scholarly journals Use of the Coulter Counter to Measure Osmotic Effects on the Swelling of Mould Spores During Germination

1967 ◽  
Vol 49 (2) ◽  
pp. 287-292 ◽  
Author(s):  
M. Barnes ◽  
M. S. Parker
2006 ◽  
Vol 12 (4) ◽  
pp. 242-243
Author(s):  
Ferran Vall-Llovera ◽  
José-Tomas Navarro ◽  
Jose-Maria Ribera ◽  
Natalia Lloveras ◽  
Jordi Junca ◽  
...  

1970 ◽  
Vol 5 (1) ◽  
pp. 1-8
Author(s):  
Gordon G.C. Robinson ◽  
Dennis J. Brown

Abstract A model “B” Coulter Counter with “J” plotter was used to determine the total volume of particulate matter and autotrophic and heterotrophic increments in particle volume in a small eutrophic lake, south of Lake Manitoba. Such increments were converted to more meaningful carbon values.


Author(s):  
Derek Burton ◽  
Margaret Burton

The blood system transports nutrients, oxygen, carbon dioxide and nitrogenous wastes; other functions include defence. Fish have a closed, single circulation in which blood is pumped by a contractile heart via a ventral aorta to the gills, then via the dorsal aorta to vessels supplying the tissues and organs, with a venous return to the heart. Large venous sinuses occur in elasmobranchs. Air-breathing fish have modifications of the circulation. Complex networks of narrow blood vessels can occur as red patches, retia, maximizing transfer of nutrients, oxygen or heat. Most fish have nucleated red blood cells (erythrocytes) with haemoglobin. The types of white blood cells (leucocytes) are similar to those of other vertebrates but there are thrombocytes rather than platelets. Nutrient transport is in the plasma, the fluid component of the blood, which may also carry antifreeze agents and molecules (e.g. urea in elasmobranchs) which counteract deleterious osmotic effects


1972 ◽  
Vol 58 (5) ◽  
pp. 599.2-600 ◽  
Author(s):  
Jannie A. De Lange ◽  
George J. Eernisse ◽  
Jan J. Veltkamp

1995 ◽  
Vol 36 (2) ◽  
pp. 204-209
Author(s):  
C.-M. Chai ◽  
T. Almén ◽  
P. Aspelin ◽  
L. Bååth

Solutions of the nonionic monomeric contrast medium iohexol (300 mg I/ml) with and without added NaCl were investigated for effects on red blood cell aggregation and blood coagulation. Three volumes of a test solution were mixed in test tubes with one volume of human blood. During 30 min samples of the mixture were taken for investigation. Six test solutions were used: 1) iohexol, 2) iohexol+glucose 280 mM, 3) iohexol+NaCl 150 mM, 4) glucose 280 mM, 5) glucose 140 mM+NaCl 75 mM, 6) NaCl 150 mM. Test solutions with NaCl caused no aggregation. Test solutions without NaCl always caused macroscopic red cell aggregates. These aggregates always disappeared when saline was added to the sample. The macroscopic red cell aggregates could be dispersed to microscopic aggregates by shaking the test tubes. During the next 30 min macroscopic aggregates returned in the glucose solution but not in the iohexol solutions. In 30 min, blood mixed with iohexol solutions never coagulated while blood layered on top of the same iohexol solutions always coagulated. Blood mixed with solutions 5 and 6, both without iohexol, always coagulated. It is concluded that adding 150 mM NaCl to iohexol did not eliminate its ability to antico-agulate whole blood, but inhibited its ability to aggregate red cells. This inhibition was not caused by the osmotic effects of the added NaCl.


1985 ◽  
Vol 86 (6) ◽  
pp. 813-832 ◽  
Author(s):  
E W Stephenson

45Ca efflux from skinned muscle fibers is stimulated transiently, by a highly Ca2+-dependent mechanism, by KCl replacement of K propionate. In the present studies, Cl replaced the much less permeant anion methanesulfonate (Mes) either (a) at constant [K], in which increased [K][Cl] permits net KCl and water flux across internal membranes, or (b) at constant [K][Cl] (choline substitution), in which the imposed gradients and diffusion potentials should dissipate slowly. 45Ca efflux and isometric force were measured simultaneously on segments of frog semitendinosus fibers skinned by microdissection. EGTA was applied to chelate released 45Ca either (a) shortly after high [Cl] (interrupted response), to minimize reaccumulation, (b) before high [Cl] (pretreated response), to evaluate Ca2+ dependence, or (c) under control conditions in KMes. KCl replacement of KMes stimulated release of 65% fiber 45Ca within 1 min in interrupted responses; EGTA pretreatment was only moderately inhibitory with substantial residual stimulation. In contrast, choline Cl replacement of KMes induced release of 26-35% fiber 45Ca in interrupted responses; EGTA pretreatment was strongly inhibitory, but release significantly exceeded control with a small, sustained increase in Ca2+-insensitive efflux. These differences in 45Ca release and EGTA inhibition suggest that Cl replacement of Mes at constant [K] stimulates efflux by osmotic effects as well as imposed diffusion potentials; at least half the stimulated 45Ca loss (above control) in interrupted KCl responses is attributable to an osmotic component with low Ca2+ sensitivity. In the highly Ca2+-sensitive stimulation at constant [K][Cl], 45Ca release (above control) in interrupted responses correlated well with that in the pretreated responses of segments from the same fiber, with a slope of 8.4. This relationship suggests that imposed diffusion potentials stimulate a small Ca2+-insensitive component that gradates a much larger Ca2+-dependent efflux. The Ca2+-insensitive component apparently reflects intermediate steps in the excitation-contraction coupling that require positive feedback to result in sufficient Ca release for contraction.


1999 ◽  
Vol 9 (2) ◽  
pp. 159-161 ◽  
Author(s):  
M Koch ◽  
A G R Evans ◽  
A Brunnschweiler
Keyword(s):  

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