Ommatidial structure in relation to turnover of photoreceptor membrane in the locust

Summary In the compound eye of the locust, Locusta, the cross-sectional area of the rhabdoms increases at dusk by 4.7-fold due to the rapid assembly of new microvillar membrane, and decreases at dawn by a corresponding amount as a result of pinocytotic shedding from the microvilli. The rhabdoms at night have more and longer photoreceptor microvilli than rhabdoms during the day. The orientations of the six rhabdomeres that comprise the distal rhabdom also change. The density of intramembrane particles on the P-face of the microvillar membrane, putatively representing mostly rhodopsin molecules, or aggregates thereof, does not change.An alteration in the size of the ommatidial field-stop, produced by the primary pigment cells, is concomitant with the change in rhabdom size. At night the increase in size of the field-stop must widen the angular acceptance of a rhabdom, increasing the capture of photons from an extended field. Conversely, during the day, when photons are more abundant, its decrease must narrow the acceptance angle, increasing angular resolution. Because of the presence of this field-stop, the optics of the ommatidium would not be greatly affected if the rhabdom were to remain always at its night size. It is argued, therefore, that the variable-size rhabdom must have resulted from some demand other than that of light/dark adaptation.Changes in size and organisation of the rhabdoms in response to various light regimes indicate that: (1) Rapid shedding of photoreceptor membrane is induced by the onset of light, but shedding also occurs slowly in darkness during the day. (2) Microvillar assembly is initiated by the onset of darkness, but also occurs at the normal time of dusk without a change in ambient lighting, provided there has been some light during the day. Therefore, both shedding and assembly of microvillar membrane are affected by the state of illumination, but also appear to be under some endogenous control.     

Ultrastructure and adaptation in the retina of Aglais urticae (Lepidoptera)

Summary The apposition eye of Aglais urticae is composed of eucone ommatidia. Serial sectioning of blocks from the laterofrontal and lateroventral eye regions and mapping at different levels revealed that there is no torsion of whole ommatidia along their long axes.The sensory part of the ommatidium comprises nine retinula cells. The most significant features of the complicated rhabdom structure (diagrammed in Fig. 3) are as follows. The vertically aligned receptor cells V₁ and V₅, which become axonal at the level at which the ninth cell begins, have microvilli arranged in bundles. The microvilli bundles of these cells generally make an angle between 30 and 55° on one or the other side of the dorsoventral axis in the ommatidium cross section. The two orientations alternate regularly along the length of the rhabdom. The repeated sweeps of these bundles in regular intervals in combination with the curvature of the V-cell microvilli is considered to be a substitute for rhabdomere twisting. The four diagonally aligned receptor cells D_2,4,6,8 have rhabdomers that are continuous, though of variable size. These rhabdomeres, like those of the horizontally aligned cells (H₃ and H₇), extend along the entire rhabdom, though there is a small (1–2 m) interruption in the H-cell rhabdomeres; the latter have the most constant orientation. Pigment granules are most abundant in the D cells, followed by the H cells and finally the V cells. RC₉ lacks pigments.Light- and dark-adaptation experiments reveal marked horizontal migration of the retinula-cell pigment (pupil reaction) and slight vertical migration. Monochromatic adaptation experiments at wavelengths =342, 436, 522, 578, and 626 nm indicate special sensitivity of the D-cells around -520 nm. There are indications for sensitivity of V cells in the UV, and possibly of H cells in the blue. The H cells are regarded as suited for the detection of polarized light. The functional significance of these findings is discussed and compared with what is known of other butterfly eyes.This work was supported by grants from the Deutsche Forschungsgemeinschaft and the Stiftung Volkswagenwerk     

Organisation of the compound eye of a tipulid fly during the day and night

Summary The ultrastructure of the compound eye of the Australian tipulid fly,Ptilogyna spectabilis, is described. The ommatidia are of the acone type. The rhabdom corresponds to the basic dipteran pattern with six outer rhabdomeres from retinular cells 1–6 (R1-6) that surround two tiered central rhabdomeres from R7 and 8. Distally, for about 8 m, the rhabdom is closed. For the remainder, where the rhabdomere of R8 replaces that of R7, the rhabdom is open, and the rhabdomeres lie in a large central ommatidial extracellular space. In the proximal two thirds of the rhabdom, the central space is partitioned by processes from the retinular cells so that the individual rhabdomeres are contained in pockets.At night the rhabdom abuts the cone cells, but during the day it migrates some 20 m proximally and is connected to a narrow (1–2 m) cone cell tract. This tract is surrounded by two primary pigment cells, which occupy a more lateral position at night and thus act like an iris. Pigment in secondary pigment cells also migrates so as to screen orthodromic light above the rhabdom during the day. Between midday and midnight, the rhabdom changes in length and cross-sectional area as a result of asynchrony of the shedding and synthetic phases of photoreceptor membrane turnover. The effects of these daily adaptive changes on photon capture ability are discussed with regard to the sensitivity of the eye.     

An ultrastructural study of the eye of Gomphiocephalus hodgsoni, a collembolan from Antarctica

The collembolan Gomphiocephalus hodgsoni is one of a few hexapods occurring in Antarctica. Male and female individuals do not differ with regard to their eyes. Both possess eight single-lens eyes. In the adults, each lens has a diameter of 10–12 m and covers an almost spherical crystalline cone made up of four unequal moieties. When we accepted homogenous refractive indices, known from pterygote insect eyes, and then calculated the focal length of the dioptric apparatus, we found that light could be focused on the retina. The retinal cells of each eye are grouped in two tiers and surround the centrally fused rhabdom. Rhabdomeric microvilli, approximately 1.3 m long, possess a diameter of 80 nm and are typically aligned in one direction. More proximally, however, two rhabdomeres with microvilli perpendicular to the larger, more distal, rhabdom appear. Signs of light-induced damage, despite the bright summer radiation in Antarctica, were not seen. Ricegrain-like screening pigment granules, measuring 0.8×0.45 m in dimensions, densely surround each rhabdom and shield the cytoplasm of the surrounding cells. The orthogonal arrangement of the microvilli suggests that G. hodgsoni could be sensitive to light-polarization. This ability might be of importance in detecting tiny amounts of meltwater in close proximity to the insect.The order of the authors names reflects the sequence in which the individuals joined in this project.     

Der Feinbau des Auges der Mehlmotte,Ephestia kuehniella Zeller (Lepidoptera,Pyralididae)

Zusammenfassung Die Retinula im Ommatidium der Mehlmotte besteht aus einer wechselnden Anzahl (9–12, meist 11) langgestreckter, prismatischer Sinneszellen. Außerdem enthält jede Retinula nahe der Basalmembran im Zentrum zwischen diesen distalen Retinulazellen noch eine basale Retinulazelle. Die Längsachse der Retinula wird von der Achsenstruktur eingenommen, die aus Mikrovilli besteht. Ihr distaler Teil ist der Achsenfaden, der breitere, proximale Teil bildet das Rhabdom. Dieses erscheint im Querschnitt meist vierstrahlig gelappt, da seine Außenseite in Längsrichtung tief gekehlt ist. Der Rhabdomquerschnitt gliedert sich in mehrere Schöpfe parallel angeordneter Mikrovilli (Rhabdomsektoren); jeder Rhabdomsektor besteht aus 1 oder 2 Rhabdomeren. Die basale Retinulazelle entsendet einen kleinen Schopf von Mikrovilli in die proximale Spitze des Rhabdoms. Die distalen Retinulazellen setzen sich proximal in Neuriten fort, welche sich in Einkehlungen der basalen Retinulazelle bzw. der Tracheenendzelle einschmiegen. Jeweils eine Tracheole durchbricht zusammen mit dem Neuritenstrang einer Retinula die Basalmembran; sie verzweigt sich distal zu ca. 30 Tracheolen, die die Retinula umhüllen.Die Kristallkegelzellen grenzen distal an die Cornea; proximal laufen die Kristallkegelzellen eines Ommatidiums in einen gemeinsamen Fortsatz aus, der zwischen den Retinulazellen unmittelbar am Achsenfaden endet. — Nur das helladaptierte Auge wurde untersucht. Hierbei erscheint im distalen Teil der Retinula nur der Achsenfaden lichtdurchlässig, das Cytoplasma der Retinulazellen hingegen von Pigmentgrana durchsetzt und für Licht undurchlässig.

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Fine structure of the eye of the meal moth, Ephestia kuehniella Zeller (Lepidoptera, Pyralididae)

Summary In each ommatidium of the meal moth a retinula is formed from a varying number (9–12, mostly 11) of elongated, prismatic sense cells. In addition, a basal retinular cell is situated near the basement membrane in the center of the other (distal) retinular cells. The axis of the retinula is occupied by many microvilli forming the axial structure, the distal section of which is the slender axial thread. Proximally, the axial structure widens (to 8.5 m instead of 1 m in diameter) and is now called rhabdom. Cross sections of the rhabdom mostly look like a petaloid with four petals; this figure is due to longitudinal infoldings along the length of the rhabdom surface. The rhabdom cross section is subdivided into several brushes of microvilli (rhabdom sectors), each one being characterized by an approximately parallel arrangement of its microvilli. One rhabdom sector may be composed of one or two rhabdomeres respectively.The basal retinular cell participates in rhabdom formation through a small brush of microvilli at the proximal end of the rhabdom. Proximally, the distal retinular cells taper into slender neurites which are embedded in grooves at the surface of the basal retinular cell and the tracheal end cell respectively. One tracheole piercing the basement membrane together with the neurites of one retinula branches into about 30 tracheoles surrounding the retinula.The crystalline cone cells touch the cornea; proximally, their cytoplasm forms a point which eventually terminates amongst the distal tips of the retinular cells, immediately at the axial thread.—Our work was restricted to light adapted eyes; in this condition, light transmission in the distal part of the retinula seems to be blocked by retinular cell pigment except inside the axial thread.

Mit Unterstützung durch die Deutsche Forschungsgemeinschaft.     

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.     

The distribution of actin immunoreactivity in rhabdomeres of tipulid flies in relation to extracellular membrane shedding

Summary Rhabdomeres of tipulid flies lose membrane during turnover from a shedding zone composed of microvillar tips. These distal domains lack intramicrovillar cytoskeletons and appear to be empty sacs of membrane. Recent concerns about the role of ninaC mechano-enzymes in the architecture of dipteran rhabodomeral microvilli and the dynamic role that they may play in the creation of shedding zones demand an examination of the distribution of actin in tipulid rhabdomeres. We compared rhabdomeres from tipulid retinae incubated before fixation for immunocytochemistry in a buffer without additives and a stabilising buffer that contained a cocktail of cysteine protease inhibitors; both were challenged by an anti-actin antibody for immunogold labelling after embedding in LR White Resin. Shedding zones thus processed collapse to structureless detritus. Stabilised and unstabilised shedding zones were immunonegative to anti-actin. To ensure that the negative results were not consequent upon conformational changes generated by the processing protocol, we examined microvilli of degenerating rhabdomeres of the Drosophila light-dependent retinal degeneration mutant rdgB ^KS222 (which separate and collapse without creating a shedding zone) and found the detritus they generate to be immunopositive to anti-actin. Stabilised and unstabilised regions of basal regions of tipulid rhabdomeres were equally immunopositive. We infer that (a) actin is absent from shedding zones; (b) actin is not degraded by microvillar cysteine proteases. The implications of these conclusions are discussed in relation to some functional models of arthropod photoreceptor microvilli.     

Segmental variations in the organization of the endoplasmic reticulum of the rat nephron

Summary The spatial organization of endoplasmic reticulum (ER) was examined in all segments of rat nephron. Tissues were fixed with glutaraldehyde, impregnated en bloc with osmium tetroxide, prepared for and examined by standard (80–100 kV) and high voltage (1 mEV) transmission electron microscopy.In all proximal tubule cells, ER forms a continuous and extensive network of canaliculi and abundant fenestrated saccules which surround mitochondria and cytoplasmic bodies; the cage-like structure of the fenestrated saccules was most evident around the spherical mitochondria of the S₃ segment. In the cells of the distal straight and convoluted tubules, the network consists mostly of canaliculi with rare non-fenestrated saccules. The ER network of canaliculi is particularly rich in intercalated cells, in contrast with its rudimentary appearance in the adjacent principal cells of the collecting tubule. In fact, in these cells there are few isolated ER cisternae and they are rarely impregnated. The nuclear envelope is well impregnated in most cells throughout the various segments. Segmental variations in ER organization and its relative abundance are most likely related to the well, established functional heterogeneity of the nephron segments. Moreover, the extensive and unique organization among mitochondria, ER and the basolateral membrane suggests that these three organelles function as a unit which is related to active electrolyte transport. In addition, because of its transepithelial organization, ER may well constitute a transcellular pathway for molecules.     

Testing the “methanochondrion concept”: are nucleotides transported across internal membranes in Methanobacterium thermoautotrophicum?

In order to test the Methanochondrion concept, uptake of adenine nucleotides in various membrane preparations of Methanobacterium thermoautotrophicum was studied. The uptake showed properties which are in general interpreted as indicative of a transport mechanism: (i) kinetics in the time range of minutes, (ii) temperature dependence, (iii) substrate specificity and (iv) failure to remove the substrate by extensive washing.However, nucleotide transport as an interpretation of this uptake can definitely be excluded. Not only an exchange mechanism of the mitochondrial type, but also a general exchange or an uniport mechanism was ruled out. In contrast, the nucleotide uptake was shown to be actually a tight and specific binding of ADP and ATP to binding sites at the interior side of the cell membrane. This was conclusively demonstrated in protoplasts obtained from M. thermoautotrophicum cells. In these protoplasts which do not contain internal membranes also nucleotide binding was observed, but only after disruption of the plasma membrane by osmotic lysis, which leads to the exposure of binding sites.     

The compound eye of Parnara guttata (Insecta,Lepidoptera, Hesperiidae): Fine structure of the ommatidium

Summary The fine structure of an ommatidium of a skipper butterfly, Parnara guttata, has been studied using the electron microscope. Each ommatidium has nine retinula cells, which were classified into three groups: two distal, six medial and one basal retinula cells. The rhabdomeres of the distal retinula cells are localized in the distal part of the rhabdom, while those of the six medial retinula cells appear throughout most of the rhabdom. The rhabdomere of the basal retinula cell occupies only the basal part of the rhabdom. The rhabdomeres of four medial cells are constructed of parallel microvilli, while fan-like microvilli form the rhabdomeres of other two medial retinula cells. The distal and basal retinula cells have rhabdomeres consisting of both parallel and fan-like microvilli. This is the first time the construction of the rhabdomeres of the distal and basal retinula cells has been described in such fine detail for a skipper butterfly. Nine retinula cell axons of each ommatidium extend to the first neuropile of the optic lobe, the lamina ganglionaris. No difference was found in the number of retinula cells of an ommatidium or the shape of the rhabdom between the dorsal and ventral regions of the compound eye.     

The eyes of mesopelagic crustaceans: I. Gennadas sp. (Penaeidae)

Summary The eye of the deep-sea penaeid shrimp Gennadas consists of approximately 700 square ommatidia with a side length of 15 n. It is hemispherical in shape and is located at the end of a 1.5 mm long eye stalk. The cornea is extremely thin, but the crystalline cone is well-developed. A clear zone between dioptric structures and the rhabdom layer is absent. A few pigment granules are found within the basement membrane; otherwise they, too, are absent from the eye of Gennadas. The rhabdom is massive and occupies 50 % of the eye. It consists of orthogonally oriented microvilli (the latter measuring 0.07 m in diameter) and is 75 m long. In cross sections adjacent rhabdoms, all approximately 8 m in diameter, form an almost continuous sheet and leave little space for retinula cell cytoplasm. In spite of a one h exposure to light, rhabdom microvilli show no disintegration or disruption of membranes. Vesicles of various kinds, however, are present in all seven retinula cells near the basement membrane. Bundles of seven axons penetrate the basement membrane. On their way to the lamina they often combine and form larger aggregations.The authors wish to thank the director of the Meat Industry Research Institute in Hamilton and his staff for the use of their electron microscope facilities     

The retina of the phalangid,Opilio ravennae,with particular reference to arhabdomeric cells

Summary The retina of the phalangid, Opilio ravennae, consists of retinula cells with distal rhabdomeres, arhabdomeric cells, and sheath cells. The receptive segment of retinula cells shows a clear separation into a Proximal rhabdom, organized into distinct rhabdom units formed by three or four retinula cells, and a Distal rhabdom, consisting of an uniterrupted layer of contiguous rhabdomeres. One of the cells comprising a retinula unit, the so-called distal retinula cell (DRC), has two or three branches that pass laterally alongside the rhabdom, thereby separating the two or three principal retinula cells of a unit. The two morphologically distinct layers of the receptive segment differ with respect to the cellular origin of rhabdomeral microvilli: DRC-branches contribute very few microvilli to the proximal rhabdom and develop extremely large rhabdomeres in the distal rhabdom only, causing the rhabdom units to fuse. Principal retinula cells, on the other hand, comprise the majority of microvilli of the proximal rhabdom, but their rhabdomeres diminish in the distal rhabdom. It is argued that proximal and distal rhabdoms serve different functions in relation to the intensity of incident light.In animals fixed 4 h after sunset, pigment granules retreat from the distal two thirds of the receptive segment. A comparison of retinae of day- and night-adapted animals shows that there is a slight (approximately 15%) increase in the cross-sectional area of rhabdomeral microvilli in dark-adapted animals, which in volume corresponds to the loss of pigment granules from the receptive segment. The length of the receptive segment as well as the pattern and shape of rhabdom units, however, remain unchanged.Each retinula unit is associated with one arhabdomeric cell. Their cell bodies are located close to those of retinula cells, but are much smaller and do not contain pigment granules. The most remarkable feature is a long, slender distal dendrite that extends up to the base of the fused rhabdom where it increases in diameter and develops a number of lateral processes interdigitating with microvilli of the rhabdom. The most distal dendrite portion extends through the center of the fused rhabdom and has again a smooth outline. All dendrites end in the distal third of the proximal rhabdom and are never present in the layer of the contiguous distal rhabdom. Arhabdomeric cells are of essentially the same morphology in day- and night-adapted animals. They are interpreted as photoinsensitive secondary neurons involved in visual information-processing that channel current collected from retinula cells of the proximal rhabdom along the optic nerve. A comparison is made with morphological equivalents of these cells in other chelicerate species.     

Freeze-etch and histochemical evidence for cycling in crayfish photoreceptor membranes

Summary Freeze-etched rhabdoms and adjacent cytoplasmic organelles from crayfish compound eyes have been studied for evidence of photoreceptor membrane cycling. The protoplasmic leaflet face (PF) of split photoreceptor membrane of the microvilli is richly particulate. The particles (92±16 A in diameter in surface fractures; 70±9 A in cross fractures; density about 8000/m²) probably indicate rhodopsin molecule localization. Closely similar particles appear in membranes of pinocytotic vesicles, multivesicular bodies (MVB) and secondary lysosomes. In contrast other retinular cell membranes like plasma membrane remote from the rhabdom are quite distinct (60±23 A particle diameter, density ca 1000/m²). Histochemical tests for acid phosphatase demonstrate its presence in well-developed (but not early stage) MVBs, mixed lamellar vesicular bodies (LVB) and lamellar bodies. Density of PF particles decreases from 8000 in MVB to roughly 4500/m² in LVB indicating a degradative sequence from rhabdom to lamellar bodies. Membrane leaflet orientations show that primary endocytosis from microvilli must be followed by secondary endocytosis of fused coated vesicles to form MVB. Morphological evidence for photoreceptor membrane resynthesis has not been found yet in crayfish but some has been obtained in other crustaceans.This research was supported by grants from the U.S. National Institutes of Health (EY 00405), the National Geographic Society and the Japan Society for the Promotion of ScienceThe authors are grateful to Mr. Washioka of the JEOL Co. Research Laboratory for his essential help in effecting the freeze-etch preparations. They also thank Professor Ryoji Kikuchi of Tokyo Women's Medical College for welcome cooperation and hospitality as well as Dr. Karl Pfenninger of Yale University for his generous assistance in interpreting the freeze-etch data. Technical advice and help were also kindly provided on the acid phosphatase histochemistry by Professor Marilyn Farquhar and others in the Yale Cell Biology Section     

Membrane topology and assembly of the outer membrane protein OmpA of Escherichia coli K12

The 325-residue outer membrane protein OmpA of Escherichia coli has been proposed to consist of a membrane-embedded moiety (residues 1 to about 170) and a C-terminal periplasmic region. The former is thought to comprise eight transmembrane segments in the form of antiparallel -strands, forming an amphiphilic connected by exposed turns. Several questions concerning this model were addressed. Thus no experimental evidence had been presented for the turns at the inner leaflet of the membrane and it was not known whether or not the periplasmic part of the polypeptide plays a role in the process of membrane incorporation. Oligonucleotides encoding trypsin cleavage sites were inserted at the predicted turn sites of the ompA gene and it was shown that the encoded proteins indeed become accessible to trypsin at the modified sites. Together with previous results, these data also show that the turns on both sides of the membrane do not possess specifically topogenic information. In two cases one of the two expected tryptic fragments was lost and could be detected at low concentration in only one case. Therefore, bilateral proteolytic digestion of outer membranes can cause loss of -strands and does not necessarily produce a reliable picture of protein topology. When ompA genes were constructed coding for proteins ending at residue 228 or 274, the membrane assembly of these proteins was shown to be partially defective with about 20% of the proteins not being assembled. No such defect was observed when, following the introduction of a premature stop codon, a truncated protein was produced ending with residue 171. It is concluded that (1) the proposed -barrel structure is essentially correct and (2) the periplasmic part of OmpA does not play an active role in, but can, when present in mutant form, interfere with membrane assembly.     

Polarization sensitivity of individual retinula cells

Summary This paper elucidates the influence of the structure of a rhabdom on the polarization sensitivity of its retinula cells. The terminology polarization sensitivity (PS) and dichroic sensitivity () needs clarification. expresses the directional property of the local microvillar medium and is independent of the gross morphology of the rhabdom. The PS of a retinula cell is that found by single cell electrophysiology and depends strongly on the gross morphology of the rhabdom. Both and PS are ratios of the effects of theE vector of linear polarized light parallel to, to that perpendicular to the microvilli. From the theoretical analysis and its correlation with experiments the following is concluded.     

Electron microscopic studies of coated membranes in two types of gill epithelial cells of lamprey

Summary Coated membranes in two types of gill epithelial cell of adult lamprey, Lampetra japonica, were studied by electron microscopy. The type 3 gill epithelial cells possess well-developed microvilli or microfolds, apical vesicles and abundant mitochondria. The cytoplasmic surface of the microvillous plasma membrane is covered by a coat of regularly spaced particles with a center-to-center distance of about 15 nm. Each particle consists of a bulbous free end, about 10 nm in diameter, and a connecting piece, about 5 nm long. Apical vesicles are covered by a surface coat which consists of fine filamentous material but lack any special coating on their cytoplasmic surface.The type 4 cells (chloride cells) are characterized by apical vesicles, abundant mitochondria and cytoplasmic tubules. These tubules possess a coat on their luminal surface which consists of spirally wound parallel rows of electron-dense materials. The rows are about 16 nm apart and wound at a pitch of about 45°. The cytoplasmic surface of these tubules does not display a special coat. These coated membranes are assumed to be the sites of active ion transport across the plasma membrane. In particular, particles in type 3 cells and linear coat materials in chloride cells may be either loci of transport enzymes or energy generating systems. Apical vesicles lack any coating on their cytoplasmic surface but a fine filamentous coat is present on their luminal surface. They contain intraluminal vesicles and are continuous with apical ends of cytoplasmic tubules.     

The nucleolar fibrillar centres in various cell types in vivo or in vitro

Summary The compound eye of male (haploid) Xyleborus ferrugineus beetles was examined with scanning and transmission electron microscopy. The eye externally consists of ca. 19 to 33 facets. Each ommatidium is composed of a thickly biconvex lenslet with about 50 electron dense and rare layers, but at the junction area between two lenslets there are only about 35 to 37 layers that can be distinguished. A very short (3.4–4.0 m) acone type crystalline cone is located directly beneath the lenslet. Each ommatidium is surrounded by pigment cells, and pigment granules also appear throughout the cytoplasm of the retinular cells. Some pigment granules are even present below the basement membrane. There are 8 retinular cells. The rhabdomeres of 2 centrally situated photoreceptor cells fuse into a rhabdom which is enveloped by the rhabdomeres of 6 peripheral retinular cells. The rhabdomeres of the 6 peripheral retinular cells join laterally to form a rhabdomeric ring around the central rhabdom. No tracheation was observed among the retinular cells. Virus-like particles are evident near the nucleus in each Semper cell of the crystalline cone.This research was supported by the Director of the Research Division, C.A.L.S., University of Wisconsin, Madison; and in part by research grant No. RR-00779 from the Division of Research Resources, National Institutes of Health and by funds from the Schoenleber Foundation, Milwaukee, WI to D.M.N.     

Degeneration of the compound eye of the termite Neotermes jouteli (Isoptera) in darkness during the phase of reproduction

Summary Long-term light deprivation of the royal pair of Neotermes jouteli during the phase of reproduction leads to a dramatic change in the organization within the compound eye. In a swarming alate, investigated with scanning and transmission electron microscopy, the eye consists of about 200 ommatidia. No differences between male and female eyes are observed. Each ommatidium is composed of a biconvex cornea, a cone of the eucone type, and a rhabdom which is located directly beneath the Semper cells. The rhabdom consists of eight rhabdomeres which are fused along the ommatidial axis. In the central part of the compound eye the rhabdom measures roughly 20 m in length. Concealed life of the imagines causes a dismantling of the cone and the rhabdom until complete destruction. This is accompanied by an increase in the number of pigment granules and a decrease in the number of mitochondria.     

Helical structure in the apical tubules of several absorbing epithelia

Summary Unique and highly ordered structures were discovered in the so-called apical tubules of several absorbing epithelia (kidney proximal tubule, visceral yolk sac and ductuli efferentes) fixed in situ with a mixture of formaldehyde, glutaraldehyde and osmium tetroxide. The apical tubules were especially numerous in the apical cytoplasm, in addition to the invaginations of the apical plasma membrane, newly formed endocytic vesicles and large endocytic vacuoles. They showed a cylindrical structure (80 nm in diameter) limited by a smooth membrane. Helically wound parallel rows of particles (11 nm in diameter) were found in the apical tubules in close proximity to their limiting membrane. The structure of the helix was determined by following the rows through serial sections and semithin sections, and was found to be a left-handed quadruple helix. These particles surround an electron-lucent cylinder (35 nm in diameter), containing at its center a single row of particles (9 nm in diameter). The apical tubules with the luminal specializations were not seen in continuity with the apical plasma membrane, but were frequently connected with the large endocytic vacuoles, which were present in the deeper levels of the apical cytoplasm. From these observations, it is suggested that the apical tubules are not derivatives of the apical plasma membrane; rather, they represent an intracellular compartment, which is morphologically related to the large endocytic vacuoles.     

Effects of photic and thermal stress on distal and proximal rhabdomeres in the crayfish eye: why are the visual membranes of the 8th retinula cell more resilient than the others?

Summary Visual membranes of the crayfish eye either belong to the small, distally placed rhabdomere of retinula cell R8 or are part of the much more voluminous proximal rhabdom, made up of rhabdomeres belonging to cells R1–R7. Under various conditions of environmental stress (e.g., prolonged darkness, elevated temperature, bright light with and without a concomitant rise in temperature, flickering lights) the visual membranes of R8 prove far more resistant to structural damage than those of R1–R7. Membrane damage is known to occur when dormant lipoxygenases become activated, for example through heat. Since R8 is the only type of visual cell in the crayfish retina that does not contain grains of screening pigment, the view that screening-pigment granules could aggravate or even trigger membrane damage in times of stress is strengthened. Functionally, R8's strong resistance to physical damage when exposed to flickering lights points to a role of the distal rhabdom in the movement detection system of the crayfish eye.