The activation of resting tsetse flies (Glossina) in response to visual and olfactory stimuli in the field

ABSTRACT Studies were conducted in Zimbabwe of the responses of Glossina morsitans morsitans Westwood and Glossina pallidipes Austen resting in a refuge to various host stimuli. Tsetse took off in response to 100% ox odour, 0.08% carbon dioxide or a visual stimulus consisting of a 0.75 × 0.75 m black target placed c . 5 m from the refuge moving at 4^o s^-1, but the level of response was low with only 35%, 19% and 29% responding, respectively. Tsetse did not take off in response to any one of 25% ox odour, 0.8% carbon dioxide, acetone (3 μg 1^-1) or octenol (0.03 μg 1^-1). In the absence of any host stimuli, flies emerged from the refuge later on hotter days (35–37^oC) than on cooler days (32–34.5^oC). Male G.pallidipes emerging later in the afternoon contained significantly more haematin than those emerging relatively earlier. There were no significant differences between the responses of G.m. morsitans and G.pallidipes. It is suggested that the initial activation of resting flies is primarily mediated through endogenous, rather than host, stimuli.     

The mating behaviour of tsetse flies (Glossina): a review

Abstract. The mode of reproduction of tsetse flies, by adenotrophic viviparity, is unusual among the Diptera and is associated with many unique aspects of the tsetse's mating system. Tsetse exist at relatively low densities in the environment but a combination of olfactory and visual stimuli brings males and virgin females together on or around host animals. The behavioural repertoire associated with mate location and identification, courtship and copulation is regulated by external physical and chemical stimuli as well as by internal physiological mechanisms. With a view to identifying stimuli that could be used to manipulate tsetse behaviour and exploited for control purposes, much progress has been made in recent years in elucidating the mating behaviour of tsetse and its regulatory mechanisms. This progress and the current state of understanding of tsetse mating behaviour is reviewed.     

Behaviour of tsetse flies (Glossina) in host odour plumes in the field

ABSTRACT. In Zimbabwe, studies were made of the responses of Glossina pallidipes Austen and G.morsitans morsitans Westwood to artificial host odour using an incomplete ring of electrocuting nets. In a plume of synthetic host odour tsetse flew generally upwind, with 50–60% flying within 35^o of due upwind. More than 80% of tsetse flew at < 50 cm above ground level. Upon losing contact with odour they executed a reverse turn within about 2 m, and upon regaining contact they turned upwind. There were no clear differences in the responses of G.m.morsitans and G.pallidipes. Using electrocuting nets lying horizontally on the ground it was found that tsetse landed in the vicinity of the odour source, the propensity to land being greater for G.pallidipes than for G.m, morsitans , greater for immature than mature flies, and greater for males than females.     

Flight responses of tsetse flies (Glossina) to octenol and acetone vapour in a wind-tunnel

Abstract. Female Glossina morsitans morsitans Westwood were video-recorded in a wind-tunnel as they entered, in crosswind flight, a broad plume of either octenol or acetone (two components of ox odour). Both odours produced upwind turning responses (in-flight anemotaxis) to a range of concentrations, with thresholds at around 10^-8mg1^-l for octenol and 10^-6mg1^-1 for acetone. Kinetic responses were unaffected by octenol at low concentrations, but flight speed was significantly reduced and sinuosity (^om^-1) and angular velocity (^os^-1) significantly increased by concentrations at or above those in ox breath; for acetone, these effects were apparent but inconsistently related to concentration. It is concluded that octenol and acetone vapour are used by tsetse flies to locate hosts by upwind anemotaxis, probably combined with kinetic responses. The behavioural basis for the 'repellency' of high octenol concentrations in the field is discussed in the context of the virtual loss of upwind anemotaxis to octenol at the highest concentration tested in the tunnel (30 × ox breath).     

Dose responses of tsetse flies (Glossina) to carbon dioxide, acetone and octenol in the field

ABSTRACT Studies were conducted in Zimbabwe of the catch of Glossina pallidipes Austen from an electric net plus target baited with mixtures of acetone plus carbon dioxide or 1-octen-3-ol (octenol) plus carbon dioxide. For acetone dispensed alone at 5–50, 000 mg h^-1, ten-fold increments in the dose increased the catch 1.7 times. For carbon dioxide dispensed alone, dose increments from 12 to 1201 h^-1 doubled the catch, but the catch was not further increased by dispensing carbon dioxide at 600–1200 1 h^-1. For mixtures of these two odours, ten-fold increments in the dose of carbon dioxide between 12 and 12, 0001 h^-1 increased the catch c . 2.5 times if acetone was also dispensed at >50 mg h^-1; changes in the dose of acetone between 50 and 50 000 mg h^-1 did not affect the catch. The addition of octenol (0.05 mg h^-1) to carbon dioxide (12–12001 h^-1) doubled the catch. Ten-fold increments in the dose of octenol between 0.05 and 5 mg h^-1 did not increase the catch significantly and the catch was independent of changes in the dose of carbon dioxide between 120 and 12001 h^-1. The behavioural basis of the dose-response curves was investigated using an incomplete ring of electric nets to assess the flight orientation of tsetse in different odours. Upwind flight was not elicited by acetone or octenol alone, or by carbon dioxide unless it was at very high doses, however, mixtures of carbon dioxide with acetone or octenol elicited upwind flight. It is suggested that the attractiveness of mixtures of acetone and carbon dioxide is a function of the region of overlap of these two odours at above threshold concentration. Acetone and octenol on their own appear to increase the responsiveness of flies to visual cues.     

Visually-guided, upwind turning behaviour of free-flying tsetse flies in odour-laden wind: a wind-tunnel study

Abstract. To test the hypothesis that tsetse flies use visual input from the apparent movement of the ground to assess wind direction while in flight, Glossina morsitans morsitans Westwood females were video- recorded in a wind-tunnel as they entered, in cross-wind flight, a broad plume of simulated host odour (C0₂ at c. 0.05%). The tunnel (2.3 times 1.2 m wide) generated winds up to 0.25 m s^-1 and had a strongly patterned floor that could be moved upwind or downwind to increase or decrease the visual input due to wind drift. Flight tracks were analysed for speed, direction relative to the wind, and angle of turn. Mean groundspeeds were c. 1.8 m s^-1. In control measurements in still air (with or without odour) flies turned 50:50 'upwind': 'downwind'. With a 0.25 m s^-1 odour-perme- ated wind, 79% turned upwind, and c. 70% left view flying upwind. When the floor was moved at 0.25 m s^-1 upwind (to mimic the visual input from the ground due to a 0.5 m s_^-1 wind), the strength of this response increased. If instead the floor was moved downwind, faster than the wind speed (to mimic the visual input due to a wind from the opposite direction), 59% turned downwind and c. 70% left view flying downwind, and thus away from the source (though progressing 'upwind' in terms of the visual input from apparent ground pattern movement). Upwind turns were on average significantly larger than downwind turns. It is concluded that tsetse navigate up host odour plumes in flight by responding to the visual flow fields due to their movement over the ground (optomotor anemotaxis), even in weak winds blowing at a fraction of their groundspeed.     

Flying mate detection and chasing by tsetse flies (Glossina)

Abstract Male tsetse flies, probably Glossina morsitans morsitans Westw., were video-recorded in the field as they took off and chased other tsetse flies. Chasers responded (took off) to a target fly at a maximum distance of c. 55 cm, when it subtended c. 1.6^o to their eye (–1 foveal ommatidial subtense). Chased targets were always within this range (mean subtense at take-off = 3.2^o) and approaching the chaser. The most significant difference between chased and non-chased targets was in the rate of approach of the target fly in terms of the increase in its image size immediately before the chaser took off ( 21^o s⁻¹), especially as its relative increase (690% s^-1 P< 0.005). No feature of the target's translational velocity, nor any relationship between that and the image size approached this level of significance. Chasers seemed to 'slipstream' their target at c. 20 cm directly behind it, perhaps suggesting target identification by speed matching. Chases were apparently abandoned when the target image shrank from covering at least two of the chaser's foveal ommatidia to covering only one. Parallax-free measurements of flight speeds indicated a preferred, stable mean groundspeed of 4.8±0.1 m s^_1 (SE), at a mean wing-beat frequency of 209±3 Hz.     

Wind speed effects on odour source location by tsetse flies (Glossina)

Abstract. Tsetse flies (mainly Glossina pallidipes Aust.) were captured by various means at sources of artificial host odour in Zimbabwe and Kenya. Their rates of arrival and flight directions were compared with simultaneous data on the wind's speed and direction, on time-scales ranging from 1 s to 30 min. It was predicted that because increasing wind speed up to 1 m s^-1 straightens out the airflow (Brady et al. , 1989) it will straighten out odour plumes, make them easier to navigate, and should therefore increase the rate of arrival of flies at an odour source. In the event, the relationship proved to be more complex, with both positive and negative correlations of arrival rate on wind speed. It seems there is a bimodal relationship: odour source finding is positively related to increasing wind speed in weak winds up to ∼0.5 m s^-1 (presumably as the odour plume straightens out), but is negatively related to increasing wind speed in strong winds above ∼1.0 m s^-1 (presumably due to increasing turbulence breaking up the odour plume).     

Flight behaviour of tsetse flies in host odour plumes: the initial response to leaving or entering odour

ABSTRACT. Free-flying, wild male and female Glossina pallidipes Aust. and G. m. morsitans Westw. were video-recorded in the field in Zimbabwe as they entered or left the side of a host-odour plume in cross-wind flight, or as they overshot a source of host odour in upwind flight (camera 2.5 m up looking down at a 3 times 2.5 m field of view at ground level). 80% of cross-wind odour leavers turned sharply ( turns 95^o), but without regard to wind direction (overshooters behaved essentially the same except that nearly 100% turned). Many fewer flies entering a plume cross wind turned ( c . 60%), and when they did they made much smaller turns ( 58^o); these turns were, however, significantly biassed upwind ( c . 70%). All three classes of fly had similar groundspeeds ( 5.5–6.5 m s^_1) and angular velocities ( 350–400^o s^-1). Clear evidence was obtained of in-flight sensitivity to wind direction: significantly more flies entering odour turned upwind than downwind, and odour losers turning upwind made significantly larger turns than average. The main basis for the different sizes of turn was the different durations of the turning flight, rather than changes in angular velocity or speed. No evidence was found of flies landing after losing contact with odour.     

Rates of progress up odour plumes by tsetse flies: a mark-release video study of the timing of odour source location by Glossina pallidipes

Abstract. The arrival of individually marked Glossina pallidipes Austen at a host odour source after their video-timed release from 30–75 m downwind was measured in the field in Zimbabwe. In the absence of odour, the proportion recaptured was <2% (= - random expectation); when synthetic ox odour was released, the probability of recapture at the source increased with proximity of release, from 6% at 75 m to 21% at 30 m (about twice this number arrived within ∼2 m of the source). There were two distinct distributions of recaptures: a 'fast' cohort which found the source within 40 s, and a 'slow' cohort which took from one to >20 min, with ∼50% of the flies in each cohort. The fastest flies probably reached the source in a single, mainly straight flight from take-off, at an overall average (straight line) displacement speed of 2.8-4.5 ms^-1 (i.e. close to the preferred flight speed of ∼5 m s^-1). The flies apparently maintained their ground speed largely independent of the wind speed they headed into. The 'slow' cohort had a constant probability of arrival at the source, presumably after losing and re-contacting the plume, and after having stopped at least once on the way. There were no marked correlations with wind parameters, although the probability of recapture increased slightly with the directness of the wind from the source, and the probability of 'slow' flight increased slightly with wind speed. It is inferred that a repeated sequence of anemotactic 'aim-then-shoot' orientation at take-off plus optomotor-steered in-flight correction of direction is used as a form of biassed random walk to bring the flies close to the odour source, rather than the use of moth-type anemotactic zigzagging.     

Copulatory behaviour of the tsetse flies Glossina morsitans and G.austeni

ABSTRACT. The copulatory behaviour of Glossina morsitans morsitans West. and G.austeni Newst. was analysed by filming. After a male and female engaged genitalia, the male performed a repertoire of five actions for 3–4 min: (1) 'rubbing' his metathoracic, tibiotarsal joint against the region of genital contact; (2) 'stroking' or hitting the female's head and thorax with his meso- and metathoracic legs; (3) 'wing flick' by moving his mesothoracic legs in a rowing motion whilst at the same time vibrating the wings as in normal flight; (4) 'wing vibration' with the wings vibrated in the closed position; (5) 'wings out' in which the wings are moved out to the flying position without any observable vibration. Each action was repeated many times, to give variable individual sequences, but declined in frequency exponentially over the first 3–4 min in copulo. The two species differed in the frequency of acts. Shortly before separation, a few hours later, actions 1 and 2 reappeared. Receptive females exhibited little overt behaviour except in the maintenance of a passive stance. Refractory females rejected a mating attempt by flexing the abdomen ventrally, vibrating their wings in the closed position, and pushing the male with meso- and metathoracic legs. The significance and possible functions of male behaviour are discussed in relation to mating in Glossina and other Diptera.     

Upwind flight of tsetse (Glossina spp.) in response to natural and synthetic host odour in the field

Abstract. In Zimbabwe, studies were made of the flight responses of tsetse ( Glossina spp.) to synthetic and natural ox odour using arrangements of electric nets.Tsetse flying away from a target showed a significant upwind bias when a blend of carbon dioxide (2/1 min), acetone (500 mg/h), octenol (0.4 mg/h), 4-methylphenol (0.8 mg/h) and 3-n-propylphenol (0.1 ma) was dispensed 15 m upwind, with c. 35% flying upwind.Without carbon dioxide this percentage was significantly reduced to 15% which was not significantly different from that with no odour (8%).This pattern was not altered by reducing the doses of acetone, octenol and phenols by 10–100 times, to levels comparable to those produced by an ox.With natural ox odour or a synthetic equivalent of ox odour dispensed from a ventilated pit 8 m upwind of the target, c. 28% flew upwind.This was reduced significantly to 15% if carbon dioxide was removed.In studies using a 17 m line of nets arranged orthogonally across the prevailing wind line, c. 50% of the catch was caught on the downwind side in the absence of odour.This increased significantly to c.60% when acetone, octenol and phenols were dispensed 15 m upwind, with or without carbon dioxide.With a shorter line (9 m) or an incomplete one (16.5 m long with 5 times 1.5 m wide gaps along its length) there was no change in the proportion caught downwind.For all three lines, dispensing odour upwind increased the catch 2–5 times on both the up-and downwind sides of the nets.It is concluded that a stronger upwind response to host odour is elicited when carbon dioxide is present.It is suggested that in nature upwind flight is very imprecisely orientated, with tsetse making flights up and down an odour plume 'searching' for a host.     

The effect of host odour on the landing responses of tsetse flies (Glossina morsitans morsitans) in a wind tunnel with and without visual targets

Abstract The effect of artificial host odour on the landing responses of males of Glossina m.morsitans West, and on their reaction to visual targets has been investigated in a wind tunnel. Landing was induced in flies that traversed steep odour gradients as they flew upwind and downwind across the edge of an odour plume, irrespective of whether visual targets were present or not; the landing response could be elicited over a wide range of odourconcentrations. When targets were present such odour gradients also tended to increase the proportion of landing flies which alighted on or near the targets; and the bigger the target, or the hungrier the flies, the greater was the propensity for target landing. In air which was more uniformly permeated with odour, the propensity to land on targets was increased only at high odour concentration.     

Orientation of tsetse flies to wind, within and outside host odour plumes in the field

Abstract Free-flying wild tsetse flies ( Glossina pallidipes Aust. and G. m. morsitans Westw.) were video recorded in Zimbabwe as they flew within an artificial host odour plume at 3, 7 or 15 m from the source, or in no odour, with and without a 0.75 m² vertical, black visual target present aligned with the wind. With no visual target present, flights in odour were strongly biased upwind, and in the absence of odour strongly biased downwind. With the target present, between 16% and 40% of the upwind approaching flies responded visually as they passed the target, by circling it, in proportion to the proximity of the source (taken to be proportional to the mean odour concentration). Crosswind approaching flies (for whom the target will have been visible for some metres away) circled more frequently (34–56%), but without obvious correlation with the odour concentration. Circling flies also responded orthokinetically, by slowing down as they passed the target. The departure directions relative to the wind of flies leaving the target were significantly affected by the odour concentration. At 3 m they left the target in all directions, except possibly avoiding due upwind. At 7 m they left with an obliquely upwind bias, but at 15 m and also in no odour, they left with a strong crosswind bias.     

The optics of tsetse fly eyes in relation to their behaviour and ecology

Abstract The visual acuity of two species of tsetse flies, Glossina morsitans morsitans Westw. and Glossina pallidipes Aust., was investigated. Male G. morsitans eyes have an acute zone in the forward region, with large hexagonal lenses (mean minimum diameter, D=33, SE±0.7 μm), relatively small interommatidial angle (Δ(φ=1.08^o) and angular receptive field of individual ommatidia (Δp) of not less than 1.14^o. A narrow band of square lenses, with intermediate diameter and Δφ, merges with smaller hexagonal lenses in the periphery (24±0.7 μm), with relatively large interommatidial angle (Δφ=3.7^o) and small angular receptive field (Δp = c. 1.6^o). G.pallidipes eyes are similar, except that the lenses in the acute zone are larger than those of G.morsitans , in proportion to their larger body size. Female eyes are not significantly different from male eyes, except that they have a narrower region of binocular overlap (maximum for males = 24^o, for females = 18^o). The eye parameter (p=DΔφ) in the acute zone of male G.morsitans = 0.62, and in the peripheral zone = 1.56. These relatively high values are consistent with fast flight, visual detection of drift due to low wind speeds, mating chases and discrimination of cryptic host animals at high light intensities. The extended region of binocular overlap in males may serve as an early warning system of the approach of potential females. From our estimates, tsetse flies ought to be able to detect small objects against the sky c. 30 min before sunrise and after sunset, and to use their peripheral vision perhaps 15 min earlier and later than this.     

The effect of wind speed on the flight responses of tsetse flies to CO2: a wind-tunnel study

Abstract. Female Glossina morsitans morsitans Westwood were video-recorded in a wind-tunnel as they entered, in cross-wind flight, a broad plume of CO₂ (a component of host odour). At a wind speed that corresponds with peak catches in the field (c. 0.6 ms-¹) odour produced both significant upwind turning responses (in-flight anemotaxis) and kinetic responses (reduced flight speed and increased sinuosity (m-¹). At a wind speed of c. 0.2 ms-¹ flies displayed anemotactic, but not kinetic, responses to odour. At very low wind speeds (0.1ms-¹) neither upwind turning responses nor kinetic responses to odour were detected. The results are discussed with regard to current theory of host-location by tsetse.     

Activity patterns in pregnant tsetse flies, Glossina morsitans

ABSTRACT. Actograph measurements of the spontaneous flight activity of isolated female Glossina morsitans morsitans Westw. were made through their first two pregnancy cycles in constant conditions under LD 12:12. Activity fell from a mean of c. 20 units/day to near zero during the 24 h preceding the day on which larvipositionoccurred. Activity on the day of larviposition rose significantly, to c. 35 units/day, then fell back to the baseline 20 units on subsequent days. The circadian pattern of activity was changed markedly by larviposition: 48 h before it, activity in the morning peak of the usual V-shaped diel pattern was twice normal; over 70% of the flies then fed, and the evening arm of their V disappeared; 24 h before larviposition, most flies were totally inactive, the few that did fly performing only 1 or 2 units/day, and only in the first and last hours of the photophase; on the day of larviposition, the morning peak of the V was reduced by c. 70%, and activity peaked instead during the post-noon 2–3 h, before and during the act of parturition. Almost all larvipositions occurred between noon and lights-out. It is suggested that the c. 48 h of pre-larviposition quiescence may play a role in the fact that pregnant G. morsitans females often survive non-residual aerosol insecticide campaigns.     

Spectral sensitivity and flicker fusion frequencies of the compound eye of salmon and wild-type tsetse flies, Glossina morsitans

ABSTRACT. The spectral sensitivity and flicker fusion frequency (FFF) of wild-type and salmon Glossina morsitans morsitans Westwood (Diptera, Glossinidae) were compared electroretinographically (ERG). Spectral sensitivity curves were similar in shape for dark-adapted wild-type and salmon flies, but salmon flies were over 100 times as sensitive as wild-type flies over much of their sensitivity range. Estimation of the spectral absorption curve (from the differences in ERG sensitivities) for the pigment absent from (or present in low concentration in) the salmon eye suggests that the pigment is an ommochrome. FFF at threshold light intensities was similar in wild-type and salmon flies, but at higher light intensity (1.3 °W/cm²) the FFF of salmon flies increased c. 200–300%, due to the capacity of the salmon eye to adapt rapidly to the flicker stimulus. Body weight had little effect upon spectral sensitivity and FFF. Wild-type males were more sensitive to yellow-green light and had higher FFF than did wild-type females. Salmon males and females did not differ in spectral sensitivity, but females had higher FFF (when tested with 520-nm light) than did males. Old wild-type females did not differ from young females in either spectral sensitivity or FFF. However, old salmon females were more sensitive but had lower FFF than young salmon females. Food deprivation reduced spectral sensitivity and FFF in wild-type males but not in salmon males. Irradiation (10.5 krad) reduced spectral sensitivity ( c. 75–375%) and FFF ( c. 30%) in wild-type males. The greatly increased spectral sensitivity and FFF in salmon flies indicate that these flies may behave differently from wild-type flies in the field. Differences in the way spectral sensitivity and flicker discrimination are affected by dark and light adaptation, and by such factors as age and sex, indicate that these measurements are of two independent phenomena.     

Host odour composition affects host location efficiency of tsetse (Diptera, Glossinidae)

Abstract. Marked Glossina pallidipes Austen were released downwind of an odour source in the field in Zimbabwe and the percentage recaptured at the source on the same day was measured.In the absence of odour, 1.3% of the marked tsetse released from a box or refuge were recaptured, independent of the distance between release point and odour source.The distance was varied from 10 to 100 m.When natural ox odour or a blend of carbon dioxide, acetone, octenol and phenols was dispensed, untransformed recapture percentages of box-released tsetse decreased from 18% for tsetse released at 10 m to 2% for tsetse released at 100 m.Recapture percentages were significantly higher than in the absence of odour at all release distances for ox odour and for release distances up to 75 m downwind for the artificial odour.When a combination of acetone, octenol and phenols or carbon dioxide on its own was dispensed, recapture percentages decreased from 6% for tsetse released at 10 m to 0% for tsetse released at 100 m.With these odours, recapture percentages were higher than in the absence of odour when tsetse were released at 20 m from the source, but were lower than recaptures in the presence of ox odour or the artificial mixture with carbon dioxide.Recapture percentages of flies spontaneously leaving refuges were higher than those of box-released tsetse.Proximity of source had no effect on the recapture percentage of refuge-leaving tsetse and host-location efficiency was close to 100% when host odour was detected at 30 m or less.The results are discussed in relation to the host location strategy of tsetse.     

Development of a system for sterilizing tsetse flies, Glossina spp., in the Held

Various autosterilizing systems were evaluated on natural populations of Glossina pallidipes Austen and G.morsitans morsitans Westwood in Zimbabwe. These involved a clear plastic tower of two or three chambers mounted at the cage position on a trap. Inside one chamber flies could be exposed to the vapour phase of the chemosterilant bisazir, P,P-bis (1-aziridinyl)-N-methylphosphinothioic amide. The system was designed to encourage flies to enter the sterilizing chamber, delaying their exit for sufficient time to expose them to a sterilizing dose. This was accomplished in the most effective system by restriction of the exit to one small hole (6 mm diameter) at the roof-side junction. The number of flies remaining in the chamber declined exponentially. The rate of exit was directly proportional to the density of flies in the sterilizing chamber and to the number of exit holes. The probability of a fly being in this chamber for at least 1 or 7 min (the times taken for female and male G.m.morsitans respectively to receive an ED50) was 0.84 and 0.67 respectively with one fly present. With sixteen flies, these probabilities were 0.76 and 0.18 respectively. Results suggest that it may be possible to develop a cheap, safe and efficient autosterilizer for use on tsetse traps.