The lateral eyes of the scorpion,Androctonus australis

Summary The dioptric apparatus of the lateral eyes of the scorpion, Androctonus austrails, consists of a cuticular lens, but lacks a vitreous body. The retina is formed by (1) retinula cells displaying a contiguous network of rhabdoms; (2) arhabdomeric cells bearing a distal dendrite that contacts retinula cells via numerous projections and ends before the rhabdomere of the retinula cells; (3) pigment cells that ensheath retinula and arhabdomeric cells with the exception of the contact regions; and (4) neurosecretory fibres possibly originating in the supraesophageal ganglion. The ratio of the number of retinula to arhabdomeric cells is determined to be close to 2 1 in the three larger anterolateral eyes, in contrast to the median eyes where the ratio is 5 1.The construction of the dioptric apparatus as well as the anatomy of the retina imply that in the lateral eyes of Androctonus australis visual acuity is reduced. A certain degree of spatial discrimination, however, may be retained by the presence of a relatively high number of arhabdomeric cells. It is suggested that the lateral eyes of A. australis mainly function as light detectors, e.g., for Zeitgeber stimuli.Supported by grant no. FL 77/8-10 from the Deutsche Forschungsgemeinschaft     

Fine structure and optical properties of an ostracode (Crustacea) nauplius eye

Summary InNotodromas monachus, the three cups of the nauplius eye are formed by four pigment cells. The insides of the cups are lined with tapetal cells, which produce several layers of reflecting crystals. The reflecting crystals form a concave mirror in each cup upon which the retinular cells rest. The two-celled rhabdoms are few and perpendicular to the tapetal layer. The axons from the tripartite eye leave the retinular cells distally in three separate groups. The eye is thus of the inverse type. Large lens cells, with a low refractive index, are present in the open part of each cup. Distal to the lens cells, highly refractive lenses are formed in the cuticle. These lenses serve to decrease the effective curvature of the mirrors, thus enabling the reflectors to produce a focused image on the retina. The ventral cup differs by the lack of a cuticular lens and has degenerated-appearing cellular elements. The investigated nauplius eye is the only one known with both a mirror and a highly refractive lens in the dioptric apparatus.This investigation has been supported by grants from the Swedish Natural Science Research Council (grant no. 2760-009) and the Royal Physiographic Society of Lund.     

Visual fields and eye morphology support color vision in a color-changing crab-spider

Vision plays a major role in many spiders, being involved in prey hunting, orientation or substrate choice, among others. In Misumena vatia, which experiences morphological color changes, vision has been reported to be involved in substrate color matching. Electrophysiological evidence reveals that at least two types of photoreceptors are present in this species, but these data are not backed up by morphological evidence. This work analyzes the functional structure of the eyes of this spider and relates it to its color-changing abilities. A broad superposition of the visual field of the different eyes was observed, even between binocular regions of principal and secondary eyes. The frontal space is simultaneously analyzed by four eyes. This superposition supports the integration of the visual information provided by the different eye types. The mobile retina of the principal eyes of this spider is organized in three layers of three different types of rhabdoms. The third and deepest layer is composed by just one large rhabdom surrounded by dark screening pigments that limit the light entry. The three pairs of secondary eyes have all a single layer of rhabdoms. Our findings provide strong support for an involvement of the visual system in color matching in this spider.     

Ocellar fine structure inCaenis robusta (Ephemeroptera), Trichostegia minor,Agrypnia varia,andLimnephilus flavicornis (Trichoptera)

Summary Three dorsal ocelli are present inCaenis robusta (Ephemeroptera), Trichostegia minor, Agrypnia varia, andLimnephilus flavicornis (Trichoptera). The dioptric apparatus of the ocelli differs between the four species. InTrichostegia andAgrypnia a biconvex corneal lens is present, inLimnephilus the corneal lens is convexo-concave complemented by an underlying haemocoelic space, whereas a cellular vitreous body is found between the cuticle and the retinal layer in the ephemerid. In the three trichopteroid species the ocelli are surrounded by an array of longitudinally arranged tracheoles; inCaenis a layer of screening pigments is found in this position. In this species the rhabdoms formed by microvilli of neighbouring retinula cells have a randomly arranged meshwork pattern; in the three trichopteroid species the rhabdoms are isolated, built up of four retinula cells. Cells with basally situated nuclei and lamellar extensions between the retinular cells are found in the ocelli ofTrichostegia, Agrypnia, andLimnephilus.     

Sexual Dimorphism in the Compound Eye of Rhagophthalmus ohbai (Coleoptera: Rhagophthalmidae): I. Morphology and Ultrastructure

The eyes of the winged males and larvi-form, wingless females of the firefly Rhagophthalmus ohbai differ from each other in several respects. Compared with the eyes of the males, those of the females contain fewer (35 versus ca. 3500) and smaller (20 μm versus 24-31 μm) facets and anatomically they are of the apposition type. Their main function appears to be to detect light intensity changes from day to nighttime; resolving power of the female eye must be poor and e-vector discrimination would be absent. The eyes of the males consist of a smaller, dorsal region of ca. 500 om-matidia of about 250 μm length and a larger, ventral region of ca. 2000 ommatidia of about 640 urn length. The microvilli of the dorsal eye region are somewhat wider than those of the ventral region (55 nm versus 45 nm) and are less regularly arranged. A tapetal reflecting layer is only present in the dorsal eye region. The small clear-zone between dioptric apparatus and retina in the dorsal eye region would not allow as good a superposition image to be produced as in the ventral eye region with its 5 times wider clear-zone. The regular orientations of the microvilli in the rhabdoms and the lack of a proper tapetum in the ventral eye region suggest that e-vector discrimination should be possible.     

Postembryonic eye growth in the seashore isopod Ligia exotica (Crustacea,Isopoda)

The eye of Ligia exotica is of the apposition type and has open rhabdoms. The facets are hexagonal, and the dioptric apparatus consists of a flat cornea and a spherical crystalline cone placed in the center of two large cone cells. Each ommatidium has seven regular retinula cells and one eccentric cell; a basement membrane forms the proximal boundary of the retina. With increases in body size from 0.6 to almost 4.0 cm, facet numbers and ommatidial diameters increased from 800 to 1500 and 35 microm to 100 microm, respectively; eye length and width grew from 1.2 to 3.2 and 0.9 to 2.5 mm, respectively; and length of dioptric apparatus and width of retinal layer changed from 70 microm to 180 microm and about 70 microm to 120 microm. Visual angles and interommatidial angles of centrally located ommatidia remained constant at about 30 and 6.9 degrees, respectively. An almost perfect linear relationship was found when eye length was plotted against the product between the square root of the total number of ommatidia and the ommatidial diameter. No difference between males and females was observed in any of the relationships, but the results suggest that, compared with smaller specimens, larger ones possess increased absolute sensitivity in single ommatidia, increased sensitivity to point sources, and overall larger angular visual fields for the eye in its totality. This means that larger individuals of L. exotica (which are also faster) have an advantage over smaller individuals at night, but that smaller individuals may cope better with bright lights. Vision in L. exotica seems useful not only in detecting potential danger, but also in locating and approaching cliffs from a distance of 2-4 m when swimming in seawater.     

The fine structure of the lateral eyes ofNeocarus texanus Chamberlin and Mulaik, 1942 (Opilioacarida,Acari, Arachnida,Chelicerata)

Summary Neocarus texanus, a primitive mite, bears two pairs of eyes, which are principally similar in ultrastructure. Each eye is covered externally by a cuticular cornea. It is underlain by flat sheath cells which send extensive processes into the retina. The retina is composed of distal and proximal cells. The 20 distal cells of the anterior eye are inversely orientated and form 10 disc-like rhabdoms. They represent typical retinula cells. Each rhabdom encloses the dendritic process of a neuron, the perikaryon of which is located outside the retina (proximal cells). The significance of this cell is not known. The retina is underlain by a crystalline tapetum. In the posterior eye 14 retinula cells form 7 rhabdoms in an arrangement similar to the anterior eye. The eyes of one side of the body are located within a capsule of pigment cells. Together the axons of the distal and proximal cells form the two optic nerves, one on each side of the body. The optic nerves leave the eyes anteriorly and terminate in two optic neuropils located in the brain.From structural evidence it is concluded, that the resolution of the eyes must be rather low.The peculiar proximal cells have not been observed previously in Acari. They probably resemble at best the eccentric cells and arhabdomeric cells of xiphosurans, scorpions, whip-scorpions and opilionids. Also, inverse retinae and tapeta of the present type have not been found in Acari until now, but are present in other Arachnida. Thus the eyes ofNeocarus texanus evidently represent a unique type within the Acari.     

The fine structure of the visual system of Lycosa (Araneae: Lycosidae)

Summary Wolf spiders have four pairs of eyes distributed in three rows. The first row which lie in the frontal region of the caparace, just above the chelicera, contains four eyes: a medial pair known as the anterior medial eyes (AM eyes or principal eyes) and two smaller eyes known as the anterior lateral eyes (AL eyes). The second row which is located also in the frontal region of the prosoma consists of two big eyes. These are the posterior median eyes (PM eyes). The third row contains the posterior lateral eyes (PL eyes) which lie in the flanks of the prosomal caparace. The AL, PM and PL eyes are the so-called secondary eyes.The electron microscope shows that the AM eye photoreceptor cells have the rhabdomere in their distal segment, just behind the vitreous body. The rhabdomere consists of closely packed microvilli about 0.5 long exhibiting a uniform diameter of 500 Å. Each rhabdom consists of two rhabdomeres. The distal segment of the photoreceptor has a prismatic shape with four or five faces depending of their location within the retina.The distribution of the rhabdoms follows two different patterns or organization. In the peripheral portion of the retina they lie oriented either parallel or perpendicular to the retinal radii. In this zone most cells have four sides while in the central region five sided cells are predominant. These cells bear microvilli in three of their five faces and the rhabdoms show no preferential mode of orientation. Each retina contains approximately 450 photoreceptors. In the secondary eyes the rhabdoms lie far from the vitreous body behind the level of the cell nuclei. A light reflecting layer or tapetum is present in the three pairs of secondary eyes. The microvilli forming the rhabdomeres of the AL eyes are 0.5 long and 500 Å wide, while the microvilli of the rhabdomeres in the PM and PL eyes are longer and thicker (1.5 long and 550–660 Å wide). In these eyes the rhabdomeres are surrounded by abundant extracellular material. Like in the principal eyes each rhabdom consists of two rhabdomeres.In the AL eyes the photoreceptor cells send out collateral branches which end, without any specialization, in contact with other photoreceptors. Clear fibers running parallely to the tapetum have been found in the secondary eyes. These fibers show specialized regions corresponding to the zones of contact with the photoreceptor cells. These areas are characterized by an increased density of the membranes and groups of vesicles (the vesicles lie within the fibers).The optic nerves consist of photoreceptor axons, glial cells and a fibrous perineural sheath. The AM and AL eyes are connected to the CNS by a single compact optic nerve while in the PM and PL eyes the optic nerve consists of several individual bundles. The total number of optic fibers entering into the brain is about 12.000.A layer of glial cytoplasm covers each photoreceptor axon and the mesaxons appear as double lines which bifurcate frequently.Research sponsored by the Air Force Office of Scientific Research, Office of Aerospace Research, United States Air Force, under AFOSR Grant Nr. 618-64.     

Development of the crayfish retina: A light and electron microscopic study

The development of the crayfish retina was examined in embryos and first, second and third instars with both and light and electron microscope. Light microscopic observations indicate that differentiation begins at the posterior portion of the optic disc and progresses in an anterior direction. Development of screening pigment, dioptric elements, and rhabdoms all parallel this posterior to anterior gradient in the retina. Tracer studies in early embryos reveal that the retina is separated from the proximal neuropil regions by a distinct vascular space. This observation suggests that the source of new cells for the retina may not be the more proximal cell proliferation zone as previously indicated. It is proposed that mitotic activity within the retina and/or differentiation of cells from the anterior surface layer of the eye may be sources for addition of new cells to the retina. Proto-ommatidial clusters of seven retinula cells occur very early at the posterior region of the embryonic retina. Initially the receptor cells extend throughout the entire thickness of the retina, but later they withdraw from beneath the cornea to occupy only the proximal portion of the retina. Microvilli of the rhabdom arise from the centrally opposed membranes of the retinula cells in each cell cluster. Each new microvillus contains a core of fine filaments which extend out into the cytoplasm at its base. As development of the microvilli continues, the core filaments appear to be lost or altered, but the cytoplasmic bundles at the base of the microvilli persist.     

Phylogeny of the Myriapoda – Crustacea – Insecta: a new attempt using photoreceptor structure*

According to molecular sequence data Crustacea and not Myriapoda seem to be the sister‐group to Insecta. This makes it necessary to reconsider how the morphology of their eyes fit with these new cladograms. Homology of facetted eye structures in Insecta (Hexapoda in the sense of Ento‐ and Ectognatha) and Crustacea is clearly supported by identical numbers of cells in an ommatidium (two corneageneous or primary pigment cells, four Semper cells which build the crystalline cone and primarily eight retinula cells). These cell numbers are retained even when great functional modification occurs, especially in the region of the dioptric apparatus. There are two different possibilities to explain differences in eye structure in Myriapoda depending on their phylogenetic position in the cladogram of Mandibulata. In the traditional Tracheata cladogram, eyes of Myriapoda must be secondarily modified. This modification can be explained using the different evolutionary pathways of insect facetted eyes to insect larval eyes (stemmata) as an analogous model system. Comparative morphology of larval insect eyes from all holometabolan orders shows that there are several evolutionary pathways which have led to different types of stemmata and that the process always involved the breaking up the compound eye into individual larval ommatidia. Further evolution led on many occasions to so‐called fusion‐stemmata that occur convergently in each holometabolic order and reveals, in part, great structural similarities to the lateral ocelli of myriapods. As myriapodan eyes cannot be regarded as typical mandibulate ommatidia, their structure can be explained as a modified complex eye evolved in a comparable way to the development to the fusion‐stemmata of insect larvae. The facetted eyes of Scutigera (Myriapoda, Chilopoda) must be considered as secondarily reorganized lateral myriapodan stemmata, the so‐called ‘pseudo‐compound eyes’. New is a crystalline cone‐like vitreous body within the dioptric apparatus. In the new cladogram with Crustacea and Insecta as sister‐groups however, the facetted eyes of Scutigera can be interpreted as an old precursor of the Crustacea – Insecta facetted eye with modified ommatidia having a four‐part crystalline cone, etc. as a synapomorphy. Lateral ocelli of all the other Myriapoda are then modified like insect stemmata. The precursor is then the Scutigera‐Ommatidium. In addition further interpretations of evolutionary pathways of myriapodan morphological characters are discussed.     

Ultrastructural study of the naupliar eye of the ostracodeVargula graminicola (Crustacea,Ostracoda)

Summary Ostracodes, like other crustaceans, have a simple naupliar eye that is built upon a theme of three eye cups surrounded by a layer of screening pigments. The single naupliar eye of the ostracodeVargula graminicola is situated medially on the dorsal-anterior side of the body and has three fused eye cups, two dorso-lateral and one ventral. Each eye cup has the following components: (1) pigment cells between the eye cups, (2) tapetal cells, (3) retinular cells with (4) microvillar rhabdomeres, and (5) axons extending into the protocerebrum. Typically two retinular cells contribute lateral microvilli to each rhabdom. The two dorso-lateral eye cups have about 40 retinular cells (20 rhabdoms) and the ventral eye cup has about 30 retinular cells (15 rhabdoms). Typical of myodocopid naupliar eyes (as reported from light microscopic studies), no lens cells or cuticular lenses were observed. The presence of tapetal cells identifies theVargula eye as a maxillopod-ostracode type crustacean naupliar eye. It is unlikely that the naupliar eye ofV. graminicola functions in image formation, rather it probably functions in the mediation of simple taxis towards and away from light.     

An apposition‐like compound eye with a layered rhabdom in the small diving beetle Agabus japonicus (Coleoptera,Dytiscidae)

The fine structure of the compound eyes of the adult diving beetle Agabus japonicus is described with light, scanning, and transmission electron microscopy. The eye of A. japonicus is mango‐shaped and consists of about 985 ommatidia. Each ommatidium is composed of a corneal facet lens, an eucone type of crystalline cone, a fused layered rhabdom with a basal rhabdomere, seven retinula cells (including six distal cells and one basal cell), two primary pigment cells and an undetermined number of secondary pigment cells that are restricted to the distalmost region of the eye. A clear‐zone, separating dioptric apparatus from photoreceptive structures, is not developed and the eye thus resembles an apposition eye. The cross‐sectional areas of the rhabdoms are relatively large indicative of enhanced light‐sensitivity. The distal and central region of the rhabdom is layered with interdigitating microvilli suggesting polarization sensitivity. According to the features mentioned above, we suggest that 1) the eye, seemingly of the apposition type, occurs in a taxon for which the clear‐zone (superposition) eye is characteristic; 2) the eye possesses adaptations to function in a dim‐light environment; 3) the eye may be sensitive to underwater polarized light or linearly water‐reflected polarized light. J. Morphol. 275:1273–1283, 2014. © 2014 Wiley Periodicals, Inc.     

Effects of bone marrow stromal cell injection in an experimental glaucoma model

We investigated if bone marrow stromal cells (BMSCs) transplanted into the vitreous body of a glaucoma model eye could be integrated in the host retina and also whether they could rescue the retinal ganglion cells (RGCs) from death induced by the elevated intraocular pressure. Glaucoma was induced in the right eye of adult Wistar rats by ligating the episcleral veins. The GFP-expressing BMSCs (GFP-BMSCs) were injected into the vitreous body of both the control and the glaucomatous eyes. After transplantation, GFP-BMSCs were mostly present along with the inner limiting membrane and only a few cells were integrated into the ganglion cell layer. At 2 or 4 weeks after transplantation, GFP-BMSCs were observed to express various trophic factors. The BMSCs injected glaucoma model eyes showed less reduction in the number of RGCs compared to the glaucomatous eyes with PBS injection. This study suggests that BMSC transplantation may be worthy as a neuroprotective tool to treat glaucoma.     

玻璃体腔联合注射赖氨酸－纤溶酶原和瑞替普酶诱导兔眼玻璃体后脱离的有效性

目的:探讨兔眼玻璃体腔联合注射赖氨酸-纤溶酶原和瑞替普酶诱导玻璃体后脱离(PVD)的有效性。方法:选取30只健康的新西兰白兔,以白兔右眼作为实验眼,左眼作为对照眼。随机分为A、B、C三组(每组10只),三组实验眼分别联合应用1万U瑞替普酶+125μg赖氨酸—纤溶酶原、2万U瑞替普酶+125μg赖氨酸—纤溶酶原、3万U瑞替普酶+125μg赖氨酸—纤溶酶原进行玻璃体腔内注射,对照眼均注射平衡盐溶液。应用视网膜电图、扫描电镜及光镜观察、比较各组诱导PVD的效果。结果:三组实验眼均形成不同程度PVD。A组实验眼注药前与注药后24 h、注药后2周的最大混合反应a波振幅、b波振幅比较均无明显差异(P0.05);B组实验眼注药后24 h的a波振幅、b波振幅均有轻度下降,2周后均恢复正常,注药前后的a波振幅、b波振幅比较均无明显差异(P0.05)。C组实验眼注药后24 h的a波振幅、b波振幅均明显低于注药前和对照眼,注药后2周的b波振幅均明显低于注药前和对照眼(P0.05)。光学组织切片观察显示:A组实验眼及所有对照眼、B组实验眼、C组实验眼的视网膜组织细胞形态正常,结构清晰,但B组神经节内核层、细胞层细胞略有减少,C组神经节内核层及细胞层细胞明显减少。结论:玻璃体腔内联合注射赖氨酸-纤溶酶原和瑞替普酶能有效诱导PVD,1万U瑞替普酶+125μg赖氨酸-纤溶酶原可诱导实现完全性PVD,不会对视功能、视网膜结构造成损害。     

Specialized ommatidia for polarization vision in the compound eye of cockchafers,Melolontha melolontha (Coleoptera,Scarabaeidae)

Summary The superposition eye of the cockchafer, Melolontha melolontha, exhibits the typical features of many nocturnal and crepuscular scarabaeid beetles: the dioptric apparatus of each ommatidium consists of a thick corneal lens with a strong inner convexity attached to a crystalline cone, that is surrounded by two primary and 9–11 secondary pigment cells. The clear zone contains the unpigmented extensions of the secondary pigment cells, which surround the cell bodies of seven retinula (receptor) cells per ommatidium and a retinular tract formed by them. The seven-lobed fused rhabdoms are composed by the rhabdomeres of the receptor cells 1–7. The rhabdoms are optically separated from each other by a tracheal sheath around the retinulae. The orientation of the microvilli diverges in a fan-like fashion within each rhabdomere. The proximally situated retinula cell 8 does not form a rhabdomere. This standard form of ommatidium stands in contrast to another type of ommatidium found in the dorsal rim area of the eye. The dorsal rim ommatidia are characterized by the following anatomical specializations: (1) The corneal lenses are not clear but contain light-scattering, bubble-like inclusions. (2) The rhabdom length is increased approximately by a factor of two. (3) The rhabdoms have unlobed shapes. (4) Within each rhabdomere the microvilli are parallel to each other. The microvilli of receptor 1 are oriented 90° to those of receptors 2–7. (5) The tracheal sheaths around the retinulae are missing. These findings indicate that the photoreceptors of the dorsal rim area are strongly polarization sensitive and have large visual fields. In the dorsal rim ommatidia of other insects, functionally similar anatomical specializations have been found. In these species, the dorsal rim area of the eye was demonstrated to be the eye region that is responsible for the detection of polarized light. We suggest that the dorsal rim area of the cockchafer eye subserves the same function and that the beetles use the polarization pattern of the sky for orientation during their migrations.     

The fine structure of the ocelli of Triatoma infestans (Hemiptera: Reduviidae)

The morphology and fine structure of the ocelli of Triatoma infestans have been analyzed by means of light and electron microscopy. The two dorsal ocelli of this species are located behind the compound eyes, looking dorsally and frontally. Externally, the ocelli are marked by the corneal lenses virtually spherical in form and limited internally by a cuticular apodeme. The lens focuses the incoming rays beyond the retina. A single layer of corneagen cells lies below the cuticular lens. The corneagen cells and photoreceptors are arranged in a cup-like fashion beneath the cuticular lens. A distal retinal zone comprises the rhabdoms, which are laterally connected in an hexagonal meshwork. A middle retinal zone comprises the receptor cell segment free of rhabdom, and a proximal zone their axons. In the middle zone, the oviform nuclei and spheroids are located. Screening pigment granules are present within the retinal cell. Spherical mitochondria are homogeneously distributed in the cytoplasm of the cell body. In the axonal zone, mitochondria are found in the peripheral region. Axons from receptor cells extend into the ocellar neuropile at the base of the ocelli, to synapse with second order neurons. The large axons of second order neurons are bundled by glial cells. The ocellar plexus exhibits a high diversity of synaptic unions (i.e. axo-dendritic, axo-axonic, dendro-axonic, and dendro-dendritic).     

Optical parameters of euphausiid eyes as a function of habitat depth

Summary The relationships between habitat depth, eye diameter relative to body length, and the dimensions of rhabdoms and crystalline cones have been examined for 13 species of three oceanic euphausiid genera with habitats ranging from near-surface waters to the deep-sea. Rate of eye growth decreases with depth. Longer rhabdoms may increase the visual sensitivity to point and extended light sources by an eye of a particular size with depth. Larger interommatidial angles suggest that visual acuity decreases at depth. Depth-related changes in euphausiid eyes are considered with respect to the probable roles of vision and bioluminescence in the deep-sea. Unusual features of the eyes of several species are described.     

Ultrastructure and orientation of ommatidia in the dorsal rim area of the locust compound eye

In many insect species, a dorsal rim area (DRA) in the compound eye is adapted to analyze the sky polarization pattern for compass orientation. In the desert locust Schistocerca gregaria, these specializations are particularly striking. The DRA of the locust consists of about 400 ommatidia. The facets have an irregular shape, and pore canals are often present in the corneae. Screening pigment is missing in the region of the dioptric apparatus suggesting large receptive fields. The rhabdoms are shorter, but about four times larger in cross-section than the rhabdoms of ordinary ommatida. Eight retinula cells contribute to the rhabdom. The microvilli of retinula cell 7 and of cells 1, 2, 5, 6, 8 are highly aligned throughout the rhabdom and form two blocks of orthogonal orientation. The microvilli in the minute rhabdomeres of retinula cells 3 and 4, in contrast, show no particular alignment. As in other insect species, microvillar orientations are arranged in a fan-like pattern across the DRA. Photoreceptor axons project to distinct areas in the dorsal lamina and medulla. The morphological specializations in the DRA of the locust eye most likely maximize the polarization sensitivity and suggest that the locust uses this eye region for analysis of the sky polarization pattern.     

The accessory lateral eye of a diplopod, Cylindroiulus truncorum (Silvestri, 1896) (Diplopoda: Julidae)

Using electron microscopy we describe an accessory lateral eye for Cylindroiulus, a diplopod. The accessory eye is situated at the cell body rind of the optic lobes, deep inside the head, and is composed of six R-cells; a dioptric apparatus is absent. Comparison reveals that many arthropods possess accessory lateral eyes in addition to the compound eyes or lateral ocelli. Their homology and distribution among the arthropod main lineages is discussed along with characters that may be useful for reconstructing phylogeny.     

The fine structure of the dorsal ocelli in the male bibionid fly

The dorsal ocelli of bibionid flies, details of which have not previously been described, were examined in males of Dilophus febrilis. The three ocelli are combined within an elevated chitin capsule, in a medial position between the enlarged dorsal compound eyes. The biconvex lenses show a multiple layering of up to 150 regularly spaced, clear and dense cuticle zones (100 nm spacing) which probably provide some spectral filtering, suggested by in vivo observations with an epifluorescence microscope. The corneagenous cells and the retina with 100-200 photoreceptor cells are adjoined proximally. A distal retina zone comprises the rhabdoms, which are laterally connected in an hexagonal network. The rhabdoms are between 4 and 15 mum in length; they decrease gradually from the dorsal to the ventral retina region. A middle retina zone comprises the receptor somata, a proximal zone, their axons. Synaptic contacts between axons and interneuron dendrites, feedback synapses to axons, and axo-axonic synapses are found, showing varying pre-synaptic structures. A possible functional role of the ocelli is discussed.