|
Global
Mercury Assessment
CHAPTER 4
Current
mercury exposures and risk evaluations for
humans
4.1
Overview
259.
As mentioned earlier, the general population is primarily exposed to
methylmercury through the diet (especially fish) and to elemental mercury vapours due to dental amalgams. Depending on
local mercury pollution load, substantial additional contributions to the
intake of total mercury can occur through air and water. Also, personal
use of skin-lightening creams and soaps, mercury use for religious,
cultural and ritualistic purposes, the presence of mercury in some
traditional medicines (such as certain Traditional Asian remedies) and
mercury in the home or working environment can result in substantial
elevations of human mercury exposure. For example, elevated air levels in
homes have resulted from mercury spills from some old gas meters and other
types of spills. Also, elevated mercury levels in the working environment
have been reported for example in chlor-alkali
plants, mercury mines, thermometer factories, refineries and dental
clinics (WHO/IPCS, 1991), as well as in mining and manufacturing of gold
extracted with mercury. Additional exposures result from the use of
Thimerosal or Thiomersal (ethylmercury thiosalicylate) as a preservative
in some vaccines and other pharmaceuticals. The national submissions to
UNEP for this assessment indicate that the relative impacts of mercury
from local pollution, occupational exposure, certain cultural and
ritualistic practices, and some traditional medicines may today vary
considerably between countries and regions in the world, and are
significant in some regions.
260.
Examples of
data on total mercury and methylmercury exposures primarily from fish
diets, but also other sources in different parts of the world, including
Sweden, Finland, the USA, the Arctic, Japan, China, Indonesia, Papua New
Guinea, Thailand, Republic of Korea, Philippines, the Amazonas and French
Guyana are provided in section 4.4. For
example, in a study of a representative group of about 1700 women in the USA
(aged 16-49 years) for years 1999-2000, about 8 percent of the women had
mercury concentrations in blood and hair exceeding the levels
corresponding to the US EPA’s reference dose (an estimate of a safe
dose, see section 4.2.1). As shown in the chapter, data indicate exposures
are generally higher in Greenland, Japan and some other areas compared to
the USA. Other examples of human exposures exist and have been submitted
for use in this report. Unfortunately, it has not been possible to present
all submitted examples here.
261.
In some of
these countries and areas, local and regional mercury depositions have
affected the mercury contamination levels over the years and
countermeasures have been taken during the last decades to reduce national
emissions. Mercury emissions are, however, distributed over long distances
in the atmosphere and oceans. This means that even countries with minimal
mercury emissions, and other areas situated remotely from dense human
activity, may be adversely affected. For example, high mercury exposures
have been observed in the Arctic, far distances from any significant
sources of releases.
262.
Data on
mercury concentrations in fish have been submitted from a number of
nations and international organisations. Additionally, many investigations
of mercury levels in fish are reported in the literature. Submitted data,
giving examples of mercury concentrations in fish from various locations
in the world, are summarised for illustrative purposes in table 4.5. The
mercury concentrations in various fish species are generally from about
0.05 to 1.4 mg/kg depending on factors such as pH and redox potential of
the water, and species, age and size of the fish. Since mercury
biomagnifies in the aquatic food web, fish higher on the food chain (or of
higher trophic level) tend to have higher levels of mercury. Hence, large
predatory fish, such as king mackeral, pike, shark, swordfish, walleye,
barracuda, large tuna (as opposed to the small tuna usually used for
canned tuna), scabbard and marlin, as well as seals and toothed whales,
contain the highest concentrations. The available data indicate that
mercury is present all over the globe (especially in fish) in
concentrations that adversely affect human beings and wildlife. These
levels have led to consumption advisories in a number of countries (for
fish, and sometimes marine mammals), warning people, especially sensitive
subgroups (such as pregnant women and young children), to limit or avoid
consumption of certain types of fish from various waterbodies. Moderate
consumption of fish (with low mercury levels) is not likely to result in
exposures of concern. However, people who consume higher amounts of
contaminated fish or marine mammals may be highly exposed to mercury and
are therefore at risk.
4.2
Evaluations of exposure levels causing risks
4.2.1
Methylmercury
263.
As mentioned,
intake of methylmercury in fish and other aquatic foods is considered the
most serious general impact on humans. Based on risk assessments and other
societal considerations, several countries and international organisations
have established risk evaluation tools such as levels of daily or weekly
methylmercury or mercury intakes considered safe (Reference Dose and
Provisional Tolerable Weekly Intake), limits/guidelines for maximum
concentrations in fish and fish consumption advisories.
264.
Table 4.1
gives an overview of examples of maximum allowed or recommended levels of
mercury in fish in various countries (based on submissions to UNEP, unless
otherwise noted). Also, examples of tolerable intake levels of mercury or
methylmercury are mentioned.
Table
4.1
Examples of maximum allowed or recommended levels of mercury (Hg)
in fish in various
countries and by WHO/FAO (based on submissions to UNEP,
unless otherwise noted).
|
|
Country/
Organization
|
Fish
type
|
Maximum
allowed/recommend levels in fish *1
|
Type
of
measure
|
Tolerable
intake levels
*1
|
|
Australia
|
Fish
known to contain high levels of mercury, such as swordfish,
southern bluefin tuna, barramundi, ling, orange roughy, rays,
shark
|
1.0 mg Hg/kg
|
The
Australian Food Standards Code
|
Tolerable
Weekly Intake: 2.8 µg Hg/kg body weight per week for pregnant
women.
|
|
All
other species of fish and crustaceans and molluscs
|
0.5 mg Hg/kg
|
|
Canada
|
All
fish except shark, swordfish or fresh or frozen tuna (expressed as
total mercury in the edible portion of fish)
|
0.5 ppm total Hg
|
Guidelines/
Tolerances of Various Chemical Contaminants in Canada
|
Provisional
Tolerable Daily Intake: 0.47 µg Hg/kg body weight per day for
most of the population and 0.2 µg Hg/kg body weight per day for
women of child-bearing age and young children
|
|
Maximum
allowable limit for those who consume large amounts of fish, such
as Aboriginal people
|
0.2 ppm total Hg
|
|
China
|
Freshwater
fish
|
0.30 mg/kg
|
Sanitation
standards for food
|
|
|
Croatia
|
Fresh
fish
Predatory
fish
(tuna, swordfish, molluscs, crustaceans)
|
1.0 mg Hg/kg
0.8 mg methylHg/kg
|
Rules
on quantities of pesticides, toxins, mycotoxins, metals and
histamines and similar substances that can be found in the food
…..
|
|
|
All
other species of fish
|
0.5 mg Hg/kg
0.4 mg methylHg/kg
|
|
Canned
fish (tin package)
Predatory
fish
(tuna, swordfish, molluscs, crustaceans)
|
1.5 mg Hg/kg
1.0 mg methylHg/kg
|
|
All
other species of fish
|
0.8 mg Hg/kg
0.5 mg methylHg/kg
|
|
European Community *2
|
Fishery
products, with the exception of those listed below.
|
0.5 mg Hg/kg
wet weight
|
Various
Commission decisions, regulations and Directives
|
|
|
Anglerfish,
atlantic catfish, bass, blue ling, bonito, eel, halibut, little
tuna, marlin, pike, plain bonito, portuguese dogfish, rays,
redfish, sail fish, scabbard fish, shark (all species), snake
mackerel, sturgeon, swordfish and tuna.
|
1 mg Hg/kg
wet weight
|
|
Georgia
|
Fish (freshwater) and fishery products
|
0.3 mg Hg/kg
|
Georgian
Food Quality Standards 2001
|
|
|
Fish (Black Sea)
|
0.5 mg Hg/kg
|
|
Caviar
|
0.2 mg Hg/kg
|
|
India
|
Fish
|
0.5 ppm total Hg
|
Tolerance
Guidelines
|
|
|
Japan
|
Fish
|
0.4 ppm total Hg/kg
0.3 ppm methylHg (as a reference)
|
Food
Sanitation Law - Provisional regulatory standard for fish and
shellfish
|
Provisional
Tolerable Weekly Intake: 0.17 mg methylHg (0.4 mg/kg
body weight per day) (Nakagawa et al., 1997).
|
|
Korea, Republic of
|
Fish
|
0.5 mg Hg/kg
|
Food
Act 2000
|
|
|
Mauritius
|
Fish
|
1 ppm Hg
|
Food
Act 2000
|
|
|
Philippines
|
Fish
(except for predatory)
|
0.5 mg methylHg /kg
|
Codex Alimentarius
|
|
|
Predatory
fish (shark, tuna, swordfish)
|
1 mg
methylHg/kg
|
|
Slovak
Republic
|
Freshwater
non-predatory fish and products thereof
Freshwater
predatory fish
Marine
non-predatory fish and products thereof
Marine
predatory fish
|
0.1 mg total Hg/kg
0.5 mg total Hg/kg
0.5 mg total Hg/kg
1.0 mg total Hg/kg
|
Slovak
Food Code
|
|
|
Thailand
|
Seafood
|
0.5 mg
Hg/g
|
Food Containing Contaminant Standard
|
|
|
Other
food
|
0.02 mg
Hg/g
|
|
United
Kingdom
|
Fish
|
0.3 mg Hg/kg
(wet flesh)
|
European
Statutory Standard
|
|
|
United
States
|
Fish,
shellfish and other aquatic animals (FDA)
|
1 ppm methylHg
|
FDA
action level
|
US
EPA reference dose: 0.1 mg
methylHg/kg body weight per day
|
|
States,
tribes and territories are responsible for issuing fish
consumption advise for locally-caught fish; Trigger level for many
state health departments:
|
0.5 ppm methylHg
|
Local
trigger level
|
|
WHO/FAO
|
All
fish except predatory fish
|
0.5 mg
methylHg/kg
|
FAO/WHO
Codex Alimentarius guideline level
|
JECFA
provisional tolerable weekly intake:
3.3 µg methylHg/kg body weight per week
(NOTE - Revised in 2003: More information here) .
|
|
Predatory
fish (such as shark, swordfish, tuna, pike and others)
|
1 mg
methylHg/kg
|
|
|
Note:
1 Units as used
in references. “mg/kg” equals “µg/g”
and ppm (parts per million). It is assumed here that fish limit values not
mentioned as “wet weight” or “wet flesh” are most likely also
based on wet weight, as this is normally the case for analysis on fish for
consumers.
2
The European Commission has recently (February 2002) revised the
previous maximum limit values for mercury in a small number of specific
fish species for consumption (Commission Regulation No 221/2002 of 6
February 2002). These changes are not reflected in the table.
Recent
risk evaluation process in USA
265.
Three
comprehensive risk evaluations on methylmercury were recently completed in
the USA by the Environmental Protection
Agency (EPA), the Agency for Toxics Substances and Disease Registry (ATSDR)
and the National Research Council (NRC). All three are summarized here
with greater detail given for the EPA evaluation, as it is a very recent
comprehensive evaluation and presents one example of a scientific approach
to estimate a safe exposure level.
266.
The
earlier-mentioned NRC evaluation was initiated by the EPA upon the request
of the US Congress, and it is has been part of a major effort by the EPA
to review the available toxicological findings on methylmercury as a basis
for a re-evaluation of the EPA reference dose (RfD). The RfD is generally
defined as an “estimate (with uncertainty spanning perhaps an order of
magnitude) of a daily exposure to the human population (including
sensitive subgroups) that is likely to be without an appreciable risk of
deleterious effects during a lifetime.” The methylmercury RfD is used by
the EPA to evaluate the potential for adverse health effects from exposure
to methylmercury for humans as well as establishing guidance for fish
consumption advisories (NRC, 2000; NIEHS, 1998; US EPA, 1997).
267.
The RfD is a
daily intake of methylmercury for which
“exposures” (intake) at or below the RfD are expected to be
safe. The risks following exposures above the RfD are uncertain, but risk
increases as exposure to methylmercury increases above the RfD (US EPA,
1997). In 1995, an RfD was set by the EPA on the basis of neurological
effects observed on children exposed prenatally (in the mothers womb) to
methylmercury in the poisoning incidence in Iraq (epidemiological data
transformed by calculations from observed mercury concentrations in
maternal hair to daily intakes – divided by a safety factor of 10 due to
biological variability and insufficient data on reproductive effects on
adults). The NRC evaluation committee concluded in 2000 that the value of
the US EPA's RfD for methylmercury, 0.1 micrograms of methylmercury per
kilogram body weight per day, “is a scientifically justifiable level for
the protection of public health". However, the committee recommended
that the above-mentioned results from the Faroe Islands study should be
used for the US EPA's determination of a new RfD instead of the Iraq study
(NRC, 2000). The NRC recommended an uncertainty factor (UF) of not less
than 10 to account for variability in human kinetics (i.e.,
pharmacokinetics) and sensitivity of the fetus’ brain to methylmercury.
The NRC review and the studies were again reviewed by an external expert
panel, and then the US EPA evaluation was presented in 2001 (US EPA,
2001b), as part of a water quality criterion.
268.
The US EPA
evaluation includes a thorough analysis of the relevant studies,
especially those conducted on children from the Faroe Islands and the
Seychelles islands. Since the results from these two studies disagree, the
merits and weaknesses of the studies were discussed, as well as possible
reasons for the conflicting results. Both studies were considered being of
high quality, and no serious flaws could be detected. In this situation,
the US EPA decided to use data from the Faroe Islands study (which showed
a negative effect on neurological development related to methylmercury
exposures) as the starting point to derive the RfD. Similar results from
the smaller New Zealand study as well as some later cross-sectional
studies from other parts of the world, contributed to this conclusion.
269.
The current RfD was derived from a benchmark dose (BMD) divided by an
uncertainty factor of 10. The BMD analysis used was based on the lower 95
percent confidence limit for a 5 percent effect level (above background)
applying a linear model to dose-response data based on cord blood mercury.
The cord blood data were converted to maternal intakes. Several of the
neuropsychological tests used, and also an integrated analysis gave
similar results with respect to benchmark doses.
Most of these endpoints yielded RfDs of about 0.1 µg/kg
body weight per day (comm-24-gov). Overall, the
EPA RfD was primarily based on a number of neurological endpoints and
the weight of evidence from the Faroe Islands and the New Zealand study,
plus an integrated analysis of those two studies plus the Seychelles
study. Other models for the benchmark analyses are possible (Budtz-Jørgensen
et al., 2000) and resulted in
lower benchmark dose limits, but the linear model was considered the most
appropriate one (Pirrone et al.,
2001). The US EPA chose an uncertainty factor of 10 accounting for
pharmacokinetic inter-individual variability, gaps of knowledge on
possible long term effects, and uncertainty concerning the relationships
between cord and maternal blood mercury concentration, and as mentioned,
the US EPA’s current RfD was set at 0.1 µg/kg body weight per day
(US EPA, 2001b, and Pirrone et al.,
2001). A daily average
methylmercury intake of 0.1 µg/kg
body weight per day by an adult woman is estimated to result in hair
mercury concentrations of about 1 µg/g,
cord blood levels of about 5 to 6 µg/l
and blood mercury concentrations of about 4-5 µg/l.
However, there are limitations, uncertainties and variability in
these estimates. These estimates were derived from data and methods presented
in US ATSDR, 1999; NRC, 2000; US EPA, 2001b and US EPA, 1997.
270.
Based on an
average daily intake of 17.5 gram of fish, the US EPA also calculated a
Tissue Residue Criterion of 0.3 mg methylmercury per kg of fish (0.3
mg/kg). This limit is weighted on all fish and shellfish consumed. For
higher intakes, a lower limit would be needed. Additionally, US EPA
calculated a set of recommendations for fish consumption limits based on
the above mentioned risk assessment, see table 4.2 (US EPA, 2001b).
271.
Consumption
limits have been calculated as the number of allowable fish meals per
month based on the ranges of methylmercury in the consumed fish tissue.
For example, when methylmercury levels in fish tissue are 0.4 mg/kg, then
two 0.23 kg meals per month can safely be consumed. The following
assumptions were used to calculate the consumption limits:
-
Consumer
adult body weight of 72 kg (less meals recommended if lower body
weight);
-
Average
fish meal size of 0.23 kg;
-
Time-averaging
period of 1 month (30.44 d);
-
EPA's
reference dose for methylmercury (0.1 µg/kg
body weight per day)
from EPA’s Water Quality Criterion for the Protection of Human
Health: Methylmercury (US EPA, 2001b).
Table
4.2
US EPA’s monthly fish consumption limits for methylmercury (US
EPA, 2001b).
|
Max.
number of fish meals/month
|
Fish
tissue concentrations
(ppm = mg/kg, wet weight)
|
|
16
|
>
0.03–0.06
|
|
12
|
>
0.06–0.08
|
|
8
|
>
0.08–0.12
|
|
4
|
>
0.12–0.24
|
|
3
|
>
0.24–0.32
|
|
2
|
>
0.32–0.48
|
|
1
|
>
0.48–0.97
|
|
0.5
|
>
0.97–1.9
|
|
None
(<0.5)*
|
>
1.9
|
* None = No consumption recommended.
>
means “above” (example ”> 0.06–0.08” means: “above 0.06 to
0.08”) |
|
272.
Using an alternative approach, the US ATSDR developed its current
Minimal Risk Level (MRL) of 0.3 µg/kg body weight per day for
methylmercury using the Seychelles Child Development Data (US ATSDR,
1999). The MRL is an estimate of the level of human exposure to a
chemical that does not entail appreciable risk of adverse non-cancer
health effects. They are intended for use by the public health officials
as screening tools to determine when further evaluation of potential
human exposure at hazardous waste sites is warranted.
Europe
273.
Guidelines
for maximum mercury concentrations in fish and consumption advice vary
somewhat among the European countries. In 2001, a group of European
scientists evaluated the risks from mercury exposure in Europe and
presented their view in this regard in their “Position Paper on
Mercury” (Pirrone et al.,
2001). Regarding methylmercury, they recommended that the US EPA
reference dose should apply in Europe also, stating that:
”We
share the view of the recent evaluations by the US EPA and NRC. No new
information has emerged that would change the risk assessment. Moreover,
the considerations made for the USA will be valid also for the European
population. We therefore consider the US EPA RfD of 0.1 µg per kg body
weight (and day) to be appropriate for Europe. It should be noted that
it is mainly relevant for fertile women, and that it includes an
uncertainty factor.
The
reference dose will be exceeded if a substantial amount of fish,
contaminated with mercury, is ingested. As an example, if the weekly
intake is about 100 g (one typical fish meal per week) of fish with >
0.4 mg/kg, the RfD will be exceeded. This suggests that fish mercury
levels should be kept below this limit.
Fish
is, however, a valuable part of the diet, in adults as well as in
children, and a source of e.g. protein, vitamin E, selenium, and omega 3
fatty acids. At high consumption of fish with low levels of mercury,
like in the Seychelles Islands, the advantages and disadvantages may
counterbalance each other. Because of the beneficial effects of fish
consumption, the long-term aim is not to replace fish in the diet by
other foods, but to reduce the methylmercury concentrations in fish. If
this is not possible, dietary restrictions with respect to fish with
high levels of methylmercury should be advised for pregnant women.”
274.
An
additional overview of some toxicological reference values (and briefs
on their background) from a number of countries, and covering a few more
mercury compounds, is given in the document “Compilation of
toxicological and environmental data on chemicals – mercury and its
derivates” (INERIS, 2000) submitted by France (can be viewed from
UNEP’s GMA home page, link: http://www.chem.unep.ch/mercury/gov-sub/Sub49govatt18.pdf).
275.
The current
EU limits for mercury in fish can be tightened for health reasons in
individual member countries. Thus, some EU member states have lower
limits than required by the directive. Because of high mercury
concentrations in fish, certain lakes and rivers are closed to sports
fishing, e.g., in Sweden. In
addition, EU member states such as Denmark, Finland, Sweden and the
United Kingdom, address specific advisories to sensitive populations.
These can include women who are pregnant, plan to become pregnant, or
who breast-feed, and children, in regard to avoiding or limiting the
intake of fish species where the EU limit of 1 mg/kg applies
(Finnish National Authority for Foodstuff, 2002)
UN
Organizations
276.
The Joint FAO/WHO
Expert Committee on Food Additives (JECFA) established a provisional
tolerable weekly intake (PTWI) of 200 µg (equivalent to 3.3 µg/kg
body weight) for methylmercury in 1978, which was confirmed in 1988. In
1999, the Committee evaluated the Faroe Islands and Seychelles studies
available at that time, as well as new neurodevelopmental toxicity
studies in animals, and concluded that the studies did not provide
consistent evidence of neurodevelopmental effects in children of mothers
whose intake of methylmercury yielded hair burdens of 20 µg/g
or less. The Committee could not evaluate the risks for the complex and
subtle neurological end-points used in these studies that would be
associated with lower intakes. In the absence of any clear indication of
a consistent risk in these recent studies, the Committee recommended
that methylmercury be re-evaluated when the 96-month evaluation of the
Seychelles cohort and other relevant data that may become available can
be considered. The Committee thus did not revise the PTWI of 3.3 µg/kg
body weight. (Note: Since publication of this report, this
PTWI has been revised. For more information, click here.)
4.2.2
Elemental mercury vapour and inorganic mercury compounds
277.
For mercury vapour, studies of occupationally exposed humans have shown
slight adverse effects on the central nervous system and kidneys at
long-term air levels of 25-30 µg/m3 or equivalent
urinary mercury levels of 30-35 µg/g creatinine. Based on the LOAEL
for effect on the central nervous system, the US EPA determined a
reference concentration (RfC) for mercury vapour of 0.3 µg/m3
for the general population (US EPA, 1997). The RfC took into account a
conversion from occupational exposure to continuous exposure for the
general population, lack of data on reproductive effects, the use of a
LOAEL instead of a NOAEL, and susceptible subgroups. The US ATSDR
established a minimum risk level (MRL) of 0.2 µg/m3,
also based on the occupational data.
Using the ATSDR document as the source document, and
complementing the information with further studies on adverse effects
observed among workers exposed to mercury vapour, and on studies on the
relationship between concentrations of mercury in urine/blood of exposed
workers and in the breathing zone air, IPCS identified 0.2 µg/m3
as a guidance value for long-term inhalation exposure of the general
public to metallic mercury vapour (WHO/IPCS, 2002).
278.
In the
European Position Paper on mercury (Pirrone et
al., 2001) it was concluded that – under European conditions –
human exposure to elemental mercury in ambient air is generally
negligible. As mentioned elsewhere, the case may be different in regions
with higher direct air pollution loads. The following risk evaluation
was presented:
“For
mercury vapour, studies of occupationally exposed humans have shown
slight adverse effects on the central nervous system and kidneys, and
probably also on the thyroid, at long-term air levels of 25-30 µg/m3
or equivalent urinary mercury levels of 30-35 µg/g creatinine. The US
EPA determined a reference concentration (RfC) for mercury vapour of 0.3
µg/m3 for the general population (US EPA, 1997). Recent
studies suggested that the limit for adverse effects (LOAEL) in
occupationally exposed subjects may be lower than indicated above. There
is no universal agreement on which uncertainty factors to use. In
ongoing work on a EU position paper on arsenic, cadmium, and nickel,
factors of 5-10 were used for similar conversion from occupational
exposure to continuous exposure, factors of 5-10 for the use of a LOAEL,
and a factor of 10 for variation of susceptibility. The total factor was
500. A similar procedure would result in a limit value for elemental
mercury of 0.05 µg/m3. We propose the use of 25 µg/m3
as starting point, a factor of 10 for continuous exposure of the general
population during a whole life-time, and uncertainty factors of 5 for
the use of a LOAEL and 10 for individual susceptibility. The proposed
limit value will then be 0.05 µg/m3, as an annual average.
This air level is rarely exceeded in ambient air in Europe, however. A
typical daily absorbed dose would be 0.6-0.8 µg of mercury for adults.
Exposure to elemental mercury from dental amalgam in most cases
represents a much higher daily uptake than this level would give rise to
(WHO/IPCS, 1991).”
279.
Studies on exposed humans do not provide sufficient information to
derive acceptable intakes for inorganic mercury compounds; therefore,
based on No adverse effects and lowest adverse effects in medium- and
long-term animal experiments, ATSDR and IPCS derived a guidance value of
0.2 µg/kg body weight per day for inorganic mercury compounds (US
ATSDR, 1999; WHO/IPCS, 2002).
4.3
Routes of mercury exposure – a general overview
280.
As mentioned above, the general population is primarily exposed to
methylmercury through the diet (especially fish) and to elemental
mercury vapours due to dental amalgams.
281.
Human
exposure to the three major forms of mercury present in the environment
is summarised in table 4.3 in section 4.3.1. Although the choice of
values given is somewhat arbitrary, this table nevertheless provides a
perspective on the relative magnitude of the contributions from various
media. Humans may be exposed to additional quantities of mercury
occupationally and in heavily polluted areas, and to additional forms of
mercury, e.g. to aryl and alkoxyaryl compounds, which are still used as
fungicides in some countries. The following paragraphs present general
contributions to human mercury exposure in a bit more detail, as
reviewed by Pirrone et al.
(2001), except for the text on occupational exposure.
Elemental
mercury vapour from ambient air and dental fillings
282.
Regarding
vapour of metallic mercury, dental fillings, and to a lesser extent, the
ambient air, represent the two major sources of human exposure for the
general population. From the atmosphere the daily amount absorbed as a
result of respiratory exposure into the bloodstream in adults is about
32 ng mercury in rural areas and about 160 ng mercury in urban
areas, assuming rural concentrations of 2 ng/m3 and
urban concentrations of 10 ng/m3 (absorption rate 80
percent).
283.
Local
contributions from airborne mercury may vary greatly depending on
emissions from local sources. For example, the Indian submission
(sub71govatt1) reports observed elevated mercury exposure in an area
influenced heavily by emissions from thermal power plants. Another
example is the submission of the Slovak Republic reporting ambient air
concentration in urban areas in Slovakia in the range of 1.7 – 20 ng/m3
(geometric mean 4.57 ng/m3) and in industrial areas in the
range of 1.5–40 ng/m3 (geometric mean 5.28 ng/m3),
with the highest levels in areas with metallurgic industry and coal
combustion (Hladiková et al.,
2001, as presented in sub10gov). Elevated
air levels may also occur downwind from some types of emissions sources
such as chlor-alkali plants.
284.
Release of mercury from amalgam fillings has been reviewed by Clarkson
et al. (1988). It was concluded that amalgam surfaces release mercury
vapour into the mouth, and this is the predominant source of human
exposure to elemental mercury in the general population. Depending upon
the number of amalgam fillings, the estimated average daily absorption
of mercury vapour from dental fillings vary between 3 and 17 µg mercury
(WHO/IPCS, 1991; Clarkson et al., 1988; Skare and Engqvist, 1994). In
rare cases the blood mercury levels due to dental amalgam may be as high
as 20 µg/l (Barregard et al. 1995, as quoted by Pirrone et al., 2001).
Effects of exposure from dental amalgam has been widely discussed and
reviewed (US Public Health Service, 1993, as quoted by Pirrone et al.,
2001; and others). However,
the Working Group for this Global Mercury Assessment, in line with its
mandate, focused on environmental exposures to mercury and their adverse
effects on health, and did not review or assess the potential effects of
exposures to elemental mercury vapour from dental amalgams or the
possible conversion to other mercury forms in the body.
Moreover, the Working Group did not reach any con-clusions about
whether or not dental amalgams cause adverse effects.
Indoor
non-occupational air exposure
285.
Very little data are available on non-occupational indoor human exposure
due to mercury vapour. However, fatalities and severe poisonings have
resulted from heating metallic mercury and mercury-containing objects in
the home. Also, incubators used to house premature infants have been
found to contain mercury vapour at levels approaching occupational
threshold limit values; the source was mercury droplets from broken
mercury thermostats. In addition, significant
exposures can occur due to use of metallic mercury in religious, ethnic,
or ritualistic practices. Exposures can occur during the practice and
afterwards from contaminated indoor air. A few of the activities
reported that result in human mercury exposures include sprinkling
elemental mercury in homes or cars, mixing mercury in bath water or
perfume or placing mercury in candles (US ATSDR, 1999).
286.
Indoor air mercury levels can also become elevated due to leaks from
central-heating thermostats and by the use of vacuum cleaners after
thermometer breakage and other spills. Another
source of exposure to mercury vapor has been the
release of mercury from paint containing mercury compounds used to
prolong shelf-life of interior latex paint, in which levels of 0.3-1.5
µg
Hg/m3 (Beusterien et al.,
1991) have been reported. However,
as explained in other sections of this report, the use of mercury in
paints has decreased substantially in many nations of the world,
therefore this source of exposure may be less common today than it was
10-30 years ago.
Drinking
water
287.
Mercury in
drinking water is usually in the range of 0.5-100 nanograms of mercury
per litre of water (ng Hg/l), the average value being about 25 ng Hg/l.
The forms of mercury in drinking water are not well studied, but Hg(II)
is probably the predominant species present as complexes and chelates
with ligands. The resulting intake from drinking water is about 50 ng
mercury per day, mainly as Hg(II); only a small fraction is absorbed.
There are reports of methylmercury in drinking water under some
conditions. It is, however, considered to be quite unusual (USA;
comm-24-gov).
Intake
from foods
288.
Concentrations
of mercury in most foodstuffs are often below the detection limit
(usually 20 ng Hg per gram fresh weight) (US EPA, 1997). Fish and
marine mammals are the dominant sources, mainly in the form of
methylmercury compounds (70-90 percent or more of the total). The normal
mercury concentrations in edible tissues of various species of fish
cover a wide range, generally from 0.05 to 1.400 mg/kg fresh wet weight
depending on factors such as pH and redox potential of the water,
species, age and size of the fish (see sections 4.4 and 4.5). Large
predatory fish, such as king mackeral, pike, shark, swordfish, walleye,
barracuda, scabbard and marlin, as well as seals and toothed whales,
contain the highest average concentrations. While large tuna typically
have levels of mercury that are similar to other large predatory fish,
data indicate that the levels usually seen in canned tuna are
substantially lower. This results from the fact that the tuna currently
used for canned tuna are those of smaller size.
289.
The intake
of mercury depends not only on the level of mercury in fish, but also
the amount consumed. Thus, many governments have provided dietary advice
to consumers to limit consumption where levels are elevated.
Fish consumption advisories typically take into account suspected
concentrations, amount of fish - or canned fish - consumed and patterns
of consumption.
290.
Intake of fish and fish products, averaged over months or weeks, results
in an average daily absorption of methylmercury variously estimated (in
the 1970's) to be between 2 and 4.7 µg
mercury (WHO/IPCS, 1976). The absorption of inorganic mercury from
foodstuffs is difficult to estimate because levels of total mercury are
close to the limit of detection in many food items and the chemical
species and ligand binding of mercury have not usually been identified.
The average daily intake of total dietary mercury has been
measured over a number of years for various age groups. The intake of
total dietary mercury (µg/day) measured during a market basket survey
(1984-1986) of the Food and Drug Administration (FDA) in the USA (WHO/IPCS,
1990), according to age group was: 0.31 µg
(6-11 months); 0.9 µg
(2 years) and 2-3 µg
in adults. In Belgium, two surveys estimated the total mercury intake
from all foodstuffs to vary between 6.5 µg
and 13 µg
mercury (Fouasuin and Fondu, 1978; Buchet et
al., 1983).
Occupational
exposure
291.
Mercury in
the working environment can lead to elevated exposures. As described in
chapter 3 on human toxicology, a significant amount of the knowledge on
the toxic effects of mercury and its compounds has been attained through
the investigation of occupational exposures. Depending on the types of
occupational activity and extent of implemented protective measures, the
severity of effects may range from the subtlest disturbances to serious
damages and death. Occupational exposures can happen in virtually all
working environments where mercury is produced, used in processes or
incorporated in products. Occupational exposure has been reported from
– among others – chlor-alkali plants, mercury mines, mercury-based
gold extraction, processing and sales, thermometer factories, dental
clinics with poor mercury handling practices and production of
mercury-based chemicals (US ATSDR, 1999).
292.
In many
countries a general improvement of protection against occupational
exposure has taken place during the last decades by introduction of a
range of working environment improvements including more closed
manufacturing systems, better ventilation, safe handling procedures,
personal protection equipment and through substitution of mercury-based
technologies. This does, however, not seem to be a universal
development, and many workers may still be exposed to mercury levels
causing risks.
293.
An example
of the potential for improvements through implementation of such
improvements and substitutions is that reported by Zavaris (1994)
concerning mercury concentrations in employees exposed to mercury in
specific industries: chlor-alkali, electric light bulbs, batteries and
control instruments. Initially about 17 percent of the workers exceeded
the legal limits for mercury in urine. After subsequent improvement in
the working environment, and in some cases substitution of the
mercury-based technology, in the industries involved, more than 98
percent of urinary levels had returned to the range of normal levels
(abstracts of occupational exposure and industrial
protection/substitution studies submitted by Brazil, sub66govatt6).
294.
A UNIDO
study has reported on the effects of mercury intoxication in the
gold-mining area of Diwalwal, dominated by Mount Diwata (also known as
Mt. Diwalwal), on the island of Mindanao - one of the major islands of
the Philippines. At the time of the study, more than 70 percent (73 of
102) of the occupationally exposed population suffered from chronic
mercury intoxication. Among the occupational sub-group of amalgam
smelter workers the percentage was even higher – 85.4 percent. Of the
non-occupationally exposed population in the area of Mt. Diwata and
downstream, approximately one-third (55 of 163) showed signs of chronic
mercury intoxication, including such classical symptoms as memory
problems, restlessness, loss of weight, fatigue, tremor, sensory
disturbances, and bluish discolouration of the gums (Böse-O’Reilly et
al., 2000).
Other
exposures
295.
Exposure to
organic mercury, inorganic mercury or elemental mercury might occur
through the use of mercury-containing skin-lightning creams, some
traditional medicines, ritualistic uses, and certain pharmaceuticals (US
ATSDR, 1999; Pelclova et al., 2002). For example, thimerosal (ethylmercury
thiosalicylate), also known as thiomersal, is used for preservation of
some types of vaccines and immunoglobulins in parts of the world.
Significant exposures can also occur from use of some Traditional
Chinese Medicines or Traditional Asian Medicines (Ernst and Coon 2001;
Koh and Woo, 2000; Garvey et al., 2001).
1.3.1
Estimated Average Exposures
296.
The WHO
(1990) estimated the daily intake of each form of mercury as shown in
table 4.3. For details on the methodology and assumptions used, see
original reference. This table presents average estimated intakes for
the different routes of exposure. However, exposures vary considerably
across populations. For example, people who consume greater amounts of
mercury-contaminated fish will obviously have greater exposures to
methylmercury than those shown in the table.
Table
4.3
Estimated average daily intake and retention in the body
(retention given in brackets) of
different mercury forms in a scenario
relevant for the general population not
occupationally exposed to
mercury, values in µg/day
(WHO/IPCS, 1991; for more details,
consult reference).
|
|
|
Elemental
Hg vapour
|
Inorganic
Hg
compounds
|
Methylmercury
|
|
Air
|
0.03
(0.024)*
|
0.002
(0.001)
|
0.008
(0.0069)
|
|
Dental
amalgams
|
3.8-21
(3-17)
|
0
|
0
|
|
-
fish
-
non-fish
|
0
|
0.60
(0.042)
3.6
(0.25)
|
2.4
(2.3)**
0
|
|
Drinking
water
|
0
|
0.050
(0.0035)
|
0
|
|
Total
|
3.9-21
(3.1-17)
|
4.3
(0.3)
|
2.41
(2.31)
|
|
|
Note: The data in brackets represent retained part of mercury input in the
body of an adult.
* If
the concentration is assumed to be 15 ng/m3 in an urban area,
the figure would be
0.3 (0.24) µg/day.
**
Assumes 100 g of fish per week with the mercury concentration of
0.2 mg/kg.
297.
When
relating the intakes of the different mercury species in table 4.3, it
should be remembered that their toxic impacts varies.
Therefore, it is not contradictory that the methylmercury intakes
are lower than other mercury intakes, but still generally constitute the
major adverse impact on humans from mercury compounds.
1.3.2
General aspects of dietary mercury intake
298.
Daily intakes and retention of mercury from food is difficult to
estimate accurately. In most food stuff mercury concentration is below
20 µg/kg. Mercury is known to bioconcentrate in aquatic organisms and it
is biomagnified in aquatic food webs.
For example, the concentration of mercury in small fish at low
food web level (such as anchovies) is below 0.085 mg/kg, while in
swordfish, shark and tuna values above 1.2 mg/kg are frequently reported
(WHO/IPCS, 1991). In Scandinavian predatory fresh-water fish (perch and
pike) average levels are about 0.5 mg/kg.
299.
The use of
fishmeal as the feed for poultry and other animals used for human
consumption may result in increased levels of mercury. In Germany, the
poultry contains 0.03 - 0.04 mg/kg. Cattle are able to demethylate
mercury in the rumen, and therefore, beef meat and milk contain very low
concentrations of mercury.
300.
One of the
major problems to accurately estimate daily intakes of various mercury
forms from diet is that national survey programmes mainly report total
mercury concentrations and the percentage of mercury as methylmercury is
not known. Total mercury daily intakes reported in various countries are
given in table 4.4. In some
national surveys the percentage of mercury originating from fish is
provided. It is assumed that in this foodstuff (fish) the percentage of
methylmercury is from 60 to 90 percent. Therefore fish and fish products
represent the major source of methylmercury. It may be concluded that in
those areas where fish consumption represent a considerable part of
diet, exposures could be considerably higher than the value of the US
EPA RfD.
|
|
Table
4.4
Selected estimates of the typical daily intake of mercury from
dietary sources in a
selection of countries (as presented by Pirrone et
al., 2001).
|
Country
|
Intake
(µg/day)
|
References
|
|
Belgium
|
All
food: 13 of which 2.9 is from fish
All
foodstuff: 6.5
|
Fouassin
and Fondu, 1978
Buchet
et al., 1983
|
|
Poland
|
5.08
( age group 1-6 years)
5.43 (age group 6-18 years)
15.8
in adults
From
fish: 7% of total dietary intake
|
Szprengier-Juszkiewicz,
1988
Nabrzyski
and Gajewska, 1984
|
|
Germany
|
0.8
from fish
0.2 from food (except fish and vegetables)
|
LAI,
1996
|
|
Croatia
|
From
fish: 27.7 (total Hg)
20.8 ( MeHg form)
|
Buzina
et al., 1995
|
|
Spain
|
4-8
(60-90 % from seafood)
in Valencia only 27% is from the seafood
18
of which about 10 is from fish (Basque country)
|
Moreiras
et al., 1996
Urieta
et al., 1996
|
|
Sweden
|
1.8
(market-basket)
|
Becker
and Kumpulainen, 1991
|
|
United
Kingdom
|
2
|
MAFF,
1994
|
|
Finland
|
2
|
Kumpulainen
and Tahvonen, 1989
|
|
The
Netherlands
|
0.7
|
Van
Dokkum et al., 1989
|
|
Czech
Rep.
|
0.7
|
Ruprich,
1995
|
|
Brazil
|
315
– 448 (Amazon, Medeira river)
|
Boishio
and Henshel, 2000
|
|
Japan
|
10
6.9
–11.0
24
(18 as MeHg)
|
Tsuda
et al., 1995
Ikarashi
et al., 1996
Nakagawa
et al., 1997
|
|
|
301.
Pirrone
et al. (2001) give the following
conclusion regarding the general exposure pattern in Europe:
“Mercury
vapour is a risk of decreasing importance in Europe, as
mercury-containing thermometers and other instruments are being
phased-out, and the emissions from the chlor-alkali industry have
decreased. In addition, only one mercury mine remains in operation in
Europe today. New developments in dental technology have resulted in
filling materials that can substitute amalgam for many purposes.
The
methylmercury risk will depend on the dietary habits and local sources
of contaminated fish and seafood. The substantial exposures documented
in the Faroe Islands, Greenland and other northern populations are
mainly due to ingestion of marine mammals. The extent of this problem
within Europe is therefore limited. However, a study from the island of
Madeira showed that the consumption of local black scabbard resulted in
average methylmercury exposures that were even higher than on the Faroe
Islands. Similarly, evidence on mercury in seafood from the Tyrrhenian
Sea have shown concentration levels which overlap with those present in
pilot whale meat. Thus, excess exposures occur in Europe and may reach
or even exceed levels observed in populations in which adverse effects
on brain development have been documented. “
302.
This
conclusion may possibly apply to large parts of the western world.
4.4
Exposure through diets of fish and marine mammals
303.
In the
following sections, examples of data on methylmercury exposure from fish
diets in different parts of the world are presented: Sweden, Finland,
USA, the Arctic, Japan, China, Indonesia, Papua New Guinea, Thailand,
Republic of Korea, the Amazonas and French Guyana. In some of these
countries or areas mercury depositions have affected mercury
contamination levels over years, and countermeasures have been set in
during the last decades to reduce national emissions. Mercury emissions
are, however, distributed over long distances in the atmosphere and by
the oceans. This means that even countries with minimal local and
national mercury emissions, and other areas situated remotely from dense
human activity, may very well be similarly affected. For example, high
mercury exposures have been observed in the Arctic, far distances from
any significant sources of releases.
304.
Data on
mercury concentrations in fish have been submitted from a number of
nations and international organisations. Additionally, many
investigations of mercury levels in fish are reported in the literature.
Submitted data giving examples of mercury concentrations in fish from
various locations in the world are summarised in this chapter. The
overview illustrates that mercury is present all over the globe in
concentrations that may affect human beings and wildlife.
4.4.1
Exposure from fish diet in Sweden and Finland
305.
According to von Rein and Hylander (2000), fish has traditionally been
an important part of the diet in Sweden thanks to a long coastline and
many lakes and rivers. Today, because of mercury contents in the fish,
detailed recommendations for the consumption are given for fresh water
fish such as pike, perch, pike-perch, burbot and eel. Women of
childbearing age are recommended not to eat these fish from Swedish
lakes at all, and the rest of the population should not eat them more
than once a week. Based on comprehensive data sets, it has been
estimated that in about 50 percent
of the approximately 100,000 Swedish lakes, pike (1 kg size) contain
mercury levels above the international WHO/FAO limit of 0.5 mg
mercury/kg wet weight, and in 10 percent of the lakes pike contains over 1 mg/kg wet weight
(Lindquist et al., 1991). It
has been calculated that the mercury deposition in Sweden must decrease
by 80 percent from the level
of the late 1980's in order to reduce the mercury content in Swedish
fish to below 0.5 mg mercury/kg wet weight. The emissions to air from
point sources in Sweden itself have decreased to about 1 metric ton/year
from peak values in the 1960's of around 30 metric tons/year, and
releases to water have been reduced similarly (Naturvårdsverket, 1991).
Most of the present mercury deposition in Sweden originates from
long-range atmospheric transport from other countries (Håkansson and
Andersson, 1990; Iverfeldt et al.,
1995). This means that in order to meet the 80 percent reduction goal,
emissions from Europe and other parts of the Northern hemisphere must
also be reduced further. There are indications of recent reductions in
deposition, and during the last few decades a general decrease of about
20 percent has been observed
in mercury concentrations in fish in Sweden (Johansson et al., 2001).
306.
Also in Finland, the accumulation of mercury in fish has been studied
during several decades (Louekari et
al., 1994). In the late 1960's about 10-15
percent of the lakes and coastal waters in Finland were affected
by elevated mercury concentrations mainly caused by direct aqueous
releases from pulp and paper industry and (related) mercury-based chlor-alkali
production. Average concentrations of mercury in northern pike in these
freshwaters and brackish coastal waters averaged as much as 1.52 mg/kg
wet weight at that time. Since the abandonment of the use of mercury
compounds for slimicides in paper production in Finland in 1968 and
decreasing demand for chlorine in the same industry, releases of mercury
have been reduced significantly. In 1990 average concentrations in pike
in these waters had decreased to 0.60 mg mercury/kg wet weight
(concentrations in pikes in freshwaters were generally higher than in
brackish waters). Louekari
et al. (1994) combined these findings with
dietary surveys and calculated estimated daily intakes of mercury in
different consumer segments, and the relative influence of pike/fish
consumption. In 1967/68, mercury intakes of the farmer segment known to
be most depending on locally caught fish were estimated at 22 μg
mercury/day in the areas with elevated mercury contamination. Similar
intakes in 1990 were estimated at 15 μg mercury/day. For office
employees, who consume less locally caught fish, corresponding intakes
were 13 and 8 μg mercury/day.
307.
The mercury
concentration limit of 0.5 mg/kg in fish, recommended by WHO/FAO, is
exceeded for one-kilo pike (Esox
lucius) in 85 per cent of the lakes in southern and central Finland
(22,000 lakes), (Lindquist et al., 1991; Verta 1990; all in Pirrone et al., 2001).
4.4.2
Exposure from fish diet in the USA
308.
In the
mid-1990’s the US EPA estimated from comprehensive national dietary
surveys that up to 5 percent of women in the child bearing age (ages 15-44 years) in
the USA consumed 100 grams of fish and shellfish per day or more. WHO
recommends "special considerations" regarding mercury exposure
for persons eating more than 100 g/day. Furthermore, the US EPA
calculated from the same dietary surveys combined with average total
mercury concentrations in the species of fish consumed, that 7
percent of US women in the child-bearing age may exceed the
exposure of the US EPA RfD (see section 4.2.1). A recent study (by the
US Centers for Disease Control and Prevention) of mercury concentrations
measured in blood and hair in a representative group of women aged 16-49
in the USA (about 1700 women) confirmed these calculations, as
approximately 8 percent of the women had hair and blood mercury levels
exceeding the levels corresponding to the US EPA RfD (CDC, 2001; Schober
et al., 2003). The CDC also collected hair and blood samples for
year 2002, but these results are not yet available. Moreover, the CDC
plans to continue the blood measurements in future years, but the hair
samples are not planned after year 2002.
309.
The US EPA
noted that the calculated results reflected the average choice of fish
species, and that "consumption of fish with mercury levels higher
than average may pose a significant source of methylmercury exposure to
consumers of such fish" (elevated mercury concentrations have been
measured in fish in quite a number of freshwater bodies in the USA). The
US EPA concluded in their risk characterisation that "most USA
consumers need not be concerned about their exposure to mercury",
but the exposure of "those who regularly and frequently consume
large amounts of fish" (especially species with high mercury
concentrations), may be of concern (US EPA, 1997).
310.
In the USA,
fish advisories (consumption recommendations) have been issued for
mercury in one or more freshwater bodies in 41 states, and 13 states
have issued statewide mercury fish advisories. Mercury is the most
frequent basis for fish advisories in the USA, representing 79 percent
of all advisories (as of December 2000; US EPA, 2001a). The US EPA has
presented a set of general recommendations for fish consumption. For
example, fish with mercury concentrations ranging from 0.48 -0.97 mg
methylmercury/kg wet weight should be eaten no more than once a month
and with 0.97 - 1.9 mg/kg wet weight only every second month, whereas
fish containing more than 1.9 mg/kg wet weight should not be eaten at
all (US EPA, 2001a); see table 4.2 in section 4.2.1 above.
311.
Fish sold in
commerce in the USA are under the jurisdiction of the Food and Drug
Administration (FDA), which issues action levels for concentration of
mercury in fish and shellfish. The current FDA action level (as per
1998) is 1 ppm (1 mg/kg) total mercury based on a consideration of
health impacts. As illustrated in table 4.5 in section 4.5, US
freshwater fish can have mercury levels which exceed the FDA action
limit of 1 ppm. The levels
in some marine species such as shark, swordfish, and king mackeral are
also typically this high. The
concentration of methylmercury in commercially important marine species
is on average close to ten times lower than the FDA action level in the
USA. Mercury levels in marine fish have been monitored by the National
Marine Fisheries Service for at least 20 years. The data in marine fish
have shown mercury levels over this time to be relatively constant in
various species. Comparable trends data for freshwater fish do not
exist, although there are data for coastal and estuarine sites (US EPA,
1997).
312.
See also the
description of Canadian experiences related to mercury in aquatic
ecosystems, including a map showing national fish mercury
concentrations, in section 5.3.
4.4.3
Exposure from marine diet in the Arctic
313.
The
comprehensive AMAP (1998) assessment report on arctic pollution issues
describes the high exposures of the Arctic population.
AMAP and other Arctic Council activities relevant to mercury
cover the whole of the Arctic region, and mercury is a priority
substance for assessment and abatement initiatives for the Council.
Here, examples of mercury exposure in Greenland are given.
314.
As for much
of the population in the region, the diet in Greenland is to a high
degree composed of marine mammals and also fish. The traditional
Greenlandic diet is also a very important part of the Greenlandic
culture and identity.
315.
The concentration and distribution of mercury in humans in Greenland
have been thoroughly studied in the last 15 years. Surveys have been
performed in adults, pregnant women and newborn babies in most parts of
Greenland including both hunting districts and more densely populated
areas. In all regions studied, the determining factors for mercury
exposure were the daily intake of meat from marine mammals. At a
regional level, the blood mercury concentrations were directly
proportional to the registered number of seals caught (and consumed),
indicating that mercury concentration in meat is probably similar in all
regions of Greenland (Hansen, 1990). In adults, whole blood
concentrations of mercury are lowest in the Southwest and increasing
towards the North where the intake of marine mammals is higher – see
figure 4.1.
Figure
4.1
Distribution (in percentiles) of whole blood mercury
concentrations in four regions in
Greenland and in Greenlanders living
in Denmark (AMAP, 1998, based on 1988
measurements). Original figure
presented courtesy of AMAP, Norway.
316.
In North Greenland, 16 percent of the adult population studied had blood
mercury concentrations exceeding 200 µg/l, which is the level regarded
by WHO as the minimum toxic blood concentration in non-pregnant adults (AMAP,
1998). More than 80 percent
of the population in North Greenland exceeded 50 µg/l blood (Hansen and
Pedersen, 1986), which almost corresponds to the benchmark dose level
from the US NRC report (2000). Blood levels of 200 µg/l are
approximately the level expected to occur following a daily average
intake of about 4 µg methylmercury per kg body weight per day. Likewise,
a daily intake of about 1 µg methylmercury per kg body weight per day is
expected to result in blood mercury levels of about 50 µg/l and hair
mercury levels of about 10 µg/g (US EPA, 1997; US ATSDR, 1999).
317.
In a small set of 20 paired samples of maternal and umbilical cord blood
taken under the AMAP programme, the mean concentrations were 24.2 and
53.8 µg/l, respectively. This level is very close to the NRC (2000)
benchmark dose level (58 µg/l) based on the NRC evaluation of the Faroe
Islands studies (see section 3.2.1).
318.
As of 1997,
no disease or symptoms had been registered which could be unequivocally
related to environmental contaminant exposure in Greenland (AMAP, 1998).
However, it should be noted that this can generally not be done for
environmental contaminants because of its complexity, except in cases of
extreme acute or sub-acute exposure. Furthermore, at that time
measurements of more subtle neurological and reproductive effects had
not yet taken place in Greenland. A recent study suggested
exposure-related neurobehavioral deficits in Inuit children in Qaanaaq,
Greenland, but the study was too small to provide solid statistical
significance of the associations (Weihe et al., 2002).
319.
The
traditional marine diet on Greenland and in parts of Arctic Canada has
very positive nutritional qualities and is not readily replaced with
other foods. Dietary advice from the Canadian Government states that the
positive health benefits of a traditional northern marine diet outweigh
the known risks associated with consumption of these foods. However, it
is clear that the risks associated with this diet increase with
increasing levels of methylmercury contamination. It is further
important to note that, beyond the physical benefits associated with the
traditional diet, it also plays an important role in the social and
cultural life of indigenous communities in the North.
320.
As
mentioned above, the investigation of mercury exposure and effects on
the Faroe Islands on the border of the Arctic area has been extensive,
and subtle neurological effects have been shown on children at low
prenatal exposure levels, see description in section 3.2.1 above.
321.
The Arctic
Council and the substantial coverage of mercury in its monitoring and
assessment programme (AMAP) and its current action plan (ACAP) are
described in section 9.5.1.
4.4.4
Examples from Asia
China,
Japan and Indonesia
322.
Feng et
al. (1998) investigated total mercury and
methylmercury concentrations in scalp hair of 243 male persons in three
areas of the Tokushima Prefecture, Japan as well as in 64 males of the
Chinese city Harbin and 55 males in the Indonesian city Medan (all
subjects were randomly chosen males aged 40-49 years). They found the
highest concentrations in subjects living in a seaside area reported to
be without local direct anthropogenic contamination. Total mercury
concentrations here ranged from 1.7-24 µg/g hair (mean 6.2 µg/g, 78
subjects), thus close to and exceeding the adverse effect benchmark
level of about 10 µg/g maternal hair derived from the Faroe Islands
studies (see section 3.2). The mean concentration for all three
investigated areas in Japan was only slightly lower: 4.6 µg/g hair (243
subjects).
323.
In Japan, where the diet is relatively high in fish and shellfish,
methylmercury constituted large parts of the total mercury measured, and
there was a high correlation between concentrations of methylmercury and
total mercury, underlining that a marine diet was the major contributor
to mercury exposure. Feng
et al. (1998)
quote the Japan General Affairs Department for 1996 dietary surveys
estimating average national consumption of fish and shellfish at 107
g/day per person, being the third highest consumption rates among 23
countries investigated.
324.
In the industrial cities of Harbin, China, and Medan, Indonesia, Feng et
al. (1998) found lower mean total mercury concentrations (means 1.7
µg/g and 3.1 µg/g hair respectively). In both of these places
methylmercury concentrations were lower – even for subjects with high
total mercury concentrations - and correlation between methylmercury and
total mercury concentrations was low, indicating that these subjects
were mainly exposed to elemental or inorganic mercury from other
sources.
Papua
New Guinea
325.
Feng et
al. (1998) quotes Suzuki (1991) for
mercury hair concentration levels found in residents of three villages
in Papua New Guinea not influenced by local direct anthropogenic
contamination. The highest concentrations were found in the seaside
village Dorogi with means at 4.1 and 4.4 µg/g hair for males and females
respectively, while concentrations were slightly lower in a riverside
village 6 kilometres from the coast and lowest in a village 25
kilometres from the coast.
Thailand
326.
For
Thailand, the national submission (sub53gov) quotes Menasveta (1993) for
an average national fish consumption rate of 61 g/day per person for
Thai people (with average weight 60 kg). There is no study on hazards
from methylmercury exposure of the Thai population.
Philippines
327.
The average estimated
national fish consumption rate is 75 g/person per day, and the average
person weighs 60 kg. Also, the exposures described in the study by UNIDO
(described in section 4.3 above) on mercury intoxication on the island
of Mindanao (a gold-mining area) are probably partially due to exposures
through the diet, especially for the non-occupationally burdened part of
the population downstream from Mt. Divalwal, where approximately a third
(55 of 163) are intoxicated (Global Mercury Assessment Working Group -
Philippines delegation, 2002).
Republic
of Korea
328.
According
to the national submission from the Republic of Korea, the supply of
fish amounted to between 74 and 94 g fish/day per person in this country
in the years 1996-1999 (Republic of Korea submission, sub76govatt2).
4.4.5
Exposure from fish diet in the Amazonas and French Guyana, South
America
329.
Several
studies in the Amazonas have reported elevated exposures to
methylmercury and total mercury in fish dependent populations in and
around areas affected by mercury-based gold extraction.
330.
Some
studies in the Amazonas have shown adverse effects from mercury exposure
on humans. For example, in the Tapajós river community of Brazil,
cognitive deficits have recently been reported in 7-year children who
were exposed, in uterus, to mercury levels corresponding to maternal
hair mercury levels below 10 µg/g
hair (Malm et al., 1999, as
quoted the in Brazilian submission sub66govatt2A). Quite a number of
studies have investigated exposures and toxic impacts from mercury in
individual areas affected by gold mining activities in the Amazonas. The
Ministry of Health, Brazil, reports to be in the process of reviewing
the available exposure data from the Amazon area with fish consumption
and mercury concentration in fish as focal points (sub66govatt2A). The
Ministry has also submitted a list of a large number of references
relevant to the impacts of mercury in the Amazon (sub66govatt2B).
331.
Akagi and Naganuma (2000) used separate measurements of methylmercury
and total mercury to distinguish between exposures through an aquatic
diet and direct exposures of elemental mercury from gold extraction
activities. They found methylmercury concentrations exceeding the
adverse effects level for adults of 50 µg/g in hair in 3.2 percent of
the 559 inhabitants surveyed, with the highest individual level being
132 µg/g. These values are substantially higher than the adverse effect
benchmark level of 10 µg/g maternal hair derived from the Faroe Islands
studies (see section 3.2.1).
332.
Vasconcellos et
al. (1998) determined total mercury
concentrations in scalp hair in 13 of the 17 tribes of Indians
inhabiting the Xingu Park in the Brazilian Amazon. In six of the
investigated groups methylmercury concentrations in hair were also
measured. Geometrical means for total mercury concentrations varied
among the tribes in the range of 3.2-21 µg/g hair, but most group means
were between 10 and 20 µg/g. In the tribes where methylmercury was also
measured, methylmercury comprised nearly all of the mercury found in the
hair samples. In the same study, three groups of inhabitants in the
Brazilian State of Amapá were also investigated. Total mercury in hair
versus numbers of fish meals per week are shown in figure 4.2 - first
for a region not affected directly by gold extraction (figure 4.2 a) and
then for another region which is affected by gold extraction (figure 4.2
b).
|
a)
Total mercury concentrations in hair versus fish consumption –
region of Serra do Navio, State of Amapá, Brazil (not directly
affected by gold extraction)
b)
Total mercury concentrations in hair versus fish consumption –
region of Vila Nova, State of Amapá, Brazil
(directly affected by gold extraction)
|

|
Figure
4.2
Total mercury concentrations in hair vs fish consumption in two
regions of the State of
Amapá, Brazil (from Vasconcellos
et al., 1998, submitted by Brazil,
sub68govatt1)
333.
Some researchers have considered if gold extraction alone could explain
the observed mercury contamination levels in the Amazonas area. Other
mercury sources mentioned are volcanic contributions and increased
mobilisation due to deforestation and other sources of soil erosion
(based on USA, comm-24-gov, 2002).
French
Guyana
334.
A study
undertaken by Fréry et al.
(1999) among the Wayana people in the higher area of the Maroni River,
French Guyana, whose diet is based mainly on fish, confirmed mercury
exposure due to consumption of river fish contaminated by mercury from
gold extraction activities. Of 242 fish samples analysed, 14.5 percent
had mercury levels over 0.5 mg/kg (with a high of 1.62 mg/kg). Based on
the Wayana’s fish consumption patterns, adults were found to consume
between 40 and 60 µg total mercury per day, nursing infants
approximately 3 µg per day, children between 1 and 3 years of age 7 µg
per day, between 3 and 6 years approximately 15 µg per day and between
10 and 15 years between 28 and 40 µg per day. Over half of the
population had hair mercury levels over the WHO recommended level of 10 µg total mercury/g, with an average of 11.4
µg/g. (Mercury levels in the
population of Guyana are approximately 3 µg/g and 1.7 µg/g in
people from urban areas.)
4.5
Submitted data on mercury concentrations in fish
335.
Information
on mercury concentrations in fish in different parts of the world has
been chosen in this report as an indicator illustrating the presence of
mercury in the global environment. Data on mercury concentrations in
fish have been submitted from a number of nations and international
organisations. Additionally, many investigations of mercury levels in
fish are reported in the literature. Submitted data giving examples of
mercury concentrations in fish from various locations in the world are
summarised in table 4.5. The available data illustrate that mercury is
present all over the globe in concentrations that may affect human
beings and wildlife.
336.
As an
illustration of how the observed concentration levels are related to
potential adverse effect levels, concentrations
at or exceeding 0.3 mg/kg wet weight – the US EPA Tissue Residue
Criterion (at 17.5 gram fish intake/day) and the Japanese guideline
value (see section 4.2.1) – have been marked
in bold text in the table. These values represent the most recent
comprehensive risk assessments regarding mercury exposure from fish
diets. As mentioned in table 4.1, FAO/WHO Codex Alimentarius guideline
levels for fish are 0.5 mg/kg wet weight for non-predators and 1 mg/kg
wet weight for predators (such as shark, swordfish, tuna, pike and
others).
Table
4.5 Examples of mercury concentrations in fish/shellfish in different
regions of the world, as
reported in submissions to the Global Mercury
Assessment. Sample collection, treatment,
and analysis methodology may
vary and may have affected results. Consult references for
details.
|
|
Geographic location
|
Fish and shellfish species
|
Concentration (-level) *3
ww: Wet weight *4
dw: dry weight *5
|
Year of sampling
|
Trophic level
*1
|
Contami-
nation
level
in habitat *2
|
References
|
|
Arctic area
|
Marine fish
|
0.01 - 0.1 mg/kg ww
Peaks: 0.1 - 0.9 mg/kg ww
|
Various
|
|
|
AMAP, 1998
|
|
Marine mussels
|
<0.009 - 0.033 mg/kg ww
|
Various
|
|
|
|
Australia
(southwest Tasmania)
|
Australian eel (Lake Gordon)
|
0.86 – 2.15 mg/kg
(mean 1.40 mg/kg, 9
samples)
|
1994
|
|
|
Bowles, 1998, in National submission from
Australia, sub63gov
|
|
Brown trout (Lake Pedder)
|
0.06 –
0.3 mg/kg
(mean 0.16 mg/kg, 20 samples)
|
1993
|
|
|
|
Brown trout (Lake Gordon)
|
0.1 – 1.4
mg/kg
(mean 0.35 mg/kg, 20
samples)
|
1994
|
|
|
|
Brown trout (Gordon River)
|
0.3 – 2.35 mg/kg
(mean 1.09 mg/kg, 25 samples)
|
1993
|
|
|
|
Redfin perch (Lake Gordon)
|
0.12 – 1.3
mg/kg
(mean 0.52 mg/kg, 20
samples)
|
1993
|
|
|
|
Baltic Sea
|
Round fish
|
0.010-0.050 mg/kg ww
|
1994-1998
|
|
Back
|
ICES, 1997, in Helcom, 2001
|
|
Marine fish
|
0.016 - 0.091 mg/kg ww (muscle, all
investigated species).
|
|
Gen
|
|
Blue mussel
|
0.005 - 0.010 mg/kg ww
|
Non
|
Back
|
|
Blue mussel
|
Slightly exceeding 0.01 mg/kg ww
|
|
Gen
|
|
Brazil
|
46 species from six
trophic levels:
|
|
1991-1993
|
|
|
Boischio and Henshel, 2000
|
|
Herbivore/Denitrivore
|
0.10/0.15 mg/kg (ww)
|
|
|
|
Planktophagus/Omnivore I
|
0.36/0.21 mg/kg (ww)
|
|
|
|
Omnivore II/Piscuvore
|
0.55/0.64 mg/kg (ww)
|
|
|
Brazil
(Amazonas)
|
River fish from pristine areas
|
Lower than 0.2 mg/kg ww of Hg
|
1990's
|
|
Back
|
Malm, as contained in NIMD Forum, 2001, in
national submission from Japan (sub6govatt1)
|
|
Predatory fish from contaminated areas (main
mined Amazonas river basin)
|
Can reach levels of
2 – 6 mg/kg or
more,
Average values above 0.5
mg/kg
|
Pre
|
Con
|
|
Côte d’Ivoire
|
Tuna species, “Thon
Albacore” (Thunnus Albacares)
Large individuals (80-91
kg):
|
0.30 - 0,36 mg/kg ww
0.8 mg/kg ww (muscle)
|
1991
|
Pre
|
Gen
|
National submission from Côte d’Ivoire
(sub72gov)
|
|
Sole, “sole”
|
0.064 - 0,090 mg/kg ww
|
Non
|
Gen
|
|
Herring, “hareng”
|
0.037 - 0,047 mg/kg ww
|
Non
|
Gen
|
|
Cyprus
|
Sword fish
|
0.20 - 2.00
mg/kg ww
(mean 0.54 of 21
samples)
|
1993-1997
|
Pre
|
Gen
|
National submission from Cyprus (about 15
species reported in all)
|
|
Sea bream
|
0.00 - 2.00
mg/kg ww
(mean 0.38 of 42
samples)
|
|
Gen
|
|
Red mullet
|
0.00 - 0.70
mg/kg ww
(mean 0.11 of 15 samples)
|
Non
|
Gen
|
|
Common dentex (dentex
dentex)
|
0.00 - 2.00
mg/kg ww
(mean 0.51 of 20 samples)
|
|
Gen
|
|
Fiji
|
Shellfish (Crassostrea
mordax)
|
<0.001-0.061 mg/kg ww
|
1987/88
|
|
Back
|
Naidu et al., 1991
|
|
Shellfish (Crassostrea
mordax)
|
0.55-0.95 mg/kg dw
|
1988
|
|
Con
|
Naidu and Morrison,
1994
|
|
Shellfish (Grafarium
tumidum)
|
0.05-0.20 mg/kg dw
|
1985/86
|
|
Back
|
Gangaiya et al.,
1988
|
|
Shellfish (Anadara
spp.)
|
0.037-0.099 mg/kg dw
|
1992/93
|
|
Back
|
Morrison et al.,
2001
|
|
Canned tuna
|
0.01-0.97 mg/kg ww
|
1990/92
|
|
?
|
IAS, 1992
|
|
Finland
|
Northern pike in freshwater and brackish
coastal waters
|
1.52 mg/kg ww of Hg
(average concentration)
|
1960's
|
|
|
Submission from the Nordic Council
of Ministers, sub84gov
|
|
0.60 mg/kg ww of Hg
(average concentration)
|
1990
|
|
|
|
France
|
Mussels
(369 samples from 96 sampling stations along
the coast of France
|
0.008 – 0.238 mg methylHg/kg dry weight
(mean 0.064 mg/kg dry weight)
|
1996
|
|
|
Claisse et al., 2001, in
national submission from France, sub49gov
|
|
Fish, Atlantic Sea:
Conger
Merlu
Rousette
|
1.2 +/- 0.3 mg/kg dw
0.4 +/- 0.1 mg/kg dw
2.0 +/- 0.6 mg/kg dw
|
|
|
|
Cossa, 1994 in national submission from France
(sub49gov).
|
|
Fish, Mediterranean Sea:
Conger
Merlu
Rousette
|
4.5 +/- 2.8 mg/kg dw
3.2 +/- 2.1 mg/kg dw
9.4 +/- 5.2 mg/kg dw
|
|
|
|
|
Fish caught in Baltic and North
Sea, English Channel, Atlantic Ocean)
Swordfish
(Xiphias gladius)
Shark
(Lamna sp.)
Red tuna
(Thunnus thynnus)
|
Mean 0.780 mg/kg ww
(41 samples)
Mean 0.692 mg/kg ww
(497 samples)
Mean 0.470 mg/kg ww
(344 samples)
|
1971 – 1980
|
|
|
Thibaud, 1992 in national submission from France (sub49gov)
|
|
Ghana
|
River species: Mostly “tilapia” (tilapia
guineensis) and “catfish” (heterobranchus spp.)
|
General: 0,55
- 1,59 mg/kg ww
Tilapia, mean: 1,17
mg/kg ww (of 8 fish)
|
2000
|
|
Con
|
National submission from Ghana and UNIDO report
sub2igoatt6part2
|
|
Guam
|
Fish
|
0.009-0.045 mg/kg
ww
|
|
|
Back
|
Denton et al.,
2001
|
|
Hong Kong
|
Mud carp (Cirrhinus
molitorella)
|
0.025 mg/kg ww
|
1995
|
|
|
Dickman and Leung, 1998
|
|
Freshwater grouper (Micropterus sp.)
|
0.195 mg/kg ww
|
|
Golden thread (Nemipterus virgatus)
|
0.219 mg/kg ww
|
|
Hair tail (Trichiurus
haumela)
|
0.146 mg/kg ww
|
|
India
|
18 groups of fish and other seafood in the Bay
of Bengal, Arabian Sea and Indian Ocean
|
0.005-0.065 mg total Hg/kg
(mean average values)
|
|
|
Back
|
Ramamurthy, 1979, in comments from India (comm.-13-gov)
|
|
Bombay, west coast
Fish
Bivalves
Gastropods
Crabs
|
0.03-0.82 mg
total Hg/kg dw
0.13-10.82 mg
total Hg/kg dw
1.05-3.60 mg total Hg/kg dw
1.42-4.94 mg total Hg/kg dw
|
|
|
|
Bhattacharya and Sarkar, 1996
|
|
Madras, southeast coast
Fish
Fish
|
Below detection limit (100 ng/g)
0.08-0.14 mg total Hg/kg ww
|
|
Sagar Island, east coast
Bivalves
|
0.06-2.24 mg total Hg/kg dw
|
|
Italy
|
Bluefin tuna (Thunnusthynnus thynnus)
|
0-4 mg total Hg/kg ww
|
|
pre
|
gen
|
Renzoni et al.,
1998
|
|
Japan
|
Scorpionfish,
inside Minamta Bay
|
0.655 mg/kg ± 0.162
0.511 mg/kg ± 0.241
|
1978
1993
|
|
|
Yasuda et
al, in national submission from Japan, sub6gov
|
|
Scorpionfish,
outside Minamata Bay
|
0.603 mg/kg ± 0.216
0.531 mg/kg ± 0.194
0.431 mg/kg ± 0.163
|
1983
1990
1999
|
|
|
|
|
Kiribati
|
Shellfish
(Anadara spp.)
|
<0.0001-0.006
mg/kg ww
|
1987
|
|
Back
|
Naidu et al., 1991
|
|
Korea, Republic of
|
Unspecified freshwater fish species from 12
places each in Keum and Nakdong River Basins, respectively
|
Mean 0.126 mg/kg total Hg
(10 species, 90 samples)
|
1989
|
|
|
National submission from Korea (sub76govatt1)
|
|
|
Mean 0.196 mg/kg total Hg
(6 species, 124 samples.
|
1985
|
|
|
|
|
7
freshwater fish species(Givel, Carp, Grey mullet, Cat fish,
Shake head, Eel, Mandarin fish) from Kangkyung area in Keum
River
|
Mean 0.351
mg/kg
(muscle, 7species, 57 samples)
|
1980
|
|
|
National submission from Korea (sub76govatt1)
|
|
Freshwater
fish species from 24 streams in South eastern area in Korea (Carassius
auratus, Zacco temmincki, plecoglossus altivelis, Moroco
lagowskii, Chaenogobius urotaenia urotaenia etc.)
|
0.02 – 0.12
mg/kg
mean 0.07 mg/kg
|
1979
|
|
|
National submission from Korea (sub76govatt1)
|
|
Kuwait
|
Shrimp, various species
|
Not detected
– 1.57
mg/kg
(average less than 0.4 mg/kg)
|
1980's
|
|
|
Khordagui and Dhari, 1991, in
UNESCWA submission, sub1igo
|
|
Mauritius
|
Shark (unspecified)
|
0.13 - 0.60
mg/kg of Hg
(52 samples of fresh shark)
|
?
|
Pre
|
Gen
|
National submission from Mauritius, sub56gov
|
|
|
Marlin
|
1.20 – 3.00 mg/kg of Hg
(in 8 samples),
0.10-0.90 mg/kg of Hg
(in 18 other samples)
|
|
|
|
|
|
|
Tuna
|
0.10 – 0.70
mg/kg of Hg
(16 samples of fresh tuna)
|
|
|
|
|
|
|
Swordfish
|
0.22 – 0.65
mg/kg of Hg
(in 17 samples of swordfish)
|
|
|
|
|
|
North East Atlantic (OSPAR waters)
|
Marine fish
|
0.01-0.2 mg/kg ww
(general)
Up to 0.9 mg/kg ww
(peak areas)
|
1993-1996
|
|
Gen
|
OSPAR, 2000b and 2000, in submission from the
Nordic Council of Ministers, sub84gov)
|
|
|
Marine mussels
|
0.01-0.1 mg/kg ww(general)
Up to 0.9
mg/kg ww
(peak areas)
|
|
Non
|
Gen
|
|
|
Norway
|
Pike
Perch
|
0.1 – 2.5
mg/kg
0.1 – 2.5
mg/kg
|
1988-1994
|
|
|
National submission from Norway, sub70gov
|
|
Philippines
|
Fish in river systems
|
0.00107 – 0.439
mg/kg totalHg
0.00071 – 0.377
mg/kg methylHg
|
1996-1999
|
|
Con (artisinal gold mining area)
|
National submission from Philippines, sub1gov
|
|
|
Taiwan clam
|
0.233 -1.208 mg/kg total Hg
|
1997-1999
|
Non
|
|
|
|
|
Tilapia
|
0.109-0.494 mg/kg total Hg
|
1996-1999
|
|
|
|
|
Seycelles
|
Various ocean species
|
Mean of 0.2-0.3 mg/kg
|
|
|
|
Cernichiari et al., 1995, as quoted by
Pirrone et al., 2001
|
|
Slovak Republic
|
Some river and lake species:
Barbel (Barbus
barbus)
|
0.053-7.329
mg/kg ww
(mean 0.728 mg/kg, 29 samples)
|
1995-2000
|
| | |