Home Contact Us Search Toxic Exposure Study Trust Foundation

WHO

Mercury Neurotoxicity Alzheimer's & Hg AD & Mercury Neurites & Hg Hg Induced AD Rep. Burton & Amalgam Hg Nephrotoxicity Heart Disease & Hg Dentist's Hg Exposure Crematoria & Hg Amalgam Hg Release Published Studies Hg Abstracts Dr. Haley On Amalgam Hg Press Releases AD Pathology & Hg ADA & Amalgam Amalgam Safe Baratz Testimony Amalgam Make Up Hg Exposure Amyloid & Metals Amalgam & TMJ Hg Free Dentists Amalgam Quotes Hg Points of View Hg Free Patents Toxic Hg Species Amalgam Lawsuits Antibiotic Resistance Amalgam Economics Amalgam vs. Composites Amalgam Debate Safety & Treatment Amalgam Protest Federal Agencies Mercury Measurement CA Dental Board Fish & Mercury Dr. Haley Responds Ban Hg Petition Dr. Vimy Responds Mercury Links Amalgam & Cavitites Amalgam & Hg Waste Hg in Medicines Rep. Watson & CDA Amalgam Waste Black Caucus Mercury Links States Fight Hg Toxic Teeth

EPA & Hg Exposure
EPA
EPA & Hospitals
CDC & Amalgam
PHS
WHO
NIST
SMRC
FDA
International
NIH
Canada
 

The World Health Organization and Mercury


Mercury

From the World Health Organization. http://www.who.int/

http://www.who.int/mercuryfull.htm#Environmental

History | Summary

Information extracted from:

Guidelines for drinking-water quality, 2nd ed.  Vol. 2. Health criteria and other supporting information.  Geneva, World Health Organization, 1996. pp. 285-298.

1. General description

Physicochemical properties

Property Value
Physical state
Dense, silver-white metal; liquid at normal temperatures and pressures
Vapour pressure 0.16 Pa at 20 °C
Stability Carbon–mercury bond in organic mercury compounds is chemically stable

Major uses

Mercury is used for the cathode in the electrolytic production of chlorine and caustic soda, in electrical appliances (lamps, arc rectifiers, mercury cells), in industrial and control instruments (switches, thermometers, barometers), in laboratory apparatus, in dental amalgams, and as a raw material for various mercury compounds. The latter are used as fungicides, antiseptics, preservatives, pharmaceuticals, electrodes, and reagents.

Environmental fate

The solubility of mercury compounds in water varies: elemental mercury vapour is insoluble, mercury(II) chloride is readily soluble, mercury(I) chloride much less soluble, and mercury sulfide has a very low solubility.

Methylation of inorganic mercury has been shown to occur in columns of fresh water and in seawater (1), and bacteria (Pseudomonas spp.) isolated from mucous material on the surface of fish and soil were able to methylate mercury under aerobic conditions. Some anaerobic bacteria that possess methane synthetase are also capable of mercury methylation (2). Once methylmercury [the generic term "methylmercury" is used throughout this text to refer to monomethylmercury compounds] is released from microbes, it enters the food chain as a consequence of rapid diffusion and tight binding to proteins in aquatic biota. The enzymology of CH3Hg+ hydrolysis and mercury(II) ion reduction is now understood in some detail. Environmental levels of methylmercury depend on the balance between bacterial methylation and demethylation (3).

2. Analytical methods

Inorganic mercury is determined by flameless atomic absorption spectrometry (4). Cold vapour atomic absorption spectrometry and atomic fluorescence spectrometry have detection limits of 50 and 1 ng/litre, respectively.

Gas chromatography is commonly used for the determination of alkylmercury compounds. The neutron activation procedure is regarded as the most accurate and is generally used as the reference method (3).

3. Environmental levels and human exposure

Air

Mercury levels in air are in the range 2–10 ng/m3.

Water

Inorganic mercury

Levels of mercury in rainwater are in the range 5–100 ng/litre, but mean levels as low as 1 ng/litre have been reported (3). Naturally occurring levels of mercury in groundwater and surface water are less than 0.5 µg/litre, although local mineral deposits may produce higher levels in groundwater. In 16 groundwaters and 16 shallow wells surveyed in the USA, mercury levels exceeded the maximum contaminant level of 2 µg/litre set by the US Environmental Protection Agency for drinking-water (5). An increase in the mercury concentration up to 5.5 µg/litre was reported for wells in Izu Oshima Island (Japan), where volcanic activity is frequent (6). The concentration range for mercury in drinking-water is the same as in rain, with an average of about 25 ng/litre (3).

Organic mercury

In a contaminated lake system in Canada, methylmercury was found to constitute a varying proportion of total mercury, depending on the lake (3). There have been no reports of methylmercury in drinking-water.

Food

Food is the main source of mercury in non-occupationally exposed populations. Fish and fish products account for most of the organic mercury in food. The average daily intake of mercury from food is in the range 2–20 µg/day, but may be much higher in regions where ambient waters have become contaminated with mercury and where fish constitute a high proportion of the diet (7).

Estimated total exposure and relative contribution of drinking-water

On the assumption of an ambient air level of 10 ng/m3, the average daily intake of inorganic mercury by inhalation would amount to about 0.2 µg. If a level in drinking-water of 0.5 µg/litre is assumed, the average daily intake of inorganic mercury from this source would amount to about 1 µg. The average daily intake of mercury from food is in the range 2–20 µg/day.

4. Kinetics and metabolism in laboratory animals and humans

Inorganic mercury

About 7–8% of ingested mercury in food is absorbed; absorption from water may be 15% or less, depending on the compound. About 80% of inhaled metallic mercury vapour is retained by the body, whereas liquid metallic mercury is poorly absorbed via the gastrointestinal tract. Inhaled aerosols of inorganic mercury are deposited in the respiratory tract and absorbed to an extent depending on particle size (8).

Inorganic mercury compounds are rapidly accumulated in the kidney, the main target organ for these compounds. The biological half-time is very long, probably years, in both animals and humans. Mercury salts are excreted via the kidney, liver, intestinal mucosa, sweat glands, salivary glands, and milk; the most important routes are via the urine and faeces (8).

Organic mercury

Dimethylmercury is almost completely absorbed through the gastrointestinal tract; after absorption it rapidly appears in the blood, where, in humans, 80–90% is bound to red cells. Demethylation of methylmercury to inorganic mercury occurs at a slow but significant rate. The greater intrinsic toxicity of methylmercury as compared with inorganic mercury is due to its lipid solubility, which enables it to cross biological membranes more easily, and especially to enter the brain, spinal cord, and peripheral nerves, and to cross the placenta (3).

Most methylmercury is excreted in the inorganic form. The site and mechanism of demethylation are still not well understood (3).

5. Effects on laboratory animals and in vitro test systems

Inorganic mercury

Short-term exposure

The toxic effects of inorganic mercury compounds are mainly in the kidney.
Lesions in the proximal tubular cells were detected after a single intraperitoneal injection of 1 µmol of mercury(II) chloride per kg of body weight (0.2 mg/kg of body weight as mercury) in male rats. Accumulation of mercury in the kidneys, however, indicated that the absorption efficiency was much greater than that expected from the gastrointestinal tract (9).

When rats were given mercury(II) chloride (3 mg/kg of body weight) by gavage twice a week for 60 days, examination by immunofluorescence showed that deposits for IgG were present in the renal glomeruli. Morphological lesions of the ileum and colon were also observed, with abnormal deposits of IgA in the basement membranes of the intestinal glands and of IgG in the basement membranes of the lamina propria (10).

When rats were exposed to mercury(II) chloride (1 mg/kg of body weight per day) by incubation or subcutaneous injection for up to 11 weeks, the rate of body weight gain decreased after 20 days, and actual weight loss occurred after 65–70 days. There were also neuropathological effects, first detected after 2 weeks, namely peripheral vacuolization of cells in the dorsal root ganglia, followed by the development of multiple small lesions in the ganglia (11).

A single dose of 1 mg/kg of body weight of mercury(II) chloride or methylmercury(II) chloride, either orally or by subcutaneous injection, resulted in leakage of dye into the nervous parenchyma within 12 h, indicating that these compounds can increase the permeability of the blood–brain barrier (11).

Long-term exposure

Rats injected subcutaneously 3 times weekly for up to 8 months with doses of inorganic mercury ranging from 0.05 to 2.5 mg/kg of body weight per injection (0.02–1.07 mg/kg of body weight per day) developed renal damage. This was characterized by an initial production of antiglomerular basement membrane antibodies, followed by the appearance of immune complex deposits in the glomerular tufts and small renal arteries accompanied by proteinuria and hypoalbuminaemia (12).

Reproductive toxicity, embryotoxicity, and teratogenicity

Controlled mating tests in which male mice were injected with single doses of mercury(II) chloride (1 mg of mercury per kg of body weight) showed a significant decrease in fertility as compared with controls (13). Normal fertility was restored after about 2 months.

Gradual changes in testicular tissues were noted in rats treated with mercury(II) chloride at doses of 0.05 or 0.1 mg/kg of body weight intraperitoneally over 90 days (14). There was a decrease in seminiferous tubule diameter, spermatogenic cell counts, and Leydig's cell nuclear diameter as compared with controls.

Of female hamsters given a total of 3–4 mg of mercuric chloride during the first estrous cycle, 60% did not ovulate by day 1 of the third cycle (15). Ovulation was inhibited in female hamsters injected with mercury(II) chloride at high doses (6.4 or 12.8 mg of mercury per kg of body weight) during day 1 of the estrous cycle (16). Female hamsters injected with 1 mg of mercury(II) chloride per day during one estrous cycle exhibited significantly higher levels of follicle-stimulating hormone in their pituitaries as compared with controls (17).

Pregnant Wistar rats were exposed intravenously to mercury(II) chloride on
different days of gestation. At mid-gestation, the minimum effective teratogenic dose of mercury (0.79 mg/kg of body weight) was high in relation to the maternal LD50, and the incidence of fetal malformations, mainly brain defects, was 23% in all live fetuses. In rats of different gestational ages, uptake of Hg2+ by the fetuses at this dose level decreased sharply between days 12 and 13 (18).

Organic mercury

Short-term exposure

In rats fed methylmercury dicyandiamide 5 days per week for 59 days, extensive damage to the renal cortex occurred with extensive inflammatory reaction surrounding the tubules and some early fibrosis even at the lowest dose of 0.6 mg/kg of body weight per day (19). Tubular degeneration of the kidney was also evident after subcutaneous injection of 10 mg/kg of body weight per day into rats for 7 consecutive days (20). In contrast to the effects of high doses of methylmercury on rats, kidney damage was not reported in cats exposed to 0.45 mg/kg of body weight (21) or in monkeys exposed to either 0.05 mg/kg of body weight per day (22) or to doses resulting in blood levels of up to 4 µg of mercury per ml of blood (23).

In cats, convulsions occurred after 60–83 days of exposure to 0.45 mg of methylmercury per kg of body weight per day; they were preceded 4–11 days earlier by progressive behavioural changes. Kittens were fed commercially available tuna contaminated with 0.3–0.5 mg of methylmercury(II) chloride per kg for 11 months. The total mercury intake over the period averaged 6.3 mg per cat or about 19 µg/day. Neurological disturbances were observed in three kittens after 7–11 months (24).

Squirrel monkeys were exposed for periods of up to 35 days to repeated oral doses of methylmercury(II) nitrate mixed in the food or by stomach tube. The threshold for both behavioural and central nervous system pathology occurred at blood mercury concentrations in the range 0.75–1.2 mg/litre (25).

Long-term exposure

In a study in which cats were fed methylmercury(II) chloride in a fish diet at doses of 0.003, 0.008, 0.020, 0.046, 0.074, or 0.176 mg/kg of body weight per day, 7 days a week for 2 years, detectable neurological impairment occurred in the group given 0.046 mg/kg of body weight per day after 60 weeks; this concentration was the lowest at which such impairment occurred. Pathological changes in the nervous system were restricted to the brain and dorsal root ganglia and were not seen at doses below 0.074 mg/kg of body weight per day (26).

Stumptail, pigtail, and squirrel monkeys were given methylmercury(II) chloride in food for periods in excess of 1000 days. This dosage regime was designed to maintain the blood mercury level at 1–4 mg/litre of blood. The critical effects seen were reduced sensitivity to visual stimuli at low luminescence and tremor on reaching for a small object. All monkeys with a blood concentration above 2 mg/litre developed symptoms with latent periods ranging from less than 20 to 200 days (23).

Cynomolgus monkeys were fed methylmercury from birth at doses of 0.05 mg/kg of body weight per day for 3–4 years. Blood concentrations of mercury peaked at 1.2–1.4 mg/litre, then declined after weaning to a steady level of 0.6–0.9 mg/litre. No overt signs of toxicity were noted but, when tested after 3–4 years, the monkeys exhibited impaired spatial vision under conditions of both high and low luminescence (22).

Reproductive toxicity, embryotoxicity, and teratogenicity

Mice were given single doses of 3.6, 5.3, 8, 12, 18, or 27 mg of methylmercury(II) chloride per kg of body weight at 9.5, 12.5, or 15.5 days post-fertilization (27). The trend among F1 females towards an adverse effect of dose on litter size, although not statistically significant, was in the direction to be expected if methylmercury(II) chloride can affect oogenesis in females exposed during fetal life.

A single dose of 2, 3, or 4 mg of mercury(II) ethanoate (about 1.3–2.5 mg of
mercury) was injected intravenously in three groups of female hamsters on day 8 of gestation (28). The exposed groups showed resorption frequencies of 12, 34, and 52%, respectively, as compared with 4% in the controls.

High doses of methylmercury given to pregnant rodents produced cleft palate (29,30). Prenatal exposure of rats can produce renal functional abnormalities detectable in offspring at 42 days of age (31).

Female rats were injected with 0, 6, or 10 mg of methylmercury(II) chloride per kg of body weight on gestational days 6–9 (32). Dams given 10 mg/kg of body weight either failed to give birth or the young were stillborn. External morphology was normal for rats given either of the two lower doses. Methylmercury produced hydrocephalus, decreased thickness of the cerebral cortex in the parietal section, and increased thickness of the hippocampus in the occipital section; with these exceptions, the brains of mercury-treated rats showed normal development.

Hamsters were given either 10 mg of methylmercury per kg of body weight on gestational day 10 or 2 mg/kg on gestational days 10–15 (33,34). In the neonatal cerebellar cortex, degenerative changes such as accumulation of lysosomes and areas of floccular cytoplasmic degradation were frequently observed in the neuroblast granular layer as well as in more differentiated neural elements in the molecular and internal granular layers. Pyknotic nuclei were seen singly and in groups throughout the external granular layer of treated animals. In the adult cerebellum, focal areas of astrogliosis were observed in the molecular layer of treated animals.

Mutagenicity and related end-points

Animal and cell culture studies confirm that methylmercury damages chromosomes if given orally at a dose of 5 mg/kg of body weight to pregnant mice (16,35), intraperitoneally at 2 mg/kg of body weight daily for 3 weeks to adult hamsters (36), and intraperitoneally at 10 mg/kg of body weight to ovulating Syrian hamsters (37). Methylmercury at low concentrations (0.05–0.1 µmol/litre) has been reported to interfere with gene expression in in vitro cultures of glioma cells (38). Non-disjunction and sex-linked recessive lethal mutations were induced in Drosophila melanogaster by treatment with methylmercury (39).

Carcinogenicity

Groups of mice were fed 15 or 30 mg of methylmercury per kg of diet for up to 78 weeks. The majority of the 30 mg/kg group died from neurotoxicity by week 26. Histopathological examination of kidney tissue from all animals surviving after 53 weeks revealed renal tumours in 13 of 16 males in the 15 mg/kg group. Of these, 11 were classified as adenocarcinomas and two as adenomas (40).

6. Effects on humans

Inorganic mercury

Acute exposure

Mercury will cause severe disruption of any tissue with which it comes into contact in sufficient concentration, but the two main effects of mercury poisoning are neurological and renal disturbances. The former is characteristic of poisoning by methyl- and ethylmercury(II) salts, in which liver and renal damage are of relatively little significance, the latter of poisoning by inorganic mercury.

In general, however, the ingestion of acute lethal toxic doses of any form of
mercury will result in the same terminal signs and symptoms, namely shock, cardiovascular collapse, acute renal failure, and severe gastrointestinal damage. Acute oral poisoning results primarily in haemorrhagic gastritis and colitis; the ultimate damage is to the kidney. Clinical symptoms of acute intoxication include pharyngitis, dysphagia, abdominal pain, nausea and vomiting, bloody diarrhoea, and shock. Later, swelling of the salivary glands, stomatitis, loosening of the teeth, nephritis, anuria, and hepatitis occur (41).

Ingestion of 500 mg of mercury(II) chloride causes severe poisoning and
sometimes death in humans (42). Acute effects result from the inhalation of air containing mercury vapour at concentrations in the range of 0.05–0.35 mg/m3 (43,44). Exposure for a few hours to 1–3 mg/m3 may give rise to pulmonary irritation and destruction of lung tissue and occasionally to central nervous system disorders (45).

Dermal exposure to alkyl mercurials may give rise to acute toxic dermatitis and eczematous changes.

Long-term exposure

Many studies involving the observation of more than 1000 individuals indicate that the classical signs and symptoms of elemental mercury vapour poisoning (objective tremors, mental disturbances, and gingivitis) may be expected to appear after chronic exposure to air mercury concentrations above 0.1 mg/m3 (8). Nonspecific neurological and physiological symptoms were also associated with lower exposure levels.

Considerable mercury exposure of children of workers at a thermometer plant has been reported (46). The median urine mercury level of 23 such children was 25 µg/litre as compared with 5 µg/litre in 39 controls. No signs of mercury intoxication were seen on clinical examination or reported by parents (3).

Organic mercury

The adverse health effects of occupational exposure to alkylmercury compounds constitute what is known as the Hunter-Russel syndrome (concentric constriction of the visual field, ataxia, dysarthria, etc.); this was seen in four workers exposed to methylmercury fungicide (47).

Methyl- and ethylmercury compounds have been the cause of the largest number of cases of mercury poisoning and of fatalities in the general population as a result of the consumption of contaminated fish or of bread prepared from cereals treated with alkylmercury fungicides. The earliest effects are nonspecific, e.g. paraesthesia, malaise, and blurred vision. These are followed by concentric constriction of the visual field, deafness, dysarthria, and ataxia. In the worst cases, the patient may go into coma and ultimately die. At high doses, methylmercury affects the peripheral nervous system in human subjects (48).

The two major epidemics of methylmercury poisoning in Japan, in Minamata Bay and in Niigata, both known as Minamata disease, were caused by the industrial release of methylmercury and other mercury compounds into Minamata Bay and into the Agano River, followed by accumulation of the mercury in edible fish. The maximum blood level of methylmercury without adverse health effects was estimated to be 0.33 µg/ml based on the epidemiological study of the Minamata disease endemic area (49). By 1971, a total of 269 cases of Minamata disease had been reported in Minamata and Niigata, of which 55 proved fatal. By March 1989, 2217 cases of Minamata disease had been officially recognized in Minamata and 911 cases in Niigata (50).

The largest recorded epidemic caused by the ingestion of contaminated bread prepared from wheat and other cereals treated with alkyl (methyl- or ethyl-) mercury fungicides took place in the winter of 1971–72 in Iraq, and resulted in the admission of over 6000 patients to hospital and over 500 deaths (51). Previous epidemics have occurred in Guatemala, Iraq, and Pakistan, and on a limited scale in other countries (3,8,52).

The Cree Indians of northern Quebec were also known to be exposed to methylmercury through the consumption of contaminated local fish. The relationship between measures of exposure and neurological abnormalities was studied in two communities. A positive association was found between neurological abnormalities and methylmercury exposure in both communities, but the relationship was statistically significant only in one of them (53,54).

The first indication of possible congenital Minamata disease was the unusual occurrence of cerebral palsy-like conditions in nine infants in the endemic areas (population about 1700) during 21 months. These infants had severe cerebral involvement (palsy and mental retardation); mild or no symptoms of poisoning were seen in their mothers, although there is a possibility that slight symptoms might have been overlooked (3).

According to an epidemiological study of an outbreak in Iraq, the clinical picture was dose-dependent. In those who were exposed to high maternal blood levels of methylmercury, the picture was one of cerebral palsy indistinguishable from that resulting from other causes (microcephaly, hyper-reflexia, and gross motor and mental impairment, associated with blindness or deafness). Milder forms were not easy to diagnose during the first few months of life, but became clearer with time. The cases showed mainly psychomotor impairment and persistence of pathological reflexes (53,55–57). The relationship between prenatal exposure to methylmercury and neurological and developmental abnormalities was also studied. Abnormality of the tendon reflex was positively associated with methylmercury exposure only in boys, without a dose–response relationship (58). Findings in the milder cases were quite similar to those associated with the minimal brain syndrome (3).

Marsh et al. (59) demonstrated a dose–response relationship between the deteriorated neurological score in children and the maximum mercury concentration during gestation in a single strand of maternal head hair.

7. Guideline value

Almost all mercury in uncontaminated drinking-water is thought to be in the form of Hg2+. Thus, it is unlikely that there is any direct risk of the intake of organic mercury compounds, and especially of alkymercurials, as a result of the ingestion of drinking-water. However, there is a real possibility that methylmercury will be converted into inorganic mercury.

In 1972, JECFA established a provisional tolerable weekly intake (PTWI) of 5 µg/kg of body weight of total mercury, of which no more than 3.3 µg/kg of body weight should be present as methylmercury (60). This PTWI was reaffirmed in 1978 (61). In 1988, JECFA reassessed methylmercury, as new data had become available; it confirmed the previously recommended PTWI for the general population, but noted that pregnant women and nursing mothers were likely to be at greater risk from the adverse effects of methylmercury. The available data were considered insufficient, however, to allow a specific methylmercury intake to be recommended for this population group (62,63).

To be on the conservative side, the PTWI for methylmercury was used to derive a guideline value for inorganic mercury in drinking-water. As the main exposure is from food, 10% of the PTWI was allocated to drinking-water. The guideline value for total mercury is 0.001 mg/litre (rounded figure).

References

1. Mercury—environmental aspects. Geneva, World Health Organization, 1989 (Environmental Health Criteria, No. 86).

2. Wood JM, Wang HK. Microbial resistance to heavy metals. Environmental science and technology, 1983, 17:82a-90a.

3. Methylmercury. Geneva, World Health Organization, 1990 (Environmental Health Criteria, No. 101).

4. International Organization for Standardization. Water quality—determination of total mercury by flameless atomic absorption spectrometry. Geneva, 1983, 1984 (ISO 5666-1,2:1983; -3:1984).

5. Ware GW, ed. Mercury. USEPA Office of Drinking Water health advisories. Reviews of environmental contamination and toxicology, 1989, 107:93-102.

6. Magara Y et al. Effects of volcanic activity on heavy metal concentration in deep well water. In: Technical Papers Water Nagoya '89; 7th Regional Conference and Exhibition of Asia-Pacific. International Water Supply Association, 1989:411-419.

7. Galal-Gorchev H. Dietary intake of pesticide residues, cadmium, mercury, and lead. Food additives and contaminants, 1991, 8:793-806. 8. Inorganic mercury. Geneva, World Health Organization, 1991 (Environmental Health Criteria, No. 118).

9. Miura K, Mori R, Imura N. Effects of selenium on mercury-induced renal lesions and on subcellular mercury distribution. Ecotoxicology and environmental safety, 1981, 5:351-367.

10. Andres P. IgA-IgG disease in the intestine of brown Norway rats ingesting mercuric chloride. Clinical immunology and immunopathology, 1984, 30:488-494.

11. Chang L, Hartmann HA. Blood–brain barrier dysfunction in experimental mercury intoxication. Acta neuropathologica, 1972, 21:179-184.

12. Makker SP, Aikawa M. Mesangial glomerulonephropathy with deposition of IgG, IgM and C3 induced by mercuric chloride. A new model. Laboratory investigation, 1979, 41:45-50.

13. Lee IP, Dixon RL. Effects of mercury on spermatogenesis studied by velocity sedimentation cell separation and serial mating. Journal of pharmacology and experimental therapeutics, 1975, 194:171-181.

14. Chowdhury AR et al. Histomorphometric and histochemical changes in the testicular tissues of rats treated with mercuric chloride. Biomedica biochimica acta, 1986, 45:949-956.

15. Lamperti AA, Printz RH. Localization, accumulation and toxic effects of mercuric chloride on the reproductive axis of the female hamster. Biology of reproduction, 1974, 11:180-186.

16. Watanabe T, Shimada T, Endo A. Effects of mercury compounds on ovulation and meiotic and mitotic chromosomes in female golden hamster. Teratology, 1982, 25:381-384.

17. Lamperti A, Niewenhuis R. The effects of mercury on the structure and function of the hypothalamo-pituitary axis in the hamster. Cell and tissue research, 1976, 170:315-324.

18. Holt D, Webb M. The toxicity and teratogenicity of mercuric mercury in the pregnant rat. Archives of toxicology, 1986, 58:243-248.

19. Magos L et al. Tissue levels of mercury in autopsy specimens of liver and kidney. Bulletin of the World Health Organization, 1976, 53(Suppl.):93-96.

20. Klein R et al. A model of acute methyl mercury intoxication in rats. Archives of pathology, 1972, 93:408-418.

21. Chang LW et al. Neurological changes in cats following long-term diet of mercury contaminated tuna. Acta neuropathologica (Berlin), 1974, 27:171-176.

22. Rice DC, Gilbert SG. Early chronic low-level methyl mercury poisoning in monkeys impairs spatial vision. Science, 1982, 216:759-761.

23. Evans HL, Garman RH, Weiss B. Methylmercury: exposure duration and regional distribution as determinants of neurotoxicity in non-human primates. Toxicology and applied pharmacology, 1977, 41:15-33.

24. Albaus L et al. Toxicity for cats of methyl mercury in contaminated fish from Swedish lakes and of methyl mercury hydroxide added to fish. Environmental research, 1972, 5:425-442.

25. Berlin MH, Nordberg G, Hellberg J. The uptake and distribution of methyl mercury in the brain of Saimari sciuresus in relation to behavioral and morphological changes. In: Miller MW, Clarkson TW, eds. Mercury, mercurials and mercaptans. Springfield, IL, Charles C. Thomas, 1973:187-205.

26. Charbonneau SM et al. Chronic toxicity of methyl mercury in the adult cat. Interim report. Toxicology, 1976, 5:337-349.

27. Gates AH, Doherty RA, Cox C. Reproduction and growth following prenatal methylmercuric chloride exposure in mice. Fundamental and applied toxicology, 1986, 7:486-493.

28. Gale TF, Ferm VH. Embryopathic effects of mercuric salts. Life sciences, 1971, 10:1341-1347.

29. Lee M et al. Effect of sodium selenite on methylmercury-induced cleft palate in the mouse. Environmental research, 1979, 19:39-48.

30. Harper K, Burns R, Erickson RP. Genetic aspects of the effects of methylmercury in mice:

the incidence of cleft palate and concentrations of adenosine 3':5' cyclic monophosphate in tongue and palatal shelf. Teratology, 1981, 23:397-401.
31. Smith MA. The effect of heavy metals on the cytoplasmic fine structure of Skeletonema costatum (Bacillariophyta). Protoplasma, 1983, 116:14-23.

32. Kutscher CL et al. Effects of the high methylmercury dose used in the collaborative behavioral teratology study on brain anatomy. Neurobehavioral toxicology and teratology, 1985, 7:775-777.

33. Reuhl KR, Chang LW, Townsend JW. Pathological effects of in utero methylmercury exposure on the cerebellum of the golden hamster. I. Early effects upon the neonatal cerebellar cortex. Environmental research, 1981, 26:281-306.

34. Reuhl KR, Chang LW, Townsend JW. Pathological effects of in utero methylmercury exposure on the cerebellum of the golden hamster. II. Residual effects on the adult cerebellum. Environmental research, 1981, 26:307-327.

35. Curle DC et al. Methylmercury toxicity: in vivo evaluation of teratogenesis and cytogenic changes. Anatomischer Anzeiger (Jena), 1983, 153:69-82.

36. Gilbert MM et al. Protective effect of vitamin E on genotoxicity of methylmercury. Journal of toxicology and environmental health, 1983, 12:767-773.

37. Mailhes JB. Methylmercury effects on Syrian hamster metaphase II oocyte chromosomes. Environmental mutagenesis, 1983, 5:679-686.

38. Ramanujam M, Prasad KM. Alterations in gene expression after chronic treatment of glioma cells in culture with methylmercuric chloride. Biochemical pharmacology, 1979, 28:2979-2984.

39. Magnusson J, Ramel G. Genetic variation in the susceptibility to mercury and other metal compounds in Drosophila melanogaster. Teratogenesis, carcinogenesis, and mutagenesis, 1986, 6:4.

40. Mitsumori K et al. Carcinogenicity of methylmercury chloride in ICR mice: preliminary note on renal carcinogens. Cancer letters, 1981, 12:305-310.

41. Stockinger HE. The metals. In: Clayton GD, Clayton FE, eds. Patty's industrial hygiene and toxicology, Vol. 2A, 3rd ed. New York, NY, John Wiley & Sons, 1981:1769-1792.

42. Bidstrup FL. Toxicity of mercury and its compounds. Amsterdam, Elsevier, 1964.

43. Neilsen-Kudsk F. Absorption of mercury vapour from the respiratory tract in man. Acta pharmacologica, 1972, 23:250.

44. Teisinger J, Fiserova-Bergerova V. Pulmonary retention and excretion of mercury vapours in man. Industrial medicine and surgery, 1965, 34:580.

45. Skerfving S, Vostal J. Symptoms and signs of intoxication. In: Friberg L, Vostal J, eds. Mercury in the environment. Cleveland, OH, CRC Press, 1972:93.

46. Hudson PJ et al. Elemental mercury exposure among children of thermometer plant workers. Pediatrics, 1987, 79:935-938.

47. Hunter D, Russel DS. Focal cerebral and cerebellar atrophy in a human subject to dose of organic mercury compounds. Journal of neurology, neurosurgery and psychiatry, 1954,17:235-241.

48. Rustam H et al. Evidence for a neuromuscular disorder in methylmercury poisoning. Archives of environmental health, 1975, 30:190-195.

49. Kitamura M. [Methylmercury accumulation in human tissues.] Advances in neurological sciences, 1974, 18:825-834 (in Japanese).

50. Japan Environmental Agency. Quality of the environment in Japan—1989. Tokyo, 1989:242-243.

51. Bakir F et al. Methylmercury poisoning in Iraq. Science, 1973, 181:230-241.

52. Greenwood MR. Methylmercury poisoning in Iraq. An epidemiological study of the 1971-1972 outbreak. Journal of applied toxicology, 1985, 5:148-159.

53. McKeown-Eyssen GE, Ruedy J, Neims A. Methylmercury exposure in northern Quebec. I. Neurologic findings in adults. American journal of epidemiology, 1983, 118:461-469.

54. McKeown-Eyssen GE, Ruedy J. Prevalence of neurological abnormality in Cree Indians exposed to methylmercury in northern Quebec. Clinical and investigative medicine, 1983, 6:161-169.

55. Marsh DO et al. Fetal methylmercury poisoning: New data on clinical and toxicological aspects. Transactions of the American Neurology Association, 1977, 102:69-71.

56. Marsh DO et al. Fetal methylmercury poisoning: clinical and toxicological data on 29 cases. Annals of neurology, 1980, 7:348-353.

57. Marsh DO et al. Dose-response relationship for human fetal exposure to methylmercury. Clinical toxicology, 1981, 18:1311-1318.

58. McKeown-Eyssen GE, Ruedy J, Neims A. Methyl mercury exposure in northern Quebec. II. Neurologic findings in children. American journal of epidemiology, 1983, 118:470-479.

59. Marsh DO et al. Fetal methylmercury poisoning, relationship between concentration in single strands of maternal hair and child effects. Archives of neurology, 1987, 44:1017-1022.

60. Evaluation of certain food additives and the contaminants mercury, lead, and cadmium: sixteenth report of the Joint FAO/WHO Expert Committee on Food Additives. Geneva, World Health Organization, 1972 (WHO Technical Report Series, No. 505).

61. Evaluation of certain food additives and contaminants: twenty-second report of the Joint FAO/WHO Expert Committee on Food Additives. Geneva, World Health Organization, 1978 (WHO Technical Report Series, No. 631).

62. Joint FAO/WHO Expert Committee on Food Additives. Toxicological evaluation of certain food additives and contaminants. Cambridge, Cambridge University Press,   1989:295-321 (WHO Food Additives Series, No. 24).

63. Evaluation of certain food additives and contaminants: thirty-third report of the Joint FAO/WHO Expert Committee on Food Additives. Geneva, World Health Organization, 1989 (WHO Technical Report Series, No. 776).

Back Home Up Next