Cadmium toxicity on synchronous populations of Chlorella ellipsoidea

1980 ◽  
Vol 58 (16) ◽  
pp. 1780-1788 ◽  
Author(s):  
H. Lue-Kim ◽  
P. C. Wozniak ◽  
R. A. Fletcher
Keyword(s):  
Cell Division ◽  
Toxic Effect ◽  
Cadmium Toxicity ◽  
Chlorophyll Concentration ◽  
Membrane Integrity ◽  
Dry Weight ◽  
Cell Number ◽  
Dark Phase ◽  
Chlorella Ellipsoidea ◽  
Synchronous Cultures

The primary phycotoxic effects of various concentrations (5–50 μM) of cadmium sulfate (CdSO4) on synchronous cultures of Chlorella ellipsoidea were determined during a 14-h light and a 10-h dark incubation cycle. At a concentration of 5 μM CdSO4 there was a slight stimulation in cell number, chlorophyll level, and dry weight whereas at higher concentrations (10–40 μM) a linear decrease in these parameters was evident. At even higher concentrations, 50 μM and above, cytolysis occurred. Inhibition of chlorophyll concentration and dry weight was greater the longer the cultures were exposed to cadmium. Cell division was completely arrested when toxic levels of cadmium were administered any time throughout the duration of the light phase. However, the severity of toxicity of cadmium, when applied during the dark phase, increased with the length of time of exposure. Cadmium toxicity also resulted in disturbances in cell division. Treated cells became larger than control cells. Unequal sporulation, microcolony and incipient microcolony formation, swelling, increased photolucence, and disruption of mitochondria occurred following treatment of cultures with toxic levels of cadmium. A further toxic effect of cadmium might relate to an increase in membrane permeability. Treatment of cultures with increasing concentrations of cadmium resulted in intracellular cadmium exceeding extracellular cadmium levels. The primary toxic effect of cadmium on synchronous cultures of C. ellipsoidea was attributed to a lack of cell division probably related to insufficient synthesis of chlorophyll and dry weight components as well as to a disruption of membrane integrity.

Some morphological, anatomical, and physiological changes in the pear fruit (Pyrus communis var. Williams Bon Chrétien) during development and following harvest

1961 ◽  
Vol 9 (2) ◽  
pp. 99 ◽  
Author(s):  
JM Bain
Keyword(s):  
Cell Division ◽  
Morphological Changes ◽  
Complex Structure ◽  
Titratable Acidity ◽  
Dry Weight ◽  
Cell Number ◽  
Pyrus Communis ◽  
Physiological Changes ◽  
Pear Fruit ◽  
Protein Nitrogen

Morphological, anatomical, and physiological changes occurring in the developing fruit of Pyrus communis var. Williams Bon Chretien were studied at frequent intervals, from blossom until after commercial maturity, in three successive seasons. Morphological changes were shown by increase in measurements of volume, long and short axis, and the width of the cortex (flesh), the morphology of the fruit being interpreted by the receptacular theory, Anatomical changes were given by the duration and distribution of cell division, differentiation of tissues, cell size, and cell number. Physiological changes were expressed as changes in fresh weight, dry weight, and moisture content for the whole fruit, and separately for the flesh, peel, and core in the second and third seasons. Total and reducing sugars, starch, titratable acidity, and total and protein nitrogen were estimated per gram of dried flesh at each sampling. Respiration rates for whole fruit were measured by the Pettenkofer method. Physiological changes could not be expressed on a per cell basis because of the complex structure of pear tissue. Data presented on the basis of the number of days from blossom showed two distinct stages in fruit growth. Stage I, the first 42-56 days of development, corresponded to the main cell division period and was characterized by more rapid morphological but slower physiological changes (except for increase in protein nitrogen) than Stage 11, the remainder of the time on the tree. Comparable trends were found in the three seasons, but drought reduced growth rate in the first season. Some ripening changes were followed on removal from the tree and after periods of cold storage at 0°C.

Factors Controlling Endosperm Cell Number and Grain Dry Weight in Wheat: Effects of Shading on Intact Plants and of Variation in Nutritional Supply to Detached, Cultured Ears

1984 ◽  
Vol 11 (3) ◽  
pp. 151 ◽  
Author(s):  
BK Singh ◽  
CF Jenner
Keyword(s):  
Cell Division ◽  
External Medium ◽  
Amino Nitrogen ◽  
Dry Weight ◽  
Cell Number ◽  
Soluble Carbohydrates ◽  
Endosperm Cell ◽  
Intact Plants ◽  
Organic Nutrients ◽  
Photon Exposure

The association between endosperm cell number and grain dry weight, and the dependence of endosperm cell division on the availability of organic nutrients, have been investigated in wheat. Two different procedures were used to vary the supply of nutrients to the grains during the phase of cell division. Detached ears were cultured in solutions of sucrose (0-60 g 1-1) and glutamine (0.125-0.75 g N 1-1), or intact plants were exposed to high (560 �mol m-2 s-1) or low (55 �mol m-2 s-1) photon irradiance. Cell number per endosperm, and grain dry weight, were both responsive to the concentration of nutrients in the external medium, and to the level of photon exposure. Average dry weight per cell was relatively independent of the level of nutrition or of photon exposure until cell division had ceased but, in the later stages of grain-filling, dry weight per cell in the cultured ears displayed a dependence upon the concentration of nutrients in the external medium. Amounts of sucrose, other soluble carbohydrates and soluble amino nitrogen were extracted from the grains and, on a per grain basis, the amounts of all fractions varied in response to variation in the level of nutrients supplied to the ears, and to photon exposure. However, concentrations of these nutrients in the developing grains, calculated on a dry weight or water basis, were not associated with the rate of cell division in the grains. While the evidence gathered supports the notion that growth (in cell number, and dry weight) of the developing endosperm is controlled inter alia by the provision of organic nutrients, the nature of the controlling mechanism is obscure. It seems that cellular division is not affected directly by nutritional supply through a mechanism involving the concentration of substrates for energy and protein synthesis within the developing grain.

scholarly journals CULTURE CONDITIONS AND THE DEVELOPMENT OF THE PHOTOSYNTHETIC MECHANISM

1946 ◽  
Vol 29 (6) ◽  
pp. 419-427 ◽  
Author(s):  
Jack Myers ◽  
Keyword(s):  
Light Intensity ◽  
Cell Volume ◽  
Unit Cell Volume ◽  
Chlorophyll Concentration ◽  
Dry Weight ◽  
Chlorella Pyrenoidosa ◽  
Cell Number ◽  
Culture Conditions ◽  
Photosynthetic Unit ◽  
Incandescent Lamps

1. Chlorella pyrenoidosa has been grown in a continuous-culture apparatus under various light intensities provided by incandescent lamps, other conditions of culture being maintained constant. The harvested cells were analyzed for cell number, dry weight, nitrogen, and chlorophyll per unit cell volume. 2. Cell nitrogen and cell volume are parallel measures of cellular material over the range of light intensity studied. 3. The dry weight per cell volume increases slowly with light intensity, showing about a 20 per cent variation. 4. Chlorophyll concentration and cell number show a concomitant decrease with increasing light intensity, varying in such a way that there are always about the same number of chlorophyll molecules per cell. It is considered that this phenomenon has bearing on the interpretation of data which has led to the theory of the photosynthetic unit.

Effects of the pseudomonad phytotoxin coronatine on tomato leaf structure and ultrastructure

1995 ◽  
Vol 53 ◽  
pp. 862-863
Author(s):  
D.A. Palmer ◽  
C.L. Bender
Keyword(s):  
Pseudomonas Syringae ◽  
Membrane Integrity ◽  
Leaf Tissue ◽  
Cell Number ◽  
Cell Ultrastructure ◽  
Response To Treatment ◽  
Prominent Symptom ◽  
Chlorophylls A And B ◽  
Cell Dimensions ◽  
Structure And Ultrastructure

Coronatine is a non-host-specific phytotoxin produced by several members of the Pseudomonas syringae group of pathovars. The toxin acts as a virulence factor in P. syringae pv. tomato, allowing the organism to multiply to a higher population density and develop larger lesions than mutant strains unable to produce the toxin. The most prominent symptom observed in leaf tissue treated with coronatine is an intense spreading chlorosis; this has been attributed to a loss of chlorophylls a and b in tobacco. Coronatine's effects on membrane integrity and cell ultrastructure have not been previously investigated. The present study describes changes in tomato leaves in response to treatment with purified coronatine, infection by a coronatine-producing strain of P. syringae pv. tomato, and infection by a cor" mutant.In contrast to H2O-treated tissue, coronatine-treated tissue showed a diffuse chlorosis extending approximately 5 mm from the inoculation site. Leaf thickness, cell number, and cell dimensions were similar for both healthy and coronatine-treated, chlorotic tissue; however, the epidermal cell walls were consistently thicker in coronatine-treated leaves (Figs, la and lb).

ABOUT SOME PECULIARITIES OF THE PHYSIOLOGICAL HETEROGENEITY OF THE POPULATION OF SCENEDESMUS QUADRICAUDA (TURP.) BREB. IN THE PRESENCE OF LOW CONCENTRATIONS OF METALS

2018 ◽  
pp. 34-43
Author(s):  
V. I. Ipatova ◽  
A. G. Dmitrieva ◽  
О. F. Filenko ◽  
T. V. Drozdenko
Keyword(s):  
Cell Division ◽  
Toxic Effect ◽  
Copper Chloride ◽  
Single Cells ◽  
Physiological State ◽  
Scenedesmus Quadricauda ◽  
Physiological Status ◽  
Lag Phase ◽  
Protective Mechanism ◽  
Low Concentrations

The structure of the laboratory population of green microalgae Scenedesmus quadricauda (Turp.) Breb (=Desmodesmus communis E. Hegew.) was studied at different stages of its growth (lag-phase, log-phase and stationary phase) at low concentrations of copper chloride and silver nitrate by the method microculture, allowing to monitor the state and development of single cells having different physiological status. The response of the culture of S. quadricauda - the change in the number of cells and the fractional composition (the fraction of dividing, «dormant» and dying cells) depended not only on the concentration of the toxicant in the medium, but also on the physiological state of the culture: the level of synchronization and the growth phase. Silver ions at low concentrations had a more pronounced toxic effect on the culture than copper ions at different phases of its development, especially at a concentration of 0.001 mg/l (10-9 M). The main mechanism of the toxic effect of metals is to inhibit the process of cell division. At low concentrations of toxicants, especially at a concentration of 0.001 mg/l, a «paradoxical» effect expressed in the predominance of the fraction of «dormant» cells was revealed. The temporary inhibition of the process of cell division can be regarded as a protective mechanism that allows preserving the integrity of the population and its ability to survive in a changing environment. The obtained data explain the effect of action of low concentrations of substances due to their inclusion in the cell, the subsequent accumulation in the cell and their low excretion.

scholarly journals Sound Waves Promote Arabidopsis thaliana Root Growth by Regulating Root Phytohormone Content

2021 ◽  
Vol 22 (11) ◽  
pp. 5739
Author(s):  
Joo Yeol Kim ◽  
Hyo-Jun Lee ◽  
Jin A Kim ◽  
Mi-Jeong Jeong
Keyword(s):  
Arabidopsis Thaliana ◽  
Cell Division ◽  
Root Growth ◽  
Apical Meristem ◽  
Cell Number ◽  
Root Apical Meristem ◽  
Control Group ◽  
Auxin Signaling ◽  
Ethylene Signaling ◽  
Sound Waves

Sound waves affect plants at the biochemical, physical, and genetic levels. However, the mechanisms by which plants respond to sound waves are largely unknown. Therefore, the aim of this study was to examine the effect of sound waves on Arabidopsis thaliana growth. The results of the study showed that Arabidopsis seeds exposed to sound waves (100 and 100 + 9k Hz) for 15 h per day for 3 day had significantly longer root growth than that in the control group. The root length and cell number in the root apical meristem were significantly affected by sound waves. Furthermore, genes involved in cell division were upregulated in seedlings exposed to sound waves. Root development was affected by the concentration and activity of some phytohormones, including cytokinin and auxin. Analysis of the expression levels of genes regulating cytokinin and auxin biosynthesis and signaling showed that cytokinin and ethylene signaling genes were downregulated, while auxin signaling and biosynthesis genes were upregulated in Arabidopsis exposed to sound waves. Additionally, the cytokinin and auxin concentrations of the roots of Arabidopsis plants increased and decreased, respectively, after exposure to sound waves. Our findings suggest that sound waves are potential agricultural tools for improving crop growth performance.

An In Vitro Cytotoxicity Assay Using Rat Hepatocytes and MTT and Coomassie Blue Dye as Indicators

1991 ◽  
Vol 19 (3) ◽  
pp. 352-360
Author(s):  
Kazuhiko Otoguro ◽  
Kanki Komiyama ◽  
Satoshi Ωmura ◽  
Charles A. Tyson
Keyword(s):  
Mtt Assay ◽  
Membrane Integrity ◽  
Cell Number ◽  
Cellular Protein ◽  
Blue Dye ◽  
Tetrazolium Salt ◽  
Sprague Dawley ◽  
Lactate Dehydrogenase Activity ◽  
Coomassie Blue

Isolated hepatocytes from male Sprague-Dawley rats suspended in culture medium supplemented with either 0.2 or 2% bovine serum albumin (BSA) were allowed to attach to collagen coated 96-well dishes. Ten test chemicals from the MEIC list and salicylic acid were added individually to the dishes, and at the end of 24 and 48 hours, cytotoxicity was determined by measuring MTT (tetrazolium salt) reduction (mitochondrial integrity) and total cellular protein using Coomassie blue dye (reflecting cell number). Total cellular lactate dehydrogenase activity was also determined in some experiments, as an indicator of plasma membrane integrity. The relative toxicities of the test chemicals were quantified by the estimation of EC10, EC20 and EC50 values for each parameter. Except for one chemical, digoxin, in the MTT assay, cytotoxic potency increased with incubation time. The hepatocytes tended to be more sensitive to the chemicals in medium containing 0.2% BSA than in medium containing 2% BSA. Simple linear regression analyses of the log transformed data from the MTT assay versus log oral LD50 in rats for the test chemicals gave the best results using EC10 at 24 hours (r2 = 0.86). With protein as the cytotoxic indicator, the best results were obtained with EC values in the medium containing 2% BSA, again at 24 hours (r2 = 0.83). These results suggest that the MTT and Coomassie blue dye assays could be useful indicators for testing the cytotoxic potential of chemicals in rat hepatocyte cultures.

scholarly journals Venous and Arterial Endothelial Cells from Human Umbilical Cords: Potential Cell Sources for Cardiovascular Research

2021 ◽  
Vol 22 (2) ◽  
pp. 978
Author(s):  
Skadi Lau ◽  
Manfred Gossen ◽  
Andreas Lendlein ◽  
Friedrich Jung
Keyword(s):  
Endothelial Cells ◽  
Umbilical Cord ◽  
Membrane Integrity ◽  
Cell Types ◽  
Cell Number ◽  
Human Umbilical Cord ◽  
Cardiovascular Research ◽  
Cardiovascular Devices ◽  
Arterial Endothelial Cells

Although cardiovascular devices are mostly implanted in arteries or to replace arteries, in vitro studies on implant endothelialization are commonly performed with human umbilical cord-derived venous endothelial cells (HUVEC). In light of considerable differences, both morphologically and functionally, between arterial and venous endothelial cells, we here compare HUVEC and human umbilical cord-derived arterial endothelial cells (HUAEC) regarding their equivalence as an endothelial cell in vitro model for cardiovascular research. No differences were found in either for the tested parameters. The metabolic activity and lactate dehydrogenase, an indicator for the membrane integrity, slightly decreased over seven days of cultivation upon normalization to the cell number. The amount of secreted nitrite and nitrate, as well as prostacyclin per cell, also decreased slightly over time. Thromboxane B2 was secreted in constant amounts per cell at all time points. The Von Willebrand factor remained mainly intracellularly up to seven days of cultivation. In contrast, collagen and laminin were secreted into the extracellular space with increasing cell density. Based on these results one might argue that both cell types are equally suited for cardiovascular research. However, future studies should investigate further cell functionalities, and whether arterial endothelial cells from implantation-relevant areas, such as coronary arteries in the heart, are superior to umbilical cord-derived endothelial cells.

scholarly journals Its What’s on the Inside That Counts: An Effective, Efficient, and Streamlined Method for Quantification of Octocoral Symbiodiniaceae and Chlorophyll

2021 ◽  
Vol 8 ◽  
Author(s):  
Rosemary Kate Steinberg ◽  
Emma L. Johnston ◽  
Teresa Bednarek ◽  
Katherine A. Dafforn ◽  
Tracy D. Ainsworth
Keyword(s):  
Protein Content ◽  
Surface Area ◽  
Water Movement ◽  
Chlorophyll Concentration ◽  
Dry Weight ◽  
Accurate Method ◽  
Host Protein ◽  
Biomass Composition ◽  
Wet Weight ◽  
Chlorophyll Concentrations

Ocean warming driven bleaching is one of the greatest threats to zooxanthellate cnidarians in the Anthropocene. Bleaching is the loss of Symbiodiniaceae, chlorophyll, or both from zooxanthellate animals. To quantify bleaching and recovery, standardised methods for quantification of Symbiodiniaceae and chlorophyll concentrations have been developed for reef-building scleractinian corals, but no such standard method has been developed for octocorals. For stony corals, quantification of Symbiodiniaceae and chlorophyll concentrations often relies on normalisation to skeletal surface area or unit of biomass [i.e., protein, ash-free dry weight (AFDW)]. Stiff octocorals do not change their volume, as such studies have used volume and surface area to standardise densities, but soft-bodied octocorals can alter their size using water movement within the animal; therefore, Symbiodiniaceae and chlorophyll cannot accurately be measured per unit of surface area and are instead measured in units of Symbiodiniaceae and chlorophyll per μg of host protein or AFDW. Though AFDW is more representative of the full biomass composition than host protein, AFDW is more time and resource intensive. Here, we provide a streamlined methodology to quantify Symbiodiniaceae density, chlorophyll concentration, and protein content in soft-bodied octocorals. This technique uses minimal equipment, does not require freeze-drying or burning samples to obtain ash weight, and is effective for down to 0.2 g wet tissue. Bulk samples can be centrifuged, the Symbiodiniaceae pellet washed, and the supernatant saved for protein analysis. This efficient technique allows for clean, easy to count samples of Symbiodiniaceae with minimal animal protein contamination. Chlorophyll a and c2 extractions occurs at different rates, with chlorophyll a taking 24 h to extract completely at 4°C and chlorophyll c2 taking 48 h. Finally, we found that where necessary, wet weight may be used as a proxy for protein content, but the correlation of protein and wet weight varies by species and protein should be used when possible. Overall, we have created a rapid and accurate method for quantification of bleaching markers in octocorals.

scholarly journals Rootstock Effects on Growth, Cell Number, and Cell Size of `Gala' Apples

2004 ◽  
Vol 129 (1) ◽  
pp. 37-41 ◽  
Author(s):  
Yahya K. Al-Hinai ◽  
Teryl R. Roper
Keyword(s):  
Cell Division ◽  
Cell Size ◽  
Agricultural Research ◽  
Fruit Size ◽  
Cell Number ◽  
Fruit Growth ◽  
Research Station ◽  
Full Bloom ◽  
Final Size ◽  
Load Effects

The effects of rootstock on growth of fruit cell number and size of `Gala' apple trees (Malus domestica Borkh) were investigated over three consecutive seasons (2000-02) growing on Malling 26 (M.26), Ottawa-3, Pajam-1, and Vineland (V)-605 rootstocks at the Peninsular Agricultural Research Station near Sturgeon Bay, WI. Fruit growth as a function of cell division and expansion was monitored from full bloom until harvest using scanning electron microscopy (SEM). Cell count and cell size measurements showed that rootstock had no affect on fruit growth and final size even when crop load effects were removed. Cell division ceased about 5 to 6 weeks after full bloom (WAFB) followed by cell expansion. Fruit size was positively correlated (r2 = 0.85) with cell size, suggesting that differences in fruit size were primarily a result of changes in cell size rather than cell number or intercellular space (IS).

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