Responses of the Toad Bufo bufo (L.) to Stationary Prey Stimuli1

In the present work toads (Bufo bufo) are shown to respond with prey catching to stationary dummies without previous or accompanying visual or olfactory stimulation. The subjects very rarely showed jerky head movements which, therefore, cannot be necessary for perception of stationary objects. Size preference with respect to stationary stimuli is about the same as in experiments with moving stimuli. However, differences exist between the effects of stationary and moving stimuli with respect to shape and orientation. If a square measuring 10 times 10 mm and a rectangle measuring 5 times 20 mm, oriented either horizontally or vertically, are presented within the frontal-vertical plane, the square is preferred to the rectangles, and among these the horizontal rectangle is to the vertical one. This latter preference is due to the negative effect of the vertical extension: If the vertical rectangle is reduced in length, it becomes more effective as compared to the horizontal rectangle. In the horizontal (X-Z) plane the square and the rectangle oriented parallel to the Z-axis are equally superior to the bar oriented parallel to the X-axis. At presentation of a pair of stimuli in both planes, the one in the frontal-vertical plane is always preferred to that in the horizontal plane. Correspondences and differences of these results to those from experiments with moving prey dummies are discussed.     

The z-model — A proposal for spatial and temporal modeling of visual threshold perception

By considering only the modulation transfer functions of stationary, uniformly moved, and time modulated sinusoidal gratings it is possible to derive a simple model, the z-model, for the spatio-temporal frequency behaviour of one-dimensional patterns. The transmission function of this model is a band pass function of a single coordinate z, which is a quadratic form of the spatial and temporal frequencies (rotational symmetry with respect to space and time). The model is determined by only three constants. Optionally a time phase which accounts for delay and phase distortion can be added. This model can also be derived from reaction time measurements for switched on sinusoidal gratings. With this model the response of a wide variety of spatio-temporal patterns have been calculated and compared with measured threshold data. For two-dimensional patterns orientational filtering has to be added to the model leading to a further parameter. This model predicts satisfactorily the threshold modulation for a great variety of arbitrary spatio-temporal patterns. However the absolute threshold value for aperiodic transient patterns differs slightly in direction of smaller sensitivity as compared with periodic stationary patterns. This suggests that the peak detection scheme usually used in threshold detection modeling should be replaced by an integrative mechanism.     

Scototaxis and target perception in the camel tickHyalomma dromedarii

The camel tick,Hyalomma dromedarii, exhibited positive scototaxis in an arena, e.g. it oriented towards a black or grey target in front of a white background. The degree of the scototactic response varied with the size and the elevation of the target, with its luminance contrast, with its shape and with the speed by which the target was moved: (1) the response to stationary and moving targets increased with increasing target size; (2) presentation of the targets at an elevation of 11^o–15^o induced the highest response; (3) the response decreased with decreasing luminance contrast of the target; (4) targets with the shape of a disk, a triangle standing on a vertex, a vertical bar or a silhouette of a dromedary caused high responses; a low response was observed when the target was a horizontal bar and there was no response to a striped pattern; (5) the smaller the size of a disk, the faster it had to be moved to elicit an optimum response.The smallest disk which elicited a significant response appeared under a visual angle of 4.8^o for a thick at the starting point. The smallest dromedary-shaped silhouette which elicited a significant response corresponded to the silhouette of a real dromedary at a distance of 18 m.     

Variation in the flash pattern of the firefly,Photuris versicolor quadrifulgens (Coleoptera: Lampyridae)

We sampled a population of signalingPhoturis versicolor quadrifulgens fireflies to quantify the variation in flash patterns emitted by males. Males produced five distinct flash patterns during their mate-searching flights. Four of the patterns consisted of two to five equal-intensity pulses and the fifth pattern type was a flicker, a group of rapid modulations in intensity. We found that the proportions of each pattern remained relatively constant from night to night throughout the season. The different flash patterns produced varied significantly with time of night; patterns having fewer pulses occurred earlier in the evening. Local density, an estimate of competition, did not significantly correlate with flash pattern type. On consecutive emissions, individuals changed their flash types with a mean probability of 0.12 (over all males), and they usually switched between patterns differing by a single pulse (from a two- to a three-pulse pattern, from a three- to a two-pulse pattern, etc.). The nightly temporal changes in flash patterns may be related to tradeoffs between female availability and energetic costs of signaling or the changes may be related to increased predation risk from visual predators. Photuris versicolor quadrifulgens was originally described by Barber (1951) as a subspecies ofP. versicolor. The genusPhoturis is currently under revision by Dr. James E. Lloyd, and this firefly will be given species status.     

Interaction between Depth Order and Density Affects Vection and Postural Sway

Objective

Vection, a feeling of self-motion while being physically stationary, and postural sway can be modulated by various visual factors. Moreover, vection and postural sway are often found to be closely related when modulated by such visual factors, suggesting a common neural mechanism. One well-known visual factor is the depth order of the stimulus. The density, i.e. number of objects per unit area, is proposed to interact with the depth order in the modulation of vection and postural sway, which has only been studied to a limited degree.

Methods

We therefore exposed 17 participants to 18 different stimuli containing a stationary pattern and a pattern rotating around the naso-occipital axis. The density of both patterns was varied between 10 and 90%; the densities combined always added up to 100%. The rotating pattern occluded or was occluded by the stationary pattern, suggesting foreground or background motion, respectively. During pattern rotation participants reported vection by pressing a button, and postural sway was recorded using a force plate.

Results

Participants always reported more vection and swayed significantly more when rotation was perceived in the background and when the rotating pattern increased in density. As hypothesized, we found that the perceived depth order interacted with pattern density. A pattern rotating in the background with a density between 60 and 80% caused significantly more vection and postural sway than when it was perceived to rotate in the foreground.

Conclusions

The findings suggest that the ratio between fore- and background pattern densities is an important factor in the interaction with the depth order, and it is not the density of rotating pattern per se. Moreover, the observation that vection and postural sway were modulated in a similar way points towards a common neural origin regulating both variables.     

Electric Organ Discharge Displays during Social Encounter in the Weakly Electric Fish Brienomyrus niger L. (Mormyridae)

We investigated the electric organ discharge (EOD) activity of the mormyrid fish Brienomyrus niger during social encounters. The fish were contained in porous ceramic shelters and tested alone and in pairs in an experimental tank designed to restrict communication to the electrosensory modality. We moved one fish toward and away from a stationary conspecific, beginning at a distance known to be outside the range of communication (250 cm). Baseline EOD activity was recorded prior to interaction and categorized as ‘variable’, ‘regular’, and ‘scallop’. When moved closer together, the fish modulated this baseline activity in four ways: (1) At 100–130 cm apart, the stationary fish emitted a maximum of sudden EOD rate increases which defined the outer limit of its communication range. (The associated Electric Field Gradient was 1 μV/cm). (2) Long EOD cessations, which we called social silence, lasted from 5–130 s and occurred most frequently when the fish were 36 to 55 cm apart (EFG: 100 μV/cm). The duration of social silence was negatively correlated (r = ? 0.862) with the responding fish's size, and was independent of the partner's sex and size. Fish whose EOD baseline pattern was ‘scallop’ were least likely to fall electrically silent, and those that were categorized as ‘regular’ or ‘variable’ were most likely to cease discharging. (3) Within electrolocation range, fish ‘regularized’ their EOD activity while the partner was ‘silent’ (EFG: 1 mV/cm). (4) Following long EOD cessations the fish resumed discharging with characteristic EOD rebound patterns. The possible ethological significance of these findings is discussed.     

A model of visual perception

In this paper we propose a model of visual perception in which a positive feedback mechanism can reproduce the pattern stimulus on a neurons screen. The pattern stimulus reproduction is based on informations coming from the spatial derivatives of visual pattern. This information together with the response of the feature extractors provides to the reproduction of the visual pattern as neuron screen electric activity. We simulate several input patterns and prove that the model reproduces the percept.     

Which retinal and extra-retinal information is crucial for circular vection?

In contradistinction to conventional wisdom, we propose that retinal image slip of a visual scene (optokinetic pattern, OP) does not constitute the only crucial input for visually induced percepts of self-motion (vection). Instead, the hypothesis is investigated that there are three input factors: 1) OP retinal image slip, 2) motion of the ocular orbital shadows across the retinae, and 3) smooth pursuit eye movements (efference copy). To test this hypothesis, we visually induced percepts of sinusoidal rotatory self-motion (circular vection, CV) in the absence of vestibular stimulation. Subjects were presented with three concurrent stimuli: a large visual OP, a fixation point to be pursued with the eyes (both projected in superposition on a semi-circular screen), and a dark window frame placed close to the eyes to create artificial visual field boundaries that simulate ocular orbital rim boundary shadows, but which could be moved across the retinae independent from eye movements. In different combinations these stimuli were independently moved or kept stationary. When moved together (horizontally and sinusoidally around the subject's head), they did so in precise temporal synchrony at 0.05 Hz. The results show that the occurrence of CV requires retinal slip of the OP and/or relative motion between the orbital boundary shadows and the OP. On the other hand, CV does not develop when the two retinal slip signals equal each other (no relative motion) and concur with pursuit eye movements (as it is the case, e.g., when we follow with the eyes the motion of a target on a stationary visual scene). The findings were formalized in terms of a simulation model. In the model two signals coding relative motion between OP and head are fused and fed into the mechanism for CV, a visuo-oculomotor one, derived from OP retinal slip and eye movement efference copy, and a purely visual signal of relative motion between the orbital rims (head) and the OP. The latter signal is also used, together with a version of the oculomotor efference copy, for a mechanism that suppresses CV at a later stage of processing in conditions in which the retinal slip signals are self-generated by smooth pursuit eye movements.     

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.     

On the invariance of visual stimulus efficacy with respect to variable spatial positions

Summary In the fly,Calliphora erythrocephala, visual stimuli presented in an asymmetrical position with respect to the fly elicit roll or tilt movements of the head by which its dorsal part is moved towards the light areas of the surroundings (Figs. 4–7). The influence of passive body roll and tilt (gravitational stimulus) on the amplitude of these active head movements was investigated for two types of visual stimuli: (1) a dark hollow hemisphere presented in different parts of the fly's visual field, and (2) a moving striped pattern stimulating the lateral parts of one eye only.The response characteristics of the flies in the bimodal situation in which the gravitational stimulus was paired with stimulation by the dark hollow hemisphere can be completely described by the addition of the response characteristics for both unimodal situations, i.e. by the gravity-induced and visually induced characteristics (Figs. 8, 9). Therefore, the stimulus efficacy of the dark hollow hemisphere is independent of (=invariant with respect to) the flies' spatial position. The advantage of this type of interaction between gravity and visual stimulation for the control of body posture near the horizontal is discussed.In contrast, the efficacy of moving patterns depends on (=non-invariant with respect to) the spatial position of the walking fly. Regressive pattern movements exhibit their stronger efficacy with respect to progressive ones only when the gravity receptor system of the legs is stimulated. The stronger efficacy of downward vs upward movements can only be demonstrated when the flies are walking horizontally, independently of whether the leg gravity receptor system is stimulated by gravity or not (Fig. 10).The results are discussed with respect (1) to the invariance and non-invariance of the efficacy of visual stimuli with respect to the direction of the field of gravity, (2) to the formation of reference lines by the gravitational field which are used by the walking fly to determine the orientation of visual patterns, and (3) to the possible location of the underlying convergence between gravitationally and visually evoked excitation. As all types of head responses occur only in walking flies, we also discussed the possible influences of some physiological processes like arousal, proprioceptive feedback during walking and various peripheral sensory inputs on the performance of behavioural responses in the fly (Fig. 11).     

Optokinetic speed control and estimation of travel distance in walking honeybees

Honeybees returning from foraging trips were video-filmed while they walked through a narrow transparent gangway to reach the hive entrance. On their way they were presented with black-and-white gratings viewed underneath as well as to both sides of the gangway. Bees could exit the gangway through one of two or three side exits installed at different distances from the gangway entrance. In one set of experiments, the substrate on which the bees walked was moved either in the bee's direction or against it. In another set of experiments, the substrate was stationary, but the pattern was moved in one or the other direction. The bee's walking speed (WS) was evaluated from the video tapes. When the substrate moved against, or the pattern in the bee's direction, in either case decreasing the speed of pattern flow (PFS), the bees increased WS, and, at the same time, they preferred the more distant exit. When the substrate moved in, or the pattern against the bee's direction, thus increasing PFS, WS decreased and the bees preferred the nearer exit. These results suggest that the speed of optic flow controls the speed of locomotion and might therefore also serve for assessing the distance travelled.Abbreviations PFS pattern-flow speed - WS walking speed Dedicated to Hans-Jochen Autrum, editor emeritus, for help in giving birth to this and many other papers over very many years, often with criticism but nevertheless with encouragement and sympathy.     

Transformation and relational-structure schemes for visual pattern recognition

Two models for visual pattern recognition are described; the one based on application of internal compensatory transformations to pattern representations, the other based on encoding of patterns in terms of local features and spatial relations between these local features. These transformation and relational-structure models are each endowed with the same experimentally observed invariance properties, which include independence to pattern translation and pattern jitter, and, depending on the particular versions of the models, independence to pattern reflection and inversion (180° rotation). Each model is tested by comparing the predicted recognition performance with experimentally determined recognition performance using as stimuli random-dot patterns that were variously rotated in the plane. The level of visual recognition of such patterns is known to depend strongly on rotation angle. It is shown that the relational-structure model equipped with an invariance to pattern inversion gives responses which are in close agreement with the experimental data over all pattern rotation angles. In contrast, the transformation model equipped with the same invariances gives poor agreement to the experimental data. Some implications of these results are considered.     

不同运动图象同时刺激左右眼时的交替视动震颤(OKN)现象

采用了同时对左右眼分别以不同的运动图象刺激的实验方法,来测量及分析其OKN眼动反应,探索在OKN反映中两眼之间的输入关系以及眼动控制机制。实验结果发现在两眼的刺激图象不一致时,眼动反应为交替的OKN反应,即中枢神经系统根据各眼的刺激速度,交替地控制产生OKN眼动反应。本文还从闭环控制上讨论了视网膜上速度误差信号的作用。     

A systematic comparison of summary characteristics for quantifying point patterns in ecology

Many functional summary characteristics such as Ripley's K function have been used in ecology to describe the spatial structure of point patterns to aid understanding of the underlying processes. However, their use is poorly guided in ecology because little is understood how well single summary characteristics, or a combination of them, capture the spatial structure of real world patterns. Here, we systematically tested the performance of combinations of eight summary characteristics [i.e. pair correlation function g(r), K‐function K(r), the proportion E(r) of points with no neighbor at distance r, the nearest neighbor distribution function D(r), the spherical contact distribution H_s(r), the kth nearest‐neighbor distribution functions D_k(r), the mean distance nn(k) to the kth neighbor, and the intensity function λ( x )]. To this end we used point pattern data covering a wide range of spatial structures including simulated (stationary) as well as real, possibly non‐stationary, patterns on tree species in a tropical forest in Panamá. To measure the information contained in a given combination of summary characteristics we used simulated annealing to reconstruct the observed patterns based only on the limited information provided by this combination and assessed how well other characteristics of the observed pattern were recovered. We found that the number of summary characteristics required to capture the spatial structure of stationary patterns varied between one (for patterns with near random structures) and three (for patterns with complex cluster and superposition structures), but with a robust ranking g(r), D_k(r), and H_s(r) that was largely independent on pattern idiosyncrasies. Stationary summary characteristics [with ranking g(r), D_k(r), H_s(r), E(r)] captured small‐ to intermediate scale properties of non‐stationary patterns, but for describing large‐scale spatial structures the intensity function was required. Our finding revealed that the current practice in ecology of using only one or two summary characteristics bears danger that essential characteristics of more complex patterns would not be detected. The technique of pattern reconstruction presented here has wide applications in ecology.     

不同运动图象同时刺激左右眼时的交替视动震颤(OKN)现象

采用了同时对左右眼分别以不同的运动图象刺激的实验方法,来测量及分析其OKN眼动反应,探索在OKN反映中两眼之间的输入关系以及眼动控制机制。实验结果发现在两眼的刺激图象不一致时,眼动反应为交替的OKN反应,即中枢神经系统根据各眼的刺激速度,交替地控制产生OKN眼动反应。本文还从闭环控制上讨论了视网膜上速度误差信号的作用。     

Television epilepsy and pattern sensitivity.

Properly functioning domestic television sets may induce seizures in epileptic patients (TV epilepsy). We investigated the effects of different types of visual stimuli on paroxysmal electroencephalographic (EEG) activity in 32 patients known to be sensitive to intermittent photic stimulation (stroboscopic light). We monitored sensitivity to patterns of horizontal and vertical lines, both stationary and vibrated (pattern sensitivity), and to normal broadcasts on a domestic, black and white (405- or 625-line) TV receiver (TV sensitivity). Twenty-three of the 32 patients were sensitive to pattern. Twenty-two were sensitive to vibrated patterns, and 11 to static patterns (P less than 0-01), All patients sensitive to pattern were also sensitive to TV; The association between sensitivity to pattern and to TV was significant. Clinical history of TV epilepsy (16 out of 32 patients) and laboratory evidence of pattern or TV sensitivity were not significantly associated. The high incidence of pattern sensitivity among flicker-sensitive patients and its association with TV sensitivity suggests that linear patterns produced by the raster of a black and white set as it scans, or "line-jitter" produced by the raster in areas of low TV-signal strength may contribute to the epileptogenic effect of TV.     

Motion-based analysis of spatial patterns by the human visual system

BACKGROUND: It is known that the visibility of patterns presented through stationary multiple slits is significantly improved by pattern movements. This study investigated whether this spatiotemporal pattern interpolation is supported by motion mechanisms, as opposed to the general belief that the human visual cortex initially analyses spatial patterns independent of their movements. RESULTS: Psychophysical experiments showed that multislit viewing could not be ascribed to such motion-irrelevant factors as retinal painting by tracking eye movements or an increase in the number of views by pattern movements. Pattern perception was more strongly impaired by the masking noise moving in the same direction than by the noise moving in the opposite direction, which indicates the direction selectivity of the pattern interpolation mechanism. A direction-selective impairment of pattern perception by motion adaptation also indicates the direction selectivity of the interpolation mechanism. Finally, the map of effective spatial frequencies, estimated by a reverse-correlation technique, indicates observers' perception of higher spatial frequencies, the recovery of which is theoretically impossible without the aid of motion information. CONCLUSIONS: These results provide clear evidence against the notion of separate analysis of pattern and motion. The visual system uses motion mechanisms to integrate spatial pattern information along the trajectory of pattern movement in order to obtain clear perception of moving patterns. The pattern integration mechanism is likely to be direction-selective filtering by V1 simple cells, but the integration of the local pattern information into a global figure should be guided by a higher-order motion mechanism such as MT pattern cells.     

Renouvellement des protéines et effet spécifique de la kinétine sur des cultures de cellules de Tabac

Determination and fractionation of proteins of tobacco cell suspensions requireing kinetin for cell division. — Cell suspensions either in stationary phase without kinetin in the medium or dividing in the presence of this factor have been compared. It was found a) that the specific rates of protein synthesis and protein degradation were not changed by the addition of kinetin during the early period of growth. A quantitative change ocurred only after the first generation period, b) Soluble proteins of these cells were mapped by polyacrylamide gel electrophoresis. The observed protein patterns were very similar as well as the patterns or radioactivity incorporated into the same proteins during the incubation period of the cells. However, a small number of specific discrepancies appeared in the pattern of cells growing in the presence of kinetin matched to the patterns of stationary cells. At least one specific difference in these patterns could be observed before the first cell division occurred.     

Age and Sex-Based Differences in the Use of Prey Sensory Cues in Wolf Spiders (Araneae: Lycosidae)

Differences in foraging patterns mediated by sensory cues were examined between adult and juvenile male and female wolf spiders (Schizocosa rovneri; Lycosidae). Patch residence time for thirty-one spiders were tested among juveniles and adults in artificial foraging patches. Patches varied in sensory information provided by live prey (crickets) as follows: visual stimuli alone; vibratory stimuli alone; visual and vibratory stimuli together; and control (no stimuli). Spiders moved between patches for one hour, but could not feed. Adult Schizocosa rovneri use primarily visual information to determine patch residence time, but juveniles use vibratory cues as well. Significant age and sex-based differences in the use of sensory cues suggest that observed divergent foraging strategies are partly due to the use of different perceptual cues in prey detection.     

A theory of the pattern induced flight orientation of the fly Musca domestica

The theory presented here describes the visual orientation behavior of fixed flying insects (the fly Musca domestica) in the presence of elementary patterns. The theory, which is based on a number of experimental results, Reichardt (1973), is a phenomenological one whose main purpose is to provide an organizational framework for treating a complex phenomenon without the need of detailed assumptions about the neural mechanisms actually involved.A simple hypothesis concerning the basic structure of the pattern fixation process leads to an equivalent stochastic equation of the Langevin type, which can be linearized for simple single-stripe panoramas. A critical experiment supports these theoretical assumptions. In addition, the effect on pattern fixation behavior of adding contrast noise to the background of the panorama, is quantitatively predicted by the theory.In the more general case of a panorama consisting of many vertical stripes, the Fokker-Planck equation associated with the Langevin equation, no longer linear, is solved. Making use of an experimentally proven superposition principle, the stationary pattern fixation behavior of the fly in an arbitrary panorama consisting of a collection of vertical stripes is predicted. In this context, concepts like pseudo-invariance and phase-transition can be applied to the insects orientation behavior. The theory presented here seems to contain rich classification properties, which might provide the foundations for an understanding of more complex pattern discrimination processes.Possible extensions of the theory, as well as some similarities to human eye fixation, are also discussed.