灰茶尺蠖成虫复眼的超微结构及其明暗适应中的变化

【目的】明确灰茶尺蠖Ectropis grisescens成虫复眼的超微结构及其明暗适应中的变化,探究其调光机制。【方法】采用超景深显微镜测定了灰茶尺蠖成虫复眼的小眼数量、间角、直径和曲率半径等外部参数,并通过组织切片、光学显微镜和透射电子显微镜等技术观察了复眼的内部超微结构;通过光学显微镜观察了灰茶尺蠖成虫复眼在明暗环境中分别适应2 h后晶锥结构及色素颗粒的位置变化。【结果】灰茶尺蠖成虫复眼呈半球形,雌、雄虫单个复眼分别有2 502±105和3 123±78个小眼。小眼自远端至近端由角膜、晶锥、透明区构成的屈光层和由15个视网膜细胞构成的感光层组成。2个初级色素细胞包裹着晶锥,自角膜近端延伸至视网膜细胞核区的远端;每个小眼外围由6个次级色素细胞围绕,自角膜近端延伸至基膜;在透明区内14个视网膜细胞聚集成束(非感杆束),远端与晶锥束末端连接,在感光层内形成闭合型感杆束,延伸至第15个视网膜细胞(基部视网膜细胞)。在明暗适应时,灰茶尺蠖复眼的晶锥细胞间出现开闭,色素颗粒进行纵向位移,以适应外界的光强度的变化。【结论】灰茶尺蠖成虫复眼属于重叠像眼,感杆束为“14+1”模式;屏蔽色素颗粒的移...     

The microanatomy of the compound eye of Munida irrasa (Decapoda: Galatheidae)

The compound eye of Munida irrasa differs in several respects from the typical decapod eye. The proximal pigment is found only in retinula cells. The eccentric cell is extremely large and expanded to fill the interstices of the crystalline tract area; thus, a typical "clear-zone" is absent. Six retinula cells course distally to screen two sides of the crystalline cone. There are approximately 12,500 ommatidia in each compound eye. There are several similarities to the typical decapod eye. Each ommatidium is composed of a typical cornea, corneagenous cells, crystalline cone cells, crystalline cone, crystalline cone tract and eight retinula cells. Distal pigment cells are present and surround the crystalline cone. The distal processes of the retinula cells also contain pigment. The retinula cell processes penetrate the basement membrane as fascicles composed of processes from adjacent retinulae.     

Fine structure of light- and dark-adapted eyes of desert ants,Cataglyphis bicolor (Formicidae,Hymenoptera)

Among ants, Cataglyphis bicolor shows the best performance in optical orientation. Its eye is of the apposition type with a fused rhabdom. Morphological studies on the general struture of the eye as well as the effect of light have been carried out with transmission and scanning electron microscopy. An ommatidium is composed of a dioptric apparatus, consisting of a cornea, corneal process and a crystalline cone, the sensory retinula, which is made up of eight retinula cells in the distal half and of an additional ninth one in the proximal half. The ommatidia are separated from each other by two primary pigment cells, which surround the crystalline cone and an average of 12 secondary pigment cells, which reach from cornea to the basement membrane. The eye of Cataglyphis bicolor possesses a light intensity dependent adaptation mechanism, which causes a radial and distal movement of the pigment granules within the retinula cells and a dilatation of cisternae of the ER along the rhabdom. Until now, no overall order in arrangement of retinula cells or direction of microvilli has been found from ommatidium to ommatidium. Such an order, however, must exist, either on the retina or the lamina level, since we have proven the ant's capacity for polarized light analysis.     

大草蛉成虫复眼的外部形态及其显微结构

用扫描电镜和光学显微镜观察了大草蛉Chrysopa pallens Ramber成虫复眼的外部形态及明、暗适应和性别对其显微结构的影响。结果发现：（1）其复眼呈半球形,位于头部两侧,略成“八”字形排列,单个复眼约由3 600个小眼组成,最前和最后小眼之间的夹角约为180°,最上和最下小眼之间的夹角约200°;（2）小眼主要由角膜、晶锥和6～8个小网膜细胞、基膜组成,外围环绕有2个初级虹膜色素细胞和6个次级虹膜色素细胞,基膜处有色素颗粒分布;（3）暗适应时,晶锥开裂程度较大,远端5～7个网膜细胞核向远端移动,与晶锥近端相接或接近,次级虹膜色素颗粒亦向远端移动包围晶锥;明适应时,晶锥开裂程度小或闭合,远端网膜细胞核向近端移动,透明带显现,大部分次级虹膜色素颗粒亦向近端移动分布在小网膜细胞柱周围,包被透明带;（4）在相同的明、暗适应下,雌、雄成虫复眼的显微结构无明显差异。结果表明大草蛉复眼为透明带明显的重叠象眼,其小眼不但具有次级虹膜色素颗粒纵向移动的常规调光机制,还存在晶锥开闭、远端网膜细胞核移动和基膜色素颗粒纵向扩散的调光新机制。     

Ultrastructure of the eye of a euphausiid crustacean

The compound eye of the Antarctic euphausiid Euphausia superba is a spherical clear zone eye. The dioptric system consists of a hexagonally-faceted cornea, two corneagenous cells, two crystalline cone cells which form the bipartite crystalline cone, and two accessory cone cells. The dioptric system of each ommatidium is separated from that of adjacent ommatidia by six distal pigment cells and a basement membrane. The proximal tip of the crystalline cone is cupped by the distal ends of the seven retinula cells whose nuclei are arranged in a staggered array slightly distal to the middle of the clear zone. In the distal half of the clear zone, each narrow retinula cell column is surrounded by large proximal extensions of the six distal pigment cells. The pigment cells narrow more proximally and terminate at the proximal basement membrane. A specialized axial channel complex extends from the crystalline cone through the clear zone, and is continuous with a conical refractive element which caps the distal end of the rhabdom. The rhabdom is fused, and made up of alternating highly birefringent layers of orthogonally-oriented microvilli. It is surrounded by a narrow extra-cellular space which is continuous with the distal refractive element and a second conical refractive element at the proximal end of the rhabdom.     

Fine-structure of the compound eye of the buprestid beetle Curis caloptera (Coleoptera, Buprestidae)

Curis caloptera is a buprestid beetle, which is active in bright sunlight. Its eye, like that of many other diurnal arthropods, is of the apposition type, in which dioptric apparatus and receptor layer are not separated by a region devoid of pigment. Perhaps to prevent damage by U. V.-radiation, the cornea is relatively thick (approximately 90 micron) and crystalline cones are of the "eucone-type". In each ommatidium the cone cell extensions occupy regular positions between the 8 retinula cells and reach down to the basement membrane where they end in bulbous swellings and contain grains of screening pigment. Pigment grains, slightly smaller than those present in the primary pigment cells, are also found within the retinula cells. Although the rhabdom possesses a uniform diameter of approximately 2 micron over its entire length of almost 300 micron, the number of rhabdomeres contributing to the rhabdom varies and depends on the level at which the rhabdom is sectioned. At the distal end, only one retinula cell possesses a rhabdomere; the same holds true for the proximal end, where a different rhabdomere (with microvilli at right angles to those of the distal cell) dominates. One retinula cell, of darker appearance in electron micrographs, occupies a distal position in each ommatidium and remains preferentially oriented within a sector of 60 degrees irrespective of the ommatidial axis. The ommatidial axis itself was found to vary 235 degrees. We provide circumstantial evidence for the view that the cell in question could be a U. V.-receptor with a role to play in an unambiguous determination of the E-vector. Separate bundles, each containing 8 axons, pass through the basement membrane together with 1 or 2 tracheoles. A traceheal tapetum is not developed.     

Ultrastructure of the larval eye of the scorpionfly Panorpa dubia (mecoptera: Panorpidae) with implications for the evolutionary origin of holometabolous larvae

The evolutionary origin of holometabolous larvae is a long‐standing and controversial issue. The Mecoptera are unique in Holometabola for their larvae possessing a pair of compound eyes instead of stemmata. The ultrastructure of the larval eyes of the scorpionfly Panorpa dubia Chou and Wang, 1981 was investigated using transmission electron microscopy. Each ommatidium possesses a cornea, a tetrapartite eucone crystalline cone, eight retinula cells, two primary pigment cells, and an undetermined number of secondary pigment cells. The rhabdomeres of the eight retinula cells form a centrally‐fused, tiered rhabdom of four distal and four proximal retinula cells. The rhabdomeres of the four distal retinula cells extend distally into a funnel shape around the basal surface of the crystalline cone. Based on the similarity of the larval eyes of Panorpidae to the eyes of the hemimetabolous insects and the difference from the stemmata of the holometabolous larvae, the evolutionary origin of the holometabolous larvae is briefly discussed. Morphol., 2012. © 2012 Wiley Periodicals, Inc.     

南五台蝎蛉成虫复眼的超微结构

采用扫描电镜和组织切片法,观察南五台蝎蛉Panorpa nanwutaina Chou成虫复眼的超微结构。南五台蝎蛉复眼近半椭球形,包括1500～1600个小眼。小眼表面光滑,由角膜、晶体、2个初级和12个次级色素细胞、视杆、以及基膜组成。角膜为多层片状纤维结构;晶体含有4个晶锥细胞;视杆由若干个视网膜细胞组成。晶体、视杆周围、和色素细胞内含有大量的色素颗粒,基膜两侧也有色素颗粒分布。南五台蝎蛉的复眼属于并列像眼。与普通蝎蛉P.communis L.小眼的次级色素细胞数目不同。讨论了南五台蝎蛉角膜的功能以及感觉毛和次级色素细胞在分类中的作用。     

Ultrastructure and migration of screening pigments in the retina of Pieris rapae L. (Lepidoptera,Pieridae)

Summary The retinal morphology of the butterfly, Pieris rapae L., was investigated using light and electron microscopy with special emphasis on the morphology and distribution of its screening pigments. Pigment migration in pigment and retinula cells was analysed after light-dark adaptation and after different selective chromatic adaptations. The primary pigment cells with white to yellow-green pigments symmetrically surround the cone process and the distal half of the crystalline cone, whilst the six secondary pigment cells, around each ommatidium, contain dark brown pigment granules. The nine retinula cells in one ommatidium can be categorised into four types. Receptor cells 1–4, which have microvilli in the distal half of the ommatidium only, contain numerous dark brown pigment granules. On the basis of the pigment content and morphology of their pigment granules, two distal groups of cells, cells 1, 2 and cells 3, 4 can be distinguished. The four diagonally arranged cells (5–8), with rhabdomeric structures and pigments in the proximal half of the cells, contain small red pigment granules of irregular shape. The ninth cell, which has only a small number of microvilli, lacks pigment. Chromatic adaptation experiments in which the location of retinula cell pigment granules was used as a criterium reveal two UV-receptors (cells 1 and 2), two green receptors (cells 3 and 4) and four cells (5–8) containing the red screening pigment, with a yellow-green sensitivity.     

The fine structure of the eyes of some bristly millipedes (Penicillata, Diplopoda): additional support for the homology of mandibulate ommatidia

The eyes of adult Phryssonotus platycephalus (Synxenidae) and Polyxenus lagurus (Polyxenidae) were investigated by light and electron microscopy. At each side of the head, various numbers of eye cups are situated on projections, the eye hills. The eye cups of P. platycephalus and P. lagurus are similarly structured and considered homologous sense organs. Each corneal lens is biconvex and formed by four to six pigmented corneagenous cells with their nuclei displaced towards the mid-periphery of the eye cup. The corneal surface displays a conspicuous nanostructure of fingerprint-like ridges in P. platycephalus. However, the corneal surface appears smooth in P. lagurus. In P. platycephalus. A rudimentary crystalline cone is observed in each eye cup, always produced by a constant number of three eucone cells. The crystalline cone is wedged between the corneal lens and the distal rhabdom and consists of three distinct compartments. Each cone compartment is connected to the voluminous proximal nuclear region by one elongated cytoplasmic process, which runs through the infraretinular space. A dual type retinula is always arranged in two distinct horizontal cell layers. The distal retinula contains an unfixed number of four to five cells in P. lagurus, whereas it contains five to eight cells in P. platycephalus. The distal retinula cells form a large and fused axial rhabdom. A constant number of three proximal retinula cells give rise to a small axial rhabdom, which looks more or less triangular in cross sections. The basal matrix is rather thin, inconspicuous and lines the bases of the eye cups. The ultrastructure of the eye cups of P. platycephalus resembles that observed in the ommatidia of the centipede Scutigera coleoptrata. The present study lends additional support to the homology of mandibulate ommatidia, because of the common possession of crystalline cone cells and a bilayered dual type retinula in the eye cups of P. platycephalus. Ommatidia or unicorneal eyes that include eucone cells with nuclei displaced outside the cone compartments, as found in Scutigeromorpha and Penicillata, might also be interpreted as an additional autapomorphy of the Myriapoda. The suggested homology of scutigeromorph and penicillate eyes implies that penicillate eye cups have to be considered modified, probably miniaturized ommatidia.     

Regional differences in a nematoceran retina (Insecta,Diptera)

Summary The compound eye of Psychoda cinerea comprises two types of ommatidia, arranged so as to divide the retina into distinct dorsal and ventral regions. The P-type ommatidium, in the ventral part of the eye, differs fundamentally from the other dipteran ommatidia so far described, and is regarded as a primitive ommatidium. The acone dioptric apparatus is the same in both types, with a spherical lens and four Semper cells, the processes of which expand below the rhabdom to form a ring of pigment sacs. Only the distal region of the rhabdom is surrounded by a continuous ring of screening pigment, formed by 2 primary and 12–16 secondary pigment cells. The highly pigmented retinula cells penetrate the basement membrane proximally at about the level of their nuclei; in this region they are separated from the hemolymph by glial elements. The rhabdomeres R1–6 are fused to form a tube. The two types of ommatidia are defined by the arrangement of the retinula cells R7/8: in the T type the central rhabdomeres are one below the other, in the usual tandem position, whereas in the P type only R8 is central, with R7 in the peripheral ring. In the proximal region of the retina, retinula cells with parallel microvilli in neighboring ommatidia are joined in rows by lateral processes from the R8 cells. All the rhabdomeres are short and not twisted, which suggests that the retinula cells are highly sensitive to direction of polarization. The eye can adapt by a number of retinomotor processes. These findings, together with observations of behavior, imply that the psychodids have well-developed visual abilities.     

Fine structural organization of the lateral ocelli in two species of Scolopendra (Chilopoda: Pleurostigmophora): an evolutionary evaluation

The lateral ocelli of Scolopendra cingulata and Scolopendra oraniensis were examined by electron microscopy. A pigmented ocellar field with four eyes arranged in a rhomboid configuration is present frontolaterally on both sides of the head. Each lateral ocellus is cup-shaped and consists of a deeply set biconvex corneal lens, which is formed by 230–2,240 cornea-secreting epithelial cells. A crystalline cone is not developed. Two kinds of photoreceptive cells are present in the retinula. 561–1,026 cylindrical retinula cells with circumapically developed microvilli form a large distal rhabdom. Arranged in 13–18 horizontal rings, the distal retinula cells display a multilayered appearance. Each cell layer forms an axial ring of maximally 75 rhabdomeres. In addition, 71–127 club-shaped proximal retinula cells make up uni- or bidirectional rhabdomeres, whose microvilli interdigitate. 150–250 sheath cells are located at the periphery of the eye. Radial sheath cell processes encompass the soma of all retinula cells. Outside the eye cup there are several thin layers of external pigment cells, which not only ensheath the ocelli but also underlie the entire ocellar field, causing its darkly pigmented. The cornea-secreting epithelial cells, sheath cells and external pigment cells form a part of the basal matrix extending around the entire eye cup. Scolopendromorph lateral ocelli differ remarkably with respect to the eyes of other chilopods. The dual type retinula in scolopendromorph eyes supports the hypothesis of its homology with scutigeromorph ommatidia. Other features (e.g. cup-shaped profile of the eye, horizontally multilayered distal retinula cells, interdigitating proximal rhabdomeres, lack of a crystalline cone, presence of external pigment and sheath cells enveloping the entire retinula) do not have any equivalents in scutigeromorph ommatidia and would, therefore, not directly support homology. In fact, most of them (except the external pigment cells) might be interpreted as autapomorphies defining the Pleurostigmophora. Certain structures (e.g. sheath cells, interdigitating proximal rhabdomeres, discontinuous layer of cornea-secreting epithelial cells) are similar to those found in some lithobiid ocelli (e.g. Lithobius). The external pigment cells in Scolopendra species, however, must presently be regarded as an autapomorphy of the Scolopendromorpha.     

龟纹瓢虫成虫的复眼形态及其显微结构

利用光镜、组织切片法观察了龟纹瓢虫Propylaea japonica(Thunberg)成虫的复眼形态及其显微结构。结果如下:(1)头正前方观,复眼外形似半球,且后方稍向内合拢。每个复眼约包括630个小眼。(2)每个小眼是由1套屈光器(1个角膜和1个晶锥)、6至8个小网膜细胞及其特化产生的视杆和基细胞等几部分组成。晶体周围及小网膜色素细胞内均含有丰富的色素颗粒。(3)小眼整体纵切显示,其上、下段色素颗粒分布相对较多,中段分布较少。(4)明、暗适应状态对小眼的色素颗粒分布有影响,性别对其分布无明显影响。明适应状态下,其色素颗粒较均匀地分布于视杆两侧上下,暗适应状态时色素颗粒则主要分布在视杆部位的上侧,显示其具有一定的重叠眼性质;而在相同的明、暗适应状态下其雌、雄成虫复眼的色素颗粒分布间无明显差异。     

Feinstruktur des Komplexauges der Roten Waldameise,Formica polyctena (Hymenoptera,Formicidae)

Zusammenfassung Die Analyse der Feinstruktur des Komplexauges der Ameise Formica polyctena ergab, daß der dioptrische Apparat der insgesamt 750 Ommatidien aus einer lamellierten Cornealinse und einem euconen Kristallkegel besteht. Zwei Hauptpigmentzellen umgeben schalenförmig den Kristallkegel, 8 Nebenpigmentzellen schirmen das Ommatidium in seiner ganzen Länge von der Cornea bis zur Basalmembran ab. Jedes Ommatidium besteht in seinem distalen Teil aus 8 Retinulazellen, 2 gegenüberliegenden schmalen und je 3 gegenüberliegenden großen Sehzellen. Weiter proximal tritt eine 9. Retinulazelle hinzu. Die Mikrovillisäume der Sehzellen verschmelzen zu einem zentralen Rhabdom. Im distalen Teil sind die Mikrovilli in 3 Richtungen angeordnet. Es wird im besonderen die Orientierung der Mikrovilli zur Augenlängsachse und zur Ommatidien-Symmetrieachse untersucht. Auch die 9. Sehzelle bildet Mikrovilli. Das Rhabdom endet an 4 basalen Pigmentzellen.Auf den Mikrovillisaum folgt im Querschnitt des dunkel adaptierten Ommatidiums ein Kranz von großen intrazellulären Vakuolen. Die anschließende cytoplasmatische Zone der Retinulazellen enthält viele Pigmentgranula und Mitochondrien; multivesikuläre und multilamelläre Körper sowie Golgiapparate treten nur selten auf. Die funktionelle Bedeutung des Ommatidienaufbaues und die Verteilung der Organellen bei Dunkeladaptation werden diskutiert.

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The fine structure of the complex eye of the ant Formica polyctena (Hymenoptera, Formicidae)

Summary The fine structure of the compound eye of the ant Formica polyctena was investigated. The eye consists of a total of 750 ommatidia, each containing a dioptric apparatus of a lamellated cornea lens, a eucone-type crystalline cone, and 8 long pigment cells which surround the ommatidium for its total length, i.e. from the cornea to the basal membrane. Each ommatidium has in its distal portion 8 retinula cells—6 large plus 2 small ones. The retinula cells are arranged in such a way that 3 pairs of large cells, and the one pair of the small cells lie opposite each other. Further proximally, a 9th retinula cell is encountered. The fused, centrally located rhabdom is built up by the microvilli of all nine retinula cells. The rhabdom ends at 4 basal pigment cells. In dark adapted ommatidia, a ring of large intracellular vacuoles is to be seen immediately peripherally to the rhabdom. The outer, cytoplasmic zone of the retinula cells contains many pigment granules and mitochondria; multivesicular bodies, onion bodies and Golgi apparatus are of relatively rare occurrence. The functional significance of the ommatidial structure and the arrangement of the cell organelles in the dark adapted condition are discussed.

Für technische Hilfe danke ich Frau Langer und Frl. Müller, Herrn Prof. H. Markl für die Durchsicht des Manuskripts.     

Fine structural description of the lateral ocellus of Craterostigmus tasmanianus Pocock, 1902 (Chilopoda: Craterostigmomorpha) and phylogenetic considerations

The lateral lens eye of adult Craterostigmus tasmanianus Pocock, 1902 (a centipede from Australia and New Zealand) was examined by light and electron microscopy. An elliptical, bipartite eye is located frontolaterally on either side of the head. The nearly circular posterior part of the eye is characterized by a plano-convex cornea, whereas no corneal elevation is visible in the crescentic anterior part. The so-called lateral ocellus appears cup-shaped in longitudinal section and includes a flattened corneal lens comprising a homogeneous and pigmentless epithelium of cornea-secreting cells. The retinula consists of two kinds of photoreceptive cells. The distribution of the distal retinula cells is highly irregular. Variable numbers of cells are grouped together in multilayered, thread-like unions extending from the ventral and dorsal margins into the center of the eye. Around their knob-like or bilobed apices the distal retinula cells give rise to fused polymorphic rhabdomeres. Both everse and inverse cells occur in the distal retinula. Smaller, club-shaped proximal retinula cells are present in the second (limited to the peripheral region) and proximal third of the eye, where they are arranged in dual cell units. In its apical region each unit produces a small, unidirectional rhabdom of interdigitating microvilli. All retinula cells are surrounded by numerous sheath cells. A thin basal lamina covers the whole eye cup, which, together with the distal part of the optic nerve, is wrapped by external pigment cells filled with granules of varying osmiophily. The eye of C. tasmanianus seemingly displays very high complexity compared to many other hitherto studied euarthropod eyes. Besides the complex arrangement of the entire retinula, the presence of a bipartite eye cup, intraocellar exocrine glands, inverse retinula cells, distal retinula cells with bilobed apices, separated pairs of proximal retinula cells, medio-retinal axon bundles, and the formation of a vertically partitioned, antler-like distal rhabdom represent apomorphies of the craterostigmomorph eye. These characters therefore collectively underline the separate position of the Craterostigmomorpha among pleurostigmophoran centipedes. The remaining retinal features of C. tasmanianus agree with those known from other chilopod eyes and, thus, may be considered plesiomorphies. Characters like the unicorneal eye cup, sheath cells, and proximal rhabdomeres with interdigitating microvilli were already present in the ground pattern of the Pleurostigmophora. Other retinal features were developed in the ancestral lineage of the Phylactometria (e.g., large elliptical eyes, external pigment cells, polygonal sculpturations on the corneal surface). The homology of all chilopod eyes (including Notostigmophora) is based principally on the possession of a dual type retinula.     

The Fine Structure of the Compound Eye of Tanais cavolinii Milne-Edwards (Crustacea: Tanaidacea)

Abstract The compound (apposition) eyes of Tanais cavolinii are not well developed: the number of ommatidia is small and there are certain irregularities in structure. The refractive components are formed by the cornea and the cone. The latter is built up by two cone cells. In addition, there are two accessory cone cells confined to the distal part of the cone. The eight pigmented retinular cells extend from the cornea to the basement membrane. Proximal to the cone, they form a fused continuous rhabdom, which in cross section has a rectangular outline. In the middle part of the rhabdom, the microvilli are arranged perpendicular to the long axis of the rhabdom when seen in cross section. The microvilli outside of this area can be arranged either parallel or perpendicular to the microvilli of the middle part. Other irregularities occur in the ommatidium, e.g. the position of the retinular cell nuclei, which are found at different levels. Extensions from the cone cells fuse and form a mesh proximal to the rhabdom. Between the mesh and basal lamina is a basal cell type enveloping the proximal parts of the retinular cells and their axons. These cells also form the basal lamina, which delimits the compound eye from the haemocoel. No special pigment cells are present in the compound eye of Tanais cavolinii.     

Post-larval development of compound eyes and stemmata of Chaoborus crystallinus (De Geer, 1776) (Diptera : Chaoboridae): Stage-specific reconstructions within individual organs of vision

During metamorphosis, the dioptric apparatus of the larval compound eye of Chaoborus crystallinus (Diptera : Nematocera) is radically reconstructed. The thin larval cornea of the ommatidia is replaced by strongly curved corneal lenses, and the eucone larval cone is replaced by an imaginal cone of the acone type. Curvature of the future lens is already apparent in very young pupae, in which the cornea consists only of a thin epicuticle with corneal nipples. Fibrillary cuticle is secreted by cone and primary pigment cells throughout pupal development. Lens formation is accompanied by movement of the nuclei of the accessory pigment cells. The larval cone disintegrates unexpectedly late in young, images. During late pupal development, 7 cone cell projections emerge. In contrast to the dioptric apparatus, the retinula cells and rhabdom remain almost unchanged during metamorphosis. The main refractive element of the larval ommatidium appears to be the cone, while that of the imaginal ommatidium is the corneal lens. In addition to the compound eyes, the pairs of stemmata are retained during the whole post-larval development. Pupal stemmata show no structural differences from the larval stemmata. The stemmata are still present in 2-day-old images (“retained stemmata”), but the primary stemma loses its dioptric apparatus and is proximally relocated to the basal region of the compound eye. The reconstructions in the visual system of Chaoborus, which occur during ontogeny, are probably connected with the change from aquatic living larvae to aerial adults, and appear to fulfill stage-specific needs of vision.     

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.     

Colour receptors in the eye of the digger wasp,Sphex cognatus Smith: Evaluation by selective adaptation

Summary Pigment granule migration in pigment cells and retinula cells of the digger wasp Sphex cognatus Smith was analysed morphologically after light adaptation to natural light, dark adaptation and after four selective chromatic adaptations in the range between 358 nm and 580 nm and used as the index of receptor cell sensitivity. The receptor region of each ommatidium consists of nine retinula cells which form a centrally located rhabdom. Two morphologically and physiologically different visual units can be described, defined by the arrangement of the rhabdomeric microvilli, the topographical relationship of the receptor cells with respect to the eye axes and the unique retinula cell screening pigmentation. These two different sets of ommatidia (type A and B) are randomly distributed in a ratio of 13 throughout the eye (Ribi, 1978b). Chromatic adaptation experiments with wavelengths of 358 nm, 443 nm, 523 nm and 580 nm and subsequent histological examination reveal two UV receptors, two blue receptors and four yellow-green receptors in type A ommatidia and two UV receptors and six green to yellow-green receptors in type B ommatidia. The pigments in cells surrounding each ommatidium (two primary pigment cells, 20 secondary pigment cells and four pigmented cone extensions) were not affected significantly by the adaptation experiments.