scholarly journals Comparative ultrastructure of the radiolar crown in Sabellida (Annelida)

Zoomorphology ◽  
2020 ◽  
Author(s):  
Ekin Tilic ◽  
Greg W. Rouse ◽  
Thomas Bartolomaeus
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Characteristic Feature ◽  
Water Currents ◽  
Internal Stabilization ◽  
Transmission Electron ◽  
Phylogenetic Lineages ◽  
Histology And Immunohistochemistry ◽  
Comparative Ultrastructure

AbstractThree major clades of tube-dwelling annelids are grouped within Sabellida: Fabriciidae, Serpulidae and Sabellidae. The most characteristic feature of these animals is the often spectacularly colorful and flower-like radiolar crown. Holding up such delicate, feathery appendages in water currents requires some sort of internal stabilization. Each of the above-mentioned family-ranked groups has overcome this problem in a different way. Herein we describe the arrangement, composition and ultrastructure of radiolar tissues for fabriciids, sabellids and serpulids using transmission electron microscopy, histology and immunohistochemistry. Our sampling of 12 species spans most of the phylogenetic lineages across Sabellida and, from within Sabellidae, includes representatives of Myxicolinae, Sabellinae and the enigmatic sabellin Caobangia. We further characterize the ultrastructure of the chordoid cells that make up the supporting cellular axis in Sabellidae and discuss the evolution of radiolar tissues within Sabellida in light of the recently published phylogeny of the group.

The comparative ultrastructure of spermatozoa from Bothrimonus sturionis Duv. 1842 (Pseudophyllidea), Pseudanthobothrium hanseni Baer, 1956 (Tetraphyllidea), and Monoecocestus americanus Stiles, 1895 (Cyclophyllidea)

1984 ◽  
Vol 62 (6) ◽  
pp. 1059-1066 ◽  
Author(s):  
Barbara M. MacKinnon ◽  
Michael D. B. Burt
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Plasma Membrane ◽  
Main Body ◽  
Posterior Portion ◽  
Transmission Electron ◽  
Dense Nucleus ◽  
Comparative Ultrastructure ◽  
Electron Lucent ◽  
Mature Spermatozoa

The mature spermatozoa from Bothrimonus sturionis (Pseudophyllidea), Pseudanthobothrium hanseni (Tetraphyllidea), and Monoecocestus americanus (Cyclophyllidea) were examined using transmission electron microscopy. Transverse sections of the sperm of B. sturionis indicate that the number of sperm axonemes varies from one to eight, with approximately one-third of the sperm containing two axonemes. Likewise, the number of peripheral microtubules lying just within the external plasma membrane varies from 12 to 20. The nucleus is electron lucent and fibrous in appearance. The spermatozoa of B. sturionis show great variation in the material examined and the majority of them are believed to be aberrant. The spermatozoon of P. hanseni contains a single axoneme with the nucleus wrapped in a crescent around it in the anterior region of the sperm. The posterior portion of the spermatozoon is characterized by a helical flange which projects from the main body of the sperm. The spermatozoon of M. americanus is elongate and slender, containing a single axoneme with an electron-dense nucleus coiled around it in the anterior one-third of the sperm. Electron-opaque bodies, which may be glycogen, fill the cytoplasm. The spermatozoa of all three species contain neither an acrosome nor mitochondria. The flagella of all the spermatozoa have a 9 + "1" arrangement of microtubules. The importance of the ultrastructure of spermatozoa in the phylogeny and taxonomy of cestodes is discussed.

Ciliation and function of the food-collecting and waste-rejecting organs of lophophorates

1978 ◽  
Vol 56 (10) ◽  
pp. 2142-2155 ◽  
Author(s):  
T. H. J. Gilmour
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Waste Material ◽  
Suspension Feeding ◽  
Food Material ◽  
Water Currents ◽  
Excess Water ◽  
Transmission Electron ◽  
Food Particles ◽  
And Function

Experiments with mixtures of colloidal graphite, stained Sephadex particles, and algae; observations by stroboscopic interference contrast optics; and scanning and transmission electron microscopy suggest that phoronids, brachiopods, and bryozoans can simultaneously reject waste material by an impingement mechanism and accept edible particles by a filtration mechanism without the ciliary reversals suggested in previous models of suspension feeding in lophophorates. Specialized laterofrontal cilia, which may detect heavy inedible particles, are found on the tentacles of all three phyla of lophophorates. In phoronids and bryozoans edible material is carried towards the esophagus by components of water currents created by the lateral cilia of the tentacles of the lophophore while inedible particles are rejected by the frontal cilia of the tentacles. The passage of food material to the mouths of brachiopods is assisted by frontal cilia located in grooves on alternate tentacles while the frontal cilia of ungrooved tentacles reject inedible material. The epistomes of lophophorates are also involved in the simultaneous acceptance of food and rejection of solid waste material and allow the escape of excess water travelling towards the mouth with food particles. This finding of a functional significance for the epistome suggests that lophophorates deserve reassessment as possible ancestors of chordates.

scholarly journals High-resolution transmission electron microscopy observations of La2Zr2O7 thin layers on LaAlO3 obtained by chemical methods

2009 ◽  
Vol 24 (4) ◽  
pp. 1480-1491 ◽  
Author(s):  
L. Rapenne ◽  
C. Jiménez ◽  
T. Caroff ◽  
C. Million ◽  
S. Morlens ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
High Resolution ◽  
Characteristic Feature ◽  
Pyrochlore Phase ◽  
Pyrochlore Structure ◽  
Coated Conductors ◽  
Thin Layers ◽  
Buffer Layers ◽  
Transmission Electron

La2Zr2O7 (LZO) films have been grown by metalorganic decomposition (MOD) to be used as buffer layers for coated conductors. LZO can crystallize into two similar structures: fluorite or pyrochlore. Coated conductor application focuses on pyrochlore structure because it is a good barrier against oxygen diffusion. Classical x-ray diffraction is not able to separate the contribution of these two structures. Transmission electron microscopy and high-resolution transmission electron microscopy were used to determine the local distribution of these two phases in epitaxial LZO layers grown on LaAlO3. A characteristic feature of LZO thin films deposited by MOD is the formation of nanovoids in an almost single-crystal structure of LZO pyrochlore phase. For comparison, LZO layers deposited by metalorganic chemical vapor deposition were also studied. In this last case, the film is compact without voids and the structure corresponds to pyrochlore phase. Thus, the formation of nanovoids is a characteristic feature of MOD grown films.

The Comparative Ultrastructure of Fibrin Induced by Thrombin and by Staphylocoagulase

1975 ◽  
Vol 34 (01) ◽  
pp. 223-235 ◽  
Author(s):  
M. J. S King ◽  
M. S Morris ◽  
M Tager
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
T Test ◽  
Test Analysis ◽  
A Value ◽  
Transmission Electron ◽  
The Mean ◽  
Comparative Ultrastructure

SummaryFibrin induced by the action of thrombin and by staphylocoagulase was studied by transmission electron microscopy.Periodic striations were consistently observed in the negatively stained preparations of both fibrins. When 4200 major periods in the thrombin fibrin system were measured the mean length was 228 Å. For 3666 major periods in the coagulase fibrin system the mean length was 223 Å. While the T test analysis of these values gave a value of 10, it is noteworthy that the differences are well within the scatter of periodicity reported in the literature for thrombin-induced fibrin.Gross inspection of the preparations indicated that the coagulase-induced fibrin had a knottier appearance and was accompanied by a greater amount of background debris than the thrombin-induced fibrin.

Techniques for Transmission Electron Microscopy of Fiber-Matrix Interfaces in Aluminum Alloy-Boron Composites by Ion Erosio

1971 ◽  
Vol 29 ◽  
pp. 204-205
Author(s):  
G. G. Shaw
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Aluminum Alloy ◽  
Electron Beam ◽  
Pure Aluminum ◽  
Ion Milling ◽  
Transmission Electron ◽  
Fiber Matrix ◽  
Ion Erosion ◽  
Row Of Fibers

The morphology and composition of the fiber-matrix interface can best be studied by transmission electron microscopy and electron diffraction. For some composites satisfactory samples can be prepared by electropolishing. For others such as aluminum alloy-boron composites ion erosion is necessary.When one wishes to examine a specimen with the electron beam perpendicular to the fiber, preparation is as follows: A 1/8 in. disk is cut from the sample with a cylindrical tool by spark machining. Thin slices, 5 mils thick, containing one row of fibers, are then, spark-machined from the disk. After spark machining, the slice is carefully polished with diamond paste until the row of fibers is exposed on each side, as shown in Figure 1.In the case where examination is desired with the electron beam parallel to the fiber, preparation is as follows: Experimental composites are usually 50 mils or less in thickness so an auxiliary holder is necessary during ion milling and for easy transfer to the electron microscope. This holder is pure aluminum sheet, 3 mils thick.

Direct Observation of Heat Exchanger Deposits by Cross Sectioning

1967 ◽  
Vol 25 ◽  
pp. 364-365
Author(s):  
R. W. Anderson ◽  
D. L. Senecal
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Heat Exchanger ◽  
Direct Observation ◽  
Cross Sections ◽  
Preparation Method ◽  
Specimen Preparation ◽  
Flowing Water ◽  
Transmission Electron ◽  
Deposit Layer

A problem was presented to observe the packing densities of deposits of sub-micron corrosion product particles. The deposits were 5-100 mils thick and had formed on the inside surfaces of 3/8 inch diameter Zircaloy-2 heat exchanger tubes. The particles were iron oxides deposited from flowing water and consequently were only weakly bonded. Particular care was required during handling to preserve the original formations of the deposits. The specimen preparation method described below allowed direct observation of cross sections of the deposit layers by transmission electron microscopy.The specimens were short sections of the tubes (about 3 inches long) that were carefully cut from the systems. The insides of the tube sections were first coated with a thin layer of a fluid epoxy resin by dipping. This coating served to impregnate the deposit layer as well as to protect the layer if subsequent handling were required.

Phase Transformations in Ti-7w/oMo-3w/oMe Alloy

1974 ◽  
Vol 32 ◽  
pp. 514-515
Author(s):  
S. Fujishiro
Keyword(s):  
Electron Microscopy ◽  
Mechanical Properties ◽  
Transmission Electron Microscopy ◽  
Tensile Strength ◽  
Mechanical Processing ◽  
Ray Method ◽  
X Ray ◽  
Transmission Electron ◽  
Water Quench ◽  
Alpha Beta

The mechanical properties of three titanium alloys (Ti-7Mo-3Al, Ti-7Mo- 3Cu and Ti-7Mo-3Ta) were evaluated as function of: 1) Solutionizing in the beta field and aging, 2) Thermal Mechanical Processing in the beta field and aging, 3) Solutionizing in the alpha + beta field and aging. The samples were isothermally aged in the temperature range 300° to 700*C for 4 to 24 hours, followed by a water quench. Transmission electron microscopy and X-ray method were used to identify the phase formed. All three alloys solutionized at 1050°C (beta field) transformed to martensitic alpha (alpha prime) upon being water quenched. Despite this heavily strained alpha prime, which is characterized by microtwins the tensile strength of the as-quenched alloys is relatively low and the elongation is as high as 30%.

Two- or three-way observations of the identical cell elements within the same sections by LM, TEM and/or SEM

1978 ◽  
Vol 36 (2) ◽  
pp. 82-83 ◽  
Author(s):  
Nakazo Watari ◽  
Yasuaki Hotta ◽  
Yoshio Mabuchi
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Fine Structure ◽  
Light Microscopy ◽  
Thin Sections ◽  
Transmission Electron ◽  
Identical Cell ◽  
Electron Microscopes ◽  
Scanning Electron

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).

Comparative Microstructures of Ion Milled and Electrochemically Thinned Composite Materials

1974 ◽  
Vol 32 ◽  
pp. 546-547
Author(s):  
R.R. Russell
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Composite Materials ◽  
Great Difficulty ◽  
Ion Milling ◽  
Transmission Electron ◽  
Ion Damage ◽  
Intermetallic Composite

Transmission electron microscopy of metallic/intermetallic composite materials is most challenging since the microscopist typically has great difficulty preparing specimens with uniform electron thin areas in adjacent phases. The application of ion milling for thinning foils from such materials has been quite effective. Although composite specimens prepared by ion milling have yielded much microstructural information, this technique has some inherent drawbacks such as the possible generation of ion damage near sample surfaces.

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