Program 1 Newsletter - Issue 17 - March 2000
Sydney
Catchment Audit Report
Following the water contamination incidents
in Sydney during late 1998, the management of water supplies for the city was
restructured by the NSW state government (1). Responsibility for management of
the catchment and storage dams was transferred from the Sydney Water Corporation
to the newly formed Sydney Catchment Authority (SCA). The Act of Parliament
establishing the SCA also required that an audit of the catchment be carried out
within a five month interval of its formation.
The audit was designed to provide
information to the SCA, state and local government departments and other
relevant organisations to assist in the future management of the catchment, and
in the development of specific programs for catchment improvement and pollution
control. The audit will also be pivotal in the preparation of a Regional
Environmental Plan for the catchment.
A team of experts led by Dr John Williams,
Deputy Chief of CSIRO Land and Water, was appointed to perform the audit. The
team was assisted by an Independent Reference Panel representing eleven
organisations with broad expertise and first-hand knowledge of the catchment.
The final report of the Catchment Audit was delivered to the NSW Minister for
the Environment in December 1999 and publicly released in January 2000
(2).
The report provides a "snapshot" of the
present state of the catchment and the many challenges that must be overcome in
order to improve the protection of public health and ecosystem integrity. It
also identifies a number of gaps in knowledge which currently hamper the
development and assessment of management strategies. In many instances these
relate not only to the specific circumstances of the Sydney catchment area, but
also to general limitations of existing knowledge of catchment
ecology.
The Terms of Reference required that the
Catchment Audit should compile and categorise information on the state of the
catchment (in terms of attributes such as water quality, physical attributes,
fauna and flora, cultural values etc), and the pressures to which the catchment
is subject (in terms of human activities, land uses, natural processes
etc).
In addition, the audit was expected to
specifically provide:
- an inventory of what is known
about the catchment (in terms of its state and available information
sources)
- an assessment
of the sufficiency of existing
information
- an
identification of information
gaps
- an identification
of the sources of pollution in the
catchment
The audit team adopted the following
process to provide a structured analysis of the state of the
catchment:
- identification of hazards to
the protection of public and catchment
health
- identification
of indicators which could be used quantify the risks associated with these
hazards
- collection,
processing and analysis of available data on these
indicators
- assessment
of both the condition of the land and water, and the risks to protection of
public and catchment health based on available
information
- identification
of hazards for which no indicators are
available
- identification
of data and knowledge needed to provide indicators for such
hazards
- integration of
the findings under the four headings listed in the paragraph
above
- recommendations
for procedures and mechanisms for monitoring strategies to ensure required data
is available and analysed for hazard and risk
analysis
- identification
of constraints to the use of this data and information in building risk
management strategies and whole-of-catchment management processes that are
critical to protecting water quality and catchment
health.
Prior to the audit, the SCA had assembled
an extensive report summarising available information sources and data
collections, and preliminary set of indicator measures had been developed in
conjunction with experts from the CRC for Freshwater Ecology. The audit team
carried out ground inspections of several areas of the catchment and made a
comprehensive helicopter inspection of major river systems, as well as examining
existing documentation. Landsat TM satellite imagery was also used to assess
the state of the catchment area.
The audit team found that a very large
volume of information was available on the catchment area in the form of
numerous reports, investigations, and monitoring data. However there had been
only limited attempts to integrate this knowledge to form a comprehensive
picture of the condition of the whole catchment.
The SCA holds detailed information on the
Special Areas (the "inner catchment" which was under the direct control of the
Sydney Water Corporation), but has very limited knowledge on the remainder of
the catchment (the "outer catchment" comprising over 70% of the total area).
Much of the information on the outer catchment compiled for the audit was
obtained from other State agencies and organisations.
Specific shortcomings in information
identified by the audit included:
- Gaps in the natural resource
information base for whole-of-Sydney water supply catchments. Effective
management of the catchment will require the establishment of an extensive
database linked to a geographic information system to document spatial,
geological and land use characteristics.
- A gap in process
knowledge of landscape, river, and ecosystem function. The SCA needs to develop
models and tools to analyse and predict the behaviour of components of the
catchment under different conditions, and build in-house expertise and
understanding of these
behaviours.
- Gaps in
approach to general water quality and quantity monitoring. A large amount of
monitoring data has been collected in the past but new methods are needed to
present and analyse trends in a more informative way. In addition, more
consideration is needed in the design of sampling programs to complement
management programs and system
modelling.
- Small but
important data gaps. The audit team noted that no information was available on
potential pollution from Commonwealth government facilities, and that there was
no existing mechanism to collect information on projected changes in intensive
farming activities. Information was also lacking on inputs of fertilisers and
pesticides, and potential high risk areas for spillages such as locations of
road intersection with
streams.
- Microbial
pathogens. A number of gaps exist in understanding of the sources, movement and
survival of microbial pathogens in the catchment. More research is needed to
define the importance of different human and agricultural
sources.
- Sediments and
related nutrient, sources, transport and delivery. Available information is
insufficient to identify erosion, source of sediment transport and delivery
across catchments, except on a broad scale which is inadequate to evaluate
hazards and set priorities.
- Hazards associated
with mining and extractive industries. Information on existing and abandoned
mines in inadequate to assess risks and assist management for the majority of
the catchment
area.
- Gaps in knowledge
of hazards associated with sewage, wastewater and solid waste disposal.
Information on the location and extent of sewage discharges and overflows from
treatment plants and septic tanks is incomplete, and this will hamper effective
management.
The audit team recommended that the first
priority for the SCA should be to assemble and organise the biogeographic
spatial data for the catchment area. This should be followed by strategic
planning of a program to fill the identified gaps in knowledge and information.
The team also proposed an expanded set of indicators based on the findings of
the audit, and recommended that these be further developed in consultation with
stakeholders and technical experts. It will be necessary to implement
assessments of small areas in order to adequately describe the diverse nature of
the catchments.
Overall, the report classified the state of
the Sydney catchments as "reasonably good", with about 10% of the total area of
16,000 square kilometres considered to be "poor" while about 25% was rated as
"excellent". However past management practices which concentrated heavily on
protection of "Special Areas" around major storage reservoirs were deemed to be
insufficient to maintain adequate protection of water quality. These areas are
largely protected from residential and agricultural development but comprise
less than 30% of the total catchment.
The audit team expressed the opinion that
past dependence on the Special Areas to protect water quality had distorted the
allocation of resources for monitoring and managing the catchment. Extensive
agricultural and residential pressures on other areas of the catchment are
contributing to increased hazards for water quality and catchment health, and a
more integrated management strategy for the whole catchment area is now urgently
required.
At present the SCA has limited powers
governing regions outside the Special Areas, and SCA regulations can be
overridden by a number of other agencies. The operations of at least 17
government instrumentalities have the potential to affect catchment health or
water quality. The report concludes that successful implementation of a
whole-of-catchment management plan will require the support of legislative power
and policy to enable vigorous control of land use.
The audit team emphasise that adequate
levels of resourcing, and active involvement and ownership by local government,
state agencies and the community will also be essential. They recommend that the
SCA builds in-house expertise and knowledge rather than relying on external
consultants. The whole-of-catchment management plan must also be incorporated
into the Regional Environmental Plan and other regional planning
processes.
According to a report in the January 5
edition of the Sydney Morning Herald, the NSW government is already moving to
strengthen the regulatory powers of the SCA. Applications for approval of
developments in the catchment will soon have to include a water cycle management
strategy explaining how water quality would be protected or improved by the
development.
However, the NSW Opposition party has
cautioned that granting broad additional powers as recommended in the Audit
Report will result in the SCA becoming a "super-power agency" overriding
existing local government, EPA and planning controls.
(1) Refer to Health Stream issues 11, 12
and 13 for reports on the contamination incidents and subsequent Sydney Water
Inquiry.
(2) Audit of the Hydrological Catchments
managed by the Sydney Catchment Authority. Final Report to the Minister for the
Environment, NSW State Government, December 1999. CSIRO Land and Water. The
report can be downloaded from:
http://www.sca.nsw.gov.au/
US Ground Water
Rule
In recent decades regulators in the US have
concentrated heavily on the microbiological health risks associated with surface
water supplies, and have introduced progressively stricter microbiological
standards for finished water and performance criteria for water treatment
plants. In contrast, regulations for groundwater supplies are less stringent
with no specific requirements for primary disinfection or maintenance of
disinfectant residuals for groundwater sources not under the influence of
surface water. However, increasing evidence of chemical and microbial
contamination of groundwater supplies, and threats to reliability from
over-pumping have resulted in an increase in regulatory attention (1).
The US EPA is now entering the final stages
of revisions to the Ground Water Rule, which governs public groundwater supply
systems. For the first time the Rule will require all public groundwater
supplies to be disinfected, even if they are not under the influence of surface
water. In addition, substantial efforts are being made to expand and coordinate
monitoring and management programs to improve understanding of the condition of
groundwater supplies.
At least 400,000 public drinking water
wells presently exist in the US, serving a population of about 110 million
people. An additional 20 million people obtain their drinking water from
private wells, making a total of 130 million (48% of the total US population of
268 million). Almost 95% of rural populations rely on groundwater for drinking
and domestic use, and over 40% of water used for crop irrigation and livestock
watering in the US comes from groundwater. Groundwater also contributes up to
half of the water flow in surface streams.
Groundwater supplies have been
traditionally viewed as having relatively low risks of microbiological
contamination compared to surface water supplies, however a recent review of
such supplies in the US has questioned this assumption (2). Researchers in the
US EPA suggest that many groundwater supplies pose health risks to consumers,
and advocate implementation of disinfection as a minimal protective measure for
all groundwater supplies.
The authors review published studies on
groundwater contamination and also note the existence of a substantial number of
unpublished surveys. Although some studies have involved sampling of large
numbers of wells, selection criteria were variable and in most cases only one
sample was taken from each site. A large survey (244 samples from public wells)
carried out by the American Water Works Association Research Foundation reported
the presence of various indicators of faecal contamination in 50% of wells
considered to be more vulnerable to contamination, and in 40% of wells
considered less vulnerable.
In another survey of 30 US public wells
thought to be vulnerable to contamination, 24% were positive for culturable
viruses, more than 50% positive for coliphage, 50% positive for E. coli
and 70% positive for enterococci in at least one monthly sample over a one year
period. Canadian researchers have also reported high rates of contamination,
with the faecal indicator Clostridium perfringens found in 20% of 300
rural wells tested (3). These and other studies suggest that many groundwater
sources are prone to faecal contamination but the fragmentary nature of the data
makes it difficult to estimate the scope of the problem on a national
level.
Groundwater supplies were responsible for
58% of the 614 drinking water related disease outbreaks in the US reported to
the Centers for Disease Control and Prevention between 1971 and 1994. About 30%
of these outbreaks were attributed to contamination of distribution systems, and
the remaining 70% to contamination of the groundwater source. During 1995 and
1996 groundwater supplies were associated with 11 of 15 drinking water related
outbreaks attributed to infectious agents (4).
In addition to recognised outbreaks
reported to CDC, it is likely that substantial numbers of people are affected by
unreported outbreaks or by small outbreaks that are not detected by health
authorities. Some epidemiological studies have suggested that waterborne
pathogens may be responsible for a significant portion of endemic
gastrointestinal illness, although the evidence on this issue is not conclusive.
The authors of the recent review (2)
believe that groundwater systems may now constitute a greater threat to public
health than surface waters because of the lower rates of use of disinfection and
absence of filtration in groundwater supplies. In order to derive an estimate
the possible magnitude of the problem, they developed a quantitative risk
assessment model based on available knowledge of groundwater contamination.
This model assumed faecal contamination
rates between 7% and 46% of wells, presence of human infectious viruses in 46%
of contaminated wells, a population of 27 million people drinking predominantly
from undisinfected groundwater systems, and dose-response models for rotavirus
infection. This model resulted in an estimate of 890,000 to 5.9 million
illnesses per year attributable to undisinfected groundwater sources, associated
with a possible mortality of 1,400 to 9,400 per year (assuming a 1% death rate
among elderly people who suffer gastroenteritis).
A number of approaches for controlling
microbial contamination of groundwater sources were also reviewed and available
evidence on their efficacy was examined. There appear to have been few
assessments of well-head protection programs, but the results suggest that such
measures have not reduced contamination rates. However US states which consider
hydrogeological criteria for siting wells had fewer reported violations of the
Total Coliform Rule (TCR) than states which did not use these criteria.
Analysis of violation rates for the TCR vs the proportion of groundwater
supplies which are disinfected in each state showed a marked inverse
relationship. The ten states with highest rates of disinfection showed an 18%
violation rate over 5 years, whereas the ten states with the least disinfection
had a violation rate of 38%.
The authors conclude that while
considerably more information is needed to establish the extent and health
impact of microbial contamination of groundwater, the introduction of
disinfection for all groundwater systems would be "prudent public health
policy".
(1) Safe Drinking Water Act, Section 1429
Ground Water Report to Congress. Office of Water, US EPA. EPA-816-R-99-016
October 1999.
(2) Current knowledge on groundwater
microbial pathogens and their control. Macler, B. A. and J. C. Merkle (2000).
Hydrogeology Journal - Special Issue: Groundwater and Microbial Processes,
8 (1) p29-40.
(3) Contamination of rural drinking water
wells by fecal origin bacteria - Survey findings. Conboy, MJ and MJ Goss (1999).
Water Qual Res J Canada 34: 281-303.
(4) Surveillance for Waterborne Disease
Outbreaks-United States, 1995-1996. (1998). MMWR 47(SS-5):
1-34.
Workshop
Report
WSAA Strategic Workshop on Viability
Testing and Genetic Typing of Cryptosporidium Oocysts.
9 & 10 March 2000,
Sydney
This workshop was attended by over 20
invited participants, representing a broad spectrum of Australian water
industry, research and public health interests. International guests included
Dr George Di Giovanni (American Water Works Service Company), Dr Rachel Chalmers
(Director of the Cryptosporidium Reference Laboratory, UK) and Dr Jim
McLauchlin (Public Health Laboratory Service, UK). The workshop produced a
series of initiatives to build a strong collaborative Cryptosporidium
research program in Australia, with potential for expansion to an international
level.
This meeting was prompted in part by a
workshop held at Tadley Court in the UK during August 1999 (1). The Tadley
Court workshop discussed observations that Cryptosporidium oocyst sources
and preparation methods may impact on viability, and highlighted the problems
associated with the use of different (and often poorly described) methods in
published studies which severely limited the comparability of results. The
participants developed a number of best practice protocols for oocyst
preparation, cell culture, disinfection and treatment studies, reporting of
results, and quality assurance and quality control for Cryptosporidium
research.
Dr John Langford, Executive Director of
WSAA, opened the Sydney workshop with a brief introduction to WSAA and a review
its research program on a range of issues relating to water quality and human
health. WSAA was a founding partner in the CRC for Water Quality and Treatment,
and is co-funding a number of projects including the Water Quality Study (a
randomised controlled trial on the effect of drinking water treatment on
gastroenteritis), and Case-control studies of risk factors for
cryptosporidiosis. In addition to its involvement in the CRCWQT, WSAA also
conducts an independent research program. The process of developing the WSAA
research agenda involves strategic workshops to discuss industry needs, define
gaps in current knowledge, and assess the feasibility of different research
approaches.
After outlining the five specific
objectives of this workshop on viability testing and genetic typing of
Cryptosporidium oocysts, Dr Langford then introduced Dr George Di
Giovanni to lead the discussion on the first objective.
Objective 1 - to define the research
and technology transfer necessary to refine and establish in vitro procedures
for the maintenance of Cryptosporidium parvum isolates of both the human
and cattle genotypes (Genotype 1 and 2).
Dr Di Giovanni has successfully combined
cell culture and PCR techniques to develop a method for the specific detection
of C. parvum oocysts that are infectious for humans (2). The method
utilises filtration and immunomagnetic separation to purify oocysts from
environmental samples, followed by inoculation into human HCT-8 enterocyte cell
monolayers in microtitre tray wells. After a 72 hour incubation to allow
replication of infectious oocysts within the human cells, the monolayers are
washed to remove any unexcysted oocysts, then the cells are lysed and PCR is
used to amplify a 361 basepair DNA product from the C. parvum heatshock protein
(hsp70) gene. The amplified segment is then DNA sequenced to determine the
genotype.
The cell culture method permits the growth
of both the Type 1 (human) and Type 2 (cattle) genotypes of C. parvum and
has been used to test the three Type 2 isolates used in human volunteer studies.
These three isolates showed large differences in infectivity in the human
volunteers, and this correlated strongly with infectivity in HCT-8 cell
cultures. Thus the technique appears to represent a relevant laboratory model
for human infection. However, the protozoa are not able to form new oocysts to
complete the entire infection cycle, and the cell cultures can be maintained
only for a limited time. Nevertheless, this method offers a more rapid and
lower cost alternative to animal infection studies.
The cell culture technique is sufficiently
sensitive to detect a single viable oocyst, and has been successfully employed
to detect viable oocysts in finished water, raw water and filter backwash
samples. Ongoing experimental work is aimed at optimising excystation and cell
culture conditions, and adapting the method to yield semi-quantitative
information on viable oocysts numbers so that it can be more easily applied to
disinfection studies.
The workshop participants agreed that
coordinated efforts should be made to establish this cell culture technique in
Australian laboratories, and carry out inter-laboratory comparisons to ensure
that results were reproducible. The following strategy was suggested for
implementation:
- development of specifications
for laboratories to participate in the program (these would include facilities
for cell culture work, willingness to collaborate, willingness to follow the
Tadley Court protocols, and willingness to help others establish the
technique).
- advertisement
for Expressions of
Interest
- selection of
several laboratories to
participate
- implementation
of a coordinated research program initially using the well characterised Iowa
(Type 2) strain to establish the technique and ensure inter-laboratory
comparability. This would be followed by inter-laboratory exchange of human
Cryptosporidium isolates (Type 1), and testing of the cell culture
technique for
these.
- organisation of
a workshop to disseminate results and enable transfer of the technique to other
laboratories.
Objective 2 - to develop strategies
for the evaluation of RT-PCR and FISH procedures for their value as a routine
procedure for their assessment of oocysts viability.
Dr Duncan Veal from Macquarie University
and Dr Paul Monis from the Australian Water Quality Centre outlined the
properties of the two methods under discussion. These procedures are already in
use in a number of Australian laboratories as surrogate markers for oocyst
viability or infectivity, however they have not yet been validated against cell
culture or animal infection methods. Some work on validation is presently
underway in the US and the UK.
The FISH method detects the presence of
ribosomal RNA sequences (rRNA) which are believed to degrade relatively quickly
after oocysts become inviable. As rRNA contains both highly conserved and
highly variable regions, it is possible to use different probes to detect either
all Cryptosporidium species, or C. parvum in particular. The
results can be scored using an epifluorescence microscope or using flow
cytometry, giving quantitative results on the number of "viable"
oocysts.
The RT-PCR method detects messenger RNA
(mRNA) which codes for the heatshock protein (hsp70). Again, this molecule is
believed to degrade relatively quickly after oocysts become inviable. The
method has the ability to detect either all Cryptosporidium species, or
C. parvum specifically depending on the probe used. The outcome is
essentially a presence /absence result for "viable" oocysts without
quantitation.
The participants agreed that following
establishment of the HCT-8 cell culture technique in Australia, a study should
be carried out to compare the results of FISH, RT-PCR and cell culture methods.
This should be carried out in a blinded fashion with samples of fresh oocysts,
killed oocysts and aged oocysts (which would be expected to have declined in
viability) from several isolates. In order to provide statistically reliable
results, it was recommended that a biometrician be involved in the study design,
and that further discussions be held when a draft protocol was available for
consideration.
Objective 3 - to develop strategies
for a multi-centre trail within Australia and overseas to compare currently
existing PCR based detection procedures for Cryptosporidium with the aim of
evaluating broad applicability in terms of specificity and
sensitivity.
and;
Objective 4 - to develop strategies
for a multi-centre trial within Australia and overseas to compare currently
existing PCR based genotyping techniques in order to determine the most useful
genetic loci.
Discussion on these objectives was
introduced by Dr Una Morgan of Murdoch University, who began by outlining the
requirements for a testing procedure in terms of sensitivity, reproducibility
and speed. A decision needs to be made on whether the method should be able to
detect all species of Cryptosporidium, all genotypes of C. parvum,
or only those genotypes currently known to infect humans with normal immune
systems (ie Genotypes 1 and 2). Ideally the method should also have the
capability to determine the genotype.
Dr Morgan then summarised the current state
of knowledge on Cryptosporidium genotyping. The taxonomy of this
organism is currently under review as increasing knowledge from molecular
characterisation reveals details of phylogenetic relationships. For C.
parvum it is likely that some of the currently recognised genotypes will
eventually be designated as separate species. At present 7 distinct major
genotypes are classified within C. parvum; Type 1 (human), Type 2
(cattle), marsupial, pig, mouse, ferret, and dog. A minor variant of Type 1
occurs in monkeys. The dog genotype is soon likely to be reclassified as a
separate species (C. canis), while the cat genotype is already recognised as
such (C. felis).
A number of genetic loci have been examined
for their ability to distinguish between different species of
Cryptosporidium, and to discriminate between major genotypes within a
species. There have been some discrepancies in results reported by different
laboratories, perhaps due to different methodology. Overall, it appears that
the 18s rRNA gene and the Hsp70 gene provide the best markers for reliably
distinguishing between species and major genotypes.
Extensive efforts have also been made by a
number of laboratories to develop markers for distinguishing between isolates
within a genotype, however the results have been disappointing. Genome
sequencing projects are underway, with the aim of determining the entire
sequence of the Iowa (Type 2) isolate and at least 65% of the sequence of the
NEMC1 (Type 1) isolate. This knowledge may assist in designing new probes for
genotyping individual isolates.
After further discussion it was agreed that
collaborating Australian laboratories would undertake to perform an analysis
with standard markers, primers, and a reference strain (and/or DNA clones) when
characterising isolates in order to provide consistent data for comparison.
These standards were agreed to comprise the 18s rRNA and Hsp70 markers, with the
Iowa strain or clones of its DNA. Collaboration will also be sought in the UK
via the National Cryptosporidium Research Steering Committee and in the
US via AWWARF. It was agreed that consideration should be given to establishing
a database of verified Cryptosporidium DNA sequence data to assist the
collaborative research effort.
On the topic of avenues for seeking new
markers to distinguish between isolates, Dr Duncan Veal suggested that the
science of "proteomics" might offer some promise. This methodology involves the
automated analysis of differences in protein content between isolates. This may
enhance the probability of finding strain-specific markers. It was agreed that
a preliminary research proposal for this approach should be
developed.
Objective 5 - to explore strategies
for determining the prevalence and distribution of human infectious and
non-infectious genotypes in different water sources, and in populations of human
and animal hosts.
Dr Andrew Thompson from Murdoch University
introduced this topic and highlighted the need for a diverse collection of
isolates from animal, human and environmental sources in order to gain the
maximum knowledge from genotyping studies.
Dr Jim McLauchlin then presented the
findings of genotyping studies done in the UK by the Public Health Laboratory
Service. Analysis of isolates from eight drinking water Cryptosporidium
outbreaks in the UK demonstrated that five outbreaks were due to Type 1 isolates
(indicating human faecal pollution) while three were due to Type 2 isolates
(human or animal faecal pollution). For five swimming pool related outbreaks
examined, two were of Type 1, two were of Type 2 and one was mixed Types 1 and
2.
Seasonal trends in prevalence in sporadic
cases (not related to outbreaks) showed that the Type 1 genotype is rarely
isolated in winter, while the Type 2 genotype is found all year round. The
incidence of reported cases and the ratio of Type 1 and Type 2 isolates varies
in different regions. Data on farm animal infections show a consistent peak of
infection in sheep during springtime (lambing season), while in cattle infection
peaks occur both in spring and in autumn.
Overall, the two major C. parvum
genotypes (Types 1 and 2) account for at least 96% of human infections in the
UK. An apparently novel genotype (Type 3) has been found recently but has not
been well characterised.
The workshop discussions then turned to
avenues for obtaining a broader range of Cryptosporidium isolates for
study:
Human sources Some participants at
the workshop have established ongoing relationships with hospitals or pathology
laboratories, but these sources are limited. A number of possible mechanisms to
obtain isolates were discussed:
- Request pathology
laboratories to forward Cryptosporidium-positive faecal specimens to
researchers after routine pathogen testing had been completed. Such specimens
would normally be discarded unless the lab was participating in a research
project.
- Request pathology
laboratories to forward faecal specimens which had not been tested for
Cryptosporidium (in most labs only a minority of faecal specimens are
tested for this organism), then test these for Cryptosporidium. This was
seen as presenting ethical difficulties concerning patient consent and
obligations to notify patients and health authorities of positive
results.
- Actively seek to collect and
test faecal specimens from settings where Cryptosporidium infection rates
might be expected to be high (eg childcare facilities). This would require
ethical approval and informed consent from parents. Patients and health
authorities would need to be notified of positive
results.
It was agreed that the first option should
be explored as the most simple and lowest cost alternative. Dr Geoff Hogg of
Melbourne University suggested that the cooperation of the Public Health
Laboratory Network should be sought initially, and then commercial pathology
labs should be approached. Cryptosporidium-positive faecal specimens
reported to Health departments in Victoria and South Australia are already being
collected as part of a CRC for Water Quality and Treatment Case-control study.
Environmental sources Some
Australian water authorities are testing environmental samples for
Cryptosporidium, but in many cases the entire sample is used in the test
procedure. Taking duplicate water samples is expensive, and the low oocyst
numbers and often poor recovery rates, oocysts may not be recovered from both
samples.
Dr Jim McLaughlin reported that he had
achieved some success with attempts to remove oocysts from slides after
microscopic examination and genotype them. Dr Chris Saint and Dr Paul Monis
from the Australian Water Quality Centre agreed to carry out preliminary
experiments of this nature to see if a reliable technique could be developed and
report back to the group.
Dr Duncan Veal noted that the SCA had
agreed to forward positive samples from their sampling program to him for
genotyping, and Dr David Roser from the University of NSW undertook to seek
similar cooperation from water authorities participating in the CRCWQT Pathogens
in Catchments Project.
Animal strains Participants with
expertise in this area reported that tests for Cryptosporidium are rarely
done in routine veterinary practice. Most isolates of this nature have to be
obtained from specific research projects. Some Australian water authorities are
supporting research programs to examine the carriage of Cryptosporidium
in catchment animals.
Conclusion Dr John Langford
concluded the workshop by summarising the agreed strategy and actions developed
for each objective, and thanked participants for their valuable input. The
proposed research strategy will now be presented to the WSAA Research Committee
for consideration and further development.
(1) Towards a standardised experimental
design for viability and inactivation studies. Report on a Workshop on
Cryptosporidium and Water Chaired by Professor Ian Bouchier Held at
Tadley Court, Tadley, Hampshire on 11-12 August
1999. http://www.dwi.detr.gov.uk/pubs/
(2) Detection of infectious
Cryptosporidium parvum oocysts in surface and filter backwash water
samples by immunomagnetic separation and integrated cell culture-PCR. Di
Giovanni, G. D., F. H. Hashemi, et al. (1999). Appl Environ Microbiol
65(8): 3427-32.
News Items
Law suits over E. coli
outbreak
The E. coli O157:H7 outbreak that hit the
Washington County Fair in August last year has resulted in lawsuits seeking
millions of dollars in damages. Over 1,000 people became ill and two people
died after drinking unchlorinated well water during the Fair. One of several
wells on the site is believed to have been contaminated by waste seepage or
runoff from a nearby dairy farm after heavy rains.
The Fairground is operated by a small
non-profit community group which holds public liability insurance of only $1
million. The group is presently engaged in a legal dispute with the insurance
company which is arguing that a policy clause exempting damage from storm and
wastewater pollution of sewer systems or streams is applicable in this
instance.
The outbreak has highlighted the risks
faced by many small water supply systems in the US, and variations in state
requirements for insurance coverage for system operators. It is believed many
small to medium operators have inadequate insurance cover and seldom hold
policies covering their officers and directors. This may leave individuals
personally liable for damages settlements in cases such as
this.
Parents advised to sue over
water
A British pediatrician has advised parents
to sue schools which do not provide drinking fountains for children. Dr Trevor
Brocklehurst of the St James University Hospital in Leeds said that many schools
have removed water fountains and substituted softdrink vending machines in their
place, leaving children with little opportunity to obtain plain water. Dr
Brocklehurst has raised the issue with the Leeds Health Authority, claiming that
children he is treating for urinary tract infections are being placed at risk of
complications by lack of access to water at school. The Leeds Health Authority
is undertaking a study on the extent of the problem, and says it is working with
local education authorities to ensure drinking water is readily available at all
schools.
US retains copper
goal
The US National Research Council has
released a report recommending that the current maximum contaminant level goal
(MCLG) of 1.3 mg/L should be retained by the EPA. Water supplies where the 90th
percentile of first flush samples exceeds the MCLG may be required to take
remedial action. The Council was asked to review the scientific and technical
basis for the level after epidemiological studies in Nebraska and Delaware
failed to show adverse effects in people consuming drinking water with high
copper levels.
Copper is an essential human nutrient but
can also cause acute gastrointestinal symptoms and longer term toxicity when
ingested at higher doses. Children are more vulnerable to copper toxicity than
adults, and people suffering from several genetic conditions may be affected
even by low levels. The committee concluded that conventional risk assessment
using chronic toxicity endpoints and safety factors was not applicable in this
case because of the essential nature of copper, its metabolic regulation and the
narrow range of acceptable intake levels. Further research is needed to better
define vulnerable groups and to estimate total copper intake from drinking water
and other sources.
US EPA asks for delay in chloroform
case
The US EPA has asked the District of
Columbia Court of Appeal to postpone hearings on the case brought against it by
the Chlorine Chemistry Council. As reported in Health Stream Issue 16, the CCC
has filed a suit asking the Court to set aside the EPA Maximum Contaminant Goal
Level of zero for chloroform, and order the EPA to set a non-zero MCLG based on
scientific evidence. The EPA is seeking to delay the case on the grounds that
the zero MCLG was set as an "interim risk management decision" in response to a
Congressional deadline, while additional scientific information was still being
sought. New evidence in the form of a report from the Science Advisory Board is
now available, and the EPA has argued that proceeding with the current court
case would be an inefficient use of time and resources for all
parties.
Water Supply in Engineering Top 20
Water supply and distribution has been
recognised as one of the top engineering achievements of the 20th century by the
US National Academy of Engineering. Water supply ranked 4th in the list of
achievements after Electrification, Automobiles and Airplanes.
EERE
2000
The 4th Annual Australian
Environmental Engineering Research Event provides postgraduate students of
Environmental Engineering and related disciplines an opportunity to present and
discuss their work in a friendly, informal atmosphere. A selection of prominent
international and local speakers has been invited.
The Event will be held in Victor Harbor,
South Australia, 21 - 24 November 2000. The theme of the event,
“Environmental disciplines working together for a sustainable
future”, will address students from a wide variety of disciplines. One
of the highlights of previous events has been the lateral communication between
postgraduate researchers of different scientific and engineering disciplines,
and we are keen to maintain this tradition.
Thus we encourage any postgraduate students
working in the environmental field to attend, whether they are Engineers or
Scientists. Postgraduate students interested in attending must either present a
poster presentation or a platform presentation. There is a call for abstracts,
which are due 19th May 2000. Sponsorship opportunities are currently
available.
|
Lionel Ho
CRC for Water Quality and
Treatment
Private Mail Bag 3
SALISBURY SA 5108
Phone: (08) 8259 0365
Fax: (08) 8259 0228
|
Rachel Prince
School of Engineering and
Science
Swinburne University of
Technology
Mail 38, PO Box 218
HAWTHORN VIC 3122
Phone: (03) 9214 8639
Fax: (03) 9819 6443
|
Sam Brooke
CRC for Water Quality and
Treatment
Private Mail Bag 3
SALISBURY SA 5108
Phone: (08) 8259 0347
Fax: (08) 8259 0228
|
|
The CRC for Water Quality and Treatment
is a Gold Sponsor of EERE 2000.
|
National Health
and Medical Research Council
Revision of the NHMRC/ARMCANZ
Australian Drinking Water Guidelines
In 1997/98, NHMRC/ARMCANZ commenced a
rolling revision of the Australian Drinking Water Guidelines (ADWG). This
rolling-revision provides an opportunity to revise individual water quality
parameters each year to ensure the guidelines represent the most up to date
scientific understanding.
The NHMRC/ARMCANZ Drinking Water
Coordinating Group is currently seeking advice in relation to priority areas to
be considered for the 2000/01 phase of the ADWG rolling-review. The following
information outlines the areas that have been revised since
1998.
In 1998/99 the following areas were
reviewed:
The revised fact sheets are due to
be completed in 2000 following a final round of public
consultation.
The 1999/2000 review program
included:
- Aluminium
- Arsenic
- Copper
- Taste and Odour
- Turbidity
|
- Coliforms
- Burkolderia Pseudomallei
- Drinking
Water Treatment Chemicals
|
|
The respective fact sheets are
also due for completion in 2000 following a final round of public consultation.
The NHMRC/ARMCANZ Drinking Water
Coordinating Group is currently considering developing a work program for
2000/01 and would welcome input into establishing priority issues for
consideration during the ADWG rolling-review process. Advice is being sought on
issues that should be considered during the forthcoming year.
If you consider:
- there are
individual water quality parameters currently in the Guidelines that require
urgent revision, or
- there are
drinking water quality issues that are not in the current Guidelines that should
be included as part of the 2000/01 revision,
please provide relevant advice
and information to support the requirement for revision. Submissions are to be
forwarded to:
Mr Phil Callan
Assistant Director
Health Advisory Unit
Office of the NHMRC
GPO Box 9848
CANBERRA ACT 2601
Fax: (02) 6289 9190
Closing date for submissions is 5 May
2000.
Coming soon ....
.. . the
Australian Drinking Water Guidelines on the Web
The NHMRC/ARMCANZ Australian Drinking
Water Guidelines (ADWG) provide the Australian community and the water
supply industry with guidance on what constitutes good quality drinking
water.
The ADWG will soon be available to download
in PDF format from the Web site of the NHMRC at:
www.nhmrc.health.gov.au/publicat/synopses/eh19syn.htm
Following its endorsement in 1996, the ADWG
has been subjected to a Rolling Revision process that ensures the Guidelines
represent the latest scientific evidence in relation to good quality drinking
water. From time-to-time, as sections of the Guidelines are reviewed, the Web
site will be updated to provide the latest information.
The production of the PDF version of the
ADWG has been organised and sponsored by the Cooperative Research Centre for
Water Quality and Treatment as a service to the Australian water industry.
From the Literature
Contact Information
The printed version of Health Stream is available free of charge - to be added to our mailing list please contact Pam Lightbody (email above or fax + 61 3 9903 0576). Past issues can be found under Publications, and there is a searchable archive of articles, news items and literature summaries.