Evidence for one-way movement detection in the visual system of Drosophila

Optomotor control of course and altitude in the fruitfly, Drosophila melanogaster, requires dense networks of elementary movement detectors (EMD's) which cover most if not all of the visual field. The predominant types of EMD's in these networks represent interactions between neighbouring visual elements along the three main directions of the hexagonal array in the compound eye. — Course control in the walking fly is achieved mainly by pairs of equivalent EMD's which occupy 2 o'clock and 4 o'clock positions with respect to the right eye (Buchner, 1976). Comparison of the turning response and the torque response in the present account confirms the particular properties of this network, and proves the presumed bidirectional sensitivity of its EMD's for the course control responses of legs and wings in the corresponding modes of locomotion. — Altitude control during flight is achieved by a less homogeneous network of EMD's which modifies lift and thrust simultaneously by the appropriate control of the wing beat amplitudes. The predominant types of EMD's in the lateral eye regions occupy 12 o'clock and 2 o'clock positions with respect to the right eye (Buchner et al., 1978). The present evaluation of the optomotor responses of thrust and wing beat confirms the preferred orientation of these EMD's and discloses a pecularity of their internal structure. The movement detectors of this network lack the bidirectional sensitivity of the EMD's in the course control system. At least the fronto-lateral network of the altitude control system seems to consist mainly of pairs of equivalent unidirectional EMD's. The detectors in 12 o'clock position increase wing beat in response to movement of the visual surroundings from inferior to superior. The opposite effect is produced by the detectors in 2 o'clock position which respond to movement from anterior-superior to posterior-inferior. These properties qualify unidirectional EMD's as the functional units of the optomotor control system in the fruitfly. Pairs of unidirectional antagonists would be sufficient to establish the bidirectional sensitivity found in the movement detectors of the course control system.     

The angular orientation of the movement detectors acting on the flight lift response in flies

The lift response of houseflies Musca domestica in fixed flight to periodic gratings movins in 12 different orientations has been measured. Two projectors were arranged symmetrically to the flies stimulating successively 18 circular patches of 50° (25°) diameter (9 for each eye) in their visual field. The shapes of the lift responses measured as a function of the orientation of the moving grating varied when different patches in the visual field were stimulated. A qualitative comparison of these response curves leads to the conclusion that the orientation of the movement detecting substrate acting on the flight lift response varies as a function of the stimulated area in the visual field. A straightforward correlation between the geometry of the ommatidial pattern and the orientation of the movement detecting substrate valid for all stimulated areas of the compound eyes does not seem very likely.     

Processing of figure and background motion in the visual system of the fly

The visual system of the fly is able to extract different types of global retinal motion patterns as may be induced on the eyes during different flight maneuvers and to use this information to control visual orientation. The mechanisms underlying these tasks were analyzed by a combination of quantitative behavioral experiments on tethered flying flies (Musca domestica) and model simulations using different conditions of oscillatory large-field motion and relative motion of different segments of the stimulus pattern. Only torque responses about the vertical axis of the animal were determined. The stimulus patterns consisted of random dot textures (Julesz patterns) which could be moved either horizontally or vertically. Horizontal rotatory large-field motion leads to compensatory optomotor turning responses, which under natural conditions would tend to stabilize the retinal image. The response amplitude depends on the oscillation frequency: It is much larger at low oscillation frequencies than at high ones. When an object and its background move relative to each other, the object may, in principle, be discriminated and then induce turning responses of the fly towards the object. However, whether the object is distinguished by the fly depends not only on the phase relationship between object and background motion but also on the oscillation frequency. At all phase relations tested, the object is detected only at high oscillation frequencies. For the patterns used here, the turning responses are only affected by motion along the horizontal axis of the eye. No influences caused by vertical motion could be detected. The experimental data can be explained best by assuming two parallel control systems with different temporal and spatial integration properties: TheLF-system which is most sensitive to coherent rotatory large-field motion and mediates compensatory optomotor responses mainly at low oscillation frequencies. In contrast, theSF-system is tuned to small-field and relative motion and thus specialized to discriminate a moving object from its background; it mediates turning responses towards objects mainly at high oscillation frequencies. The principal organization of the neural networks underlying these control systems could be derived from the characteristic features of the responses to the different stimulus conditions. The input to the model circuits responsible for the characteristic sensitivity of the SF-system to small-field and relative motion is provided by retinotopic arrays of local movement detectors. The movement detectors are integrated by a large-field element, the output cell of the network. The synapses between the detectors and the output cells have nonlinear transmission characteristics. Another type of large-field elements (pool cells) which respond to motion in front of both eyes and have characteristic direction selectivities are assumed to interact with the local movement detector channels by inhibitory synapses of the shunting type, before the movement detectors are integrated by the output cells. The properties of the LF-system can be accounted for by similar model circuits which, however, differ with respect to the transmission characteristic of the synapses between the movement detectors and the output cell; moreover, their pool cells are only monocular. This type of network, however, is not necessary to account for the functional properties of the LF-system. Instead, intrinsic properties of single neurons may be sufficient. Computer simulations of the postulated mechanisms of the SF-and LF-system reveal that these can account for the specific features of the behavioral responses under quite different conditions of coherent large-field motion and relative motion of different pattern segments.     

Connections between wide-field monocular and binocular movement detectors in the brain of a hawk moth

Summary Recordings were made in the brain of Sphinx ligustri of pairs of directionally selective movement detectors, and the spike trains analysed with a computer for possible synaptic connections between two classes of movement detector. (1) Neurones with large binocular fields which arise in the medial protocerebrum and project to the medulla or lobula of one optic lobe, or to the ventral nerve cord. (2) Movement detectors which project from the lobula complex of one optic lobe to the opposite medial protocerebrum. The majority of the second group had back-to-front preferred directions over the ipsilateral eye, and of these many were weakly sensitive to stimuli to the opposite eye. The ipsilateral receptive field covered most of the eye.Optic lobe output cells with the appropriate preferred direction provide a powerful excitatory input to the binocular movement detectors centrifugal to the medulla. Each centrifugal movement detector probably receives excitatory inputs from no more than two optic lobe output cells with back-to-front preferred direction. The same set of optic lobe output neurones probably feeds several cells projecting to the medulla and lobula of both optic lobes, and, possibly, to the ventral nerve cord.Evidence was obtained that the optic lobe output cells themselves receive few excitatory inputs, and that therefore the receptive fields of their input cells are large.Two moving stimuli were presented in different areas of the receptive field. Movement through the null direction in one area inhibited the response to movement in the preferred direction in another area. This suppression was stronger in optic lobe output cells with front-to-back preferred direction than in units with back-to-front preferred direction. Thus the optic lobe output cells, or wide-field units feeding them, receive inhibitory inputs from wide-field units with the opposite preferred direction.Similar tests in which moving stimuli were presented to both eyes gave results indicating that the binocular centrifugal movement detectors may receive inhibitory inputs from movement detectors with back-to-front preferred direction. The possible functional significance of these inhibitory inputs is discussed.I am very greatful to F. A. Miles for helpful discussion and criticism. Financial support came from the U. K. Science Research Council.     

Comparison between the movement detection systems underlying the optomotor and the landing response in the housefly

Flies evaluate movement within their visual field in order to control the course of flight and to elicit landing manoeuvres. Although the motor output of the two types of responses is quite different, both systems can be compared with respect to the underlying movement detection systems. For a quantitative comparison, both responses were measured during tethered flight under identical conditions. The stimulus was a sinusoidal periodic pattern of vertical stripes presented bilaterally in the fronto-lateral eye region of the fly. To release the landing response, the pattern was moved on either side from front to back. The latency of the response depends on the stimulus conditions and was measured by means of an infrared light-beam that was interrupted whenever the fly lifted its forelegs to assume a preprogrammed landing posture (Borst and Bahde 1986). As an optomotor stimulus the pattern moved on one side from front to back and on the other side in the opposite direction. The induced turning tendency was measured by a torque meter (Götz 1964). The response values which will be compared are the inverse latencies of the landing response and the amplitude of the yaw torque.

1. Optomotor course-control is more sensitive to pattern movement at small spatial wavelengths (10° and 20°) than the landing response (Fig. 1a and b). This suggests that elementary movement detectors (EMDs, Buchner 1976) with large detection base (the distance between interacting visual elements) contribute more strongly to the landing than to the optomotor system.
2. The optimum contrast frequencies of the different responses obtained at a comparatively high pattern contrast of about 0.6 was found to be between 1 and 10 Hz for the optomotor response, and around 20 Hz for the landing response (Fig. 2a and b). This discrepancy can be explained by the fact that the optomotor response was tested under stationary conditions (several seconds of stimulation) while for the landing response transient response characteristics of the movement detectors have to be taken into account (landing occurs under these conditions within less than 100 ms after onset of the movement stimulus). To test the landing system under more stationary conditions, the pattern contrast had to be reduced to low values. This led to latencies of several seconds. Then the optimum of the landing response is around 4 Hz. This is in the optimum range of the optomotor course-control response. The result suggests the same filter time constants for the movement detectors of both systems.
3. The dependence of both responses on the position and the size of the pattern was examined. The landing response has its optimum sensitivity more ventrally than the optomotor response (Fig. 3a and b). Both response amplitudes increase with the size of the pattern in a similar progression (Fig. 3c and d).

In first approximation, the present results are compatible with the assumption of a common set of movement detectors for both the optomotor course-control and the landing system. Movement detectors with different sampling bases and at different positions in the visual field seem to contribute with different gain to both responses. Accordingly, the control systems underlying both behaviors are likely to be independent already at the level of spatial integration of the detector output.     

Temporal modulation of luminance adapts time constant of fly movement detectors

The time constant of movement detectors in the fly visual system has been proposed to adapt in response to moving stimuli (de Ruyter van Steveninck et al. 1986). The objective of the present study is to analyse, whether this adaptation can be induced as well, if the luminance of a stationary uniform field is modulated in time. The experiments were done on motion-sensitive wide-field neurones of the lobula plate, the posterior part of the third visual ganglion of the blowfly, calliphora erythrocephala. These cells are assumed to receive input from large retinotopic arrays of movement detectors. In order to demonstrate that our results concern the properties of the movement detectors rather than those of a particular wide-field cell we recorded from two different types of them, the H1- and the HSE-cell. Both cell types respond to a brief movement stimulus in their preferred direction with a transient excitation. This response decays about exponentially. The time constant of this decay reflects, in a first approximation, the time constant of the presynaptic movement detectors. It was determined after prestimulation of the cell by the following stimuli: (a) periodic stationary grating; (b) uniform field, the intensity of which was modulated sinusoidally in time (flicker stimulation); (c) periodic grating moving front-to-back; (d) periodic grating moving back-to-front. The decay of the response is significantly faster not only after movement but also after flicker stimulation as compared with pre-stimulation with a stationary stimulus. This is interpreted as an adaptation of the movement detector's time constant. The finding that flicker stimulation also leads to an adaptation shows that movement is not necessary for this process. Instead the adaptation of the time constant appears to be governed mainly by the temporal modulation (i.e., contrast frequency) of the signal in each visual channel.     

Sexual difference of lifetime movement in adults of the Japanese skimmer,Orthetrum japonicum (Odonata: Libellulidae), in a forest-paddy field complex

The mark-and-recapture method was used to study the lifetime movement of the Japanese skimmer,Orthetrum japonicum, in a forest-paddy field complex in the warmtemperate zone of Japan. The flight season was from mid April to late June. The age structure showed that the maiden flight occurred towards the forest from the emergence sites (paddy fields) for both sexes. The insects returned to the paddy fields after maturation. The total number of skimmers estimated in the whole survey area was about 1000–2000, of which about 200 males were found in the paddy fields. The average lengths of the immature and reproductive periods were about 10 and 20 days in both sexes, respectively. Most mature males tended to stay in the paddy fields and showed territorial behavior, while most mature females moved frequently between the forest and the paddy fields. The average extent of each territory was about 19 m², being established mainly in the shady paddy fields. Few males were sneakers. The available habitat throughout the life span for the skimmers was both the paddy fields and the forest.     

Visually induced height orientation of the fly Musca domestica

The visually controlled height orientation of fixed flying flies (Musca domestica) was investigated. The flight lift force measured by a transducer drives the vertical motion of a panorama. The dynamical conditions of the free flight are electronically simulated for the fly with respect to this degree of freedom of motion. In most of the experimentally investigated cases the panorama consists of a horizontally oriented narrow dark stripe on a bright background. The fly orientates with respect to the stripe, transporting it into a stable fixation position just below the equatorial plane of its compound eyes. It is experimentally demonstrated that the formalism of the linearized theory of the pattern induced flight orientation — Poggio and Reichardt (1973a) — can be applied to describe the height orientation of the fly. The experimental evidence concerning the simultaneous perception of stripes moving in a well defined manner in front of each of the two compound eyes is consistent with the hypothesis that the two halves of the visual system are perceptually additive.     

Elementary detectors for vertical movement in the visual system of Drosophila

Optomotor thrust responses of the fruitfly Drosophila melanogaster to moving gratings have been analysed in order to determine the arrangement of elementary movement detectors in the hexagonal array of the compound eye. These detectors enable the fly to perceive vertical movement. The results indicate that, under photopic stimulation of a lateral equatorial eye region, the movement specific response originates predominantly from two types of elementary movement detectors which connect neighbouring visual elements in the compound eye. One of the detectors is oriented vertically, the other detector deviates 60° towards the anterior-superior direction (Fig. 5b). The maximum of the thrust differences to antagonistic movement is obtained if the pattern is moving vertically or along a superior/anterior — inferior/posterior direction 30° displaced from the vertical (Fig. 3d,e, Fig. 6). Only one of the detectors coincides with one of the two detectors responsible for horizontal movement detection. This indicates that a third movement specific interaction in the compound eye of Drosophila has to be postulated. — The contrast dependence of the thrust response (Fig. 2) yields the acceptance angle of the receptors mediating the response. The result coincides with the acceptance angle found by analysis of the turning response of Drosophila (Heisenberg and Buchner, 1977). This value corresponds to the acceptance angle expected, on the basis of optical considerations, for the receptor system R 1–6. — The movement-specific neuronal network responsible for thrust control is not homogeneous throughout the visual field of Drosophila. Magnitude and preferred direction of the thrust response in the upper frontal part of the visual field seem to vary considerably in different flies (Fig. 6).     

Properties of individual movement detectors as derived from behavioural experiments on the visual system of the fly

The performance of the fly's movement detection system is analysed using the visually induced yaw torque generated during tethered flight as a behavioural indicator. In earlier studies usually large parts of the visual field were exposed to the movement stimuli; the fly's response, therefore, represented the spatially pooled output signals of a large number of local movement detectors. Here we examined the responses of individual movement detectors. The stimulus pattern was presented to the fly via small vertical slits, thus, nearly avoiding spatial integration of local movement information along the horizontal axis of the eye. The stimulus consisted of a vertically oriented sine-wave grating which was moved with a constant velocity either clockwise or counterclockwise. In agreement with the theory of movement detectors of the correlation type, the time-course of the detector signal is modulated with the spatial phase of the stimulus pattern. It can even assume negative values for some time during the response cycle and thus signal the wrong direction of motion. By spatially integrating the response over sufficiently large arrays of movement detectors these response modulations disappear. Finally, one obtains a signal of the movement detection system which is constant while the pattern moves in one direction and only changes its sign when the pattern reverses its direction of motion. Spatial integration thus represents a simple means to obtain a meaningful representations of motion information.     

Behavior underpins the predictive power of a trait‐based model of butterfly movement

1. Dispersal ability is key to species persistence in times of environmental change. Assessing a species' vulnerability and response to anthropogenic changes is often performed using one of two methods: correlative approaches that infer dispersal potential based on traits, such as wingspan or an index of mobility derived from expert opinion, or a mechanistic modeling approach that extrapolates displacement rates from empirical data on short‐term movements.
2. Here, we compare and evaluate the success of the correlative and mechanistic approaches using a mechanistic random‐walk model of butterfly movement that incorporates relationships between wingspan and sex‐specific movement behaviors.
3. The model was parameterized with new data collected on four species of butterfly in the south of England, and we observe how wingspan relates to flight speeds, turning angles, flight durations, and displacement rates.
4. We show that flight speeds and turning angles correlate with wingspan but that to achieve good prediction of displacement even over 10 min the model must also include details of sex‐ and species‐specific movement behaviors.
5. We discuss what factors are likely to differentially motivate the sexes and how these could be included in mechanistic models of dispersal to improve their use in ecological forecasting.

     

The quantal content of optomotor stimuli and the electrical responses of receptors in the compound eye of the fly Musca

Summary Physical measurements of the energy content of effective optomotor stimuli for the fly Musca support the notion that single light quanta trapped by the photopigment of the retinal receptors generate adequate sensory messages. The results of an electrophysiological experiment on single retinula cells in the fly's eye are presented to strengthen confidence in certain assumptions it was necessary to adopt with regard to receptor optical and spectral properties in order to calibrate the complex movement stimuli. This experiment also emphasizes the small amplitude of electrical signals generated in the receptors by dim but behaviourally effective pattern illumination levels.     

Sex determination in<Emphasis Type="Italic"> Drosophila melanogaster</Emphasis> and<Emphasis Type="Italic"> Musca domestica</Emphasis> converges at the level of the terminal regulator<Emphasis Type="Italic"> doublesex</Emphasis>

Sex-determining cascades are supposed to have evolved in a retrograde manner from bottom to top. Wilkins 1995 hypothesis finds support from our comparative studies in Drosophila melanogaster and Musca domestica, two dipteran species that separated some 120 million years ago. The sex-determining cascades in these flies differ at the level of the primary sex-determining signal and their targets, Sxl in Drosophila and F in Musca. Here we present evidence that they converge at the level of the terminal regulator, doublesex (dsx), which conveys the selected sexual fate to the differentiation genes. The dsx homologue in Musca, Md-dsx, encodes male-specific (MdDSX^M) and female-specific (MdDSX^F) protein variants which correspond in structure to those in Drosophila. Sex-specific regulation of Md-dsx is controlled by the switch gene F via a splicing mechanism that is similar but in some relevant aspects different from that in Drosophila. MdDSX^F expression can activate the vitellogenin genes in Drosophila and Musca males, and MdDSX^M expression in Drosophila females can cause male-like pigmentation of posterior tergites, suggesting that these Musca dsx variants are conserved not only in structure but also in function. Furthermore, downregulation of Md-dsx activity in Musca by injecting dsRNA into embryos leads to intersexual differentiation of the gonads. These results strongly support a role of Md-dsx as the final regulatory gene in the sex-determining hierarchy of the housefly.Edited by D. Tautz     

Thoracic morphology of a flightless mexican grasshopper,Barytettix psolus: Comparison with the locust,Schistocerca gregaria

The thoracic morphology of a flightless grasshopper, Barytettix psolus, is described and compared to that of locusts, Schistocerca gregaria, to evaluate modifications to skeleton, muscles, and the nervous system which have accompanied secondary loss of flight. Barytettix lacks hindwings, has immobile vestiges of forewings and is devoid of skeletal specializations for wing movement and flight. Its pterothoracic musculature resembles that of Schistocerca except for the absence of those muscles which, in locusts, have the primary function of moving the wings, the dorsal longitudinal, tergosternal, first basalar, pleuroalar, and dorsal accessory muscles. Pterothoracic ganglia of Barytettix resemble those of Schistocerca in their gross features, number, and primary branching pattern of nerves, with differences in detail relating to reduction of the flight muscles. The combination of features exhibited in Barytettix represents an extreme reduction in the specialization for wing movements and flight displayed by most acridids, at a level which exceeds that of many brachypterous and some apterous species. While skeletal fusion and loss of muscles indicate loss of flight, the accompanying thoracic stiffening and increase in overall body density may promote more efficient jumping as a means of locomotion.     

Neighborhood size in a beetle pollinated tropical aroid: effects of low density and asynchronous flowering

Summary Genetic neighborhood size and area were estimated from pollinator movements over 3 years in a scarab beetle-pollinated clonal herb, Dieffenbachia longispatha (Araceae) at the La Selva Biological Station, Costa Rica. This species was characterized by low densities of reproductive individuals and asynchronous flowering within the population. The pollinator flight distributions were characterized by relatively long mean distances between consecutive visits to inflorescences (83 m) and movements to the nearest neighboring inflorescence in the appropriate phase of flowering. Pollinator movement distributions between consecutive visits to inflorescences were significantly leptokurtic in 2 of the 3 years. I calculated neighborhood sizes incorporating the levels of kurtosis and found minimal estimates of N _e to be 227–611 ramets and neighborhood area to be 88 000–180 000 m². The three beetle species that made 94% of the visits (Cyclocephala gravis, C. amblyopsis, and Erioscelis columbica) varied in their flight distributions and in their contributions to the estimates of neighborhood size. Cyclocephala amblyopsis exhibited the greatest degree of kurtosis in its movement patterns, and neighborhood size based on its movement was large relative to N _e calculated from movement distributions of the other two beetle species. Long-distance movements of C. amblyopsis (>300 m) accounted for 68% of the neighborhood size.     

Changes in visual fields associated with web reduction in the spider family uloboridae

When visual fields of the primitive orb-weaver, Waitkera waitkerensis, are reconstructed using measurements taken from intact lenses and cross and longitudinal sections of the prosoma, they show that this species has complete visual surveillance, but that none of the visual fields of its eight eyes overlap. The more advanced orb-weaver, Uloborus glomosus, also has eight eyes, but each eye has a greater visual angle, giving this species a complex pattern of overlapping visual fields. Uloborids that spin reduced webs are characterized by reduction or loss of the four anterior eyes and other carapace modifications necessary for them to effectively monitor and manipulate their reduced webs. The eyes of these uloborids have greater visual angles than those of orb-weavers, resulting primarily from perimetric expansion of their retinal hemispheres. Additionally, the axes of their visual fields are more ventrally directed due to greater dorsal than ventral retinal expansion and to ventral redirection of the entire eye. Consequently, even though the anterior lateral eyes of the triangle-weaver Hyptiotes cavatus lack retinae, the species' six functional eyes permit complete visual surveillance and exhibit visual overlap. The single-line-weaver, Miagrammopes animotus, has lost its four anterior eyes, and with them much of the anterior vision and all of the visual overlap found in the other species. However, changes similar to those of H. cavatus permit this species to retain most if its dorsal and ventral visual surveillance. Thus, ocular changes act in consort to maintain relatively complete visual surveillance in the face of eye loss and other major carapace modifications necessary for the operation of reduced webs.     

The effects of nitrogen addition on the growth of two exotic and two native forest understory plants

Many studies have linked the spread of exotic, invasive species to high nitrogen supply, but most of this work does not distinguish between various inorganic forms and different concentrations of available nitrogen. Previous research has suggested that exotic, invasive species common in eastern deciduous forests may preferentially utilize nitrate in contrast to native species that preferentially make use of ammonium. We tested this hypothesis by comparing the growth response of two common forest invaders, Berberis thunbergii and Microstegium vimineum, and two co-occurring native species (Vaccinium pallidum and Hamamelis virginiana) to different forms of nitrogen under varying concentrations in a greenhouse experiment. Two forms of nitrogen (nitrate or ammonium) were added at different concentrations (22, 106, and 212 mg N l⁻¹) to all species. Growth response variables included survival, stem length, stem diameter, above and belowground biomass, and estimated seed production (Microstegium only). Unexpectedly the exotic species did not respond preferentially to nitrate addition. Microstegium responded most strongly to both nitrogen forms depending on the response variable. Berberis and Hamamelis surprisingly reacted similarly to nitrogen additions. As expected, Vaccinium fared poorly under most treatment conditions, but did show some growth in NH₄ ⁺ treatments. Our findings suggest species response to nitrogen addition is complex, and that exotic species do not all respond similarly to nitrogen inputs. In this study, the response of exotic and native species to available nutrients does not provide a general mechanism of invasion success.     

Temporal changes in pollen flow and neighbourhood structure in a population of Saxifraga hirculus L.

Summary The population are of flowering shoots of the perennial herb, Saxifraga hirculus, reaches a max. of 134 m² and an overall density of flowers/m² of 11.4. The flower is mainly visited by a syrphid sp., Eurimyia lineata, and to a lesser extent by another syrphid Neoscia tenur, a moth, Zygaena trifolii, and a fungus gnat, Asindulum nigrum. The distribution of the interfloral flight distance is leptokurtic. The mean flight distance of the visitors is 101 cm. 10% of the flights are much longer (2–8 m: cross-flower patch, and about 20 m: cross-population flights). If they are not included, the mean of flights (<1.7 m) becomes 28 cm. These flights become shorter with increasing flower density. The visitors do not have a nearest-neighbour foraging pattern. They visit on average the 8th nearest neighbour. The distribution of flight directions is uniform. Seed dispersal distances have a leptokurtic distribution and a mean dispersal distance of 13 cm. The ecological neighbourhood area is 66.4 m² and 64.9 m² assuming normality and allowing for leptokurtosis. Z. trifolii with its large proportion of long flights increases the size of the neighbourhood area considerably. The mean flight distance (<1.7 m) is correlated with neighbourhood area. The evolutionary impact of moths and butterflies to plant population structure is stressed.     

Flight pattern induced by temperature in a single-gene mutant of Drosophila melanogaster

Simultaneous intracellular recordings were made from the six dorsal longitudinal flight muscle (DLM) fibers in the temperature-sensitive mutant of Drosophila melanogaster, shibire^{ts 1} (shi). The DLM firing pattern induced by temperature in shi was compared with the DLM pattern of a wild-type fly in stationary flight. The firing pattern, induced at temperatures between about 26 and 27°C, was very similar to that of the wild-type pattern. At higher temperatures, the pattern became abnormal, characterzed by many synchronous firings among the fibers and occasional bursting.