Ecophysiology and Mercury Accumulation of Rainbow Trout (Salmo gairdneri) When Exposed to Mercury in Various Concentrations of Chloride

1986 ◽  
Vol 43 (3) ◽  
pp. 710-714 ◽  
Author(s):  
Barbara Z. Walczak ◽  
U. Theodore Hammer ◽  
P. Ming Huang

Rainbow trout (Salmo gairdneri) mortality was 100% when exposed to HgCl2 (2–10 μg∙Hg2+∙L−1) for 14 d in a natural low chloride medium. There was no mortality if the medium contained 100, 200, or 400 mg Cl−∙L−1 or more. Accumulation of mercury was highest in kidneys (0.65–13 μg∙g−1), spleen (0.31–4.2), gills (0.46–4.15), and liver (0.53–2.1) but accumulations differed for periods of exposure (14 or 42 d) and chloride concentration in the medium (100 or 200 mg Cl−∙L−1). In rainbow trout exposed to HgCl2 for 42 d, there were significant increases in plasma sodium level at 200 mg Cl−∙L−1 and significant decreases in plasma potassium, albumin, α1-globulin, and β-globulin levels in 100 mg Cl−∙L−1. No significant changes occurred in these parameters at other chloride concentrations or in erythrocytes, hematocrit, mean corpuscular volume, white blood cell counts, or chloride plasma levels. Although chloride concentrations in the media affect mercury accumulation by different organs as well as affecting physiological functions, there appears to be no direct relationship except for reduced mortality.

1963 ◽  
Vol 25 (4) ◽  
pp. 457-464 ◽  
Author(s):  
W. N. HOLMES ◽  
D. G. BUTLER

SUMMARY The effects were studied of cortisol, corticosterone and aldosterone on the concentrations of sodium and potassium in muscle and blood plasma and on water content of muscle in the fresh-water rainbow trout (Salmo gairdneri). These steroids appeared to cause a loss in plasma sodium throughout the 96 hr. experimental period. An initial rise in muscle sodium was observed during the first 24 hr. after commencement of the treatments. The subsequent decline in muscle sodium was interrupted by a transient rise followed by a continuing decline. The effect of these hormones on the potassium concentrations in plasma was variable, although there was a significant rise in the potassium concentration in muscle during the period of decline in sodium concentration. The significance of these results in relation to the possible enhanced adrenocortical activity of the trout during adaptation to a marine environment is discussed.


1980 ◽  
Vol 37 (4) ◽  
pp. 746-750 ◽  
Author(s):  
C. Michel

With the aid of published information, we have developed a standardized and reproducible experimental model of furunculosis in rainbow trout (Salmo gairdneri). The infective doses (LD50 = 200 to 2000 germs, i.m.) employed strains of Aeromonas salmonicida, the virulence of which was maintained by passage in 15-g fingerlings. The number of viable cells in the dose was conveniently determined using the drop-plate enumeration technique; however, meaningful cell counts could only be obtained if broth cultures used for infecting the fish were harvested early in the exponential growth phase (OD < 1.000 at 525 nm). Better results were obtained with intramuscular injection than with intraperitoneal injection. The infection procedure involved injecting a dose of 10 LD50, intramuscularly, into each of 30 fish held at 15 °C and recording the mortalities for 10 d. Protection tests in which Tribrissen (28 mg sulfadiazine and 5.6 mg trimethoprim/kg fish for 8 d) was fed or tetracycline (1 mg per fish) i.m. injected into the infected fish served to demonstrate the value of the model. Results were in agreement with field observations with no death for treated fish and a mortality of 96%, for untreated fish. Key wordss rainbow trout, Salmo gairdneri; Aeromonas salmonicida, furunculosis, experimental infection


1973 ◽  
Vol 30 (4) ◽  
pp. 485-492 ◽  
Author(s):  
J. C. MacLeod ◽  
E. Pessah

Mercury toxicity in rainbow trout fingerlings was related to temperature and chemical formulation of the mercury. At 10 C, the 24-hr TLm concentration (median tolerance limit) for mercuric chloride (HgCl2) was approximately 30 times that for phenyl mercuric acetate (PMA). The 96-hr TLm values for mercuric chloride at 5, 10, and 20 C were 0.40, 0.28, and 0.22 mg Hg/liter. The velocity of mortality, (V = reciprocal of time to death in hours), was linearly related to temperature. For a mercuric chloride concentration of 0.5 mg Hg/liter, V =.002 +.0023t, where t = temperature in centigrade degrees.Temperature also affected accumulation rate of mercury in the fish muscle. At 5, 10, and 20 C a mercuric chloride concentration of 0.1 mg Hg/liter in the water produced biological magnification factors (conc. in fish ÷ conc. in water) of 4, 10, and 22 ×, respectively, PMA produced higher magnification factors of 80–100 × at 10 C.Active metabolic rate, though increased by higher temperatures, was depressed by mercuric chloride, and higher temperatures augmented the depressant effect.


1984 ◽  
Vol 41 (11) ◽  
pp. 1678-1685 ◽  
Author(s):  
Michael A. Giles

Rainbow trout (Salmo gairdneri) were exposed to 3.6 and 6.4 μg Cd/L for periods up to 178 d. Transitory changes in plasma calcium and magnesium were observed in fish exposed to 3.6 μg Cd/L although the differences were not significant. Exposure to 6.4 μg Cd/L, however, resulted in significantly lowered plasma sodium, potassium, calcium, and chloride and elevated magnesium concentrations. Analyses of urine indicated that the rate of urine production, osmolality, and sodium, potassium, chloride, magnesium, calcium, and protein concentrations were unaffected by exposure to 3.6 μg Cd/L although slight changes were observed in the first week of exposure. Urine production rate and urinary concentrations of potassium and chloride were unaffected in trout exposed to 6.4 μg Cd/L but sodium, protein, and osmolality were elevated and calcium and magnesium concentrations reduced in these fish. The results demonstrate that the majority of the cadmium-induced electrolyte imbalances do not result from impairment of renal function.


1961 ◽  
Vol 39 (1) ◽  
pp. 1-8 ◽  
Author(s):  
John R. Beaton

Further observations on metabolic alterations in fasted rats cooled under ice to rectal temperatures approximating 15 °C are reported. In the hypothermic rats, metabolism of injected lactic acid does not appear to be impaired. There is however: increased concentration of inorganic phosphorus in blood but not in liver; increased concentration of glutathione in liver but not in blood; increased plasma chloride concentration; decreased red cell potassium concentration; increased red cell water content; decreased plasma water content. Hypothermia, under these conditions, did not alter concentrations of liver acid-extractable glycogen, red cell sodium, plasma sodium, plasma potassium, nor serum calcium. Administration of urea in saline prior to cooling elevated plasma sodium and potassium concentrations in hypothermic rats. These observations are discussed in relation to previously reported effects of hypothermia on carbohydrate metabolite levels.


1985 ◽  
Vol 42 (4) ◽  
pp. 710-717 ◽  
Author(s):  
Bruce A. Barton ◽  
Gary S. Weirter ◽  
Cars B. Schreck

Acid-stressed fish appear to be more sensitive to additional stressors than unstressed fish. When juvenile rainbow trout, Salmo gairdneri, were exposed to acid conditions (pH 5.7–4.7) for 5 d, plasma cortisol was affected only slightly during the initial hours of exposure, but plasma glucose and hematocrit increased, and plasma sodium decreased. However, when fish held at pH 4.7 were subsequently subjected to a 30-s handling stress, poststress plasma cortisol rose to a peak level of more than twice that in handled fish held at ambient pH (6.6). Effects of handling on plasma glucose or sodium were not apparent against levels already altered by the chronic acid exposure, judging by the corticosteroid response, we conclude that the acid-stressed fish were more sensitive to additional handling, even though they appeared to be physiologically normal after 5 d. Thus, as a management consideration, when fish are stocked in acidified waters, care should be taken to avoid situations where the fish may encounter additional disturbances in the new environment. Plasma glucose and sodium were better indicators of chronic acid stress alone than plasma cortisol, but the greater cortisol response to handling at low pH may be a useful method of detecting increased interrenal activity during early stages of environmental acidification.


2003 ◽  
Vol 98 (5) ◽  
pp. 1077-1084 ◽  
Author(s):  
Hiroshi Morimatsu ◽  
Jens Rocktäschel ◽  
Rinaldo Bellomo ◽  
Shigehiko Uchino ◽  
Donna Goldsmith ◽  
...  

Background Clinicians calculate the anion gap (AG) and the strong ion difference (SID) to make acid-base diagnoses. The technology used is assumed to have limited impact. The authors hypothesized that different measurement technologies markedly affect AG and SID values. Methods SID and AG were calculated using values from the point-of-care blood gas and electrolyte analyzer and the central hospital laboratory automated blood biochemistry analyzer. Simultaneously measured plasma sodium, potassium, and chloride concentrations were also compared. Results Mean values for central laboratory and point-of-care plasma sodium concentration were significantly different (140.4 +/- 5.6 vs. 138.3 +/- 5.9 mm; P &lt; 0.0001), as were those for plasma chloride concentration (102.4 +/- 6.5 vs. 103.4 +/- 6.0 mm; P &lt; 0.0001) but not potassium. Mean AG values calculated with the two different measurement techniques differed significantly (17.6 +/- 6.2 mEq/l for central laboratory vs. 14.5 +/- 6.0 mEq/l for point-of-care blood gas analyzer; P &lt; 0.0001). Using the Stewart-Figge methodology, SID values also differed significantly (43.7 +/- 4.8 vs. 40.7 +/- 5.6 mEq/l; P &lt; 0.0001), with mean difference of 3.1 mEq/l (95% limits of agreement, -3.4, 9.5 mEq/l). For 83 patients (27.6%), differences in AG values were as high as 5 mEq/l or more, and for 46% of patients whose AG value was outside the reference range with one technology, a value within normal limits was recorded with the other. Conclusions Results with two different measurement technologies differed significantly for plasma sodium and chloride concentrations. These differences significantly affected the calculated AG and SID values and might lead clinicians to different assessments of acid-base and electrolyte status.


1987 ◽  
Vol 24 (1) ◽  
pp. 34-43 ◽  
Author(s):  
M. Albassam ◽  
J. Moore ◽  
A. Sharma

Rainbow trout (Salmo gairdneri) of two age groups were exposed to a cationic acrylamide-based flocculant at various concentrations in static bioassay chambers. At lethal concentrations the flocculant produced severe gill alterations in all fish. The principal alterations were necrosis and separation of the respiratory epithelial cells covering secondary lamellae. Many necrotic chloride cells were also seen, their apical plasma membrane was destroyed, and mitochondria were swollen with separated cristae. An influx of a large amount of fluid into the interstitial spaces caused partial or complete separation of subepithelial spaces from the covering epithelial cells and basement membranes of underlying blood vessels. Clinicopathological alterations included marked decreases in blood pH, partial pressure of oxygen, bicarbonate and plasma sodium, and chloride concentrations. Hematocrit, total protein, and blood glucose were increased. Fish exposed to sublethal concentrations had gill alterations characterized by hypercellularity and thickening of the secondary lamellae. These were due to undifferentiated cell proliferation and macrophage and lymphocyte infiltration between the covering epithelial cells and the underlying blood vessels. Macrophages and undifferentiated cells had large phagolysosomes containing cytoplasmic organelles, an indication of cell injury and increased turnover.


1964 ◽  
Vol 46 (1) ◽  
pp. 12-24 ◽  
Author(s):  
Dorothy E. Woolley ◽  
Paola S. Timiras

ABSTRACT Ovariectomy, hypophysectomy and administration of oestradiol, progesterone, testosterone or methylandrostenediol altered water or electrolyte concentrations in plasma, liver, cerebral cortex, brain stem and cerebellum in the rat. High daily doses of the steroids (500 μg/100 g body weight) increased plasma sodium levels. Oestradiol, followed by progesterone, then testosterone and methylandrostenediol, was most effective in producing hypernatraemia. Lower doses of oestradiol (10–200 μg/100 g body weight) did not change plasma sodium concentrations. Plasma potassium was increased by ovariectomy and decreased by low doses of oestradiol in ovariectomized, but not in hypophysectomized, rats. All doses of oestradiol lowered per cent plasma water in intact adult male rats and ovariectomized adult females, but not in hypophysectomized rats. High doses of the steroids, especially of oestradiol plus progesterone, raised concentrations of water, sodium, potassium and chloride in the liver, whereas water, sodium and potassium concentrations remained constant in brain. Each of the steroids elevated brain chloride concentrations. Of the brain areas analyzed, the cerebral cortex most consistently showed increased chloride after injections. Testosterone and progesterone, followed by oestradiol and then methylandrostenediol, were most potent in increasing brain chloride concentrations. Because the sex hormones have previously been shown to alter brain excitability, it is postulated that some of these alterations may be correlated with concomitant changes in brain anionic concentrations.


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