Descending neurons supplying the neck and flight motor of diptera: Organization and neuroanatomical relationships with visual pathways

In dipterous insects, a volume of behavioral and electrophysiological studies promote the contention that three wide‐field motion‐sensitive tangential neurons provide a necessary and sufficient input to specific channels that drive the torque motor during flight. The present studies describe the results of neuroanatomical investigations of the relationships between motion‐sensitive neuropil in the fly optic lobes and descending neurons that arise from a restricted area of the brain and supply segmental neck and flight motor neuropil. The present observations resolve at least 50 pairs of descending neurons supplying flight motor centers in the thoracic ganglia. The majority of descending neurons receive a distributed output from horizontal motion‐sensitive neurons. However, the same descending neurons are also visited by numerous small‐field retinotopic neurons from the lobula plate as well as hitherto undescribed small tangential neurons. Neuroanatomical studies, using cobalt, Golgi, and Texas red histology, demonstrate that these smaller inputs onto descending neurons have dendrites that are organized at specific strata in retinotopic neuropil and that these correspond to horizontal and vertical motion sensitivity layers. Conclusions that only a restricted number of wide‐field neurons are necessary and sufficient for visually stabilized flight may be premature. Rather, neuroanatomical evidence suggests that descending neurons to the flight motor may each be selectively tuned to specific combinations of wide‐ and small‐field visual cues, so providing a cooperative descending network controlling the rich repertoire of visually evoked flight behavior.

[1]  R. Murphey,et al.  Neurospecificity in the cricket cercal system. , 1984, The Journal of experimental biology.

[2]  L. Tolbert,et al.  Patterns of glial proliferation during formation of olfactory glomeruli in an insect , 1989, Glia.

[3]  K. Hausen The Lobula-Complex of the Fly: Structure, Function and Significance in Visual Behaviour , 1984 .

[4]  J P Miller,et al.  Relationships between neuronal structure and function. , 1984, The Journal of experimental biology.

[5]  N. J. Strausfeld,et al.  The resolution of neuronal assemblies after cobalt injection into neuropil , 1977, Proceedings of the Royal Society of London. Series B. Biological Sciences.

[6]  C. Wehrhahn,et al.  Microsurgical lesion of horizontal cells changes optomotor yaw responses in the blowfly Calliphora erythrocephala , 1983, Proceedings of the Royal Society of London. Series B. Biological Sciences.

[7]  R. Hengstenberg Spike responses of ‘non-spiking’ visual interneurone , 1977, Nature.

[8]  Roland Hengstenberg,et al.  Roll-Stabilization During Flight of the Blowfly’s Head and Body by Mechanical and Visual Cues , 1984 .

[9]  G. Geiger,et al.  Visual orientation behaviour of flies after selective laser beam ablation of interneurones , 1981, Nature.

[10]  Vacuolation of an identified peptidergic (proctolin-containing) neuron , 1981, Brain Research.

[11]  V. Rodrigues,et al.  The Antennal Glomerulus as a Functional Unit of Odor Coding in Drosophila Melanogaster , 1989 .

[12]  K. Hensler Corrective Flight Steering in Locusts: Convergence of Extero- and Proprioceptive Inputs in Descending Deviation Detectors , 1989 .

[13]  J Palka,et al.  The cerci and abdominal giant fibres of the house cricket, Acheta domesticus. I. Anatomy and physiology of normal adults , 1974, Proceedings of the Royal Society of London. Series B. Biological Sciences.

[14]  W. Gronenberg,et al.  Descending neurons supplying the neck and flight motor of diptera: Physiological and anatomical characteristics , 1990, The Journal of comparative neurology.

[15]  J. Bacon,et al.  Receptive fields of cricket giant interneurones are related to their dendritic structure. , 1984, The Journal of physiology.

[16]  E. Buchner,et al.  Anatomical Localization of Functional Activity in Flies Using 3H-2-Deoxy-d-Glucose , 1983 .

[17]  N. Strausfeld Atlas of an Insect Brain , 1976, Springer Berlin Heidelberg.

[18]  M. Egelhaaf On the neuronal basis of figure-ground discrimination by relative motion in the visual system of the fly , 1985 .

[19]  Martin Egelhaaf,et al.  Visual course control in flies relies on neuronal computation of object and background motion , 1988, Trends in Neurosciences.

[20]  N. Strausfeld Insect Vision and Olfaction: Common Design Principles of Neuronal Organization , 1989 .

[21]  N. Strausfeld,et al.  Cobalt-coupled neurons of a giant fibre system in Diptera , 1983, Journal of neurocytology.

[22]  R. Murphey Competion and the dynamics of axon arbor growth in the cricket , 1986, The Journal of comparative neurology.

[23]  Alexa Riehle,et al.  Directionally Selective Motion Detection by Insect Neurons , 1989 .

[24]  N. Strausfeld,et al.  Cluster organization and response characteristics of the giant fiber pathway of the blowfly Calliphora erythrocephala , 1990, The Journal of comparative neurology.

[25]  C. H. F. Rowell,et al.  DESCENDING INTERNEURONES OF THE LOCUST REPORTING DEVIATION FROM FLIGHT COURSE: WHAT IS THEIR ROLE IN STEERING? , 1989 .

[26]  Rodney K. Murphey,et al.  Positional information, compartments, and the cercal sensory system of crickets , 1986 .

[27]  Martin Egelhaaf,et al.  Neural Mechanisms of Visual Course Control in Insects , 1989 .

[28]  Erich Buchner,et al.  Behavioural Analysis of Spatial Vision in Insects , 1984 .

[29]  Martin Egelhaaf On the neuronal basis of figure-ground discrimination by relative motion in the visual system of the fly. 2: Figure-dectection cells, a new class of visual interneurones , 1985 .

[30]  N. Strausfeld,et al.  The neck motor system of the fly Calliphora erythrocephala. I: Muscles and motor neurons , 1987 .

[31]  Nicholas J. Strausfeld,et al.  Organizational principles of outputs from Dipteran brains , 1984 .

[32]  C. Wehrhahn,et al.  Neural circuits mediating visual flight control in flies. II. Separation of two control systems by microsurgical brain lesions , 1990, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[33]  A. Spurr A low-viscosity epoxy resin embedding medium for electron microscopy. , 1969, Journal of ultrastructure research.

[34]  Erich Buchner,et al.  [3H]2-Deoxyglucose mapping of odor-induced neuronal activity in the antennal lobes of Drosophila melanogaster , 1984, Brain Research.

[35]  N. Strausfeld The optic lobes of Diptera. , 1970, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[36]  Nicholas J. Strausfeld,et al.  The neck motor system of the fly Calliphora erythrocephala. II: Sensory organization , 1987 .