A specific area of the compound eye in the cricket Gryllus bimaculatus sends photic information to the circadian pacemaker in the contralateral optic lobe

1996 ◽  
Vol 180 (1) ◽  
pp. 63-70 ◽  
Author(s):  
K. Tomioka ◽  
M. Yukizane
2002 ◽  
Vol 205 (9) ◽  
pp. 1305-1314 ◽  
Author(s):  
A. S. M. Saifullah ◽  
Kenji Tomioka

SUMMARYThe bilaterally paired optic lobe circadian pacemakers of the cricket Gryllus bimaculatus mutually exchange photic and circadian information to keep their activity synchronized. The information is mediated by a neural pathway, consisting of the so-called medulla bilateral neurons,connecting the medulla areas of the two optic lobes. We investigated the effects of serotonin on the neural activity in this coupling pathway. Spontaneous and light-induced electrical activity of the neurons in the coupling pathway showed daily variations, being more intense during the night than the day. Microinjection of serotonin or a serotonin-receptor agonist,quipazine, into the optic lobe caused a dose- and time-dependent inhibition of spontaneous and light-induced responses, mimicking the day state. The amount of suppression was greater and the recovery from the suppression occurred faster during the night. Application of metergoline, a non-selective serotonin-receptor antagonist, increased spontaneous activity and light-evoked responses during both the day and the night, with higher effect during the day. In addition, metergoline effectively attenuated the effects of serotonin. These facts suggest that in the cricket's optic lobe, serotonin is released during the daytime and sets the day state in the neurons regulating coupling between the bilaterally paired optic lobe circadian pacemakers.


2012 ◽  
Vol 27 (6) ◽  
pp. 467-477 ◽  
Author(s):  
Yoshiyuki Moriyama ◽  
Yuichi Kamae ◽  
Outa Uryu ◽  
Kenji Tomioka

Development ◽  
1984 ◽  
Vol 83 (1) ◽  
pp. 189-211
Author(s):  
D. J. Emery ◽  
K. A. Bell ◽  
W. Chapco ◽  
J. D. Steeves

A reduced-eye (re) mutant grasshopper of Melanoplus sanguinipes has been characterized by small flat compound eyes lacking facets, no lateral ocelli and only a remnant of the median ocellus. The re grasshoppers walk, jump, fly and feed in a normal manner, but do not respond to visual and auditory stimuli, suggesting they may be blind and deaf. Extracellular recordings from the ventral nerve cord of re mutants verified the lack of neural activity in response to visual and auditory inputs, yet the mutants detected mechanical and tactile stimuli. Electroretinograms implied that a visual deficit may be within the photoreceptors of the compound eye. Histological examination of the compound eyes and ocelli indicated that the cells of the mutant compound eye incompletely differentiate. The optic lamina underlying the retina is missing, as is the outer optic chiasma. The medulla and lobula of the mutant optic lobe are present, however, the neuropil of the medulla lacks the characteristic axonal projection patterns of wild-type grasshoppers. The re grasshopper also lacks all ocellar nerves. Ocellar nerves are normally formed from processes of second order ocellar neurons (SONs), suggesting that if the mutant SONs are present within the protocerebrum, their morphology is drastically altered. Comparison of embryos and juvenile nymphs supports the suggestion that the alterations in the re visual system are the result of abnormal differentiation during development. Even though there is clear evidence of morphological alterations in second and third order optic lobe interneurons, one higher order visual interneuron of the midbrain, the descending contralateral movement detector (DCMD), has the same morphology as the DCMD in a wildtype brain. In this instance, the complete deprivation of the primary sensory input does not appear to alter cellular development.


Development ◽  
1981 ◽  
Vol 66 (1) ◽  
pp. 235-255
Author(s):  
Robert J. Stark ◽  
Michael I. Mote

The compound eyes of Periplaneta americana are connected by optic fibre tracts to an optic lobe composed of three sequential ganglia, the lamina, the medulla and the lobula respectively. The eyes and optic ganglia are organized into repeating sub-units arranged in a regular pattern. During postembryonic development, the number of subunits in the eye (ommatidia) increases from between 50 and 60 to over 2000, with a concomitant increase in the size of the optic lobe ganglia. The patterns of cell growth and proliferation were examined in serial section autoradiagraphs prepared following long and short exposures to [3H]thymidine during each developmental stage. Aspects of structural differentiation were examined in reduced silver-stained sections of nymphs at each developmental stage. Growth of the eye and optic ganglia resulted from the continuous proliferation of new cells throughout postembryonic development. Unlike other body tissues, growth of this system was independent of the moulting cycle. The pattern of growth observed in the optic ganglia directly reflected the growth of the eye. Growth of the compound eye occurs from a special zone of proliferation and differentiation located along all but its posterior margin. The lamina and medulla both grow by cell proliferation from a single neuroblast region located at the apex of the angle subtended by them. Cells which proliferate distally from this region differentiate into lamina neurons, while those that proliferate proximally differentiate into medulla neurons. Axons growing from these two adjacent regions meet at and add new new fibres to the distal end of the medulla neuropil. Specificity of the interneuronal connexions appears to result from a precise temporospatial sequencing of growth with the formation of the optic ganglia dependent on retinal development.


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