Morpho-anatomy of the cypselae of native species of Mutisieae (Asteraceae) from Mexico

Phytotaxa ◽  
2020 ◽  
Vol 436 (1) ◽  
pp. 1-20
Author(s):  
ROSARIO REDONDA-MARTÍNEZ ◽  
TERESA TERRAZAS ◽  
ALICIA ROJAS-LEAL
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Native Species ◽  
Vascular Bundles ◽  
Anticlinal Wall ◽  
Periclinal Wall ◽  
Mexican Species ◽  
Anatomical Trait ◽  
Scanning Electron

The aims of this study were to describe and illustrate cypselae of 15 Mexican species of Mutisieae from observations using optical and scanning electron microscopy. The cypselae are heteromorphic with pilose, sericeous or glandular indumentum. The primary sculpture of the surface has two microstructural patterns: reticulate and plicate. The secondary sculpture is striate in 13 taxa, but in two species, Chaptalia estribensis and C. mexicana, differences were found in the secondary sculpture of the external and internal cypselae. The most distinctive anatomical trait is in the epicarp, which has rectangular or square-shaped cells that have a convex periclinal wall in most species of Chaptalia. The mesocarp has vascular bundles with fibers in all species of Chaptalia, but fibers are absent in Adenocaulon, Gerbera and Leibnitzia. In addition, the cells of the mesocarp inner layer have either thick walls or only an anticlinal wall in nine species of Chaptalia. The micromorphological characteristics of the primary or secondary sculpture of the surface, the type of trichomes and the variation they present have taxonomical value for recognizing closely-related taxa, whereas anatomical traits of the mesocarp distinguish Adenocaulon, Gerbera and Leibnitzia from most Chaptalia species.

Seed morphology of Epilobium and Chamaenerion (Onagraceae) in Turkey

Phytotaxa ◽  
2017 ◽  
Vol 331 (2) ◽  
pp. 169 ◽  
Author(s):  
KAMİL COŞKUNÇELEBİ ◽  
SERDAR MAKBUL ◽  
SEDA OKUR
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Seed Morphology ◽  
Morphological Features ◽  
Seed Shape ◽  
Generic Level ◽  
Specific Level ◽  
Periclinal Wall ◽  
First Time ◽  
Scanning Electron

Macro- and micro-morphological features of seeds belonging to 26 taxa from Turkey were observed under the light and scanning electron microscopy. Present findings partly agree with segregation of Epilobium and Chamerion at generic level. The members of the genus Epilobium were distinguished by seeds with conical, semispherical, cylindrical or crest-like papillae or without papillae, granulate periclinal surfaces, papillae with parallel, radial, irregular or spirally furrow and the members of Chamerion were distinguished by seeds crest-like papillae or without papillae and without granulate periclinal surfaces and without furrow. The results also showed that seed shape, presence/absence of papillae and beak, papillae shape and ornamentation, and periclinal wall features are valuable for delimiting the examined taxa specific level within both genera. A key to Turkish Epilobium and Chamerion taxa based on seed morphology is presented for the first time

Chvalaea yolkamini sp. nov. (Diptera: Hybotidae), the first Mexican species of genus discovered on Instagram

Zootaxa ◽  
2020 ◽  
Vol 4748 (3) ◽  
pp. 592-600 ◽  
Author(s):  
SANTIAGO JAUME-SCHINKEL ◽  
MATHEUS M.M. SOARES ◽  
LUANA M. BARROS
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Social Network ◽  
New Species ◽  
Hunting Behavior ◽  
First Time ◽  
Mexican Species ◽  
A New Species ◽  
Scanning Electron

A new species of Chvalaea Papp & Földvári, 2002 is discovered after a photo on a social network and later collected in nature. Chvalaea yolkamini sp. nov. is described and illustrated here. In addition, for the first time we describe eggs with scanning electron microscopy and report on adult hunting behavior. 

scholarly journals Micromorphology of the floral elements, the structure of the nectary, and the apicultural value of Elaeagnus commutata Bernh. ex Rydb.

2012 ◽  
Vol 64 (1) ◽  
pp. 27-34
Author(s):  
Mirosława Chwil ◽  
Elżbieta Weryszko-Chmielewska
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Honey Bees ◽  
Epidermal Cells ◽  
Sugar Concentration ◽  
Vascular Bundles ◽  
Stomatal Development ◽  
Adaxial Side ◽  
Abaxial Side ◽  
Scanning Electron

The investigations were carried out using light and scanning electron microscopy. The flowers of <i>Elaeagnus commutata</i> grow in clusters of 1-4 in the leaf axils. They are actinomorphic, four-lobed, with a single perianth that is yellow from the adaxial side, while the abaxial side is silvery-white. Peltate hairs of different structure are found on both surfaces of the sepals. The conical epidermal cells of the lobes are covered with a thick striated cuticle. Cylindrical hairs were observed on the edges of the lobes. Peltate hairs also grew on the style. The dish-shaped nectary gland is located at the base of the style. Nectar is secreted through numerous, evenly distributed stomata located above or at the level of other epidermal cells. Different stages of stomatal development are evidence of the asynchronous functioning of the stomata. The nectary consists of small epidermal cells and 5-6 layers of secretory parenchyma. The deeper layers of the gland are composed of larger cells of subglandular parenchyma in which vascular bundles supplying the nectary run. Honey bees were the main pollinators of silverberry. Ten silverberry flowers produced an average of 12 g of nectar with a sugar concentration in the 29.5-34.5% range. The weight of pollen produced by 10 flowers was 3.33 mg.

scholarly journals The Pulp Stones: Morphological Analysis in Scanning Electron Microscopy and Spectroscopic Chemical Quantification

Medicina ◽  
2021 ◽  
Vol 58 (1) ◽  
pp. 5
Author(s):  
Aleksandra Palatyńska-Ulatowska ◽  
Marcos Cook Fernandes ◽  
Krystyna Pietrzycka ◽  
Agata Koprowicz ◽  
Leszek Klimek ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Chemical Composition ◽  
Chemical Elements ◽  
Deciduous Teeth ◽  
Vascular Bundles ◽  
Pulp Cavity ◽  
Pulp Stones ◽  
Chemical Quantification ◽  
Scanning Electron

Background and objectives: Pulp stones are hard tissue structures formed in the pulp of permanent and deciduous teeth. Few studies have evaluated their morphology and chemical composition. However, their formation, composition, configuration and role played in overall health status are still unclear. Clinically, they may be symptomatic; technically, they impede access during endodontic therapy, increasing the risk of treatment errors. Thus, this study aimed to morphologically analyze pulp stones and present their chemical quantification, identifying their main chemical elements. It also correlates the results with their possible induction mechanisms. Materials and Methods: Seven pulp nodules were collected from molar teeth needing endodontic treatment. The morphology of the stones was analyzed by scanning electron microscopy (SEM), and their chemical composition was determined by X-ray dispersive energy spectroscopy (EDX). Results: These structures varied considerably in shape, size and topography. The site of the stones in the pulp cavity was the factor that most affected the morphology. The majority of the stones found in the pulp chambers presented nodular morphology, while those in the root canals presented a diffuse shape, resembling root canal anatomy. The topography of the nodules showed heterogeneous relief, revealing smooth and compact areas contrasting with the rugged and porous ones. The chemical composition varied depending on the location of the nodule in the pulp cavity and the relief of the analyzed area. Radicular stones presented considerably lower calcium and phosphorus content than coronary nodules. Conclusions: The high cellularity rate of the coronal pulp predisposes this region to nodular mineralizations around injured cells. The presence of larger caliber vascular bundles and higher collagen fiber content in radicular pulp determines a diffuse morphological pattern in this region. Understanding the morphology and chemical composition of the pulp stones allows future translational pathways towards the prevention or treatment of such conditions.

Pathogenesis of Human Hair Defects

1974 ◽  
Vol 32 ◽  
pp. 12-13
Author(s):  
P.S. Porter ◽  
T. Aoyagi ◽  
R. Matta
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Human Hair ◽  
Standard Techniques ◽  
Scanning Electron

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.

Ultrastructural Analysis of the Salivary Glands of Gromphadorhina Portentosa (Schaum)

1977 ◽  
Vol 35 ◽  
pp. 638-639
Author(s):  
P.J. Dailey
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Salivary Glands ◽  
Secretory Vesicles ◽  
The Past ◽  
Transmission Electron ◽  
Means Of Transmission ◽  
Gromphadorhina Portentosa ◽  
Scanning Electron ◽  
Topographical Relief

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.

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).

Spontaneous Cataract in Nude Athymic Mice

1977 ◽  
Vol 35 ◽  
pp. 512-513
Author(s):  
Ronald H. Bradley ◽  
R. S. Berk ◽  
L. D. Hazlett
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Nude Mouse ◽  
Cellular Immunity ◽  
Phosphate Buffer ◽  
Osmium Tetroxide ◽  
Athymic Mice ◽  
Transmission Microscopy ◽  
Mouse Lens ◽  
Scanning Electron

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.

Scanning and Transmission Microscopy of Nematocyst Batteries in Epitheliomuscular Cells of Hydra

1971 ◽  
Vol 29 ◽  
pp. 410-411 ◽  
Author(s):  
Jane A. Westfall ◽  
S. Yamataka ◽  
Paul D. Enos
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Osmium Tetroxide ◽  
External Surface ◽  
Three Dimensional ◽  
Surface Structures ◽  
Transmission Microscopy ◽  
Transmission Electron ◽  
Freeze Dried ◽  
Scanning Electron

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).

Microbulldozing and Microchiseling

1969 ◽  
Vol 27 ◽  
pp. 134-135
Author(s):  
J.N. Ramsey ◽  
D.P. Cameron ◽  
F.W. Schneider
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Material Handling ◽  
Microprobe Analysis ◽  
Foreign Matter ◽  
Specific Location ◽  
Potential Problems ◽  
Knoop Indenter ◽  
Scanning Electron ◽  
Microhardness Tester

As computer components become smaller the analytical methods used to examine them and the material handling techniques must become more sensitive, and more sophisticated. We have used microbulldozing and microchiseling in conjunction with scanning electron microscopy, replica electron microscopy, and microprobe analysis for studying actual and potential problems with developmental and pilot line devices. Foreign matter, corrosion, etc, in specific locations are mechanically loosened from their substrates and removed by “extraction replication,” and examined in the appropriate instrument. The mechanical loosening is done in a controlled manner by using a microhardness tester—we use the attachment designed for our Reichert metallograph. The working tool is a pyramid shaped diamond (a Knoop indenter) which can be pushed into the specimen with a controlled pressure and in a specific location.

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