scholarly journals Struktur Sel Sekresi Daun Jeruk Kalamansi (Citrus microcarpa Bunge.) di Pulau Ambon

2021 ◽  
Vol 6 (2) ◽  
pp. 138-145
Author(s):  
Christina Horowidi ◽  
Hermalina Sinay ◽  
Ritha Lusian Karuwal ◽  
Lona Parinussa
Keyword(s):  
Secretory Cell ◽  
Cell Structure ◽  
Secretory Cells ◽  
Cell Diameter ◽  
Fresh Sample ◽  
Cell Structures ◽  
Secretory Cavities ◽  
Cell Shapes ◽  
Citrus Leaves ◽  
Dark Green

 Perbedaan lokasi tumbuh dapat mengakibatkan perbedaan penampilan fenotipik tanaman yang dapat diamati secara morfologi dan anatomi seperti struktur anatomi sel sekretori. Tujuan penelitian ini adalah untuk mengetahui struktur sel sekretori daun jeruk kalamansi di pulau Ambon. Metode jelajah dilakukan pada 13 lokasi di Pulau Ambon untuk koleksi sampel, dan pada setiap lokasi diambil 3 tanaman sebagai 3 ulangan. Tiap tanaman diambil 5 daun pada setiap sisi pohon tanaman jeruk kalamansi dengan ukuran panjang 5-7 cm dan warna hijau tua. Pembuatan preparat mengikuti metode free hand section. Pengamatan menggunakan kamera Optilab pada mikroskop Olympus dengan perbesaran 400x. Pengukuran diameter sel menggunakan fitur measure pada software Image Ruster. Data kualitatif berupa struktur sel sekresi daun jeruk Kalamansi ditampilkan dalam bentuk gambar dan dideskripsikan sesuai hasil yang terlihat, sedangkan data hasil pengukuran diameter sel sekresi adalah rerata 3 ulangan dan ditampilkan sebagai mean ± standar deviasi (SD). Hasil penelitian menunjukkan adanya sel sekretori yang berjumlah satu sel. Struktur sel sekretori terdiri dari sel epitel, sel selubung, dan rongga sekretori. Bentuk sel sekresi ada yang bulat dan lonjong. Diameter rongga sekretori berkisar antara 106,08-167,60 µm.  Berdasarkan hasil penelitian, maka dapat disimpulkan bahwa sel sekresi pada daun jeruk kalamansi pada lokasi-lokasi berbeda di Pulau Ambon bervariasi baik bentuk maupun ukurannya. Differences in habitat can induce differences in the phenotypic appearance of plants that can be observed morphologically and anatomically such as the anatomical structure of secretory cells. The purpose of this study was to determine the structure of the secretory cells in the leaves of Calamansy citrus in Ambon island. Tracking method was done for sample collections, and at each location 3 plants were taken as replicates. Each plant was taken 5 leaves with a length of 5-7 cm and dark green color. Prior to be observed, the fresh sample was done with free-hand section method.   Microscopy observations were done by a light microscope at 400x magnification. Measurement of cell diameter was done by the measure feature in Image Ruster software.  Qualitative data such as secretory cell structures of Calamansy citrus leaves were shown in form of images and described according to the results, while the data of the measurement of secretory cell diameters is the average of 3 replications and was shown as mean ± standard deviation (SD).  The results showed the presence of secretory cells which amounted to one cell. The secretory cell structure is composed of epithelial cells, sheath cells, and secretory cavities. Cell shapes vary, including round and oval. The diameter of the secretory cell cavity ranges from 106.08-167.60 µm.   

Computational and Experimental Studies of Cellular Samples Manufactured Using Additive Methods for Use in Advanced Lightweight Designs of Engine Parts

2020 ◽  
Author(s):  
Liubov Magerramova ◽  
Michael Volkov ◽  
Oleg Volgin ◽  
Pavel Kolos
Keyword(s):  
Fatigue Testing ◽  
Low Cycle Fatigue ◽  
Cell Structure ◽  
Experimental Studies ◽  
Cellular Structures ◽  
Uniaxial Tensile ◽  
Porous Structures ◽  
Lattice Cell ◽  
Cell Structures ◽  
Homogeneous Materials

Abstract The use of cellular structures is one way to reduce the weight of engine parts. Cellular structures are used to provide rigidity and strength for parts subject to compression, bending, and shock loads. Failure of the individual elements of a lattice/cell structure does not result in the destruction of the entire part; this stands in contrast to the structure of a conventional homogeneous metal object, in which cracks will continue to increase with increasing load, causing the destruction of the entire part. Lattice/cell structures have relatively high characteristics of rigidity and strength, excellent thermal insulation properties, energy absorption characteristics, and high fatigue resistance. The use of this type of structure in engine part construction opens up new opportunities for advanced aviation applications. However, the deformation behavior of porous and metallic structures differs significantly from that of conventional homogeneous materials. Samples with cellular and porous structures are themselves designs. Therefore, procedures for strength testing and interpretation of experimental results for cellular and porous structures differ from those for samples derived from homogeneous materials. The criteria for determining the properties of cellular structures include density, stiffness, ability to accumulate energy, etc. These parameters depend on the configuration of the cells, the size of each cell, and the thickness of the connecting elements. Mechanical properties of cellular structures can be established experimentally and confirmed numerically. Special cellular specimens have been designed for uniaxial tensile, bending, compression, shear, and low-cycle fatigue testing. Several variants of cell structures with relative densities ranging from 13 to 45% were considered. Specifically, the present study examined the stress-strain states of cell structures from brands “CobaltChrome MP1” powder compositions obtained by laser synthesis on an industrial 3D printer Concept Laser M2 Cusing Single Laser 400W. Numerical simulations of the tests were carried out by the finite element method. Then, the most rational cellular structures in terms of mass and strength were established on the basis of both real and numerical experiments.

scholarly journals Struktur Anatomi dan Uji Histokimia Terpenoid dan Fenol Dua Varietas Sirih Hijau (Piper betle L.)

BIOSCIENTIAE ◽  
2021 ◽  
Vol 17 (2) ◽  
pp. 1
Author(s):  
Gusti Puspa Dewi ◽  
Evi Mintowati Kuntorini ◽  
Eny Dwi Pujawati
Keyword(s):  
Copper Acetate ◽  
Anatomical Structure ◽  
Secretory Cells ◽  
Cell Diameter ◽  
Piper Betle ◽  
Vascular Bundles ◽  
Palisade Parenchyma ◽  
Betel Leaf ◽  
Epidermal Tissue ◽  
Pith Parenchyma

This study aims to determine the anatomical structure and histochemical test of terpenoid and phenol compounds in two varieties of green betel plants (Piper betle). Making leaves anatomical structure preparations using the fresh method, testing terpenoid compounds with 5% copper acetate, testing phenol with ferric trichloride 10% and some grains of sodium carbonate. The observations of the anatomical structure of green betel leaf varieties 1 and varieties 2 have similarities consisting of the upper epidermis, upper hypodermis, palisade parenchyma, parenchymal sponges, vascular bundles (xylem and phloem), sclerenchyma, cholenchyma, lower epidermis, lower hypodermis, secretory cells, trichoma, stoma and calcium oxalate crystals, and in varieties 2 look more trichomes. The anatomical structure of the variety 1 betel stem and varieties 2 are arranged from the outside in the direction of the epidermal tissue, colenchymal tissue, cortical bundles, sclerenchyma, cortex, medullary and peripheral vascular files, pith, the central part of the stem is a secretory gland. Phenol in betel vine varieties 1 and varieties 2 is positive in the secretion cell part which is spread in the parenchymal tissue of the mother's leaf bone and lamina, whereas in the stem is spread around the cortex and pith parenchyma. Positive secretion cells contain phenol not as much as secretory cells containing terpenoids. Based on quantitative observations the size of oil cell density and secretion cell diameter, the essential oils contained in the cell secretions in the leaves of variety 1 are more than varieties 2 while in the varieties 2, there are more varieties 1.

Anatomy, ultrastructure, and functional morphology of the metathoracic tracheal defensive glands of the grasshopper Romalea guttata

1991 ◽  
Vol 69 (8) ◽  
pp. 2100-2108 ◽  
Author(s):  
Douglas W. Whitman ◽  
Johan P. J. Billen ◽  
David Alsop ◽  
Murray S. Blum
Keyword(s):  
Secretory Cell ◽  
Tactile Stimulation ◽  
Defensive Secretion ◽  
Smooth Endoplasmic Reticulum ◽  
Duct Cell ◽  
Secretory Cells ◽  
Glandular Tissue ◽  
Golgi Bodies ◽  
Romalea Guttata ◽  
Defensive Glands

In the lubber grasshopper Romalea guttata, the respiratory system produces, stores, and delivers a phenolic defensive secretion. The exudate is secreted by a glandular epithelium surrounding the metathoracic spiracular tracheal trunks. Embedded in the glandular tissue are multiple secretory units, each comprised of a basal secretory cell and an apical duct cell. Secretory cells have numerous mitochondria, a tubular, smooth endoplasmic reticulum, well-developed Golgi bodies, and a microvillilined vesicle thought to transfer secretion to the intracellular cuticular duct of a duct cell. Ducts empty into the metathoracic tracheal lumina where the exudate is stored behind the closed metathoracic spiracle. Tactile stimulation elicits secretion discharge, which begins when all spiracles except the metathoracic pair are closed and the abdomen is compressed. Increased hemostatic and pneumatic pressures drive air and secretion out of the spiracle with an audible hiss. Both metathoracic spiracles discharge simultaneously. The secretion erupts first as a dispersant spray, then as an adherent froth, and finally assumes the form of a slowly evaporating repellent droplet. Discharge force and number vary with eliciting stimuli, volume of stored secretion, and age, disturbance state, and temperature of the insect. Molting grasshoppers are unable to discharge because the stored exudate is lost with the shed cuticle. The advantages and limitations of a tracheal defensive system are discussed.

Sensitivity of mammary secretory cell turnover to protein restriction and re-alimentation during early lactation

1997 ◽  
Vol 1997 ◽  
pp. 130-130
Author(s):  
M.G. Goodwill ◽  
N.S. Jessop ◽  
J.D. Oldham
Keyword(s):  
Cell Proliferation ◽  
Mammary Gland ◽  
Milk Production ◽  
Secretory Cell ◽  
Protein Restriction ◽  
Secretory Cells ◽  
Early Lactation ◽  
Cell Turnover ◽  
Lactational Performance

Milk production depends on both the number and activity of secretory cells within the mammary gland. Our earlier work showed the sensitivity of lactational performance to changes in diet during lactation (Goodwill et al, 1996). This study investigated the influence of protein undernutrition and re-alimentation on secretory cell proliferation and death in the mammary gland of rats during early lactation.

Describing the lactation curve of dairy animals

1999 ◽  
Vol 1999 ◽  
pp. 197-197 ◽  
Author(s):  
G. E. Pollott
Keyword(s):  
Secretory Cell ◽  
Empirical Models ◽  
Secretory Cells ◽  
Cell Numbers ◽  
Biological Meaning ◽  
Lactation Curve ◽  
Dairy Animals ◽  
The Difference ◽  
Daily Milk Yield ◽  
Daily Milk

Most functions used to describe the lactation curve of dairy animals are empirical in approach and result in parameters with little or no biological meaning. A new model for describing lactation based on the biology of the pregnant and lactating animal is proposed and compared to several empirical models (Wood, 1967; Grossman and Koops, 1988; Morant and Gnanasakthy, 1989).Lactation is thought of as the balance between an increase in secretory cell numbers (NSCP) and their later decline (NSCD). The difference between them is the number of active secretory cells, each of which secretes milk at a particular rate (S kg/cell/day). Thus daily milk yield (MY) = (NSCP – NSCD) x S.

Technological Exercise of Cell Structure Forming

2017 ◽  
Vol 736 ◽  
pp. 122-126 ◽  
Author(s):  
S.N. Larin ◽  
V.I. Platonov ◽  
G.A. Nuzgdin
Keyword(s):  
Liquid Fuel ◽  
Cell Structure ◽  
Experimental Studies ◽  
Single Layer ◽  
Processing Parameters ◽  
Utilization Factor ◽  
Specific Strength ◽  
Cell Structures ◽  
Critical Strain Rate ◽  
Material Utilization

Single-layer and multi-layer cell structures are used for manufacturing of shells of liquid fuel tankers, as well as of "dry" shells of products, wings, fairings, etc. However, conventional methods of production by means of milling do not allow achieving the required specific strength. In this connection, diffusion bonding by means of gas pressure and gas forming at specified temperature and speed conditions are extremely important. Studies conducted by authors help model the processes and calculate the necessary processing parameters: pressure, critical strain rate, deformation rate (deformation time). This paper describes the manufacturing technology for these products, in which the solutions are based on theoretical and experimental studies, which provide: an increase in specific strength; reduction in weight of the product; reduction of labor intensity and increase in material utilization factor.

Cell structure and mechanical properties of microcellular PLA foams prepared via autoclave constrained foaming

2020 ◽  
pp. 026248932093032
Author(s):  
Jinwei Chen ◽  
Ling Yang ◽  
Dahua Chen ◽  
Qunshan Mai ◽  
Meigui Wang ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Cell Size ◽  
Cell Structure ◽  
Saturation Pressure ◽  
Tensile Modulus ◽  
Cell Structures ◽  
Wide Range ◽  
The Mean ◽  
Constrained Foaming ◽  
The Relationship

Microcellular polylactic acid (PLA) foams with various cell size and cell morphologies were prepared using supercritical carbon dioxide (sc-CO2) solid-state foaming to investigate the relationship between the cell structure and mechanical properties. Constrained foaming was used and a wide range of cell structures with a constant porosity of ∼75% by tuning saturation pressure (8–24 MPa) was developed. Experiments varying the saturation pressure while holding other variables’ constant show that the mean cell size and the mean cell wall thickness decreased, while the cell density and the open porosity increased with increase of pressure. Tensile modulus of PLA foams decreased with increasing the saturation pressure, but the specific tensile modulus of PLA foams was still 15–80% higher than that of solid PLA. Tensile strength and elongation at break first increased with increasing saturation pressure up to 16 MPa and then decreased with further increasing saturation pressure (20 MPa and 24 MPa) at which opened-cell structure produced. Compressive modulus, compressive strength, and compressive yield stress also followed the same variation trend. The results indicated that not only cell size plays an important role in properties of PLA foams but also cell morphology can influence these properties significantly.

scholarly journals Knockdown of p180 Eliminates the Terminal Differentiation of a Secretory Cell Line

2009 ◽  
Vol 20 (2) ◽  
pp. 732-744 ◽  
Author(s):  
Payam Benyamini ◽  
Paul Webster ◽  
David I. Meyer
Keyword(s):  
Cell Line ◽  
Mammalian Cells ◽  
Secretory Cell ◽  
Terminal Differentiation ◽  
Secretory Cells ◽  
Rnai Technology ◽  
Apo E ◽  
Secretory Phenotype ◽  
Rough Er ◽  
Necessary And Sufficient

We have previously reported that the expression in yeast of an integral membrane protein (p180) of the endoplasmic reticulum (ER), isolated for its ability to mediate ribosome binding, is capable of inducing new membrane biogenesis and an increase in secretory capacity. To demonstrate that p180 is necessary and sufficient for terminal differentiation and acquisition of a secretory phenotype in mammalian cells, we studied the differentiation of a secretory cell line where p180 levels had been significantly reduced using RNAi technology and by transiently expressing p180 in nonsecretory cells. A human monocytic (THP-1) cell line, that can acquire macrophage-like properties, failed to proliferate rough ER when p180 levels were lowered. The Golgi compartment and the secretion of apolipoprotein E (Apo E) were dramatically affected in cells expressing reduced p180 levels. On the other hand, expression of p180 in a human embryonic kidney nonsecretory cell line (HEK293) showed a significant increase in proliferation of rough ER membranes and Golgi complexes. The results obtained from knockdown and overexpression experiments demonstrate that p180 is both necessary and sufficient to induce a secretory phenotype in mammalian cells. These findings support a central role for p180 in the terminal differentiation of secretory cells and tissues.

Novel exocrine glands in the hindleg tarsi of the ant Nothomyrmecia macrops

2000 ◽  
Vol 48 (6) ◽  
pp. 661 ◽  
Author(s):  
Johan Billen ◽  
Fuminori Ito ◽  
Christian Peeters
Keyword(s):  
Golgi Apparatus ◽  
Secretory Cell ◽  
Anterior Part ◽  
Duct Cell ◽  
Exocrine Gland ◽  
Secretory Cells ◽  
Exocrine Glands ◽  
The Third ◽  
Duct Cells

The third tarsomere of the hindlegs of both workers and queens of Nothomyrmecia macrops is almost entirely filled with a hitherto unknown exocrine gland (which does not occur in the closely related Myrmecia). Each of the approximately 30 secretory cells is connected to the outside via a duct cell. These open individually via large cuticular pores at the mesoventral side of the anterior part of the tarsomere. The diameter of the duct cells is narrow near the secretory cell, but gradually increases towards their opening site. The rounded secretory cells show a well developed Golgi apparatus and numerous clear vesicles. The function of this gland is not yet known, although its opening site may be indicative of the deposition of marking substances. At the mediodistal side of tarsomeres 2, 3 and 4 in the three pairs of legs, a glandular thickening of the epidermal epithelium occurs; this represents another novel exocrine structure in ants. This epithelial gland occurs in both Nothomyrmecia and Myrmecia.

scholarly journals Histological and histochemical aspects of the penial glands of Girardia biapertura Sluys, 1997 (Platyhelminthes, Tricladida, Paludicola)

2002 ◽  
Vol 62 (3) ◽  
pp. 547-555 ◽  
Author(s):  
S. T. SOUZA ◽  
A. M. LEAL-ZANCHET
Keyword(s):  
Secretory Cell ◽  
Ejaculatory Duct ◽  
Distal Portion ◽  
Proximal Region ◽  
Secretory Cells ◽  
Type I ◽  
Type Ii ◽  
Cell Type ◽  
Median Region

Girardia biapertura was described with sperm ducts penetrating the penis bulb, subsequently opening separately at the tip of the penis papilla and receiving the abundant secretion of penial glands. In the present work, the penial glands of this species have been histologically and histochemically analysed, and four types of secretory cells are distinguished. The openings of the penial glands into the intrabulbar and intrapapillar sperm ducts, designated here as intrapenial ducts, allow for the distinction between three histologically differentiated regions. The most proximal region possibly corresponds to the bulbar cavity of other freshwater triclads whereas the median and distal portions correspond to the ejaculatory duct. The proximal region of the intrapenial ducts receives mainly the openings of a secretory cell type (type I) that produces a proteinaceous secretion. A second type of secretory cell (type II) that secretes neutral mucopolyssacharides opens into the median region of the intrapenial ducts. The distal portion of the ducts receives two types of secretory cells (types III and IV) which secret glycoprotein and glycosaminoglycans, respectively. Types III and IV open also directly into the male atrium through the epithelium of the penis papilla. A comparison with the results presented here and those of other authors for species of Girardia is provided and the importance of the study of the penial glands for taxonomic characterisation of freshwater triclads is emphasised.

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