Scanning electron microscope studies of some skink papillae basilares

Summary The papilla basilaris of scincid lizards is relatively long, slightly curved or bowed, and characteristically has an apical terminal expansion. A limbus-attached tectorial membrane is present but is apparently not continuous with the tectorial material covering the hair cells of the papilla. The hair cells of the apical expansion are covered by a thick spongy mass of tectorial material, while the hair cells above (dorsal to) the apical region are covered by thickened tectorial material that is in the form of uniquely sculptured, twisted or folded drape-like masses (sallets). The surface of the basal (dorsal) quarter of the papilla is unusual in that it is concave rather than convex. The expanded terminals of the hair cell kinocilia are also unusual in being arrowhead-shaped.Kinocilial orientation of the non-apical papillary hair cells is simply bidirectional; the hair cells on each side of the papillary axial midline are oriented toward the midline. Kinocilial orientation of the hair cells of the apical expansion is more complex with the peripheral neural and abneural rows both being abneurally directed, and the central rows being at first neural in orientation, but becoming abneurally oriented as the apical tip is approached. At the apical tip region, most all hair cells are abneurally oriented.I would like to thank Ms Maria Maglio for her skill in handling the technical aspects of the electron microscope, Mr. David Akers for expert photographic assistance, and Ms. Michiko Kasahara for aid in all aspects of the work. Research sponsored by United States Public Health Service Grant NS-09231.     

Further scanning electron microscope studies of lizard auditory papillae

The papillae basilares of 12 species of lizards from seven different families were studied by SEM. The iguanids, Sceloporus magister and S. occidentalis, have typical “iguanid type” papillae with central short-ciliated unidirectional hair cell segments and apical and basal long-ciliated bidirectional hair cell segments. These species of Sceloporus are unique among iguanids in that the bidirectional segments consist of but two rows of hair cells. The agamids, Agama agama and Calotes nigrolabius, have an “agamid-anguid type” papilla consisting of an apical short-ciliated unidirectional hair cell segment and a longer basal bidirectional segment. Agama agama is unusual in having a few long-ciliated hair cells at the apical end of the apical short-ciliated segment. The agamid, Uromastix sp., has an “iguanid type” papilla with a central short-ciliated unidirectional segment and apical and basal bidirectional segments. The anguid, Ophisaurus ventralis, has an “iguanid” papillar pattern with the short-ciliated segment centrally located. All the short-ciliated hair cells of the above species are covered by a limbus-attached tectorial network or cap and the long-ciliated hair cells, only by loose tectorial strands. The lacertids, Lacerta viridis and L. galloti, have papillae divided into two separate segments. The shorter apical segment consists of opposingly oriented, widely separated short-ciliated cells covered by a heavy tectorial membrane. The apical portion of the longer basal segment consists of unidirectionally oriented hair cells, while the greater part of the segment has opposingly oriented hair cells. The xantusiids, Xantusia vigilis and X. henshawi, have papillae made up of separate small apical segments and elongated basal segments. The apical hair cells are largely, but not exclusively, unidirectional and are covered by a heavy tectorial cap. The basal strip is bidirectional and the hair cells are covered by sallets. The kinocilial heads are arrowhead-shaped. The papilla of the cordylid, Cordylus jonesii, is very similar to that of Xantusia except that the apical segment is not completely separated from the basal strip. The papilla of the Varanus bengalensis is divided into a shorter apical and a longer basal segment. The hair cells of the entire apical and the basal three quarters of the basal segment are opposingly oriented, not with reference to the midpapillary axis but randomly to either the neural or abneural direction. The apical quarter of the basal segment contains unidirectional, abneurally oriented hair cells. The entire papilla is covered by a dense tectorial membrane. The functional correlations of the above structural variables are discussed.     

Scanning electron microscope studies of some internal surfaces in human skin

Summary The scanning electron microscope has been used to investigate the surfaces of epidermis, hair follicles, fat cells, glands and blood vessels in sections of human skin. The appearances of structures associated with these surfaces have been described. The results demonstrate that this new instrument can become an important tool in the investigation of surface changes that might accompany the application of loads (extensive, compressive or torsional), or physiological or pathological abnormalities.We wish to thank Prof. R. M. Kenedi for his continued encouragement of this work. One of us (I.A.B.) is also grateful to the Science Research Council for the provision of a post-graduate student grant.     

Scanning electron microscope studies of the papilla basilaris of some turtles and snakes

The papillae basilares of three species of turtles and four species of snakes were studied by SEM. The papillae of turtle are relatively large among reptiles and are characterized by a long, horizontal middle section resting on wide basilar membrane. Both terminal ends of the papilla extend onto the surrounding limbus in the form of a forked or "T" -shaped end or as a curved, "hook"- like processes. Details vary with the species. In the three species of turtles studied, there were between 1,100 and 1,400 hair cells on a papilla. The tectorial membrane covering the horizontal portion of the papilla is heavy in appearance and tightly attached to the kinocilial bulbs. The terminal ends of the papilla are covered by a thin gelatinous material. In addition, mat-like tectorial network covers the supporting cells and extends from the microvilli of the supporting cells to the overlying tectorial membrane. All hair cells are unidirectionally and abneurally oriented. The supporting cell surfaces form a large part of the papilla and, thus, hair cell density is low. The papillae of the two boid snake species studied are moderately long among snakes and contain a moderate number of hair cells (574 in Epicrates and 710-780 in Constrictor). Papillar form is elongate, avoid, or canoe-shaped. The tectorial membrane may be either highly fenestrated or moderately dense and covers all but a few of the terminal hair cells. A tectorial-like mat covers all but a few of the terminal hair cells. Most hair cells are unidirectionally and abneurally oriented. A few terminal cells in boids may show reverse orientation. Hair cell density is similar to that of turtles.     

Scanning and transmission electron microscope studies on the sensory sucker papillae of the fish parasite Entobdella soleae (monogenea)

Summary The ventral surface of the posterior sucker of Entobdella soleae, a monogenean skin parasite of the sole Solea solea, is covered with more than 800 papillae ranging in size from 2.5–19 m in diameter. The papillae are penetrated by nerves which double over themselves to form a stack-like array of lamellae running parallel to the surface of the haptor. No cilia or associated structures are present within these presumed sense organs and the papillae have no opening to the exterior. The much larger sucker papillae of a related species, E. hippoglossi, have been shown to have a similar ultrastructure. The possibility that the papillae may be contact receptors or strain receptors, providing proprioceptive information assisting the coordination of the attachment organ, is discussed and the papillae are compared with vertebrate touch receptors.I should like to thank Colin Ogden of the British Museum of Natural History for the generous assistance with the scanning electron microscopy and the Director and Staff of the Plymouth Laboratory and Ken Mackenzie and Rod Wootten of the Marine Laboratory, Aberdeen for help in obtaining material.     

Scanning electron microscope studies on the internal structures of the stomachs of some atyid and palaemonid prawns

Abstract

This paper deals with the internal structures of the stomachs of the atyid prawns Caridina africana, Atyaephyra desmaresti desmaresti and A. d. orientalis and of the palaemonid prawns Palaemon elegans and Palaemonetes antennarius. The various regions of the stomach are described and discussed in relation to diet.     

Scanning electron microscope studies on the parasitic cycle of Coccidioides immitis

The process involved in the in vivo conversion of the arthroconidia of Coccidioides immitis into endosporulating spherules was studied with the aid of a scanning electron microscope. By the fifth and sixth day after inoculation of laboratory mice, complete conversion had occurred in their kidneys, lungs, and spleens. The progressive stages of cleavage that occurred in the enlarged arthroconidia were initiated by invagination at several points of the cytoplasmic membrane that covers the inner surface of the developing spherule's cell wall. Through repeated branching of the cleavage cell walls, the spherule's cytoplasm was divided into progressive smaller segments. These segments were aggregated in packets and enclosed in a membranous sac. At maturity the membrane dissolved, and the endospores were freed within the spherules. Finally, the spherule wall ruptured, and the endospores were released.     

Scanning electron microscope observations of the spores of some species of Polystichum

Five species of Polystichum are studied under the scanning electron microscope and a comparison made with the light microscope studies of the same species published earlier. The SEM studies present a clear picture of the surface topography, supplying additional information.     

Light and electron microscope studies on ovarian follicles in the lizard Chalcides ocellatus

The development of ovarian follicles in a skink has been studied with light and electron microscopy. In early stages the previtellogenic oocyte has a follicular covering (granulosa) comprising only two cell types, small cells and pyriform cells. A complex microvillous interdigitation between follicle cells and oocyte is present from very early stages but regresses as a mature size is reached. The outer thecal layer differentiates into distinct interna and externa as growth proceeds. Occasional biovular follicles are formed. Pyriform cells establish direct continuity with the oocyte via cytoplasmic bridges which traverse the layer of microvilli interdigitating in the zona pellucida. Such bridges appear most frequently just before the onset of yolk deposition; the organelles and cytoplasmic constituents presumed to be transferred across them may stimulate this activity. As the follicles grow, the pyriform cells shrink and disappear to leave just the small cells forming the single layered granulosa. There is asynchrony in recruitment and/or early growth rates of follicle crops and uniformity of oocyte size appears only as vitellogenesis nears completion (with up to five oocytes, about 1 cm in diameter, on each side). Yolk deposition may involve transformation of golgi vesicles or pinocytotic vesicles but there is no evidence to show mitochondria as foci for deposition.     

Scanning electron microscope studies of the endometrium of the cyclic mare.

Endometrial biopsies obtained from mares at different stages of the oestrous cycle, during anoestrus and in various abnormal conditions were examined with the scanning electron microscope. Preliminary observations suggest that the patterns of secretory and ciliary activity in the uterine epithelium are similar to those observed by electron microscopical techniques in laboratory and other large domestic animals. The response of the epithelial cells to hormonal variations and infections is compared with that of the endometrium as seen with the light microscope.     

Scanning electron microscope studies of the surface of the sea urchin egg

Summary The surface of the egg of the two sea urchin species,Strongylocentrotus droebachiensis andS. pallidus, was studied with SEM. Clear differences were observed between the two species, in both the number and form of the microvilli. The changes in the egg surface which follow insemination are described.     

Scanning electron microscope studies of Echinococcus multilocularis cysts (author's transl)]

In the present paper, morphologic studies on experimental echinococcosis are reported. Following i.p. infection of gerbils (Meriones unguiculatus) with Echinococcus multilocularis scolices, the development of cysts within the internal organs of the experimental animals could be readily visualized by scanning electron microscopy.     

Scanning electron microscopic and histochemical studies of foliate papillae in the rabbit, rat and mouse

The foliate papillae of the rabbit, rat and mouse were studied by scanning electron microscopy and histochemistry. The papillae consisted of folds and grooves located on the posterolateral margin of the tongue in front of the circumvallate papillae. The numbers of folds and taste buds varied among the three animals species. Scanning electron microscopy showed that in longitudinal sections the taste buds were oval in shape and their pores were surrounded by microvilli. The reaction product of alkaline phosphatase could only be demonstrated in the superficial epithelium of the rabbit as well as in the mouse foliate papillae, but it also diffused into the taste buds in the rat. The intensity and distribution of the reactions of adenosine triphosphatase, acetylcholinesterase and butyrylcholinesterase were identical to those reported by other investigators in spite of differences in animal species and histochemical techniques employed.     

Scanning electron microscope studies on blastodisc formation in the zebrafish,Brachydanio rerio

Upon fertilization, the zebrafish egg undergoes marked physiological and structural changes, one of which involves blastodisc formation. Before fertilization, yolk globules are rounded and the endoplasm extends throughout the oocyte. During blastodisc formation, the yolk globules become angular and the endoplasm is restricted to streamers among the yolk globules. The streamers are oriented in an anterior-posterior axis of the egg. During blastodisc formation the cytoskeleton consists of an extensive array of filamentous structures of variable width in both the cortex as well as within elongate endoplasmic streamers. Although the filamentous components in the cortex and endoplasmic streamers probably include both microfilaments and microtubules, frequently they are somewhat wider than the usual dimensions, and possible reasons for this are suggested. From their arrangement in both the cortex and endoplasm, it seems likely that the components of the cytoskeleton (e.g., microfilaments and microtubules) may provide, through contraction, the major force responsible for the streaming of the endoplasm into the forming blastodisc. It is assumed that the surface tension of the vegetal hemisphere exceeds that of the animal hemisphere, thus forcing, through differential contraction, the endoplasm to flow in the direction of the forming blastodisc. No distinct barrier between the yolk and forming blastodisc was observed. The compressed condition of the larger and many-sided yolk globules could prevent their movement into the blastodisc. Scanning electron microscopy is limited in the resolution with which it can depict the cytoskeleton, but nonetheless it provides useful information about structural interrelationships.     

Scanning electron microscope study of human cervical mucus

The ultrastructure of human cervical mucus was studied by scanning electron microscopy. In fertile women, naturally occurring midcycle cervical mucus showed an arrangement of parallel fibers oriented along the main axis of the mucus sample. Sperm migration through a column of cervical mucus in vitro was also studied. It was found that sperm present among the longitudinal fibers were oriented parallel to the them and to the main axis of the mucus sample.     

Scanning electron microscope studies of sperm incorporation into the zebrafish (Brachydanio) egg

Morphological studies on the gametes and entry of the spermatozoan into the egg of the zebra danio, Brachydanio rerio, were conducted primarily with scanning electron microscopy. The spermatozoan showed a spherical head, which lacked an acrosome, a midpiece containing several mitochondria, and a flagellum. Observations of the unfertilized egg confirmed and extended prior studies showing a distinct cluster of microvilli on the plasma membrane, identified as the sperm entry site, beneath the inner micropylar aperture (Hart and Donovan, '83). The fertilizing spermatozoan attached to the sperm entry site within 5 seconds of the mixing of a gamete suspension. Binding to the egg microvilli appeared restricted to the equatorial surface of the spermatozoan. Fusion between the plasma membranes of the interacting gametes was followed by the formation of a distinct, nipple-shaped fertilization cone. The sperm head was partially incorporated into the fertilization cone cytoplasm by 60 seconds postinsemination. The incorporation of the entire sperm head, midpiece, and a portion of the flagellum occurred between 1 and 2 minutes. During this time, the fertilization cone shortened and was transformed into a massive, blister-like cytoplasmic swelling. Concurrently, upward movements of the ooplasm resulted in the gradual disappearance of the original depression in the egg surface containing the sperm entry site. The second polar body, fully developed by 10 minutes postinsemination, formed approximately 10-15 microns from the site of sperm penetration. Development of the fertilization cone, formation of the second polar body and exocytosis of cortical granules at the sperm entry site readily occurred in parthenogenetically activated eggs, indicating that these surface rearrangements do not require sperm binding and/or fusion.     

Scanning electron microscope evidence of telocytes in vasculature

Here, we here present scanning electron microscope data for the existent telocytes (TCs) on the endothelial surface of the wall of pig coronary arteries, internal thoracic arteries and carotid arteries. These cells have a small (8.39 ± 1.97 μm/4.95 ± 0.91 μm) cell body of different shapes (from round to triangular, depending on the number of cellular prolongations) with very long (of about 30 μm) and thin cellular processes called telopodes (Tps), which have uneven calibre. The number of Tps ranges between 2 and 6. Tps typically present the alternation of podoms and podomers, and also have a dichotomic branching pattern. These data could influence the current attempts for elucidating the role(s) of TCs.     

Scanning electron microscope study of the liver microcirculation

During the experimental investigation performed in dogs and rats, by means of scanning electron microscopy of corrosive anatomical preparations, the spatial organization of all parts of the hepatic vascular bed (arterial, venous and lymphatic) has been studied, specific features of their components construction have been described. Within the limits of one hepatic lobule the number of vessels included in the portal vein system exceeds that of the arterial ones, originating from the proper hepatic artery system. In every part of the vascular bed the gradient of the form, orientation and pronouncement of the nuclei-containing zones in endotheliocytes and myocytes has been established. Various appliances participating in the blood and lymph stream regulation in different parts of the vascular bed have been revealed. As initial elements of the lymph bed, closed digital or loop-like capillaries should be regarded, they localize in the organ's connective tissue framework. Around the portal and hepatic veins and their branches, as well as around the biliary ducts, well developed plexuses of the lymphatic and blood capillaries and vessels localize, they are the main draining pathways of the organ. The degree of development and pronouncement of these plexuses depends on the lumen size in the formation they accompany.