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  • 11
    Electronic Resource
    Electronic Resource
    Springer
    Journal of comparative physiology 147 (1982), S. 479-484 
    ISSN: 1432-1351
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Drosophila melanogaster is able to perform osmotropotaxis under open-loop conditions. With an ‘optimal’ stimulus the average turning tendency to the side of higher concentration corresponds to a circular track with radiusr=0.8 cm. The response amplitude does not decrease within 1 or 2 h. Unilaterally antennectomized flies in an homogeneous odor field show a permanent turning tendency towards their intact side. The smallest concentration ratio to elicit osmotropotaxis in normal flies ranges between 6∶10 and 9∶10 at high and between 2∶10 and 5∶10 at an about 50 times lower odor intensity. No negative tropotaxis (i.e. turning to the side of lower concentration) is observed, even with strong repellents.
    Type of Medium: Electronic Resource
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  • 12
    Electronic Resource
    Electronic Resource
    Springer
    Journal of comparative physiology 139 (1980), S. 177-191 
    ISSN: 1432-1351
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary InDrosophila polarization sensitivity as revealed in optomotor experiments is mediated by retinula cells R1–6. In the optomotor turning response of the walking fly the response amplitude is a sinusoidal function of E-vector orientation of the stimulus light. For the effect to occur the area of the visual field in which moving vertical stripes are presented must be embedded in an illuminated surround which covers a large part of the visual field. The phase and amplitude of this sinus function do not reflect directly the polarization sensitivity of the photoreceptors mediating it since a) the amplitude is much larger than could be expected from the measured properties of fly retinula cells, b) the effect can be elicited in parts of the visual field viewed by photoreceptors of which half are oriented in mirror symmetry to the other half (equator, frontal area), c) presentation of the stimulus to either eye (at the same height) does not lead to a phase shift in the sinus functions. (A phase shift of 90 ° would be expected in our experiments if the response reflected the fly's bilateral symmetry.) The data suggest that the fly has an “inner” representation of E-vector orientation. In a closed loop situation in which the fly is illuminated from above by linearly polarized light and is allowed to turn the orientation of the E-vector plane relative to its body axis by its yaw torque it can maintain its optomotor balance (i.e. it can fly straight). Often flies keep their longitudinal body axis roughly parallel or perpendicular to the E-vector plane during the whole experiment (4 min). Flies perform discrete 360 °-loops although the rotating polarizing filter has a 180 ° period. Viewed in the context of the first experiment this observation suggests that the fly, like the bee, evaluates the polarization pattern as a whole and designs its loons accordingly. At least on clear daysDrosophila can make use of the polarization pattern of the free sky in flight orientation. Polarization sensitivity is not restricted to the upper part of the eye: Also with the lower part the fly can use a polarization pattern for course control.
    Type of Medium: Electronic Resource
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  • 13
    Electronic Resource
    Electronic Resource
    Springer
    Journal of comparative physiology 169 (1991), S. 699-705 
    ISSN: 1432-1351
    Keywords: Operant orientation behavior ; Initiating activity ; Learning by doing ; Sensory-motor correlation ; Drosophila melanogaster
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Operant behavior is studied in tethered Drosophila flies using visual motion, heat or odour as operandum and yaw torque, thrust or direction of flight as operans in various combinations (Fig. 1). On the basis of these results a conceptual framework of operant behavior is proposed: (1) It requires a goal (desired state) of which the actual state deviates. (2) To attain the goal a range of motor programs is activated (initiating activity, see Fig. 7). (3) Efference copies of the motor programs are compared to the sensory input referring to the deviation from the desired state (e.g. by cross-correlation). (4) In case of a significant coincidence the respective motor program is used to modify the sensory input in the direction towards the goal. (5) Consistent control of a sensory stimulus by a behavior may lead to a more permanent behavioral change (conditioning). In this scheme operant activity (1–4) and operant conditioning (1–5) are distinguished.
    Type of Medium: Electronic Resource
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  • 14
    Electronic Resource
    Electronic Resource
    Springer
    Journal of comparative physiology 80 (1972), S. 119-136 
    ISSN: 1432-1351
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Phototaxis and optomotor reactions of the mutantsebony and opm 2 are investigated. LikeMusca, Drosophila has two complementary visual input systems, one specialized (e. g.) in optimal contrast transfer (high acuity system, HAS, retinula cells 7 and 8) the other in high sensitivity (HSS, retinula cells 1–6). Inebony the HSS seems to be blocked for phototaxis and optomotor responses (Figs. 1 A, 5). However, even the HAS has a higher threshold intensity than in wild type (Fig. 5). In opm 2 the HSS is disturbed for phototaxis (Fig. 1) but is operating for the optomotor response (Fig. 6). However the HAS seems to be largely suppressed for the optomotor response (Table 2). In the double mutantebony-opm 2 both visual input systems seem to be impaired for movement detection (Fig. 7). Two other properties of the visual system of opm 2 are described. The visual fields of the sampling stations for movement detection are about twice as large as in wild type (Figs. 2A, B). This can not be explained by a disturbance of the optics. In other mutants of this type the visual field size is slightly different. In opm 2 the reaction to movement from front to back (progressive) is specificly suppressed, whereas, at least in flight, the reaction to movement from back to front (regressive) is normal (Table 1, Figs. 3, 4). The degree of suppression of the reaction to progressive movement is variable in individual flies and differs for the three mutants of the opm 2-group (Table 1). In a simple example the use of these mutants for system analysis experiments is demonstrated.
    Type of Medium: Electronic Resource
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  • 15
    Electronic Resource
    Electronic Resource
    Springer
    Journal of comparative physiology 98 (1975), S. 217-241 
    ISSN: 1432-1351
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Partially blind mutants can be used to investigate the processing of visual information in the fruit flyDrosophila. This approach requires (1) procedures for the selection of a variety of partially blind mutants, and (2) a strategy for the identification and coordination of visual malfunctions by comparison of interrelated traits of behaviour. The two selection techniques so far employed to recover partially blind mutants use either the fast phototaxis or the optomotor response as selection determining behaviour. The second method is described here and is applied specifically to select mutants in which one of the two autonomous subsystems of vision designated asHigh Sensitivity System andHigh Acuity System is defective. (The mutants obtained are apparently normal with respect to their HAS whereas the HSS is blocked.) Two sets of experiments have been developed in order to test interrelated traits of behaviour in a comparatively large number of flies. One set of experiments measuresslow phototaxis as a function of light intensity. The other is to determine the optomotor response to moving patterns of different spatial periods as functions of both the average brightness and the speed of the movement. Further techniques such as electroretinography and optical inspection of the eyes are used to complement the behavioural approach. By combination of the different tests a first step has been made in the characterization and classification of partially blind mutants with neuronal disorders obtained by different selection procedures and in different laboratories.
    Type of Medium: Electronic Resource
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  • 16
    Electronic Resource
    Electronic Resource
    Springer
    Naturwissenschaften 70 (1983), S. 70-78 
    ISSN: 1432-1904
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Natural Sciences in General
    Notes: Abstract Initiation as a basic property of behavioral activity is functionally analyzed and discussed at the level of voluntary behavior. Fixed action patterns often are not released by stimuli but are generated by the animal itself through brain processes of the Darwinian type. Analogous to mutations, behavioral “subroutines” are brought up by chance and are subjected to selection either by the change in the situation (trial and the elimination of error) or by mental activity suppressing inappropriate behavior even before it is executed.Initiation improves the chance of survival. It is a prerequisite of goal-oriented behavior, an essential constituent of operant conditioning and presumably the first step in the evolution of thought. According to I. Kant a person is free if, by following his own directive, he does what has to be done. This definition meets the two central criteria of initiation: the independence of releasing stimuli and the adaptive value of the behavior generated.
    Type of Medium: Electronic Resource
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  • 17
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    BioEssays 19 (1997), S. 1065-1073 
    ISSN: 0265-9247
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: In neuroethology, the nervous system and behavior are analyzed in the context of the animal's natural habitat and evolutionary history. For the last 30 years the influence of genetics on neuroethology has steadily grown, particularly in Drosophila. Genetic variants reveal new properties of neurons; they help to dissect neuronal circuits and complex behavioral systems; genetics provides new methods to visualize certain brain structures and to assign behavioral functions to them; and, finally, genetic variants can be used to test ecological models. While single-gene mutations can have highly specific behavioral effects, molecular analysis of the corresponding genes reveals that the latter normally have a much broader functional scope. The ‘graininess’ of a functional model of the brain, therefore, is defined by the independent regulatory units of the genes rather than by the genes themselves.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 18
    Publication Date: 2022-07-19
    Language: English
    Type: article , doc-type:article
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  • 19
    Publication Date: 2022-07-19
    Language: English
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  • 20
    Publication Date: 2022-07-19
    Language: English
    Type: article , doc-type:article
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