Ultrastructure d'une glande sternale tubuleuse des mâles de Speonomus hydrophilus (Coleoptera, Bathysciinae)

1983 ◽  
Vol 61 (3) ◽  
pp. 673-681 ◽  
Author(s):  
Monique Cazals ◽  
Lysiane Juberthie-Jupeau

The tubular sternal glands of S. hydrophilus are tegumentary glands present only in the males and were until today unknown. They lie in the segments 6–8 and open between the 8th and 9th segment. They consist of a ramified epithelium made up of prismatic cells. The gland opening is composed of a porous plate connected to an internal cuticular complex. The porous plate itself consists of an epicuticular layer perforated by tiny pores, a mesocuticular layer with large pore canals reaching the pores, then a part with cuticular filaments. All around the porous plate, the mesocuticle makes up a cylindrical excrescence directed towards the secretory part, the free edge of which is prolonged by long mesocuticular plates called pseudomembranes; they are thin, parallel, and penetrate each of the gland cavities. Thus the tubular sternal glands appear as a ramified epidermal invagination; only the internal part of the cuticle is accompanying this invagination. The pseudomembranes might play the same role as an end apparatus for the secretory products. These glands may produce a sex pheromone which would allow the female to recognize the male.

1946 ◽  
Vol s2-87 (348) ◽  
pp. 393-439
Author(s):  
J. W. BEAMENT

The main regions of the Ehodnius prolixus egg-shell have been defined; a concise definition has been obtained for the term ‘chorion’. The formation and structure of the unspecialized chorion has been followed from the time of differentiation of the follicle cells, up to the completion of the shell, and an assessment made of the chemistry and permeability of each component shell layer. The follicle cells are binucleate; changes in morphology and histology prior to secretion of the shell are outlined. The secretory products of the follicle cells fall naturally into an endochorion and an exochorion; the endochorion consists of five modifications of a proteinaceous substance. They are, in order of secretion: 1. The Inner Polyphenol Layer, which consists of a series of tanned granules of average diameter 2µ, containing large quantities of polyphenols. The layer is discontinuous and has no effect on permeability. 2. The Resistant Protein Layer, a tanned and possibly vulcanized layer of protein, 1 to 2µ, thick, containing diffuse polyphenols. It is resistant to strong acids and bases, and permeable to water, ions, and large water-soluble molecules. 3. The Outer Polyphenol Layer, which is similar to the inner layer, but has more minute granules. 4. The Amber Layer.--This is the only coloured layer of the shell, and is less than 0-1µthick. It consists of tanned protein to which oil is added after secretion. It is therefore a lipidized protein, which is excessively resistant to acids and alkalies, and permeable to oils and oil-soluble material and to small ions and water. 5. The Soft Protein Layer.--This is a thick laminated layer some 8µ. thick, similar to, but less resistant than, the resistant protein layer. It contains polyphenols and tyrosine. The layer is freely permeable to water-soluble substances. Throughout the secretion of the endochorion, the follicle cells stain deeply and appear to be filled with the protein components of the shell. The exochorion consists of two layers of the lipoprotein ‘chorionin’. 6. The Soft Exochorion Layer is a lipoprotein which is soluble in potash but not in strong acids; the layer is permeable to lipoid solvents and to water and small ions, but not to larger particles. It is 8µ thick at its maximum thickness, but contains follicular pits which, during secretion, are filled by long processes from the follicle cells. 7. The Eesistant Exochorion Layer is a more resistant form of chorionin. It lines the pits and covers the surface of the shell, giving rise to the polygonal markings corresponding to the follicle cells, each with a pit at its centre. The follicle cells contain quantities of lipoprotein during this phase of secretion, and are difficult to stain. A method of staining is described which shows that pore canals of two varieties are present in the exochorion layers only. They run from the walls of the pits but do not reach the endochorion. None of the layers of the chorion waterproofs the shell. In the rear end of the shell, the outer polyphenol layer is displaced towards the exochorion, thus increasing the resistant protein layer and reducing the soft protein layer. It is shown that all seven layers are present in the neck, and in the central region of the cap, and that the order of secretion is the same. Modifications are produced by variations in the thickness of the various layers. In the neck, the soft protein layer is reduced; in the cap, the resistant protein layer is reduced while the amber layer is 2µ thick, giving the cap a brown appearance. The soft protein layer is extremely thin and irregular while the exochorion layers are 16 µ thick. Pore canals are again present in two varieties. Some analysis is made of the formation of follicular pits; this appears to be correlated with the thickness of the exochorion and endochorion layers.


1947 ◽  
Vol 23 (3-4) ◽  
pp. 213-233 ◽  
Author(s):  
J. W. L. BEAMENT

An investigation has been made of the junction between the shell and cap in the egg-shell of Rhodnius prolixus. This complex region consists of the thickened rim of the cap connected by a thin sealing bar to the rim of the shell. The secretion of this part of the shell has been followed and compared with the formation of less specialized portions of the shell. The shell has been divided into units, each the product of an individual follicle cell. It has been found that all the seven layers which make up the unspecialized parts of the shell are present in the seal complex; that these consist of five endochorion layers and two exochorion layers in their normal order. The exochorion is secreted around long villi, one from each follicle cell. These give rise to follicular pits in the shell. In this complex region, cells start to secrete at various stages in the seven-phase cycle; their initial secretion is apparently related to the material with which they make contact at that time. After secretion has started, each cell completes the remainder of the cycle. The rim of the cap is the product of four rings of follicle cells; the additional thickness is achieved by an increase in the exochorion layers, secreted around a series of very long follicular pits. The sealing bar, which is produced by one ring of follicle cells, is composed of the inner four layers of the chorion only; the cells do not produce soft endochorion, or exochorion layers. At the cap end of the sealing bar there is the predetermined hatching line. It is apparently produced by the presence in the follicle of cells which are inactive during the secretion of the inner layers, and so prevent co-ordination between the active cells on either side. A weak point is also present at the base of the sealing bar, at the site of other inactive cells, though this fissure is not used at hatching. The rim of the shell is similarly produced by an expansion of the exochorion layers secreted around four rings of follicular villi. Of these, three rings of pits are filled in towards the end of secretion, but the fourth, lying on the upper portion of the rim, remains. These pits become the micropyles and associated structures. There are 200 pits in the completed rim, divided into two groups. About fifteen are micropyles; the remainder are cavities closed at each end, and to which the name ‘pseudomicropyle’ has been given. The pseudomicropyles are formed in a similar way to normal follicular pits, but start in the resistant protein layer, 0.5µ from the inside of the shell. They end in the resistant exochorion, where they are connected to the external surface by small bunches of pore canals. They probably play some part in the respiration of the embryo. The true micropyles form the only free path through the shell. The inner portion of each tube is lined with hydrophilic protein, and the outer portion, which lies slightly posterior to the pseudomicropyles, is composed of hydrophobic lipoprotein. The number of true micropyles is not constant, there being between ten and twenty scattered irregularly around the rim. However, eggs produced by older females contain fewer micropyles; this may account for a higher rate of sterility among these eggs. The cells which form the micropyles and pseudomicropyles are the only ones which do not adhere to the typical cycle of seven secretory products. But in omitting three phases, the attachment of the exochorion to a protein layer is retained. Evidence suggests that the cells forming the micropyles are determined in the earliest stages of secretion by being squeezed out of the pseudomicropylar ring of cells.


2015 ◽  
pp. 15-19
Author(s):  
F. N. Zosimov ◽  
S. K. Turenko

A new model of hard-to-recover oil reserves generation in the dome part of the structure is described. It is shown that in the dome part of the structure thin pore canals are saturated with oil thanks to high overpressure, while in the transition and undersaturated zones the same size canals are filled with water. When producing oil by contour water-flooding the water effectively displaces the oil from large pore canals, but fine pores remain oil-saturated. It is shown that to recover oil from thin pore canals some new methods of the formation stimulation should be developed.


2008 ◽  
Vol 34 (2) ◽  
pp. 220-228 ◽  
Author(s):  
Christer Löfstedt ◽  
Jan Bergmann ◽  
Wittko Francke ◽  
Erling Jirle ◽  
Bill S. Hansson ◽  
...  
Keyword(s):  

1974 ◽  
Vol 52 (6) ◽  
pp. 695-705 ◽  
Author(s):  
Jean E. Percy

The sex-pheromone-producing gland of Choristoneura fumiferana, as in other moths, is a modified intersegmental membrane between the eighth and ninth abdominal segments. Gland cells differ from epidermal cells in unmodified intersegmental membranes in their size, shape, and structure. One to 2 days before emergence of the adult, the gland cells have few microvilli and the cytoplasm contains mainly rough endoplasmic reticulum. By 1 h before emergence, the cells have the adult characteristics. The basal region below the nucleus contains Golgi complexes, lipid droplets, glycogen deposits, and rough endoplasmic reticulum. The apical region contains many microbodies and extensive smooth tubular endoplasmic reticulum. The apical surface has numerous well-developed microvilli, each of which contains a core of smooth endoplasmic reticulum. In contrast to gland cells, unmodified epidermal cells only contain rough endoplasmic reticulum and their apical projections are small and ill-defined. Cuticle of the gland and unmodified intersegmental membrane does not change after deposition but continues to resemble that of the developing gland 1 to 2 days before emergence. Pore canals are present as gaps in the endocuticle and follow the helicoidal arrangement of the microfibrils. Near the microvilli the pore canals contain a filamentous structure which is replaced by epicuticular filaments near the first lamella of the endocuticle. Groups of epicuticular filaments terminate at an oval depression in the dense epicuticle. Each oval depression opens at the surface of the inner cuticulin. Epicuticular filaments are not the immediate precursors of the pheromone. The probable role of the epicuticular filaments in pheromone synthesis and release is discussed.


2006 ◽  
Vol 11 (4) ◽  
pp. 331-343 ◽  
Author(s):  
M. S. Alam ◽  
M. M. Rahman ◽  
M. A. Samad

The problem of combined free-forced convection and mass transfer flow over a vertical porous flat plate, in presence of heat generation and thermaldiffusion, is studied numerically. The non-linear partial differential equations and their boundary conditions, describing the problem under consideration, are transformed into a system of ordinary differential equations by using usual similarity transformations. This system is solved numerically by applying Nachtsheim-Swigert shooting iteration technique together with Runge-Kutta sixth order integration scheme. The effects of suction parameter, heat generation parameter and Soret number are examined on the flow field of a hydrogen-air mixture as a non-chemical reacting fluid pair. The analysis of the obtained results showed that the flow field is significantly influenced by these parameters.


2019 ◽  
Vol 22 (9) ◽  
pp. 1197-1206
Author(s):  
Fathimunnisa ◽  
Sirangala Ganesh Rakesh ◽  
Neetu Srivastava

Author(s):  
J. Buggaramulu ◽  
M. Venkatakrishna ◽  
Y. Harikrishna

The objective of this paper is to analyze an unsteady MHD free convective heat and mass transfer boundary flow past a semi-infinite vertical porous plate immersed in a porous medium with radiation and chemical reaction. The governing equations of the flow field are solved numerical a two term perturbation method. The effects of the various parameters on the velocity, temperature and concentration profiles are presented graphically and values of skin-frication coefficient, Nusselt number and Sherwood number for various values of physical parameters are presented through tables.


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