The optic neuropiles and chiasmata of Crustacea

Summary On the basis of ontogeny and adult morphology, an interpretation of the arrangement of optic neuropiles and fibre connexions of the Crustacean compound eye is presented. In the embryo of phyllopods and decapods, the ommatidia, the lamina ganglionaris, and the medulla externa are developed synchronously from a common medial proliferation zone. As this zone persists in all investigated adult Crustacea that possess compound eyes, such a derivation of the mentioned structures is taken to be universal within the group. The direction of growth of the lamina ganglionaris is parallel with the row of ommatidia, the growth direction of the medulla externa is perpendicular to it and parallel with the long axis of the eyestalk. This arrangement is more or less retained in most adult non-Malacostracan Crustacea, and the axons of fully developed neurons pierce the optic neuropiles and leave and enter on the neuropile side. As a result, there is no chiasma in the non-Malacostracan groups.The Malacostraca have an extra neuropile, the medulla interna, derived from the medulla terminalis. Chiasmata occur between the lamina ganglionaris and the medulla externa, and between the medulla externa and the medulla interna. This difference from the non-Malacostracans depends on the course of the fibres. Those coming from the lamina ganglionaris leave the lamina on the neuropile side and enter medulla externa between the cell bodies in the perikaryon layer of the medulla externa neurons and the neuropile of the medulla. The fibres from the medulla externa to the lamina come from T-shaped neurons and emanate from the perikaryon layer side, entering the lamina on its neuropile side. The fibre relations between the medulla externa and the medulla interna are similar. Thus in both cases, chiasmata are present from the beginning, but they become obvious when the medulla externa rotates through part of a circle.The directed growth of the optic neuropiles and the course of the fibre connexions are consequently crucial to the understanding of the topographic relations between the neuropiles. A pattern with short neurons connecting neighbouring optic neuropiles and long neurons connecting the medulla externa with the central nervous system is common to all crustaceans.In memoriam Bertil Hanström.This work has been supported by a grant from the Swedish Natural Science Research Council 2760-3, 99-35.     

A Golgi-electron-microscopical study of the structure and development of the lamina ganglionaris of the locust optic lobe

Summary The gross structure as well as the neuronal and non-neuronal components of the lamina ganglionaris of the locust Schistocerca gregaria are described on the basis of light- and electron-microscopical preparations of Golgj (selective silver) and ordinary histological preparations. The array of optic cartridges within the lamina neuropile — their order and arrangement — and the composition of the cartridges are described. There are six types of monopolar neurons: three whose branches reach to other cartridges and three whose branches are confined to their own cartridges. Retinula axons terminate either in the lamina or the medulla neuropiles. There are three types of centrifugal neurons, two types of horizontal neuron, as well as glia and trachea in the lamina neuropile. The development of the lamina neuropile is described in terms of developing monopolar and centrifugal axons, growing retinula fibres, and composition of the developing optic cartridges.MSN was supported in part by a Fulbrights-Hays Scholarsship. We are grateful to the Science Research Council for its grant to PMJS.     

Neuronal connectivity patterns in the compound eyes of Artemia salina and Daphnia magna (Crustacea: Branchiopoda)

Summary The neuronal types and patterns in the visual system of the species Artemia salina and Daphina magna have been studied with the Golgi method and electron microscopy. The lamina contains five classes of neurons: photoreceptor axons, monopolar, centrifugal, tangential and amacrine neurons. The terminals of the receptor axons are distributed in two (A. salina) or three (D. magna) layers. The dilated terminals have an extensive and wide array of fine branches. One axon from each ommatidium bypasses the lamina and terminates in the medulla in A. salina. A. salina has four types of monopolar neurons, two of which are stratified, whereas in D. magna only two types are found, one of which is bistratified. Tangential T-neurons connect the lamina with the protocerebrum. D. magna has in addition one tangential T-neuron connecting both the lamina and the medulla with the protocerebrum. In both species monopolar-type centrifugal neurons connect the medulla and the lamina, whereas that of A. salina has a wide laminar distribution. Both species also have amacrine cells in the lamina. The medulla contains, besides those shared with the lamina, transmedullary neurons (two types in A. salina), amacrine cells and neurons originating in the protocerebrum.Cartridge-type synaptic compartments are lacking in the investigated species, although a periodic arrangement is discernible in the distal portion of the lamina of A. salina. The receptors from three types of specialized contacts in Artemia, one of which involves a dyad. D. magna has only one-to-one synapses. Neurosecretory fibres are absent in A. salina.The investigation was supported by the Swedish Natural Science Research Council (Grant No. 2760-009)     

Monoaminergic neurons in the nervous system of crustaceans

Summary Certain neurons in the nervous system of the malacostracan crustaceans give rise to a predominantly green and a sparse yellow fluorophore in the histochemical fluorescence method of Falck-Hillarp. The same applies to the whole of Crustacea. The green fluorophore is probably a catecholamine; the yellow to brown-yellow has not yet been identified.The biogenic amine responsible for the green fluorescence, besides being found in diffusely distributed fibres, also appears in distinct areas of fibre concentrations in the central nervous system. The protocerebrum of the malacostracans contains three areas: the central body and two areas in the top of the brain, one anterior and one posterior. The latter two are not recognized as separate areas in ordinary histological preparations. In addition, the optic neuropiles are fluorescent, some with a distinct stratification of the fluorophore. The deuto and tritocerebrum and the ventral nerve cord also contain monoaminergic neurons. Of the brightly fluorescent areas in the whole of Crustacea, only the central body consistently exists in all species. The other areas of concentrated fluorescent neuropile are restricted to smaller taxonomic units and differ from each other. p The monoaminergic neurons in Crustacea are sensory, motor, and internuncial, and also belong to a fourth type which mimics the neurosecretory neurons in neurohaemal organs. Only one example of a monoaminergic sensory neuron is known (in Anemia, a non-malacostracan, Aramant and Elofsson 1976), a few motor and a few neurosecretory mimics (the latter in malacostracans). Most are internuncials. Acknowledgement. We have enjoyed the laboratory facilities at the Department of Histology, Faculty of Medicine, and express our sincere thanks to Prof. Bengt Falck.-Grants from the Swedish Natural Science Research Council (2760-007) and the Swedish Medical Research Council (04X-712) supported the work     

Monoamine-containing neurons in the optic ganglia of crustaceans and insects

Summary With the fluorescence method of Falck and Hillarp, the presence and localization of monoaminergic neurons in the optic ganglia of several crustaceans and insects have been investigated. It was found that in both classes the monoaminergic terminals, when present, appeared (especially in the medullae externa and interna of the crustaceans and the medulla of the insects) in strata specific for each species. So far, the only monoamine (visualized by this technique) present in the crustacean optic ganglia is dopamine, whereas in the Insecta, the catecholamines dopamine and noradrenaline, and the indolamine, 5-hydroxytryptamine, are found in the optic lobe. But in the Insecta, different species show different content of these amines.This work was supported by grants 2760-3 and 2760-4 from the Swedish Natural Science Research Council (R.E.), by a fellowship from Deutsche Forschungsgemeinschaft, and a grant from the Swedish Medical Research Council B72-14X-712-D7B (N.K.). We are very grateful to the director of the Department of Histology, Faculty of Medicine, Lund, Professor Bengt Falck, who put all his facilities and knowledge at our disposal.     

The development of the compound eyes ofPenaeus duorarum (Crustacea: Decapoda) with remarks on the nervous system

Summary The development of the compound eyes and nervous system of the penaeid shrimp,Penaeus duorarum, from the first nauplius to the first postlarva, has been studied. The first anlage of the compound eyes is a pair of optic discs on the front of the animal. These increase in size through cell-division until the second protozoea stage, where the eye-stalks appear with ommatidia and optic neuropiles developed. The original neuroectoderm of the optic discs is retained in the shape of a proliferation zone throughout the life of the animal. From the optic discs, develop the ommatidia, the lamina ganglionaris, and the medulla externa. The medullae interna and terminalis develop from cells coming from the brain anlage. From the second protozoea and onwards, the development is less rapid. The final shape of the adult eye is reached during the postlarval stages and includes the appearance of a few more pigments and a perfecting of several features. A scheme for the development of crustacean compound eyes is laid down. Further, the medulla externa of the Malacostraca and the single medulla of non-malacostracan crustaceans are homologized.The continuous growth of the nervous system is traced in the development of the neuropile. The appearance of glomeruli structures is reported, as are also, to some extent, neurosecretory organs. The development of the SPX-organ conforms to that of other decapods.For the sake of simplicity, the findings reported below in Results are grouped under two headings, namely the eye-stalk and the nervous system. Under the eye-stalk will be described both the structures coming from the optic discs comprising the ommatidia, the lamina ganglionaris, and the medulla externa, and the contributions from the nervous system comprising the medulla terminalis and medulla interna. Under the nervous system will be described the rest of the nervous system. The term anlage of the compound eyes is the same as the optic discs and denotes all contributions from this area in the early larva.     

Distribution of GABA-like immunoreactive neurons in the optic lobes of Periplaneta americana

Summary Specific antisera against protein-conjugated -aminobutyric acid (GABA) were used in immunocytochemical staining procedures to study the distribution of the putative GABA-like immunoreactive neurons in the optic lobes of Periplaneta. GABA-like immunoreactive structures are evident in all three optic neuropil regions. Six different populations of GABAergic neurons, whose perikarya are grouped around the medulla, are found within the optic lobe. The number of these immunoreactive cells varies greatly and corresponds to the number of ommatidia of the eye. In the proximal part of the lamina, a coarse network of GABA-positive fibres is recognizable. These are the processes of large field tangential cells whose fibres pass through the distal surface of the medulla. A second fibre population of the lamina is made up of the processes of the centrifugal columnar neurons whose perikarya lie proximally to the medulla. The medulla contains 9 layers with GABAergic elements of variable immunoreactivity. Layers 1, 3, 5, 7 and 9 exhibit strong labelling, as a result of partial overlapping of the processes of centrifugal and centripetal columnar neurons, tangential fibres and/or lateral processes of perpendicular fibres and (possibly) processes of amacrines. A strong immunoreactivity is found in the proximal and distal layers of the lobula.     

A novel wide-field neuron with branches in the lamina of the <Emphasis Type="Italic">Drosophila</Emphasis> visual system expresses myoinhibitory peptide and may be associated with the clock

Although neuropeptides are widespread throughout the central nervous system of the fruifly Drosophila, no records exist of peptidergic neurons in the first synaptic region of the visual system, the lamina. Here, we describe a novel type of neuron that has wide-field tangential arborizations just distal to the lamina neuropil and that expresses myoinhibitory peptide (MIP). The cell bodies of these neurons, designated lateral MIP-immunoreactive optic lobe (LMIo) neurons, lie anteriorly at the base of the medulla of the optic lobe. The LMIo neurons also arborize in several layers of the medulla and in the dorso-lateral and lateral protocerebrum. Since the LMIo resemble LN_v clock neurons, we have investigated the relationships between these two sets of neurons by combining MIP-immunolabeling with markers for two of the clock genes, viz., Cryptochrome and Timeless, or with antisera to two peptides expressed in clock neurons, viz., pigment-dispersing factor and ion transport peptide. LMIo neurons do not co-express any of these clock neuron markers. However, branches of LMIo and clock neurons overlap in several regions. Furthermore, the varicose lamina branches of LMIo neurons superimpose those of two large bilateral serotonergic neurons. The close apposition of the terminations of MIP- and serotonin-producing neurons distal to the lamina suggests that they have the same peripheral targets. Our data indicate that the LMIo neurons are not bona fide clock neurons, but they may be associated with the clock system and regulate signaling peripherally in the visual system.     

The Fine Structure of Photoreceptor Terminals in the Compound Eye of Pandalus borealis (Crustacea)

Seven of the photoreceptor axons of each ommatidium in the compound eye of the prawn Pandalus borealis end in two layers in the optic lamina. They have expanded terminals in the optic cartridges; four distally and three proximally in each cartridge. All seven receptor terminals are presynaptic to one lamina monopolar neuron (M₂) of the cartridge. This monopolar neuron is situated centrally in the cartridge and has a thick axis fibre with radially arranged branches, and its axon has a terminal in medulla externa. At the synapses, an arrowlike presynaptic bar is found facing three postsynaptic profiles. The receptor terminals have several characteristics. Their cytoplasm is filled with empty and coated vesicles, and contains numeorus large mitochondria and clusters of tubular elements. There is a longitudinally arranged fascicle of filaments partly surrounded by electron-dense amorphous material in the terminals. Centrally towards M₂, numerous neural spines invaginate into the terminal. Along the entire terminal periphery, there are invaginations from the glial cells. The terminals also form small knoblike protrusions extending into the surrounding glial cells.     

The optic lobe of Drosophila melanogaster. I. A Golgi analysis of wild-type structure

Summary Golgi studies of the neurons in the optic lobes of Drosophila melanogaster reveal a large number of neuronal cell types. These can be classified as either columnar or tangential. Columnar elements establish the retinotopic maps of the lamina, medulla, and lobula-complex neuropiles. They are classified according to the position of their cell bodies, the number, width, and level of their arborizations, and their projection areas. Tangential elements are oriented perpendicularly to the columns. The arborizations of different tangential neurons are restricted to different layers of the optic neuropiles, within such layers their dendritic fields may span the entire retinotopic field or only part of it. The abundance of cell types inside each of the columnar units of the optic lobe is discussed with regard to its possible functional significance. By means of their stratified arborizations the columnar neurons form what appear to be multiple sets of retinotopically organized parallel information processing networks. It is suggested that these parallel networks filter different kinds of visual information and thus represent structurally separated functional subunits of the optic lobe. Such a parallel organization of visual functions increases the sites for function-specific gene actions and may explain the behavioral phenotypes of recently isolated structural mutants of the optic lobe.     

Function of an eyestalk ganglion,the Medulla terminalis,in olfactory integration in the lobster,Panulirus argus

Summary Ipsilateral antennular dysfunction resulting from total unilateral eyestalk ablation in spiny lobsters does not occur when visual input is restricted by an opaque cap over one eyestalk, or when optic ganglia alone (eg. lamina ganglionaris, medulla externa, medulla interna) are removed. Antennular dysfunction appears only when connections between the most proximal of the four eyestalk ganglia, the medulla terminalis, and the remainder of the cerebral ganglia (brain) are interrupted. We conclude that neural processing of olfactory input from the antennule involves structures in the medulla terminalis.Contribution number 430 from the Bermuda Biological Station for Research, Inc. This work was supported by USPHS Grant NB-06017.     

Localization of substance P-like,leucine-enkephalin-like,methionine-enkephalin-like,and FMRFamide-like immunoreactivity in the eyestalk of the fiddler crab,Uca pugilator

Summary The occurrence and distribution of substance P (SP)-like, methionine-(Met)- and leucine-(Leu)-enkephalinlike, and FMRFamide-like immunoreactivities were determined in the neuroendocrine complex of the eyestalk of the fiddler crab, Uca pugilator, by immunocytochemistry. SP-like immunoreactivity was found in the optic peduncle, sinus gland, medulla externa, medulla interna, lamina ganglionaris, and retinular cells. Met-enkephalin-like and Leuenkephalin-like immunoreactivity was observed in most of the retinular cells, optic peduncle, sinus gland, medulla terminalis, and lamina ganglionaris. However, Met-enkephalin-like, but no Leu-enkephalin-like, immunoreactivity was seen in the medulla terminalis X-organ. FMRFamide-like immunoreactivity could be seen in all parts of the eyestalk except in the sinus gland, lamina ganglionaris, and retinular cells. FMRF-amide-like activity was especially strong in the three chiasmatic regions connecting the optic ganglia. The possibility that these four peptides may function as neuroregulators in the fiddler crab is discussed.This investigation was supported in part by Grant No. PCM-8300064 from the National Science Foundation to MF and Biomedical Research Support Grant No. 2 SO7RRO5373 SUB from the University of Kansas Medical Center to LLV     

Localization of monoaminergic neurons in the central nervous system of Astacus astacus Linné (Crustacea)

Summary The cellular localization of biogenic monoamines in crustaceans was studied by means of a highly specific and sensitive fluorescence method devised by Falck and Hillarp. It was found that neurons displaying specific fluorescence in the central nervous system were confined to the protocerebrum, the medulla externa and interna and the ventral nerve cord. The method allows a distinction between the fluorophores of 5-hydroxytryptamine (and 5-hydroxytryptophan), which emit the yellow light, and the fluorophores deriving from the catecholamines (and DOPA), which emit the green light. Green-fluorescent neurons occurred abundantly in the aforementioned parts of the central nervous system while yellow-fluorescent neurons were sparsely present in the same parts.The present work has been carried out at the departments of Histology and Zoology at the University of Lund. The authors take great pleasure in expressing their warmest thanks for laboratory facilities, provided by Professors Erik Dahl (Zoological Institute) and Bengt Falck (Histological Institute).The research reported in this document has been sponsored by the Air Force Office of Scientific Research under Grant AF EOAR 66-14 through the European Office of Aerospace Research (OAR), United States Air Force and by a grant from the Swedish Natural Science Research Council 99-32 (nr 5995).     

Immunohistochemical localization of dopamine in the brain of the insect Locusta migratoria migratorioides in comparison with the catecholamine distribution determined by the histofluorescence technique

Summary As part of a follow-up study to our previous investigation of the catecholaminergic neurosecretory cells in the brain of adult female locusts (Locusta migratoria migratorioides) by means of the formaldehyde-induced fluorescence method, we have attempted to specify the identity of the amines present in these cells by an immunohistological technique. Using a recently developed anti-dopamine serum, we have demonstrated that the majority of the cate cholaminergic median neurosecretory cells contain dopamine. Moreover, dopamine is present in some cell bodies of other zones of the brain, i.e. the median subocellar neurosecretory cells, perikarya in external areas of the protocerebrum, below the calyces, around the pedunculus, in the optic lobes (between the lobula and the medulla, between the medulla and the lamina), and in external zones of the tritocerebrum. Among the structured neuropils, which were particularly fluorescent in the formaldehyde-induced fluorescence method, only the pedunculus, the posterior part of the central body, the external zones of the - and lobes and the proximal part of the lamina contain little dopamine.     

The first optic ganglion of the bee

Summary The organization, characterization and connectivity patterns of four different interneurone types were studied with the use of Golgi light- and electron-microscopic techniques. All four cell types originate in the outer chiasma; they have an efferent end-branch in the lamina and an afferent one terminating in the distal region of the second optic ganglion, the medulla. These interneurones are referred to as:(i) Garland-cell: The efferent fibre has on its tangential branch numerous centripetal side branches, so-called garlands, which synapse with first- and second-order visual cells. (ii) Y-cell: The lamina branch bifurcates before entering the lamina. It innervates two neighbouring cartridges. Synaptic contacts were seen in two different laminar strata where bottle-brush-like collaterals occurred. (iii) Single bottle-brush cell: The efferent part has only one centrifugal branch, which can be compared morphologically and in terms of synaptology with those of the Y-cell. (iv) Triptychcell: The lamina component innervates three neighbouring cartridges at three different laminar layers interconnecting different first- and second-order visual neurones.The present study provides some essential qualitative and quantitative fine-structural information, which — when compared with adequate physiological data — may lead to a better understanding of the function of the first visual information-processing centre of the bee.     

Neural organisation in the first optic ganglion of the nocturnal bee <Emphasis Type="Italic">Megalopta genalis</Emphasis>

Each neural unit (cartridge) in the first optic ganglion (lamina) of the nocturnal bee Megalopta genalis contains nine receptor cell axons (6 short and 3 long visual fibres), and four different types of first-order interneurons, also known as L-fibres (L1 to L4) or lamina monopolar cells. The short visual fibres terminate within the lamina as three different types (svf 1, 2, 3). The three long visual fibres pass through the lamina without forming characteristic branching patterns and terminate in the second optic ganglion, the medulla. The lateral branching pattern of svf 2 into adjacent cartridges is unique for hymenopterans. In addition, all four types of L-fibres show dorso-ventrally arranged, wide, lateral branching in this nocturnal bee. This is in contrast to the diurnal bees Apis mellifera and Lasioglossum leucozonium, where only two out of four L-fibre types (L2 and L4) reach neighbouring cartridges. In M. genalis, L1 forms two sub-types, viz. L1-a and L1-b; L1-b in particular has the potential to contact several neighbouring cartridges. L2 and L4 in the nocturnal bee are similar to L2 and L4 in the diurnal bees but have dorso-ventral arborisations that are twice as wide. A new type of laterally spreading L3 has been discovered in the nocturnal bee. The extensive neural branching pattern of L-fibres in M. genalis indicates a potential role for these neurons in the spatial summation of photons from large groups of ommatidia. This specific adaptation in the nocturnal bee could significantly improve reliability of vision in dim light. B.G. is grateful for travel awards from the Royal Physiographic Society, the Per Westlings Fond, the Foundation of Dagny and Eilert Ekvall and the Royal Swedish Academy of Sciences. E.J.W. acknowledges the receipt of a Smithsonian Short-Term Research Fellowship and thanks the Swedish Research Council, the Crafoord Foundation, the Wenner–Gren Foundation and the Royal Physiographic Society of Lund for their ongoing support. W.T.W. was supported by general research funds from the Smithonian Tropical Research Institute     

The appearance of monoamines in the adult and developing neurohypophysis of Gallus gallus

Summary Most of the specific monoamine fluorescence of the fowl neurohypophysis is found in the eminentia mediana and the infundibular stem. The densest accumulation of fluorescent structures is located to the zona externa and the subependymal layer, whereas generally only scattered fluorescence is demonstrable in the fiber layer. The neural lobe tissue is provided with very fine smooth fibers often difficult to distinguish. Spectrofluorimetric determinations have shown that noradrenaline is the major catecholamine in the chick neurohypophysis. From the embryological studies it is evident that the monoamine fluorescence first appears in the subependymal layer, the fiber layer and the neural lobe (after about 15 days of incubation). The zona externa fluorescence is not visible until just before hatching. 10 days after hatching the fluorescence intensity of the chick neurohypophysis is similar to that of the adult. Some comparisons are also made with the appearance of monoamines in the mouse.The authors take great pleasure in expressing their warmest thanks for laboratory facilities and good advice provided by Dr. Bengt Falck at the Institute of Histology, Lund, Sweden.This work was supported by grants from the Swedish Natural Science Research Council (project no. 99-35 and 2180-16), from the United States Public Health Service (NB-06701-02) and from the Swedish Medical Research Council (B-69-14 x -56-05 C).     

Comparative anatomy of pigment-dispersing hormone-immunoreactive neurons in the brain of orthopteroid insects

Summary In a comparative study, the anatomy of neurons immunoreactive with an antiserum against the crustacean -pigment-dispersing hormone was investigated in the brain of several orthopteroid insects including locusts, crickets, a cockroach, and a phasmid. In all species studied, three groups of neurons with somata in the optic lobes show pigment-dispersing hormone-like immunoreactivity. Additionally, in most species, the tritocerebrum exhibits weak immunoreactive staining originating from ascending fibers, tritocerebral cells, or neurons in the inferior protocerebrum. Two of the three cell groups in the optic lobe have somata at the dorsal and ventral posterior edge of the lamina. These neurons have dense ramifications in the lamina with processes extending into the first optic chiasma and into distal layers of the medulla. Pigment-dispersing hormone-immunoreactive neurons of the third group have somata near the anterior proximal margin of the medulla. These neurons were reconstructed in Schistocerca gregaria, Locusta migratoria, Teleogryllus commodus, Periplaneta americana, and Extatosoma tiaratum. The neurons have wide and divergent arborizations in the medulla, in the lamina, and in several regions of the midbrain, including the superior and inferior lateral protocerebrum and areas between the pedunculi and -lobes of the mushroom bodies. Species-specific differences were found in this third cell group with regard to the number of immunoreactive cells, midbrain arborizations, and contralateral projections, which are especially prominent in the cockroach and virtually absent in crickets. The unusual branching patterns and the special neurochemical phenotype suggest a particular physiological role of these neurons. Their possible function as circadian pacemakers is discussed.     

A note on the preservation of chromatic information in the lamina of the worker honeybee (Apis mellifera)

Summary Extracellular recordings were taken from a sustained unit in the first optic chiasma of the optic lobe of the worker honeybee. This unit received information from onlyone of the four retinal photopigments, despite the anatomical convergence in the retina and lamina ganglionaris.Supported by AFOSR contract F44620-70-C-0113 and NSF grant GB 30732.     

The unusual visual system of the Strepsiptera: external eye and neuropils

Adult males of the insect order Strepsiptera are characterized by an unusual visual system that may use design principles from compound as well as simple eyes. The lenses of this eye are unusually large and focus images onto extended retinae. The light-gathering ability of the lens is sufficient to resolve multiple points of an image in each optical unit. We regard each unit as an independent image-forming eye that contributes an inverted partial image. Each partial image is re-inverted by optic chiasmata between the retinae and the lamina, where the complete image could be assembled from the neighboring units. The lamina, medulla and lobula are present, but their organization into cartridges is not clearly discernable. Fluorescent fills, whole-tissue stains, and synaptotagmin immunohistochemistry show that the optic neuropils nevertheless are densely packed, and that several parallel channels within the medulla underlie each of the lenses. The size and shape of the rhabdoms, as well as a relatively slow flicker-fusion frequency could suggest that these eyes evolved through a nocturnal life stage.Abbreviations O object size - U object distance - I image size - f focal length - A lens aperture - D lens diameter - interommatidial angle - S light sensitivity of optical system