TY - JOUR
T1 - Recurrent inversion of visual orientation in the walking fly, Drosophila melanogaster
AU - Bülthoff, Heinrich
AU - Götz, Karl G.
AU - Herre, Manfred
PY - 1982/12
Y1 - 1982/12
N2 - Movement-induced visual orientation in flies depends largely upon predictable responses which establish simple "optomotor balance" or complex "pseudo search" in the appropriate visual environment. Less conspicuous course diverting spontaneous actions of the flies become important in pattern-induced visual orientation. The apparently stochastic spontaneous actions of the housefly Musca domestica still allow powerful probabilistic predictions of orientation during stationary flight (Reichardt and Poggio 1981). The predominance of non-stochastic spontaneous actions such as "body saccades", focussing and shift of "visual attention", plasticity of response components etc. in the fruitfly Drosophila melanogaster (Heisenberg and Wolf 1979-1980) accounts for complementary behavioural options which reduce the relevance of probabilistic predictions of orientation in this fly. The conjecture of "complementary options" is based on a striking antagonism between orientation towards a visual object (fixation), and orientation in the opposite direction (anti-fixation), in the walking fly. Forced choice in a multiple-Y-maze quite definitely elicits fixation in the wild type, and antifixation in the "optomotor blind" mutant ombH31 (Fig. 3). However, these effects cannot be attributed to a continuous predominance of attraction in the wild type and repellence in the mutant. This is shown under comparable conditions of free choice in an arena: The flies of either strain alternate between fixation and anti-fixation of an inaccessible visual object (Fig. 4a), and keep running to and fro between two of these objects in "Buridan's paradigm" (Fig. 4b, c), even if the objects are not alike (Fig. 4d). The sequence of approach, retreat and transition may be repeated a few thousand times to the point of exhaustion (Fig. 5). The process resembles the recurrent alternation of ambiguous figures such as the Necker cube in human perception. The recurrent transition between competitive objects counteracts the accumulation of spontaneous preferences, and is likely to explain the apparent lack of pattern-discrimination under operant and non-operant conditions of continued free choice in Drosophila. The conspicuous dichotomy of fixation and anti-fixation in the same environment is, as yet, incompatible with the phenomenological theory of visually controlled orientation in larger flies.
AB - Movement-induced visual orientation in flies depends largely upon predictable responses which establish simple "optomotor balance" or complex "pseudo search" in the appropriate visual environment. Less conspicuous course diverting spontaneous actions of the flies become important in pattern-induced visual orientation. The apparently stochastic spontaneous actions of the housefly Musca domestica still allow powerful probabilistic predictions of orientation during stationary flight (Reichardt and Poggio 1981). The predominance of non-stochastic spontaneous actions such as "body saccades", focussing and shift of "visual attention", plasticity of response components etc. in the fruitfly Drosophila melanogaster (Heisenberg and Wolf 1979-1980) accounts for complementary behavioural options which reduce the relevance of probabilistic predictions of orientation in this fly. The conjecture of "complementary options" is based on a striking antagonism between orientation towards a visual object (fixation), and orientation in the opposite direction (anti-fixation), in the walking fly. Forced choice in a multiple-Y-maze quite definitely elicits fixation in the wild type, and antifixation in the "optomotor blind" mutant ombH31 (Fig. 3). However, these effects cannot be attributed to a continuous predominance of attraction in the wild type and repellence in the mutant. This is shown under comparable conditions of free choice in an arena: The flies of either strain alternate between fixation and anti-fixation of an inaccessible visual object (Fig. 4a), and keep running to and fro between two of these objects in "Buridan's paradigm" (Fig. 4b, c), even if the objects are not alike (Fig. 4d). The sequence of approach, retreat and transition may be repeated a few thousand times to the point of exhaustion (Fig. 5). The process resembles the recurrent alternation of ambiguous figures such as the Necker cube in human perception. The recurrent transition between competitive objects counteracts the accumulation of spontaneous preferences, and is likely to explain the apparent lack of pattern-discrimination under operant and non-operant conditions of continued free choice in Drosophila. The conspicuous dichotomy of fixation and anti-fixation in the same environment is, as yet, incompatible with the phenomenological theory of visually controlled orientation in larger flies.
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U2 - 10.1007/BF00619785
DO - 10.1007/BF00619785
M3 - Article
AN - SCOPUS:0006914395
SN - 0340-7594
VL - 148
SP - 471
EP - 481
JO - Journal of Comparative Physiology A: Neuroethology, Sensory, Neural, and Behavioral Physiology
JF - Journal of Comparative Physiology A: Neuroethology, Sensory, Neural, and Behavioral Physiology
IS - 4
ER -