MUSCLE SAMPLES FOR SCANNING ELECTRON MICROSCOPY: PREPARATIVE TECHNIQUES AND GENERAL MORPHOLOGY

2008 ◽  
Vol 41 (4) ◽  
pp. 867-873 ◽  
Author(s):  
SUSAN B. JONES ◽  
ROBERT J. CARROLL ◽  
JAMES R. CAVANAUGH
Author(s):  
J.F. Putterill ◽  
J.T. Soley

The heads of nine 2.5 to 3-year-old Nile crocodiles (Crocodylus niloticus) were obtained from a commercial farm where crocodiles are raised for their skins and meat. The animals from which these specimens originated were clinically healthy at the time they were slaughtered. A detailed description of the macroscopic and microscopic features of the palate and gingivae of the Nile crocodile is presented and the results are compared with published information on this species and other Crocodylia. The histological features are supplemented by information supplied by scanning electron microscopy. Macroscopic features of interest are the small conical process situated at the base of the first two incisors of the maxilla, the distribution of cobbled units on the palate, and the broad dentary shelf forming the rostral aspect of the mandible. Histologically the palate and gingivae did not differ significantly from each other and both regions showed a presence of Pacinian-type corpuscles. Two types of sensory structures (taste receptors and pressure receptors) were identified in the regions examined, both involving modification of the epithelium and the underlying connective tissue.


1999 ◽  
Vol 73 (1) ◽  
pp. 51-57 ◽  
Author(s):  
I. Kanev ◽  
B.S. Dezfuli ◽  
M. Nestorov ◽  
B. Fried

Scanning electron microscopy (SEM) was used to study the collar region of Deropristis inflata (Molin, 1858), an intestinal digenean of fish, and Echinostoma revolutum (Froelich, 1802), an intestinal digenean of birds. The results showed basic differences in the following morphological features. The collar of D. inflata was open ventrally and dorsally whereas that of E. revolutum was closed dorsally and ventrally, forming a kidney-like ring. The collar of D. inflata was located posterior to the oral sucker, some distance behind the anterior end of the body. That of E. revolutum was located terminally around the oral sucker. The collar of D. inflata had numerous collar spines which varied in size, shape and position. That of E. revolutum had 37 collar-spines, mainly homogenous in their general morphology and with a typical arrangement pattern for 37-collar-spined echinostomes. The collar of D. inflata had few tegumentary papillae whereas that of E. revolutum had abundant papillae. A ventral depressed area occurred in D. inflata, between the acetabulum and oral sucker, dividing the collar into two left and right independent parts. The ventral depression in E. revolutum extended from the ventral sucker to the posterior end of the collar, and was not divided. In D. inflata, tegumentary spines were located on the oral sucker, and the collar was posterior to the sucker. In E. revolutum, the oral sucker and the collar lacked tegumentary spines. The region immediately posterior to the collar also lacked spines in E. revolutum. The collar pattern of D. inflata is undoubtedly more primitive than that of E. revolutum.


Zootaxa ◽  
2007 ◽  
Vol 1509 (1) ◽  
pp. 17-30 ◽  
Author(s):  
DÉBORA A. FRANCISCO ◽  
SÉRGIO L.S. BUENO ◽  
TERUE C. KIHARA

The post-embryonic development in Aegla franca is epimorphic, in which the hatching form is a juvenile that very much resembles the adults in general morphology. Newly-hatched juveniles were obtained under laboratory conditions from ovigerous females bearing eggs at late embryonic stage, and collected from the wild. Upon hatching, some juvenile specimens were cleared, stained, dissected and prepared for light microscopy on semi-permanent slides and each appendage was described in detail and illustrated accordingly. Some specimens were also prepared for scanning electron microscopy to obtain detailed information concerning setal morphology and ultrastructure of some cephalothoracic appendages. Comparison of the present results to previous descriptions of the first juvenile of other aeglid species show some interesting features observed only in Aegla franca. These features include the presence of pores on the first and second pairs of antennae; the rudimentary condition of the mandible and the long setae with a subterminal pore and scaly outgrowth distally on the basal bilobed endite of the maxilla.


1985 ◽  
Vol 63 (10) ◽  
pp. 2483-2487 ◽  
Author(s):  
M. Wiles ◽  
D. K. Cone ◽  
P. H. Odense

Specimens of the kinetophragminophorid ciliates Chilodonella cyprini (Moroff, 1902) from goldfish (Carassius auratus) in Nova Scotia and Chilodonella hexasticha (Kiernik, 1909) from channel catfish (Ictalurus punctatus) in Arkansas were examined by scanning electron microscopy. They are round to foliate, ventrally flattened protozoa well suited for adherence to, and movement over, a flat host surface. Organelles including ventral ciliary rows, dorsal cilia, excretory pores, and a prominent cytopharynx are described. Dorsal surfaces of both species have a distinct reticulate pattern which represents a modification of the pellicle. Ventrolateral margins of C. cyprini contain rows of short cuticular proturberances not seen in C. hexasticha. Our specimens of the two species were distinguished by their total ventral ciliary row number (12–14 in C. hexasticha, 21 in C. cyprini). General morphology as revealed by scanning electron microscopy is compared with previous light microscopical observations. The taxonomic separation of the two species, C. cyprini and C. hexasticha, is confirmed.


2017 ◽  
Vol 9 (10) ◽  
pp. 10792
Author(s):  
Balasaheb V. Sarode ◽  
Nikhil U. Joshi ◽  
Swapnil S. Boyane ◽  
Subodh S. Gaikwad ◽  
Pratik P. Pansare ◽  
...  

Dicranocephalus lateralis (Signoret), 1879, a bug from the family Stenocephalidae, is briefly redescribed with colour and scanning electron microscopy (SEM) illustrations of general morphology, including details of male and female genitalia, metathoracic scent gland (MTG), exoskeletal male abdominal glands, eggs and nymphal stages.  The status of other species of this genus in India is also discussed.  This will be the first well-illustrated account of the morphology and life cycle of this bug from India.


Author(s):  
P.S. Porter ◽  
T. Aoyagi ◽  
R. Matta

Using standard techniques of scanning electron microscopy (SEM), over 1000 human hair defects have been studied. In several of the defects, the pathogenesis of the abnormality has been clarified using these techniques. It is the purpose of this paper to present several distinct morphologic abnormalities of hair and to discuss their pathogenesis as elucidated through techniques of scanning electron microscopy.


Author(s):  
P.J. Dailey

The structure of insect salivary glands has been extensively investigated during the past decade; however, none have attempted scanning electron microscopy (SEM) in ultrastructural examinations of these secretory organs. This study correlates fine structure by means of SEM cryofractography with that of thin-sectioned epoxy embedded material observed by means of transmission electron microscopy (TEM).Salivary glands of Gromphadorhina portentosa were excised and immediately submerged in cold (4°C) paraformaldehyde-glutaraldehyde fixative1 for 2 hr, washed and post-fixed in 1 per cent 0s04 in phosphosphate buffer (4°C for 2 hr). After ethanolic dehydration half of the samples were embedded in Epon 812 for TEM and half cryofractured and subsequently critical point dried for SEM. Dried specimens were mounted on aluminum stubs and coated with approximately 150 Å of gold in a cold sputtering apparatus.Figure 1 shows a cryofractured plane through a salivary acinus revealing topographical relief of secretory vesicles.


Author(s):  
Nakazo Watari ◽  
Yasuaki Hotta ◽  
Yoshio Mabuchi

It is very useful if we can observe the identical cell elements within the same sections by light microscopy (LM), transmission electron microscopy (TEM) and/or scanning electron microscopy (SEM) sequentially, because, the cell fine structure can not be indicated by LM, while the color is; on the other hand, the cell fine structure can be very easily observed by EM, although its color properties may not. However, there is one problem in that LM requires thick sections of over 1 μm, while EM needs very thin sections of under 100 nm. Recently, we have developed a new method to observe the same cell elements within the same plastic sections using both light and transmission (conventional or high-voltage) electron microscopes.In this paper, we have developed two new observation methods for the identical cell elements within the same sections, both plastic-embedded and paraffin-embedded, using light microscopy, transmission electron microscopy and/or scanning electron microscopy (Fig. 1).


Author(s):  
Ronald H. Bradley ◽  
R. S. Berk ◽  
L. D. Hazlett

The nude mouse is a hairless mutant (homozygous for the mutation nude, nu/nu), which is born lacking a thymus and possesses a severe defect in cellular immunity. Spontaneous unilateral cataractous lesions were noted (during ocular examination using a stereomicroscope at 40X) in 14 of a series of 60 animals (20%). This transmission and scanning microscopic study characterizes the morphology of this cataract and contrasts these data with normal nude mouse lens.All animals were sacrificed by an ether overdose. Eyes were enucleated and immersed in a mixed fixative (1% osmium tetroxide and 6% glutaraldehyde in Sorenson's phosphate buffer pH 7.4 at 0-4°C) for 3 hours, dehydrated in graded ethanols and embedded in Epon-Araldite for transmission microscopy. Specimens for scanning electron microscopy were fixed similarly, dehydrated in graded ethanols, then to graded changes of Freon 113 and ethanol to 100% Freon 113 and critically point dried in a Bomar critical point dryer using Freon 13 as the transition fluid.


Author(s):  
Jane A. Westfall ◽  
S. Yamataka ◽  
Paul D. Enos

Scanning electron microscopy (SEM) provides three dimensional details of external surface structures and supplements ultrastructural information provided by transmission electron microscopy (TEM). Animals composed of watery jellylike tissues such as hydras and other coelenterates have not been considered suitable for SEM studies because of the difficulty in preserving such organisms in a normal state. This study demonstrates 1) the successful use of SEM on such tissue, and 2) the unique arrangement of batteries of nematocysts within large epitheliomuscular cells on tentacles of Hydra littoralis.Whole specimens of Hydra were prepared for SEM (Figs. 1 and 2) by the fix, freeze-dry, coat technique of Small and Màrszalek. The specimens were fixed in osmium tetroxide and mercuric chloride, freeze-dried in vacuo on a prechilled 1 Kg brass block, and coated with gold-palladium. Tissues for TEM (Figs. 3 and 4) were fixed in glutaraldehyde followed by osmium tetroxide. Scanning micrographs were taken on a Cambridge Stereoscan Mark II A microscope at 10 KV and transmission micrographs were taken on an RCA EMU 3G microscope (Fig. 3) or on a Hitachi HU 11B microscope (Fig. 4).


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