Fecal Nickel Excretion by Healthy Adults

1973 ◽  
Vol 19 (4) ◽  
pp. 429-430 ◽  
Author(s):  
Eva Horak ◽  
F William Sunderman

Abstract Nickel was measured by atomic absorption spectrometry in three-day collections of feces from healthy hospital workers (age 22-65) who had lived for more than a year in Hartford, Connecticut. None of the 10 subjects (4/♂ , 6/♀.) had occupational exposure to nickel. Fecal nickel averaged 3.3 µg/g (wet weight); SD, ±0.8; and range, 2.1 to 4.4 µg/g. Corresponding figures on a dry-weight basis were 14.2 µg/g; SD, ±2.7; and range, 10.8 to 18.7 µg/g. The fecal excretion of nickel averaged 258 µg/day (SD, ±126; range, 80 to 540 µg/day). Fecal excretion is evidently the major route for elimination of nickel from the human body. Comprehensive evaluations of environmental or occupational exposures to nickel should also include analyses of nickel in serum, urine, and hair.

1954 ◽  
Vol 37 (3) ◽  
pp. 381-399 ◽  
Author(s):  
Ruth Hubbard

The sedimentation behavior of aqueous solutions of digitonin and of cattle rhodopsin in digitonin has been examined in the ultracentrifuge. In confirmation of earlier work, digitonin was found to sediment as a micelle (D-1) with an s20 of about 6.35 Svedberg units, and containing at least 60 molecules. The rhodopsin solutions sediment as a stoichiometric complex of rhodopsin with digitonin (RD-1) with an s20 of about 9.77 Svedberg units. The s20 of the RD-1 micelle is constant between pH 6.3 and 9.6, and in the presence of excess digitonin. RD-1 travels as a single boundary also in the electrophoresis apparatus at pH 8.5, and on filter paper at pH 8.0. The molecular weight of the RD-1 micelle lies between 260,000 and 290,000. Of this, only about 40,000 gm. are due to rhodopsin; the rest is digitonin (180 to 200 moles). Comparison of the relative concentrations of RD-1 and retinene in solutions of rhodopsin-digitonin shows that RD-1 contains only one retinene equivalent. It can therefore contain only one molecule of rhodopsin with a molecular weight of about 40,000. Cattle rhodopsin therefore contains only one chromophore consisting of a single molecule of retinene. It is likely that frog rhodopsin has a similar molecular weight and also contains only one chromophore per molecule. The molar extinction coefficient of rhodopsin is therefore identical with the extinction coefficient per mole of retinene (40,600 cm.2 per mole) and the E(1 per cent, 1 cm., 500 mµ) has a value of about 10. Rhodopsin constitutes about 14 per cent of the dry weight, and 3.7 per cent of the wet weight of cattle outer limbs. This corresponds to about 4.2 x 106 molecules of rhodopsin per outer limb. The rhodopsin content of frog outer limbs is considerably higher: about 35 per cent of the dry weight, and 10 per cent of the wet weight, corresponding to about 2.1 x 109 molecules per outer limb. Thus the frog outer limb contains about five hundred times as much rhodopsin as the cattle outer limb. But the relative volumes of these structures are such that the ratio of concentrations is only about 2.5 to 1 on a weight basis. Rhodopsin accounts for at least one-fifth of the total protein of the cattle outer limb; for the frog, this value must be higher. The extinction (K500) along its axis is about 0.037 cm.2 for the cattle outer limb, and about 0.50 cm.2 for the frog outer limb.


Toxics ◽  
2019 ◽  
Vol 7 (4) ◽  
pp. 58
Author(s):  
Suhendrayatna ◽  
Arahman ◽  
Sipahutar ◽  
Rinidar ◽  
Elvitriana

The purpose of this study was to investigate the toxicity and the distribution of mercury (Hg) in the main tissues of freshwater fish (Oreochromis niloticus) after being exposed to water containing Hg(II). A sample group of 10 fish, of mean weight 80–100 g wet weight, were exposed to different concentrations of Hg (0.0012; 0.0049; 0.0141; 0.0524; 0.1126; and 0.5110 mg-HgII/L) for 72 hours under controlled conditions using the static method in ponds. A control medium was also prepared in two replications. Mortality of fish was closely monitored, and the test was repeated three times. For the toxicity test, observations were based on behavior, mortality, and anatomical pathology. The methodology was based on the OECD guidelines for testing of chemicals and lethal concentration (LC50) and particularly using the probit method. Thus, the mean value was obtained from two replications and then further calculated by a software (MiniTab® 16 version). Prior to analysis, samples were first lyophilized. The total concentration of Hg accumulation in the fish organs was analyzed using heat-vaporization atomic absorption spectrometry (HV-AAS) and a MA2000 automatic mercury analyzer. Results showed that toxicity (LC50) of freshwater fish was 0.1435 mg-Hg(II)/L. The internal organs showed some pathological changes including pale gills, anemic eyes, and a whitish body color after the exposure. Furthermore, histopathologically, exposure to mercury might also affect other organs, such as gills, liver, and hepatopancreas. Mercury was found in trace amounts, and its accumulation was found to be at least in the gills. Meanwhile, the highest accumulation was found in the muscle tissue with approximately 5.7183 µg/g dry weight. If they are put in order, the mercury accumulation in the tissue organs was varied from the highest to lowest one: Muscle > eye > bone > head > gill. Finally, it can be concluded that the Hg exposure could affect the histopathological condition of the tested fish.


2015 ◽  
Vol 39 (1) ◽  
pp. 15-22
Author(s):  
Nichaya Praditsup ◽  
Gullaya Wattayakorn

Concentrations of monobutyltin (MBT), dibutyltin (DBT) and tributyltin (TBT) compounds were analyzed in surface sediment samples collected from twelve stations along the Eastern Gulf of Thailand. The total butyltin (∑BTs) concentrations ranged between <1 and 109.7 ng g (dry weight). The overall concentration ranges found in the sediments were from <1 to 79.81 ng g-1 for MBT, from <1 to 9.5 ng g -1 for DBT, and from <1 to 29.8 ng g-1 for TBT, on a dry weight basis. MBT generally prevailed in most of the samples, suggesting the occurrence of old inputs of butyltin compounds in the area. Butyltin compounds were also measured in Nassarius sp., where ∑BTs concentrations were found to range between <1 and 238 ng g-1 (wet weight). The level of butyltin compounds in gastropod tissue samples tended to be related to that of the sediments and percentage of imposex incidence.


2010 ◽  
Vol 20 (2) ◽  
pp. 449-453 ◽  
Author(s):  
Michael A. Fidanza ◽  
David L. Sanford ◽  
David M. Beyer ◽  
David J. Aurentz

Fresh mushroom compost is a byproduct of the edible mushroom (Agaricus bisporus) industry and represents the composted growing substrate that remains after a crop has been harvested to completion. Thirty samples were obtained from commercial mushroom farms in southeastern Pennsylvania and sent to a laboratory for analysis to determine plant nutrient content, bulk density, and particle size distribution of fresh mushroom compost. Fresh mushroom compost had an average pH of 6.6, with an average carbon:nitrogen ratio of 13:1. Organic matter content averaged 25.86% (wet weight), 146.73 lb/yard3 (wet volume) or 60.97% (dry weight). For the primary macronutrients, average total nitrogen content averaged 1.12% (wet weight), 6.40 lb/yard3 (wet volume) or 2.65% (dry weight), phosphorus measured 0.29% (wet weight), 1.67 lb/yard3 (wet volume) or 0.69% (dry weight), and potassium was 1.04% (wet weight), 5.89 lb/yard3 (wet volume) or 2.44% (dry weight). Average soluble salt content was 13.30 mmho/cm (wet weight basis). However, on a per acre basis, the calculated sodium absorption ratio of 0.38 was considered very low. The average bulk density of fresh mushroom compost was 574.73 lb/yard3 (wet volume basis), and 91% of the material measured ≤3/8 inch in diameter as determined on a wet weight basis. Overall, fresh mushroom compost is suitable as a natural organic fertilizer and soil amendment for agriculture and horticulture.


2017 ◽  
Vol 2 (2) ◽  
pp. 158
Author(s):  
Wira Wanti Bangalino ◽  
Lydia Ninan Lestario ◽  
Cucun Alep Riyanto

<p style="text-align: justify;">The purpose of this study was to determine the effect of alginate and CaCl2 concentration of antioxidant activity and betacyanin content of restructuring product of red dragon fruit, and to determine the best formulation of the product restructuring that produces antioxidant activity and the content of the highest betacyanin on product restructuring. Data were analyzed by 4x2 Factorial Design and Randomized Completely Block Design (RCBD) with 4 replications. As the first factor is the alginate concentration which are 2 %, 3 %, 4 % and 5 %. The second factors are calcium cloride (CaCl2 ) 0.5 % and 0.75 %, while as the block is the time analysis. To test the differences between treatments means, the Honestly Significant of Differences (HSD) were used at 5% level of significant.The results showed that the higher concentrations of alginate and CaCl2 causes declining content of antioxidant activity and betacyanin, the best results are obtained is at a concentration of 2% alginate and CaCl2 0.5% with betacyanin levels 0.537 ± 0.062 mg/g dry weight basis and 0.132 ± 0.011 mg / g wet weight basis. The antioxidant activity of H. polyrhyzus restructuring amounted to 77.452% ± 0.624. ©2016 JNSMR UIN Walisongo. All rights reserved.</p>


1989 ◽  
Vol 52 (3) ◽  
pp. 204-206
Author(s):  
ANTHONY LOPEZ ◽  
HARRIET L. WILLIAMS

Ten essential elements were determined in dry and canned butter beans (Phaseolus limensis L.) by atomic absorption spectrophotometry. Samples were taken at different stages during the canning process to determine where changes in element content occurred. The content of each sample was compared statistically to other samples taken within the process. Element retention, excluding chloride and sodium, ranged from 51 to 84% on a dry weight basis, and 14 to 24% on wet weight basis.


1988 ◽  
Vol 51 (7) ◽  
pp. 574-576 ◽  
Author(s):  
ANTHONY LOPEZ ◽  
HARRIET L. WILLIAMS

Ten essential elements were determined in dry and canned chick peas (Cicer arietinum L.) by atomic absorption spectrophotometry. Samples were taken at different stages during the canning process to determine where changes in element content occurred. The content of each sample was compared statistically to other samples taken within the process. Element retention, excluding chloride and sodium, ranged from 12 to 127% on a dry weight basis and 4 to 45% on wet weight basis.


1960 ◽  
Vol XXXIV (III) ◽  
pp. 465-472 ◽  
Author(s):  
Joel Bitman ◽  
T. Randall Wrenn ◽  
Helene C. Cecil ◽  
J. F. Sykes

ABSTRACT Studies were made of H2O, Na, K, and Cl in rat uteri with and without deciduoma and in uteri from ovariectomized rats. Samples of whole uterus, endometrium and myometrium were obtained. The proportion of endometrium increased from 6.6 % to 27.2 % when deciduoma were present. Uterine horn weight increased from about 300 mg to over 900 mg. With the development of deciduoma the following effects occurred in whole uterus and myometrium: H2O content increased about 3.5 %. Na and Cl increased 22 % on a dry weight basis, although there were no differences when based upon wet weight. K increased 16 % on a wet weight and 40 % on a dry weight basis. The water and electrolyte content of uteri from ovariectomized rats was very similar to that of uteri without deciduoma. Endometrium could only be obtained from uteri with decidual tissue. H2O, Na, and Cl were about equal to the concentrations in whole uterus with deciduoma, but K was considerably higher than that observed in whole uterus. The ionic changes which the rat uterus exhibits during the development of deciduoma are characteristic of tissue growth. Similar changes have been observed in uterine growth under the influence of progesterone in the rabbit and the cow.


2015 ◽  
Vol 59 (3) ◽  
pp. 357-360 ◽  
Author(s):  
Józef Szkoda ◽  
Maciej Durkalec ◽  
Agnieszka Nawrocka ◽  
Mirosław Michalski

AbstractA total of 85 mussel samples of eight species were examined. Analysis of mercury in the freeze-dried samples was carried out by atomic absorption spectrometry method using direct mercury analyser AMA 254. The analytical procedure for determination of mercury was covered by the quality assurance programme of research and participation in national and international proficiency tests. Concentrations of total mercury in all investigated samples were found to be generally low, in the range of 0.033-0.577 mg/kg of dry weight and of 0.003-0.045 mg/kg of wet weight. The results indicate that obtained levels of mercury in bivalve molluscs are not likely to pose a risk to the health of consumers.


Author(s):  
I.M. Ritchie ◽  
C.C. Boswell ◽  
A.M. Badland

HERBACE DISSECTION is the process in which samples of herbage cut from trials are separated by hand into component species. Heavy reliance is placed on herbage dissection as an analytical tool ,in New Zealand, and in the four botanical analysis laboratories in the Research Division of the Ministry of Agriculture and Fisheries about 20 000 samples are analysed each year. In the laboratory a representative subsample is taken by a rigorous quartering procedure until approximately 400 pieces of herbage remain. Each leaf fragment is then identified to species level or groups of these as appropriate. The fractions are then dried and the composition calculated on a percentage dry weight basis. The accuracy of the analyses of these laboratories has been monitored by a system of interchanging herbage dissection samples between them. From this, the need to separate subsampling errors from problems of plant identification was, appreciated and some of this work is described here.


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