection of solvent vapors. Although the sensor presents a high sensitivity to ethanol, it was unable to follow variations in concentration (see the dashed curve in Figure 4B). The problem came from the sensor housing. The TGS2620 is commercialized with a cap that has a flame-proof stainless steel gauze. The response time is slow because, in practice, it takes a certain time for the gas to diffuse through the gauze and reach the metal oxide surface. Recovery is also slow because it takes time to clean the sensor when the gas is trapped inside the cap. We therefore removed the cap and this modification improved the dynamics significantly (see the plain curve in Figure 4B). Still, there was a factor ten between the EAG and the TGS2620 (10 Hz versus 1 Hz). This comparison is nevertheless qualitative as the EAG and the TGS2620 were not tested in the same conditions.

We then assessed the stability over time of our whole-insect preparation (n = 12 moths) as compared to excised antennae (n = 7 antennae). The EAG was recorded periodically in response to pheromone stimulations (duration 500 msec, dose 1 μg). Raw EAGs (in mV) were converted to relative EAGs (percentages of initial value obtained at time t = 0). Figure 5 shows very good stability of our whole-insect preparation within a working day. In contrast, EAGs recorded on isolated antennae decrease rapidly over time so that the signal falls to one half of its initial value after only 1.5 hr. This time dependence is well described by an exponential decay with a lifetime of 2 hr.

Finally, we tested the ability of the EAG robotic plateform to search for an odor source (pheromone compound Z7-12:OAc) using a reactive search strategy (Figure 6A). The search strategy combines upwind surge every time the pheromone is detected with spiral casting in the absence of detections²⁸. The presence of pheromone is detected from the EAG by the neuromorphic detector, as described in step 4.3. Two examples of EAG recorded during the search are shown in Figure 6B. Without the odor source, the EAG remains around zero (i.e. 2.5 V) with very few or no detections. The robot performs spiral casting and generally leaves the search space before reaching the target location (in 92% of the trials, n = 26 trials, Figure 6C right). With the odor source (Figure 6C left), the EAG presents bursts of activity (detections) intertwined with periods of silence (no detections). Spiral casting mainly occurs at the plume contour (Figure 6C left, red line) and appears to be an efficient strategy for relocating the plume centerline when the odor is lost. In this condition, the source is generally found (success rate = 96%, n = 44 trials).

Figure 1. Whole-insect EAG preparation and robotic setup. A) The electroantennogram (EAG) is recorded from a whole-insect preparation (see text for details). B) The preparation is mounted on the robot. Please click here to view a larger version of this figure.

Figure 2. Hardware-software interface. A) Eagle schematic of the hardware. The circuit consists of six sections (see text for details). It allows filtering (frequency band 0.1-500 Hz, notch at 50 Hz), amplification (total gain 250X) and signal conditioning in the range 0-5 V. B) Eagle layout showing lines of copper (the top is in red and the bottom in blue) and holes (in green). C) Printed circuit board (PCB) showing the discrete elements. D) Graphical user interface (GUI) written in Qt-C++ for data visualization (red trace = EAG input, green trace = neuron model output), filter design and signal detection. Please click here to view a larger version of this figure.

Figure 3. Signal detection from the EAG. A) Electroantennogram (EAG) model. The EAG is modeled by a nonlinear cascade²⁷ that consists of a static nonlinearity followed by a 1^st order low pass filter with exponential impulse function . The EAG output is given by the convolution integral with . B) Engineering approach. The deconvolution filter writes and , see text for details. Odor encounters (hits) are detected wheneverexceeds a predefined threshold. C) Bio-inspired approach. A Hodgkin–Huxley type neuron model with five internal currents (leak, K⁺, Na⁺, Ca²⁺ and SK) is used to reproduce the observed firing pattern of excitation-inhibition (E-I) observed experimentally¹³. For signal detection, the EAG signal is used as input current and hits are detected whenever a burst of excitation is followed by inhibition in the firing activity.

Figure 4. EAG response time. A) EAG recordings in response to 20 msec pheromone pulses (dose 1 μg and 10 μg) delivered at different rates (1, 2, 4, 6, 8, and 10 pulses/sec). The normalized EAG power spectrum is shown for a stimulus pulsed at 1 and 10 Hz (dose 1 μg and 10 μg). The EAG resolves individual pulses up to 10 Hz. B) Recordings from gas sensor TGS2620 in response to ethanol (fluctuating concentration). The dashed and plain curves are the sensor response with and without the cap, respectively. The sensor with the cap has a response time of tens of seconds and thus cannot follows the fluctuations in the gas concentration. The TGS2620 without cap resolves individual fluctuations up to 1 Hz. Please click here to view a larger version of this figure.

Figure 5. EAG stability (whole insect preparation vs excised antenna). The EAG was recorded every hour during 8 hr for the whole-insect preparation (n = 12 moths) and every 20 min during 3.2 hr for excised antennae (n = 7 antennae). The figure shows relative EAGs (percentages of initial value obtained at time t = 0). The time dependence for excised antennae is well fitted by an exponential decay with a lifetime of 2 hr (half-life of 1.5 hr).

Figure 6. Robotic experiments. A) The surge-casting strategy combines upwind surge in the presence of the odor with spiral casting in its absence²⁸. B) Typical EAG recorded during the search while the robot is moving (with and without the odor). C) Robot trajectories with odor (n = 44 trials) and without odor (n = 26 trials). The red dashed line represents the plume contour where 90% of all detections occurred during the trials. Experimental conditions : search space = 4 m x 2.5 m, robot’s speed = 5.6 cm/sec, target = 10 μg of pheromone deposited on a paper filter and replaced every 2 trials, robot initial location = 2 m from target, wind velocity = 0.9 ± 0.2 m/sec at target location. Please click here to view a larger version of this figure.

Discussion

Almost twenty years ago, Kanzaki and his colleagues pioneered the idea of using EAGs on olfactory robots^29-30. Their technique was originally based on excised antennae. Here, we recorded from intact antennae to improve the sensitivity and the lifetime of the preparation. Other studies^31-32 also noticed the superiority of whole-body preparations over isolated antennae. In our robotic experiments, we experienced stable recordings within a day. In contrast, EAGs recorded on isolated antennae have a lifetime of 2 hr (Figure 5).

Our EAG-robotic platform was primarily developed to test biological hypotheses about olfactory coding and search strategies in insects¹³. Similar to central neurons receiving input from insect antennae, we connected a neuron model to a real moth antenna on a robot and performed pheromone detection based on its firing pattern. Detection and non-detection events were then used to drive the robot toward the source of pheromone. The reactive search strategy considered here was inspired by the behavioral patterns of male moths attracted by a sex pheromone. It performed well in laboratory conditions (Figure 6), allowing the localization of a low emission source (pheromone dose of 10 μg in our case versus 10 mg in previous work²⁴) in a relatively large search space (initial distance from source of 2 m versus 10 cm in previous experiments^20-21).

These robotic experiments should be considered as a proof of concept showing that insect antennae are suitable for robotic olfactory searches. Although insect antennae are known to respond to toxic gases, drugs and explosives^9-11, several extensions are needed for coping with real world applications. First, a more sophisticated search method^34-36 may be more efficient at distances beyond 10 m, when the reacquisition of the plume becomes very unlikely. Second, it may be necessary to combine EAGs from different species in a bio-electronic nose configuration¹⁴ in order to detect odorants of interests. Third, stereo sensing capabilities obtained by recording from the two antennae of the same insect may prove beneficial in terms of effectiveness. Two sensors employed in parallel may indeed increase directionality. Fourth, extensions of the search strategy to collective robotic searches³⁷ are ought to be considered for practical applications even if they are not biologically relevant in the case of moths.

Materials

Name	Company	Catalog Number	Comments
Agrotis ipsilon	PISC http://www-physiologie-insecte.versailles.inra.fr/indexenglish.php		moth
Robot Khepera III	K-team www.k-team.com		Khe3Base + KorBotLE + KorWifi
KoreIOLE	K-team		Input/output extension board
EAG-robot interface	LORIA www.loria.fr		Custom-made hardware and software
Sirene	LORIA		neuronal simulator sirene.gforge.inria.fr
Eagle	CadSoft www.cadsoftusa.com		PCB design software
Micromanipulator	Narishige / Bio-logic	UN-3C
Magnet base	Narishige/ Bio-logic	USM-6
Adapter	Narishige/ Bio-logic	UX-6-6
Rotule	Narishige/ Bio-logic	UPN-B
Micro scisors	MORIA / Phymep	15371-92
Stereo microscope Zeiss Stémi 2000	Fisher Scientific	B19961
Light source 20 W KL200	Fisher Scientific	W41745
Narishige PC-10 Na PC-1	Narishige	Narishige PC-10
Capillaries Na PC-1	Fisher scientific	C01065
Pheromone cis-7-Dodecenyl acetate(Z7-12:OAc)	Sigma-Aldrich	259829
Pack of 3 pipettes: 2-20 µl/ 50-200 µl/ 100-1,000 µl	Eppendorf	4910000514	For pheromone dilution and deposition on paper filter
Gas sensor TGS2620	Figaro www.figarosensor.com		Optional, for comparison with EAG
Electrode puller	Narishige	PC-10