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Selenium, mercury interactions

Suzuki, K. T., Ogra, Y. Metabohsm of selenium audits interaction with mercury mechanisms by a speciation study. Phosphorus, Sulfur Silicon Relat Elem 2001, 171-172, 135-169. [Pg.271]

Beijer, K. and A. Jernelov. 1978. Ecological aspects of mercury-selenium interactions in the marine environment. Environ. Health Perspec. 25 43-45. [Pg.1623]

Klaverkamp, J.F., D.A. Hodgkins, and A. Lutz. 1983a. Selenite toxicity and mercury-selenium interactions in juvenile fish. Arch. Environ. Contam. Toxicol. 12 405-413. [Pg.1629]

Lucu, C. and M. Skreblin. 1981. Evidence of the interaction of mercury and selenium in the shrimp Palaemon elegans. Mar. Environ. Res. 5 265-274. [Pg.1629]

Selenium is readily available in a variety of foods including shrimp, meat, dairy products, and grains, with a recommended daily intake of 55 to 70 jug. It occurs in several forms with Se+6 being biologically most important. Selenium is readily absorbed by the intestine and is widely distributed throughout the tissues of the body, with the highest levels in the liver and kidney. It is active in a variety of cellular functions and interacts with vitamin E. Selenium appears to reduce the toxic effects of metals such as cadmium and mercury and to have anticarcinogenic activity. Selenium produces notable adverse effects both in deficiency and excess thus recommended daily intake for adults is approximately 70 Jg/day but should not exceed 200 pg/day. [Pg.124]

Parizek, J. (1978). Interactions between selenium compounds and those of mercury or cadmium. Environ. Health Perspect. 25, 53-55. [Pg.341]

Regression analysis on the data was used to estimate the coefficients in a predictive model equation. The dependent variable was chosen as the difference between the computer-calculated value for mercury (or selenium or ytterbium) and the true value. Independent variables were the elements plus plausible interactions (e.g., the interaction of selenium... [Pg.117]

Ganther HE. 1980. Interactions of vitamin E and selenium with mercury and silver. Ann NY Acad Sci 355 212-226. [Pg.145]

Ridlington JW, Whanger PD. 1981. Interactions of selenium and antioxidants with mercury, cadmium and silver. Fundam Appl Toxicol 1 368-375. [Pg.159]

Whanger PD. 1985. Metabolic interactions of selenium with cadmium, mercury, and silver. Adv Nutr Res 7 221-250. [Pg.167]

Interactions Overabundance of one trace element can interfere with the metabolic use of another element available at normal levels. For example, addition of large amounts of zinc to a diet interferes with (antagonizes) intestinal copper absorption, resulting in copper deficiency from a diet with adequate copper content. Copper deficiency can provoke iron deficiency and anaemia. Molybdenum deficiency in animals can be induced by co-administration of large amounts of the similar element tungsten. Iron deficiency can also increase retention of cadmium and lead, and selenium has been proposed to protect against cadmium and mercury toxicity. [Pg.60]

Biological, chemical, and physical effects of airborne metals are a direct function of particle size, concentration, and composition. The major parameter governing the significance of natural and anthropogenic emissions of environmentally important metals is particle size. Metals associated with fine particulates are of concern particles larger than about 3-fjim aerodynamic equivalent diameter are minimally respirable, are ineffective in atmospheric interactions, and have a short air residence time. Seventeen environmentally important metals are identified arsenic, beryllium, cadmium, chromium, copper, iron, mercury, magnesium, manganese, nickel, lead, antimony, selenium, tin, vanadium, and zinc. This report reviews the major sources of these metals with emphasis on fine particulate emissions. [Pg.146]

The environmental scientist has at his disposal a variety of sensitive, multi-elemental analytical methods that can lead to a massive amount of data on airborne metals. Optimum use of these tools for environmental monitoring calls for focusing resources only on those metals that are environmentally important. Considerations of toxicity along with their ability to interact in the air, leading to the formation of secondary pollutants, and their presence in air have led to the identification of 17 environmentally important metals nickel, beryllium, cadmium, tin, antimony, lead, vanadium, mercury, selenium, arsenic, copper, iron, magnesium, manganese, titanium, chromium, and zinc. In addition to the airborne concentration, the particle size of environmentally important metals is perhaps the major consideration in assessing their importance. [Pg.167]

In the diet and at the tissue level, ascorbic acid can interact with mineral nutrients. In the intestine, ascorbic acid enhances the absorption of dietary iron and selenium reduces the absorption of copper, nickel, and manganese but apparently has little effect on zinc or cobalt. Ascorbic acid fails to affect the intestinal absorption of two toxic minerals studied, cadmium and mercury. At the tissue level, iron overload enhances the oxidative catabolism of ascorbic acid. Thus, the level of dietary vitamin C can have important nutritional consequences through a wide range of inhibitory and enhancing interactions with mineral nutrients. [Pg.551]

Concerning interactions with other chemicals, there is an ongoing debate about the value of fish in the diet versus the risk from increased exposure to methylmercury that may be in the fish. One recent study reported a beneficial effect from increased fish consumption even though mercury body burdens were increased to some extent (Davidson et al. 1998). One possible factor in the fish that could improve health is omega 3-fatty acid. Children and adults both benefit from a healthy diet, but there may more emphasis on the benefits to growing children. Other interactions for mercury include the effect of various substances on its gastrointestinal absorption (e.g., iron, zinc) or possibly protective effects from prevention or repair of mercury related oxidative damage (e.g., interactions with selenium as an antioxidant). No information was identified that specifically addresses differences in these interactions for children compared to adults. [Pg.341]

Cuvin-Aralar MLA, Furness RW. 1991. Mercury and selenium interaction A review. Ecotoxicol Environ Safety 21(3) 348-364. [Pg.595]

Magos, L., and M. Webb. 1980. The interaction of selenium with cadmium and mercury. Crit. Rev. Toxicol. 8(1) 1-42. [Pg.87]

A wide variety of interactions of selenium with essential and nonessential elements, vitamins, xenobiotics, and sulfur-containing amino acids have been demonstrated in numerous studies. Selenium has been reported to reduce the toxicity of many metals including mercury, cadmium, lead, silver, and to some extent, copper (Frost 1972). Most forms of selenium and arsenic interact to reduce the toxicity of both elements (Levander 1977). Because of selenium s role in the antioxidant glutathione peroxidase enzymes, selenium also reduces the toxicity of metals in vitamin E-deficient animals (Diplock et al. 1967). [Pg.195]

DOE. 1996. Mercury-selenium interactions in the environment. Upton, NY U.S. Department of Energy, Office of Fossil Energy. NTIS DE 96 006 148. [Pg.332]

Magos L, Webb M. 1980. The interactions of selenium with cadmium and mercury. CRC Crit Rev Toxicol (Nov) 1980 1-42. [Pg.365]


See other pages where Selenium, mercury interactions is mentioned: [Pg.356]    [Pg.356]    [Pg.5]    [Pg.238]    [Pg.381]    [Pg.379]    [Pg.502]    [Pg.171]    [Pg.136]    [Pg.403]    [Pg.411]    [Pg.1604]    [Pg.136]    [Pg.403]    [Pg.411]    [Pg.1650]    [Pg.19]    [Pg.377]    [Pg.180]    [Pg.190]    [Pg.291]    [Pg.342]    [Pg.529]    [Pg.98]    [Pg.197]   
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Selenium interaction with mercury

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