Postembryonic development of the visual system of the locust, Schistocerca gregaria

Development ◽  
1978 ◽  
Vol 46 (1) ◽  
pp. 147-170
Author(s):  
Hilary Anderson

In the compound eye of the locust, Schistocerca gregaria, neurons from the retina project to the lamina in a precise topographical mapping. The formation of this projection was investigated in grafting experiments which altered the spatial or temporal relationship between the retina and the lamina. The results show that retina axons tend to grow along the paths of adjacent axons, with no indication of specificity for their normal termination sites. It is suggested that the orderly sequence of retina differentiation during normal development plays a major role in imposing pattern both upon the developing projection and, through some form of inductive interaction between retina and lamina neurons, upon the lamina.

Development ◽  
1978 ◽  
Vol 45 (1) ◽  
pp. 55-83
Author(s):  
Hilary Anderson

The visual system of the locust, Schistocerca gregaria, has a highly ordered and predictable arrangement of neurons. The retina and the outermost layer, or lamina, of the optic lobe are each composed of repeating units, ommatidia and cartridges respectively. Each ommatidium has eight photoreceptor cells, which send axons directly to a group of five neurons in the lamina to form the cartridge. The importance, for the development of this precise pattern, of the mode of growth of the two arrays and of interactions between them was investigated. The spatial and temporal sequences of cell proliferation, differentiation and death in the developing retina and optic lobe were examined quantitatively under normal and experimental conditions. The retina grows from its anterior margin by addition of new ommatidia formed from recruited epidermal cells. The lamina also grows by addition of new neurons to its anterior margin, but these neurons are derived from a stem cell population. The parallel pattern of growth of the retina and lamina may be important for the formation of neuronal connexions between them. The retina grows and differentiates even when deprived of the underlying lamina. In laminae deprived of the ingrowth of new axons from the retina, the production of new neurons is also autonomous, but these neurons do not differentiate, but degenerate. A limited amount of cell death occurs in the laminae of control insects. These two observations suggest that a plausible mechanism for coordinating the sizes of the two arrays during normal development might be production of lamina neurons in excess of requirements and death of those remaining non-innervated.


Development ◽  
1976 ◽  
Vol 36 (2) ◽  
pp. 409-423
Author(s):  
S. Eley ◽  
P. M. J. Shelton

Intercellular junctions in the developing retina of the locust Schistocerca gregaria have been examined by electron microscopy. Different types of junction appear in a well-defined sequence during development. Five stages of ommatidial development are described. Close junctions and punctate junctions are present throughout development. Gap junctions appear transiently amongst the undifferentiated cells, before clearly defined preommatidia can be distinguished. The subsequent disappearance of gap junctions may be correlated with cell determination. Lanthanum studies confirm these findings. The later sequential appearance of adhesive junction types is described. These include septate desmosomes and two types of desmosomes. In the fully differentiated ommatidium only two types of junction remain, these are: desmosomes and rhabdomeric junctions.


2004 ◽  
Vol 91 (1) ◽  
pp. 1-12 ◽  
Author(s):  
Thomas Matheson ◽  
Stephen M. Rogers ◽  
Holger G. Krapp

We demonstrate pronounced differences in the visual system of a polyphenic locust species that can change reversibly between two forms (phases), which vary in morphology and behavior. At low population densities, individuals of Schistocerca gregaria develop into the solitarious phase, are cryptic, and tend to avoid other locusts. At high densities, individuals develop instead into the swarm-forming gregarious phase. We analyzed in both phases the responses of an identified visual interneuron, the descending contralateral movement detector (DCMD), which responds to approaching objects. We demonstrate that habituation of DCMD is fivefold stronger in solitarious locusts. In both phases, the mean time of peak firing relative to the time to collision nevertheless occurs with a similar characteristic delay after an approaching object reaches a particular angular extent on the retina. Variation in the time of peak firing is greater in solitarious locusts, which have lower firing rates. Threshold angle and delay are therefore conserved despite changes in habituation or behavioral phase state. The different rates of habituation should contribute to different predator escape strategies or flight control for locusts living either in a swarm or as isolated individuals. For example, increased variability in the habituated responses of solitarious locusts should render their escape behaviors less predictable. Relative resistance to habituation in gregarious locusts should permit the continued responsiveness required to avoid colliding with other locusts in a swarm. These results will permit us to analyze neuronal plasticity in a model system with a well-defined and controllable behavioral context.


The compound eyes of the solitaria phase individuals of the desert locust, Schistocerca gregaria (Forskål), are vertically striped with mostly 6 and 7, rarely 5 and 8, dark brown stripes, and a number of cream-coloured interstripes. In phase gregaria the interstripes, which are more or less invaded by brown pigment, are partially or wholely masked, the eye in the latter case presenting an almost uniformly dark brown appearance. The postembryonic development of the striped eyes, is described stage by stage. There is no stripe at the time of hatching. In the 6-striped eye one stripe is developed in the first-stage hopper and, subsequently a stripe is added at each of the five moults. In the 7-striped eye the one-moult-one stripe relationship holds good in most stages, but the extra seventh stripe is produced in two ways: (i) By the addition of two stripes at the second moult (i. e. the third-stage hopper has four stripes instead of three); and (ii) by the interposition of an extra-moult, usually in the third stage and rarely in the fourth, during which a new stripe is added (stripe-positive extra-moult). But extra-moulting does not necessarily lead to the addition of a stripe; stripe-neutral extra-moults are not infrequent. The development of the dorsal spot and the subdorsal streak are described. The mechanism of growth and the homology and nomenclature of the stripes and interstripes are discussed. The structure of the compound eyes and the pigmentary basis of stripe formation are described, and their effects on vision in solitaria and gregaria individuals discussed. Vision is discussed on the basis of ommatidial structure and pigmentation. In gregaria eyes a perfect apposition image is formed, the image being sharply defined. An ‘anti-halation’ device, produced by the post-retinular layer of pigment, is present. The eye is suited for diurnal vision, and strong direct sunlight is not avoided. In solitaria eyes the image is of the apposition type in its mode of formation but of the superposition type in effect; it has been termed a ‘pseudo-superposition’ image, and is more diffuse but brighter than in gregaria eyes. The ‘anti-halation’ device is weak and ineffective. The eye is suited for vision in subdued light and perceives movements rather than sharp images. Solitaria individuals, especially hoppers, avoid strong, direct sunlight. The effects of these differences in vision on the behaviour of gregaria - and solitaria -phase individuals are as follows: the former, owing to mutual visual impact induced by the formation of sharp images, tend to be gregarious; and further, owing to the presence of light-absorbing mechanisms, they do not avoid strong sunlight; the latter, on the other hand, owing to the want or comparative ineffectiveness of the above-mentioned features, neither tend to congregate nor to go out boldly into the bright open.


Development ◽  
1969 ◽  
Vol 21 (1) ◽  
pp. 1-21
Author(s):  
Vladimír J. A. Novák

One of the basic assumptions of the author's gradient-factor theory of insect morphogenesis is that the effects of the hypothetical gradient-factor on tissue growth can be reproduced by the juvenile hormone, not only during postembryonic development, but also in the course of embryogenesis (Novák, 1951 a, b, 1956, 1966). This concept was originally based on the more or less indirect evidence supplied by the findings of Pflugfelder (1947) in Dixippus morosus and by those of Novák (1951 b) in Oncopeltus fasciatus. Recently, however, direct evidence has been made available by the work of Sláma & Williams (1966) on Pyrrhocoris apterus and of Riddiford (1966) on Hyalophora cecropia. Using the ‘paper factor’ in the first case and cecropia oil in the second, the above authors succeeded in demonstrating that these substances were able to block embryogenesis when applied to the egg surface or to the female before egg-laying commenced.


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.


Development ◽  
1981 ◽  
Vol 62 (1) ◽  
pp. 241-258
Author(s):  
Mark S. Nowel

There is a topographical mapping of neural elements onto the lamina neuropile of the optic lobe of the cockroach, such that adjacent ommatidia project to adjacent points (optic cartridges) in the lamina neuropile. Postembryonic growth of the compound eye occurs by addition of new ommatidia to its growing margin. Retinula axons grow from the newly formed ommatidia to the lamina. By transplantation experiments in which the position or the orientation of retinal material is altered, it is shown that retinula axons do not make connections in the lamina with respect to their old position and orientation, but rather, in keeping with their new situations, apparently maintaining a retinotopic mapping upon the optic lobe.


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