Ultrastructure and role of the aeropyle and shell of the egg of Galleria mellanella

The structure of the eggshells and particularly the morphogenesis and the fine structure of an aeropyle were studied in the wax moth Galleria mellonella.Galleria has eggs whose chorion shows an inner trabecular layer and the walls of aeropyles are coated by threads. During oviposition air enters the trabecular layer in a sufficient quantity to allow the development of the caterpillar if the egg is immersed in boiled water or paraffin oil. This layer is in communication with the atmosphere by means of 150 to 200 aeropyles.     

Morphology of the egg shell and the developing embryo of the Red Palm Weevil,Rhynchophorus ferrugineus (Oliver)

The harvested eggs of Rhynchophorus ferrugineus are ovo-cylindrical shaped, averaged 1.09 mm in length and 0.43 mm in width, with ratio of L\W 4.42. The chorionic layer of electron dense material is seen covering the exochorion structure of the eggs. The egg main body chorion exhibits a polygonal pattern and architecture surface of the egg is supported by a system of irregular interconnecting grooves. The micropylar apparatus of the eggs of the Red Palm Weevil, R. ferrugineus is described in the present study for the first time. Two micropylar openings are found closed to the center of the posterior wide pole of the egg. Each micropylar opening presents a single small orifice and its surrounding chorion is porous and densely set with tiny projections allowing the spermatozoa to penetrate the egg. Respiratory aeropyles are distributed on the borders of reticulations in the area chorionic surface of egg capsule. The hatching region is detected on the anterior part at the opposite side of the egg. Changes in the appearance and shape of R. ferrugineus eggs as well as the incidence of embryonic development are observed.     

Egg structure of Zorotypus caudelli Karny (Insecta, Zoraptera, Zorotypidae)

The structural features of eggs of Zorotypus caudelli Karny are described in detail. The egg is elliptic with long and short diameters of 0.6 and 0.3 mm respectively, and creamy white. The egg shows a honeycomb pattern on its surface, without any specialized structures for hatching such as an operculum or a hatching line. The fringe formed by a fibrillar substance secreted after the completion of the chorion encircles the lateral surface. The egg layer is composed of an exochorion, an endochorion, and a vitelline envelope. The exochorion and endochorion are electron-dense and homogeneous in structure. The exochorion shows a perforation of numerous branching aeropyles. The exo- and endochorion are connected by numerous small columnar structures derived from the latter. The vitelline envelope is very thin and more electron-dense than the chorion. A pair of micropyles is present at the equator on the dorsal side of the egg. Originating at the micropyle, the micropylar canal runs through the chorion obliquely. The structural features of the eggs of Zoraptera were compared with those of other polyneopteran and paraneopteran orders.     

Ultrastructural and histochemical studies of the egg capsules of Perla marginata (Panzer, 1799) and Dinocras cephalotes (Curtis, 1827) (Plecoptera : Perlidae)

Eggshells of stone flies P. marginata and D. cephalotes (Plecoptera : Perlidae), inhabiting mountain streams, were examined using scanning and transmission electron microscopes, a phase-contrast light microscope and histochemical methods to detect proteins, lipids and polysaccharides.The eggshells of the species investigated consist of a vitelline envelope, chorion and gelatinous sheet decorated on its outer surface with mushroom-like structures. An anchoring structure (attachment disc) is situated on the posterior pole of the egg. The structure and function of the attachment disc, as well as the possible taxonomic applications, are discussed. The morphology and histochemical composition of all these elements of the shell clearly demonstrate good adaptation to land and aquatic habitats; the chorion consists of 2 layers, the internal layer being finely perforated by numerous aeropyles. The external layer, with fewer, regularly placed aeropyles, protects the egg interior against dehydration in the land habitat. The gelatinous sheet seems to provide additional protection. Mushroom-like structures, situated on its surface, correspond with the positions of aeropylar openings. These and other interrelations between chorion structure and function are discussed.     

Eggshell fine structure of three lepidopteran pests: Cydia pomonella (L.) (Tortricidae), Heliothis virescens (Fabr.), and Spodoptera littoralis (Boisd.) (Noctuidae)

The eggshells of 3 moths, Cydia pomonella (Tortricidae), Heliothis virescens, and Spodoptera littoralis (Noctuidae) were investigated by scanning (SEM) and transmission (TEM) electron microscopy. The surface of the noctuid eggs shows structural elements (micropylar rosette, ribs, cross-ribs, and aeropyles) and regional differentiation, all typical of Lepidoptera. The egg of C. pomonella shows a different regional morphology due to its watch-glass shape and its position, lying on the flank. The micropylar structures are on the lower egg face in contact with the substrate. For S. littoralis, the surface structure (sculpturing) of the egg is not species-specific, being indistinguishable from that of S. frugiperda (Salkeld, 1984).In all 3 moths, the eggshell fine structure is basically identical, as revealed by TEM. Both the vitelline envelope and the chorion consist of several distinct layers. The vitelline envelope, bi-layered and several μm thick, undergoes a marked structural change when embryogenesis begins. At the same time, Golgi vesicles bearing dense particles, appear in the periplasm of the egg cell in fertilized eggs of H. virescens and S. littoralis. The chorion of all 3 species consists of a basal layer (C-1), a cavity layer (C-2) supported by trabecles and opening to the exterior via aeropylar canals, and a lamellar layer (C-3), which probably consists of helicoidally arranged stacks of fibrils. In H. virescens and S. littoralis, an additional epicuticle-like layer (C-4) is present. Available data from the literature are summarized and a basic scheme of the radial eggshell fine structure of ditrysian Lepidoptera is proposed.     

Absorption and cannibalism: do phytoseiids conserve egg resources when prey densities decline rapidly?

The number of eggs oviposited or left in the opisthosomas of dead mites (total eggs) was assessed for Metaseiulus occidentalis (Nesbitt), Neoseiulus fallacis (Garman), Typhlodromus pyri Scheuten or Amblyseius andersoni Chant when each was caged with either (1) no Tetranychus urticae Koch, (2) only odours of T. urticae, (3) ten eggs of M. occidentalis or (4) ten nymphs of M. occidentalis (T. pyri for M. occidentalis). The total eggs for the no prey versus odour tests did not differ within species; the levels were the greatest for N. fallacis > T. pyri > A. andersoni > M. occidentalis. Among treatments, egg means did not differ for M. occidentalis but they did for N. fallacis and T. pyri and similar trends were seen for A. andersoni. Egg means were usually less for mites held with ten predator nymphs than mites held with ten predator eggs or with no prey. Were adult females with nymphs absorbing rather than ovipositing their eggs or dying with them in their opisthosomas? Activity levels (walking) for adult females were no more for mites held with nymphs versus no food. The data indicated that interference by nymphs was not increasing the energy use of females and thus reducing egg levels. However, tests with ten nymphs, one egg and no adult female had egg losses from nymphal predation that could account for fewer eggs in cage tests. Overall, no evidence for absorption was found. If it occurs, it must be among younger eggs or mites exposed to less rapid prey losses than were the mites tested here; in addition, other stimuli may cause absorption. The total eggs in sticky-tape tests were greatest for N. fallacis > M. occidentalis > T. pyri > A. andersoni. Cage versus stick-tape data differed most for M. occidentalis because of cannibalism. All four mites cannibalized eggs but M. occidentalis did most rapidly and extensively. When starved, it laid all of its eggs before the other three species did. Such behaviours may enhance survival of M. occidentalis when prey become scarce.     

Patterns of inner chorion structure in Anastrepha (Diptera: Tephritidae) eggs

The inner chorion structure of Anastrepha eggs from 16 species of various infrageneric taxonomic groups is described by scanning and transmission electron microscopy. The layers of the chorion, the outer egg membrane, are structurally similar. Furthermore, an additional trabecular layer (ATL) that exists in some species, together with other characteristics, facilitates the recognition of four patterns of chorion structuring: Pattern I, in which the ATL layer is absent, is found in Anastrepha amita, the Anastrepha fraterculus complex, Anastrepha obliqua, Anastrepha sororcula, Anastrepha suspensa and Anastrepha zenildae (fraterculus group), and Anastrepha bistrigata and Anastrepha striata (striata group); Pattern II in Anastrepha serpentina (serpentina group), Anastrepha grandis (grandis group) and Anastrepha pseudoparallela (pseudoparallela group), in which the ATL presents large open spaces with pillars; Pattern III, found in Anastrepha consobrina (pseudoparallela group), in which the ATL is composed of round cavities; and Pattern IV, found in Anastrepha alveata and Anastrepha pickeli (spatulata group), where the large ATL cavities are reticulated. Comparatively, the chorion structure in Anastrepha eggs is more complex than in eggs of other fruit flies, e.g., Bactrocera, Rhagoletis and Ceratitis.     

Comparative morphology of the egg of the castniid palm borer,Paysandisia archon (Burmeister, 1880) (Lepidoptera: Castniidae)

Paysandisia archon (Burmeister, 1880) is an attractive neotropical castniid moth whose presence in Europe was recently reported. Its larvae are endophagous, feeding inside the trunks and branches of several species of palm trees (Arecaceae). The present paper deals with the morphology and biometry of the egg of this moth, comparing them with those of other castniid species.

The egg is a typical castniid egg, fusiform, upright sensu Döring, light cream or creamy pink when freshly laid, 4.69 ± 0.37 mm long and 1.56 ± 0.11 mm wide. Larvae emerge by gently splitting the chorion along one of the longitudinal ridges, on the half closer to the micropyle. SEM, TEM and LSCM photographs showing ultrastructural details of the egg are shown for the first time. The micropylar rosette (c. 54 μm in diameter) has generally 14–17 cells; in its centre lies the micropylar pit (c. 6 μm in diameter) which bears 12–16 micropylar canal openings (= micropyles) around its periphery. The pathways followed by those canals through the chorion have been figured. Eggs sampled in the wild (so laid by several females) were found to have a slightly variable number of ridges: most bore seven ridges (68.87%), although a significant portion (30.46%) bore eight and 1 egg (0.67%) bore only six; this against the currently accepted rule of five‐ridged eggs for Castniini (i.e. Neotropical castniids) to which Paysandisia archon belongs. It has also been found that the same female specimen has the capability of producing six‐, seven‐ or eight‐ridged eggs. Five types of egg irregularities affecting the longitudinal ridges are also figured and described. Transverse striae on the egg of P. archon are about 122. Aeropyles (c. 4 μm in diameter) occur on the ridges, at the intersections between the latter and two contiguous (left and right of the ridge) transverse striae, amounting to c. 854 on a seven‐ridged egg and to c. 976 on an eight‐ridged egg. Occasionally minute aeropyles ('microaeropyles') (c. 1.96–3.13 μm in diameter) also occur on transverse striae located close to both egg poles.

The chorion of P. archon shows the typical ditrysian fine structure with very thin basal layer (C‐1), 0.3–0.2 μm thick, gas‐filled trabecular layer (C‐2), c. 0.9 μm thick, and lamellar layer (C‐3), its thickness varying between 18.5 and 13 μm due to the bumpy external surface of the chorion. Aeropylar canals, that penetrate layer C‐3, connect the air‐containing inner chorionic meshwork (the trabecular layer C‐2) with the surrounding air; their outer part forms a big bulbous cavity (which opens to the outside through the small opening seen in external SEM images) and, underneath, a narrow canal follows, leading into the trabecular layer (C‐2).     

Egg shells in mites: vitelline envelope and chorion in Acaridida (Acari)

This study deals with the formation of vitelline envelope (VE) and chorion compartments in several free living and parasitic acaridid mites.In all investigated mites, the VE is of primary origin (produced by oocyte itself), whereas exochorion material is of tertiary origin (oviduct or chorion gland secretion).In acarid mites Acarus siro and Tyrophagus perniciosus, VE formation starts with the oviductal oocytes in which vitellogenesis already proceeds. It is characterized by stratification (Acarus) or coarse fibrillar texture (Tyrophagus). Oocyte microvilli penetrating VE material were not observed. When the vitellogenesis terminates, VE becomes homogeneous and is transformed into chorion. This is the only layer protecting the deposited egg in A. siro, whereas in T. perniciosus the chorion-coated eggs passing through the distal portion of the oviduct are additionally covered by exochorion material deposited in three distinct forms: dense patches, granules, and most conspicuous locular chambers. In Tyrophagus longior, the egg surface closely resembles that of T. perniciosus, but the locular chambers are smaller. In Aleuroglyphus ovatus the exochorion material forms tiny spherical patches instead of locular chambers.In Sarcoptes scabiei, Notoedres cati and Falculifer rostratus, flocculent VE appears on vitellogenic oocytes in the oviduct. VE development is characterized by formation of numerous lenticular perivitelline spaces, which initially grow to disappear later. Then VE material transforms into fully homogeneous chorion. Chorion glands in Sarcoptes and Notoedres produce multivesicular secretory bodies; their content is released onto the egg surface to form a vesicular monolayer (exochorion) during the egg passage. The chorion gland in Falculifer is composed of two secretory cell types. Its secretion possibly glues the eggs to the host feather barb during highly ordered deposition, and forms the appendage ending with a ribbed plate, here considered to be a print of female undulate lamina acting as an ovipositor. The hatching suture is present. Neither distinct micropyle nor aeropyles have been found in eggs of species under study.The exochorion is proposed to be an adhesive layer which fixes the eggs to the substratum. The same role plays the chorion gland secretion in F. rostratus. It can be argued, however, that locular chambers of Tyrophagus exochorion may participate in reduction of water loss rather than in egg adherence or plastron respiration, as previously suggested in the literature.     

Respiratory morphology of the Abedus herberti Hidalgo egg chorion (Hemiptera: Belostomatidae)

Although giant water bugs (Hemiptera: Belostomatidae) are large, aquatic insects known for their obligate paternal egg brooding behaviors, little research has focused on the structure of their eggs. The respiratory requirements of developing embryos likely created selection for brooding, so a thorough understanding of the respiratory morphology of belostomatid eggs could help explain how brooding behaviors facilitate embryonic gas exchange. This study used scanning electron microscopy to document the respiratory microstructure of the eggs of Abedus herberti, a back brooding giant water bug. The exochorion is similar to that of other belostomatids in texture and organization except that the respiratory region is confined to the uppermost quarter of the egg. This is the area exposed to the atmosphere by encumbered males. A plastron network made up of densely packed vertical projections demarcates the boundary between the respiratory and nonrespiratory regions of the chorion. The internal chorion is composed of alternate air‐filled and denser layers that likely facilitate the movement of oxygen from the aeropyles at the top of the eggs to the developing embryonic tissues. J. Morphol., 2011. © 2011 Wiley‐Liss, Inc.     

Fine structure of the egg shells of Habrophlebia fusca (curtis) and h. consiglioi Biancheri (Ephemeroptera : Leptophlebiidae)

The eggs of 2 mayflies, Habrophlebia fusca and H. consiglioi (Ephemeroptera : Leptophlebiidae) were observed with scanning and transmission electron microscopes. The external surface of the eggs in both species had longitudinally oriented costae. The chorion of H. fusca had different structures in its costal and intercostal zones. Three distinct layers could be recognized: an inner layer close to the vitelline coat, consisting of electron-dense lamellae perpendicular to the egg surface; an intermediate layer, consisting of loosely structured fibrillar material; and an outer highly electron-dense layer, consisting of 2 separate laminae, divided by an electron-transparent line. In the egg of H. fusca, the costal area of the chorion shows a columnar structure. The columns merge distally to create wide chambers. This organization has been observed with the SEM in H. consiglioi as well. The chambers are interconnected and communicate with the exterior through openings along the costal edges. Masses of mucus-like substance are present both in the chambers and outside the chorion; they show fibrillar material and electron-dense bodies with a paracrystalline structure.     

Surface morphology of eggs of Euproctis chrysorrhoea (Linnaeus, 1758)

Candan, S., Suludere, Z. and Bayrakdar, F. 2007. Surface morphology of eggs of Euproctis chrysorrhoea (Linnaeus, 1758). —Acta Zoologica (Stockholm) 88 : 000–000. Filaments covering the egg batches and chorion structure were studied both by light and scanning electron microscopy in the brown‐tailed moth Euproctis chrysorrhoea (Linnaeus, 1758). Females lay eggs in masses on the underside of apple leaves. The egg batches are covered with brown hairs derived from the bodies of the female. Each female lays about 200–400 eggs. The spherical eggs are about 0.84 mm long and 0.47 mm wide. Newly deposited eggs are golden‐yellow and darken after the onset of embryonic development. The micropylar area appears somewhat depressed and has a circular outline. The region is surrounded by a rosette of 10–12 petal‐shaped primary cells, which are completely surrounded by a series of secondary and tertiary cells. The remainder of the egg is largely smooth, but shows aeropyles. These are located in the corners of ill‐defined polygons.     

Choriogenesis in the medfly Ceratitis capitata (Wiedermann) (Diptera : Tephritidae)

Four chorionic stages (11, 12, 13, 14) can be discerned in the medfly Ceratitis capitata (Diptera : Tephritidae) by light microscope. More detailed staging (stages 11A, 11B, 12A, 12B, 12C, 13A, 13B, 13C, 14A and 14B) is possible only by electron microscope. Throughout these stages, the first chorionic layer (wax layer) is formed at stage 11A, followed by the formation of the innermost chorionic layer (stage 12A), the inner endochorion, the pillars and the cavities of the first trabecular layer (stage 12), creation of the second trabecular layer and the chorionic network (stage 13), and finally the secretion of the exochorionic layers (stage 14). Pulse-chase autoradiography has revealed that the follicle cells are responsible for the synthesis of all proteinaceous layers. No extensive regional complexity is observed besides the existence of the micropylar apparatus and aeropyles in the anterior pole. Biochemical analysis has revealed several eggshell proteins and their stage-specific synthesis: two intermediate molecular-weight proteins are the major chorion proteins; in addition, there are 2 more groups comprising 6 proteins, which might be characteristic for the different chorion layers as can be deduced by their stage-electrophoretic pattern.     

Intra- and interspecific predation on four life stage groups by the adult females of Metaseiulus occidentalis, Typhlodromus pyri, Neoseiulus fallacis and Amblyseius andersoni

Do adult females of oligophagous species such as Neoseiulus fallacis (Garman) and Metaseiulus occidentalis (Nesbitt) show less intra- and interspecific predation on phytoseiids when other foods are scarce than polyphagous species such as Amblyseius andersoni Chant and Typhlodromus pyri Scheuten? We caged single adult females of each species without food with ten of their own eggs or larvae, with ten eggs or larvae of the other species or with ten nymphs or adult females of M. occidentalis (T. pyri for M. occidentalis). We assessed the ambulatory activity, survival time, egg levels and prey loss in each test. Polyphages (in particular T. pyri) lived longer than oligophages (in particular N. fallacis) without food. The small T. pyri detected its own stages and benefited most by feeding on small active stages of other species. Amblyseius andersoni, the largest mite, fed and gained the most of any species when held with nymphs and female adults. Metaseiulus occidentalis fed on eggs of all four species to enhance survival. The large hyperactive N. fallacis gained the least from these behaviours. Each mite seemed uniquely adapted to survive conditions of scarce prey and these behaviours may explain their roles in phytoseiid mite complexes. Overall, oligophagous adult females fed less and gained less by feeding on phytoseiids than did polyphagous adult females.     

Switch in pattern formation after puncturing the anterior pole of Smittia eggs (Chironomidae, Diptera).

The aberrant pattern, “double abdomen,” previously induced in the egg of Smittia by uv irradiation of anterior pole regions was also produced by puncturing of the egg at the anterior pole. Double abdomens and embryos with anterior defects developed in eggs in which puncturing had locally prevented the regular arrangement of cleavage nuclei in the periplasm. The resulting gap in the blastoderm at the anterior pole was subsequently closed under exclusion of a small amount of egg material. Double abdomens did not develop in eggs where exclusion of anterior egg material was not observed. Thus a basic switch in the developmental program of the egg appears to depend upon the functional elimination of some crucial components in the anterior egg region.     

Pathogenicity of entomopathogenic hyphomycetes, Paecilomyces fumoso-roseus and Nomuraea rileyi, to eggs of noctuids, Mamestra brassicae and Spodoptera littoralis

Bioassays were conducted to determine the susceptibility of egg masses of Mamestra brassicae and Spodoptera littoralis to different spore doses of Paecilomyces fumoso-roseus and Nomuraea rileyi at 20° and 25°C. P. fumoso-roseus was highly virulent against eggs, whereas N. rileyi provoked only a deferred mortality of larvae hatched from treated eggs. Nevertheless, larval mortality of S. littoralis caused by N. rileyi at 25°C was more effective after first-instar larval contamination than after egg mass treatment. The duration of the egg stage could explain differences of susceptibility between the two noctuids at 25°C. Scanning electron microscopical observations suggested two ways of contamination of newly hatched larvae. First, fungal germinations on the chorion surface suggested that newly hatched larvae might be infected by penetration of the egg integument before hatching. Second, conidia on the egg cuticle could be an entomopathogenic inoculum for newly emerging larvae which fed upon chorions. Results showed that pathogenicity of Hyphomycetes to noctuid eggs might be a promising area of investigation for biological control.     

Function of shell structures of pig louse and how egg maintains a low equilibrium temperature in direct sunlight

The functional significance of the structures of the eggshell of the pig louse, Haematopinus suis, and those of some other Anoplura and some Mallophaga, is described.The shell of the pig louse has an outer air-filled meshwork. The air in this meshwork is isolated from that in the respiratory system. This layer does not function as an insulator. Calculations show that the temperature drop across the layer is only about $\text{1}\text{75}\text{°}\text{C}$.The air-filled outer meshwork functions as a reflector. The eggs are often exposed to direct sunlight because of the wide spacing of the pig's bristles. The outer reflecting layer has an enormous selective advantage for the egg in two quite different ways: (1) it slows down the rate at which equilibrium temperature is reached, and (2), much more important, it enables the egg to lower equilibrium temperature.Assuming that reflectance = 0.9 and sunlight = 10³ Wm^?2, the heat input is $\text{3.1 ×}\text{r}{}^2\text{100}\text{J/sec}$, and the time required for a rise of 20°C, assuming no heat loss, is 4.3 min. Assuming a more realistic energy flux (sunlight = 500 Wm^?2) for the latitudes in which most pigs are bred, and even assuming a reflectance of only 20%, the time required for a rise of 20°C in direct sunlight, with no heat loss, is increased by 1 min 4 sec.Lowering the equilibrium temperature is of much greater selective advantage than merely slowing down the rate at which it is reached. Reflectance + emissivity = 1. Nevertheless, the egg can achieve a reflectance of, say, 0.8 at the same time as it achieves an emissivity of 0.8 from the energy absorbed by the chorion and especially the aqueous embryo or pharate first instar larva, either of which will function as a black body and absorb all of the infra-red not absorbed by the chorion. Calculations show that if a heat input of 200 Wm^?2 is assumed, at an ambient temperature of 27°C, the equilibrium temperature can be maintained at 47°C.The chorionic hydropyle of the pig louse, like that of apparently all other Phthiraptera, is most unusual in that the hygroscopic spumaline secreted by the accessory glands flows through the hydropyle canals of the chorion into the interior of the egg while the egg is still in the common oviduct. Molecules as large as those of fast green (mol. wt 809) pass through the spumaline into the interior of the egg and then pass through the serosal hydropyle. The amount of spumaline secreted greatly exceeds that necessary to glue the egg to the bristle. Once absorption is seen as another function of the spumaline, its amount no longer becomes difficult to understand: under many natural conditions it will enable the egg quickly to replace losses of water that result from exposure to high temperatures in direct sunlight.The egg of the pig louse, like those of other species of Haematopinus, has a very well-developed plastron or permanent physical gill. A number of the aeropyles are covered by spumaline, but even assuming that 30% of them are so covered, the water-air interface for small eggs is 3.5 × 10⁶ μm²/mg and for large eggs 2.6 × 10⁶ μm²/mg. Thus the relation of water-air interface to weight of tissue is the most favourable so far reported in insects.     

Ultrastructure and resistance to water loss in eggs of Acanthoscelides obtectus Say (Coleoptera: Bruchidae)

The mature oöcyte of Acanthoscelides obtectus is surrounded by three envelopes: an external layer, a chorion and a vitelline membrane. The external layer is secreted by the walls of the lateral oviducts. The chorion and vitelline membrane are secreted by the follicular cells. The vitelline membrane becomes very compact during the hour following fertilization and laying. The chorion is composed of three layers, one of which has a paracrystalline ultrastructure.Mature, unfertilized, chorion-containing oöcytes, whose vitelline membranes are loose, dehydrate rapidly in a dry atmosphere after laying or after removal from the lateral oviducts. Fertilized eggs are quite resistant to desiccation: after 12 days at 25°C and 5% relative humidity, viable larvae are obtained.The compact vitelline membrane is the most effective protection against dehydration. The chorion and the external layer are much less effective in preventing water loss from the egg.The retention of eggs in the lateral oviducts does not seem to lead to any modification of the structure of their envelopes.     

L'oeuf de Myrmeleotettix maculatus Thunb. (Orthoptera : Acrididae): Absorption d'eau et structure fine des enveloppes

Water absorption and fine structure of the egg shell have been studied in the eggs of Myrmeleotettix maculatus (Orthoptera : Acrididae). At the anterior pole of these eggs, there is a respiratory plastron and at the posterior end, behind the ring of micropyles, many minute holes can be seen. Eggs of M. maculatus incubated on wet filter paper at 30°C absorb water before diapause between the 5th and the 25th day after oviposition. The period of water absorption coincides with the serosal cuticle secretion. The increase in volume of the egg does not seem to involve any fragmentation in the chorion. The chorion is composed of 3 layers (upper, middle and lower). The middle layer, the thickest one, contains twisted elements with a paracrystalline structure. During the first days of incubation, the vitelline membrane becomes changed. In the newly laid egg, it is granular and homogeneous. Five days later, 4 layers with different structures can be distinguished. After 30 days, the serosal cuticle presents a thin epicuticule and a thick lamellated endocuticule with many pore canals.     

Bemerkenswerte endogene Farbveränderung der Eischale von Chioninia delalandii (Duméril & Bibron, 1839) (Reptilia: Sauria: Scincidae)

The paper describes an unusual endogenous eggshell colouration observed in an egg of the Cap Verde skink Chioninia delalandii.A female specimen, kept in a terrarium, laid three eggs. Two of them were considered as fertilized (oval germ-disk, weakly pink). They were embedded 1 cm deep in a layer of moistened clay granules (substrate/water 2:1) and kept under different temperatures (egg 1 “cool”, 26–27 °C; egg 2 “warm”, 29–30 °C). There was a normal embryonic development in both eggs from their volume-enlargement and characteristic allometric growth (egg wide > egg length). The young hatch after 51 and 56 days.A change in eggshell colour, however, occurred in the “warm” kept egg during the last third of its incubation period. It started with a small spot (2–3 mm) in the outer area of the animal egg pole and spread into a dark-violet colouration over the whole eggshell within 15 days. After hatching of the young the shells of both eggs were examined. In the non-coloured egg there was no great difference in colour between the inner and outer egg layer, while in the coloured egg there was a distinct difference between the inner part, which was dark violet-gray, and the pale gray calcareous deck-layer. From the macroscopic view along the edge of the eggshell it was not identifiable, if the colour pigment was infiltrated into protein fibrils of the condensed surface layer.A possible explanation for the eggshell colouration could be an unusual embryonic pigmentation. This assumption is based on the first appearance of a restricted, point-like coloured area and its further regular extension. It might be that dark pigments (melanophores?) reached the eggshell (membrana testacea) and infiltrated the border-area to the condensed surface layer.