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Australian Drinking Water Guidelines
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  • Australian Drinking Water Guidelines
  • Copyright
  • Table of updates
  • Contents
  • Figures
  • Tables
  • Boxes
  • Introduction
    • Chapter 1: Introduction
      • 1.1 Guiding principles
      • 1.2 About the Guidelines
        • 1.2.1 Scope of the Guidelines
        • 1.2.2 Purpose of the Guidelines
        • 1.2.3 Structure of the Guidelines
      • 1.3 Water quality characteristics
        • 1.3.1 Introduction
        • 1.3.2 Health-based targets
        • 1.3.3 Microbial health-based targets
        • 1.3.4 Physical and chemical guideline values
        • 1.3.5 Radiological screening and reference values
      • 1.4 Community consultation
      • 1.5 Development of the Guidelines
        • 1.5.1 Acknowledgments
      • 1.6 Future revisions of the Guidelines
      • 1.7 References
  • Part 1: Management of Drinking Water Quality
    • Chapter 2: Framework for Management of Drinking Water Quality: overview
      • 2.1 A preventive strategy from catchment to consumer
      • 2.2 Structure of the Framework
      • 2.3 Benefits of the Framework
      • 2.4 The need for multi-agency involvement
      • 2.5 Applying the Framework
      • 2.6 Correlations of the Framework with other systems
    • Chapter 3: Framework for Management of Drinking Water Quality: the twelve elements
      • 3.1 Commitment to drinking water quality management (element 1)
        • 3.1.1 Drinking water quality policy
        • 3.1.2 Regulatory and formal requirements
        • 3.1.3 Engaging stakeholders
      • 3.2 Assessment of the drinking water supply system (element 2)
        • 3.2.1 Water supply system analysis
        • 3.2.2 Assessment of water quality data
        • 3.2.3 Hazard identification and risk assessment
      • 3.3 Preventive measures for drinking water quality management (element 3)
        • 3.3.1 Preventive measures and multiple barriers
        • 3.3.2 Critical control points
      • 3.4 Operational procedures and process control (element 4)
        • 3.4.1 Operational procedures
        • 3.4.2 Operational monitoring
        • 3.4.3 Corrective action
        • 3.4.4 Equipment capability and maintenance
        • 3.4.5 Materials and chemicals
      • 3.5 Verification of drinking water quality (element 5)
        • 3.5.1 Drinking water quality monitoring
        • 3.5.2 Consumer satisfaction
        • 3.5.3 Short-term evaluation of results
        • 3.5.4 Corrective action
      • 3.6 Management of incidents and emergencies (element 6)
        • 3.6.1 Communication
        • 3.6.2 Incident and emergency response protocols
      • 3.7 Employee awareness and training (element 7)
        • 3.7.1 Employee awareness and involvement
        • 3.7.2 Employee training
      • 3.8 Community involvement and awareness (element 8)
        • 3.8.1 Community consultation
        • 3.8.2 Communication
      • 3.9 Research and development (element 9)
        • 3.9.1 Investigative studies and research monitoring
        • 3.9.2 Validation of processes
        • 3.9.3 Design of equipment
      • 3.10 Documentation and reporting (element 10)
        • 3.10.1 Management of documentation and records
        • 3.10.2 Reporting
      • 3.11 Evaluation and audit (element 11)
        • 3.11.1 Long-term evaluation of results
        • 3.11.2 Audit of drinking water quality management
      • 3.12 Review and continual improvement (element 12)
        • 3.12.1 Review by senior executive
        • 3.12.2 Drinking water quality management improvement plan
      • 3.13 References
    • Chapter 4: Framework for the Management of Drinking Water Quality: application to small water supplies
      • 4.1 Introduction
      • 4.2 Applying the Framework
        • 4.2.1 Assessment of the drinking water supply
        • 4.2.2 Preventive measures for drinking water quality management
        • 4.2.3 Implementation of operational procedures and process control
        • 4.2.4 Verification of drinking water quality
      • 4.3 Individual household supplies
      • 4.4 Reference
  • Part 2: Description of Water Quality
    • Chapter 5: Microbial Quality of Drinking Water (Updated 2022)
      • 5.1 Introduction
      • 5.2 Microorganisms in drinking water
      • 5.3 Assessing microbial risk
      • 5.4 Enteric pathogens
        • 5.4.1 Enteric pathogens of concern in drinking water
        • 5.4.2 Contamination of source waters with enteric pathogens
        • 5.4.3 Management of risk from enteric pathogens
      • 5.5 Opportunistic pathogens
      • 5.6 Cyanobacteria
      • 5.7 Nuisance organisms
        • 5.7.1 Organisms causing taste and odour problems
        • 5.7.2 Organisms causing colour problems
        • 5.7.3 Deposits due to iron and manganese bacteria
        • 5.7.4 Corrosion problems due to iron and sulphur bacteria
        • 5.7.5 Problems caused by large numbers of microorganisms
      • 5.8 References
    • Chapter 6: Physical and Chemical Quality of Drinking Water
      • 6.1 Introduction
      • 6.2 Physical quality of drinking water
        • 6.2.1 An overview of physical characteristics
        • 6.2.2 Approach used in derivation of guidelines values for physical characteristics
      • 6.3 Chemical quality of drinking water
        • 6.3.1 Inorganic chemicals
        • 6.3.2 Organic compounds (Revised 2011)
        • 6.3.3 Approach used in derivation of guideline values for chemicals
      • 6.4 Differences between Australian and WHO guideline values
      • 6.5 National and international guideline values (2016)
      • 6.6 References
    • Chapter 7: Radiological Quality of Drinking Water (Updated 2022)
      • 7.1 Introduction
      • 7.2 Sources of radiation in the environment and in drinking water
      • 7.3 Health effects of radiation
      • 7.4 Exposure to radiation
      • 7.5 Units of radioactivity and radiation dose measurement
        • 7.5.1 Units of radioactivity and radiation dose
        • 7.5.2 Converting intake to radiation dose
        • 7.5.3 Average dose of radiation
      • 7.6 Approach for derivation of reference levels and screening values for radionuclides
        • 7.6.1 System for radiation protection
        • 7.6.2 Estimation of the dose from radionuclides in water
        • 7.6.3 Estimation of risk from low-level radiation
        • 7.6.4 Reference levels and screening values for drinking water
        • 7.6.5 Application of reference levels
        • 7.6.6 Remedial measures
      • 7.7 References
    • Chapter 8: Drinking Water Treatment Chemicals (Revised 2006)
      • 8.1 Introduction
      • 8.2 Scope and limit of application of this chapter
      • 8.3 Overview of chemical treatment processes
        • 8.3.1 Control of algae
        • 8.3.2 Coagulation and flocculation
        • 8.3.3 Adsorption
        • 8.3.4 Softening
        • 8.3.5 Oxidation
        • 8.3.6 Disinfection
        • 8.3.7 Adjustment of pH
        • 8.3.8 Addition of buffering capacity
        • 8.3.9 Corrosion inhibition
      • 8.4 Public health measures
        • 8.4.1 Fluoridation
      • 8.5 Assessment of Chemicals acceptable for use in drinking water treatment (revised 2016)
        • 8.5.1 Chemicals assessed prior to 2004
        • 8.5.2 New water treatment chemicals
      • 8.6 Quality assurance for drinking water treatment chemicals
        • 8.6.1 Risks associated with drinking water chemicals
        • 8.6.2 Managing risks
        • 8.6.3 Specifications for the supply of drinking water treatment chemicals
      • 8.7 Monitoring and analytical requirements
      • 8.8 Contaminants in drinking water treatment chemicals
      • 8.9 Useful contacts
      • 8.10 References
  • Part 3: Monitoring
    • Chapter 9: Overview of monitoring (Revised 2021)
      • 9.1 Introduction
      • 9.2 Monitoring overview
        • 9.2.1 Monitoring priorities
        • 9.2.2 Principles of monitoring frequency
        • 9.2.3 Catchment-to-consumer monitoring
      • 9.3 Developing a monitoring program
      • 9.4 Operational monitoring
        • 9.4.1 Operational characteristics
        • 9.4.2 Target criteria
        • 9.4.3 Critical limits at critical control points
        • 9.4.4 Corrective action
        • 9.4.5 Operational monitoring frequency
        • 9.4.6 Chlorination as a critical control point: an example
      • 9.5 Verification of drinking water quality
        • 9.5.1 Monitoring consumer satisfaction
        • 9.5.2 Drinking water quality monitoring
      • 9.6 Water quality issues beyond the point of supply
      • 9.7 Investigative studies and research monitoring
      • 9.8 Validation of barrier performance
      • 9.9 Incident and emergency response monitoring
      • 9.10 Reliability of monitoring data
        • 9.10.1 Sample integrity
        • 9.10.2 Methods
        • 9.10.3 Detection limits
        • 9.10.4 Measurement uncertainty
        • 9.10.5 Field testing
      • 9.11 Monitoring advice for small, remote or community-managed water supplies
      • 9.12 Assessing the significance of short-term exceedances of health-based guideline values
      • 9.13 References
    • Chapter 10: Monitoring for specific characteristics in drinking water (Updated 2022)
      • 10.1 Introduction
      • 10.2 Assessing safety: short-term evaluation of monitoring
        • 10.2.1 Short-term evaluation of operational monitoring
        • 10.2.2 Short-term evaluation of drinking water quality monitoring
      • 10.3 Assessing performance: long-term evaluation of monitoring
        • 10.3.1 Long-term evaluation of microbial performance
        • 10.3.2 Long-term evaluation of health-based chemical performance
        • 10.3.3 Long-term evaluation of aesthetic performance
        • 10.3.4 Long-term evaluation of consumer satisfaction
        • 10.3.5 Improvement plan
        • 10.3.6 Performance reporting
        • 10.3.7 Summary of guideline values for microbial, chemical and physical characteristics
        • 10.3.8 Summary of reference levels and screening values for radiological characteristics
      • 10.4 Reference
  • Part 4: Information sheets
    • 1. Disinfection
      • 1.1: Introduction to water treatment
      • 1.2: Overview of disinfection
      • 1.3: Disinfection with chlorine
      • 1.4: Chloramines
      • 1.5: Disinfection with chlorine dioxide
      • 1.6: Disinfection with ozone
      • 1.7: Disinfection with ultraviolet light
      • 1.8: Other disinfectants
    • 2. Sampling
      • 2.1: Sampling Information – handling requirements and preservation
      • 2.2: Radiological monitoring and assessment of performance (updated 2022)
    • 3. Statistics
      • 3.1: Statistics – Visualising data
      • 3.2: Statistics – Assessing data
      • 3.3: Statistics – Statistical principles
      • 3.4: Statistics – Control charts and trends
      • 3.5: Number of samples required
      • 3.6: Guidance for issuing and lifting boil water advisories
      • Attachments
  • Part 5: Fact sheets
    • Microorganisms
      • Microbial indicators
        • Bacteroides
        • Coliphages
        • Clostridium perfringens
        • Escherichia coli
        • Heterotrophic plate counts
        • Intestinal enterococci
        • Thermotolerant coliforms
        • Total coliforms
      • Bacteria
        • Aeromonas
        • Burkholderia pseudomallei
        • Campylobacter
        • Escherichia coli (E. coli) (pathogenic)
        • Helicobacter pylori
        • Klebsiella
        • Legionella
        • Mycobacterium
        • Pseudomonas aeruginosa
        • Salmonella
        • Shigella
        • Vibrio
        • Yersinia
      • Protozoa
        • Acanthamoeba
        • Blastocystis
        • Cryptosporidium
        • Cyclospora
        • Giardia
        • Naegleria fowleri
      • Cyanobacteria and their toxins
        • Cyanobacteria and their toxins
        • Cylindrospermopsin
        • Microcystins
        • Nodularin
        • Saxitoxins
      • Viruses
        • Adenovirus
        • Enterovirus
        • Hepatitis viruses
        • Norovirus
        • Rotavirus
    • Physical and chemical characteristics
      • Acephate
      • Acrylamide
      • Aldicarb
      • Aldrin and Dieldrin
      • Aluminium
      • Ametryn
      • Amitraz
      • Amitrole
      • Ammonia
      • Antimony
      • Arsenic
      • Asbestos
      • Asulam
      • Atrazine
      • Azinphos-methyl
      • Barium
      • Benomyl
      • Bentazone
      • Benzene
      • Beryllium
      • Bioresmethrin
      • Boron
      • Bromacil
      • Bromate
      • Bromoxynil
      • Cadmium
      • Captan
      • Carbaryl
      • Carbendazim/Thiophanate-methyl
      • Carbofuran
      • Carbon tetrachloride
      • Carboxin
      • Carfentrazone-ethyl
      • Chloral hydrate (Trichloroacetaldehyde)
      • Chlorantraniliprole
      • Chlordane
      • Chlorfenvinphos
      • Chloride
      • Chlorinated furanones
      • Chlorine
      • Chlorine dioxide, Chlorite, Chlorate
      • Chloroacetic acids: chloroacetic acid, dichloroacetic acid (DCA), trichloroacetic acid (TCA)
      • Chlorobenzene
      • Chloroketones
      • Chlorophenols
      • Chloropicrin
      • Chlorothalonil
      • Chlorpyrifos
      • Chlorsulfuron
      • Chromium
      • Clopyralid
      • Colour (True)
      • Copper
      • Cyanide
      • Cyanogen chloride
      • Cyfluthrin, Beta-cyfluthrin
      • Cypermethrin isomers
      • Cyprodinil
      • 2,4-D [(2,4-Dichlorophenoxy) acetic acid]
      • DDT (1,1,1-trichloro-di-(4-chlorophenyl) ethane)
      • Deltamethrin
      • Diazinon
      • Dicamba
      • Dichlorobenzenes
      • Dichloroethanes: 1,1-dichloroethane, 1,2-dichloroethane
      • Dichloroethenes: 1,1-dichloroethene (1,1-DCE), 1,2-dichloroethene (1,2-DCE)
      • Dichloromethane (methylene chloride)
      • 1,3-Dichloropropene
      • Dichlorprop/Dichlorprop-P
      • Dichlorvos
      • Diclofop-methyl
      • Dicofol
      • Diflubenzuron
      • Dimethoate
      • Diquat (ion), Diquat dibromide
      • Dissolved oxygen
      • Disulfoton
      • Diuron
      • 2,2-DPA
      • Endosulfan
      • Endothal
      • Epichlorohydrin
      • EPTC
      • Esfenvalerate
      • Ethion
      • Ethoprophos
      • Ethylbenzene
      • Ethylenediamine tetraacetic acid (EDTA)
      • Etridiazole
      • Fenamiphos
      • Fenarimol
      • Fenchlorphos
      • Fenitrothion
      • Fenthion
      • Fenvalerate
      • Fipronil
      • Flamprop-methyl
      • Fluometuron
      • Fluoride
      • Flupropanate
      • Formaldehyde
      • Glyphosate
      • Haloacetonitriles
      • Haloxyfop
      • Hardness (as calcium carbonate)
      • Heptachlor and heptachlor epoxide
      • Hexachlorobutadiene
      • Hexazinone
      • Hydrogen sulfide, Sulfide
      • Imazapyr
      • Iodine, Iodide
      • Iprodione
      • Iron
      • Lanthanum
      • Lead
      • Lindane
      • Maldison (Malathion)
      • Mancozeb
      • Manganese
      • MCPA
      • Mercury
      • Metaldehyde
      • Metham
      • Methidathion
      • Methiocarb
      • Methomyl
      • Methyl bromide
      • Metiram
      • Metolachlor/s-Metolachlor
      • Metribuzin
      • Metsulfuron-methyl
      • Mevinphos
      • Molinate
      • Molybdenum
      • Monochloramine
      • Naphthalophos
      • Napropamide
      • Nicarbazin
      • Nickel
      • Nitrate and nitrite
      • Nitrilotriacetic acid (NTA)
      • N-Nitrosodimethylamine (NDMA)
      • Norflurazon
      • Omethoate
      • Organotins: dialkyltins, tributyltin oxide
      • Oryzalin
      • Oxamyl
      • Paraquat
      • Parathion
      • Parathion-methyl
      • Pebulate
      • Pendimethalin
      • Pentachlorophenol
      • Per-fluoroalkyl and poly-fluoroalkyl substances (PFAS)
      • Permethrin
      • pH
      • Picloram
      • Piperonyl butoxide
      • Pirimicarb
      • Pirimiphos methyl
      • Plasticisers
      • Polihexanide
      • Polycyclic aromatic hydrocarbons (PAHs)
      • Profenofos
      • Promecarb
      • Propachlor
      • Propanil
      • Propargite
      • Propazine
      • Propiconazole
      • Propyzamide
      • Pyrasulfotole
      • Pyrazophos
      • Pyroxsulam
      • Quintozene
      • Radionuclides, Specific Alpha and Beta Emitting
      • Radium (radium-226 and radium-228)
      • Radon-222
      • Selenium
      • Silica
      • Silver
      • Simazine
      • Sodium
      • Spirotetramat
      • Styrene (vinylbenzene)
      • Sulfate
      • Sulprofos
      • Taste and Odour
      • Temephos
      • Temperature
      • Terbacil
      • Terbufos
      • Terbuthylazine
      • Terbutryn
      • Tetrachloroethene
      • Thiobencarb
      • Thiometon
      • Thiram
      • Tin
      • Toltrazuril
      • Toluene
      • Total dissolved solids
      • Triadimefon
      • Trichlorfon
      • Trichlorobenzenes
      • 1,1,1-Trichloroethane
      • Trichloroethylene (TCE)
      • Triclopyr
      • Trifluralin
      • Trihalomethanes (THMs)
      • Turbidity
      • Uranium
      • Vernolate
      • Vinyl chloride
      • Xylenes
      • Zinc
    • Drinking water treatment chemicals
      • Aluminium chlorohydrate
      • Aluminium sulfate (alum)
      • Ammonia
      • Ammonium sulfate
      • Calcium hydroxide
      • Calcium hypochlorite
      • Calcium oxide
      • Carbon, granulated activated
      • Carbon, powdered activated
      • Chlorine
      • Copper sulfate
      • Ferric chloride
      • Ferric sulfate
      • Hydrochloric acid
      • Hydrofluorosilicic acid
      • Hydrogen peroxide
      • Hydroxylated ferric sulfate
      • Ozone
      • Polyacrylamide
      • Polyaluminium chloride
      • Polyaluminium silica sulfates
      • Polydiallyldimethylammonium chloride
      • Potassium permanganate
      • Sodium aluminate
      • Sodium bicarbonate
      • Sodium carbonate
      • Sodium fluoride
      • Sodium fluorosilicate
      • Sodium hexametaphosphate
      • Sodium hydroxide
      • Sodium hypochlorite
      • Sodium silicate
      • Sodium tripolyphosphate
      • Sulfuric acid
      • Zinc orthophosphate
  • Appendices
    • Appendix 1: Additional guidance
      • A1.1 Introduction
      • A1.2 Water supply system analysis
      • A1.3 Assessment of water quality data
      • A1.4 Hazard identification
      • A1.5 Risk assessment
      • A1.6 Preventive measures and multiple barriers
      • A1.7 Critical control points
      • A1.8 Chlorination as an example of a critical control point
      • A1.9 References
    • Appendix 2: Further sources of information on drinking water quality management
      • A2.1 Drinking water quality management - general
      • A2.2 Catchment management and source water protection
      • A2.3 Groundwater protection
      • A2.4 Risk assessment and management
      • A2.5 System analysis and management process control and optimisation
      • A2.6 Monitoring and verification
      • A2.7 Materials and chemicals
      • A2.8 Incident and emergency management
      • A2.9 Employee training and awareness
      • A2.10 Research and development
      • A2.11 Documentation and reporting
      • A2.12 Community consultation and communication
      • A2.13 Hazard analysis and critical control point (HACCP)
      • A2.14 Quality management continuous improvement
      • A2.15 Reference web sites
    • Appendix 3: Derivation of microbial treatment targets for enteric pathogens
      • A3.1 Introduction to Quantitative Microbial Risk Assessment (QMRA)
      • A3.2 Adopting the QMRA approach in the Guidelines
      • A3.3 QMRA framework for the calculation of log₁₀ reduction values (LRVs)
      • A3.4 Defining the health outcome target
      • A3.5 Selection of reference pathogens
      • A3.6 Level of reference pathogen contamination in Australian source waters
      • A3.7 Consumption volume of unheated (unboiled) water per person per day
      • A3.8 Dose response relationships
      • A3.9 Disability Adjusted Life Years (DALY) burden per case
      • A3.10 Calculation of LRVs using the QMRA framework
      • A3.11 Interpretation of calculated LRVs for practical treatment guidance
      • A3.12 Understanding log₁₀ reductions
      • A3.13 References
  • Glossary
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Australian Drinking Water Guidelines 6 2011, v3.9

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On this page
  • Sampling locations for drinking water quality monitoring
  • Figure 9.3 Example of sample locations in a typical distribution system
  • Microbial quality – sampling frequency
  • Table 9.4 Recommended minimum frequency of E. coli monitoring
  • Drinking water quality (non-microbial) – sampling frequency
  • Table 9.5 Generic frequencies for monitoring non-microbial drinking water quality as supplied to the consumer
  1. Part 3: Monitoring
  2. Chapter 9: Overview of monitoring (Revised 2021)
  3. 9.5 Verification of drinking water quality

9.5.2 Drinking water quality monitoring

Drinking water quality monitoring is used to provide assurance that the quality of drinking water in the distribution system, as supplied to the consumer, is meeting guideline values, agreed levels of service, and/or any regulatory requirements. It can provide an additional means of detecting any unrecognised problems that may be occurring upstream or within the distribution system, and can trigger the necessary corrective actions.

Drinking water quality monitoring cannot prevent unsafe water being supplied to consumers, as results are typically not available for days to weeks after collecting the sample, so that any corrective actions occur after the water has been supplied. Drinking water quality monitoring should not, therefore, be used in place of or as a substitute for operational monitoring.

As it is neither physically nor economically feasible to test for all drinking water quality characteristics equally, monitoring effort and resources should be directed at significant or ā€˜key’ characteristics – that is, those characteristics identified in the system-specific hazard identification and risk assessment process as likely to be present. These key characteristics require more frequent monitoring. Characteristics that the risk assessment shows are unlikely to be present, or pose a low risk, are monitored very infrequently, or may not need to be included in the drinking water quality monitoring program.

Generally, sampling and analysis are required most frequently to assure microbial safety and less often for chemical and radiological compounds. This is because of the acute and almost universal health risk posed by waterborne microbial pathogens, whereas the guideline values for most (but not all) chemical characteristics are based on lifetime exposure. In the absence of a specific event (e.g. spills, chemical overdosing at a treatment plant), episodes of chemical contamination that would constitute an acute health concern are rarer.

Sampling locations for drinking water quality monitoring

Drinking water quality monitoring confirms the final quality of water that is supplied to consumers. As such, it needs to be undertaken throughout the distribution system at points representative of the quality of water supplied to consumers’ properties (e.g. at or close to water meters).

The location and number of sampling points within a distribution system are determined by the complexity of the system. For purposes of management, monitoring and reporting, large and complex distribution systems should be divided into discrete water quality monitoring zones. These zones are typically:

  • supplied from a single source, and/or

  • hydraulically separated from other zones (single or multiple sources).

As the priority for monitoring drinking water quality is to confirm microbial safety, the design of the microbiological sampling program often dictates the location of sampling points. Sampling points are normally placed well into the distribution system to be representative of what most consumers have received. They should also be spread geographically to give coverage across the system or zone.

Circumstances where microbial quality has the potential to change within a distribution system need to be considered. This is most likely where the system is depressurised, increasing the chance for ingress (e.g. at a service tank). Sample points should, therefore, be included downstream of any tanks (often called a subzone) even though the source water may be unchanged.

Samples for physical and chemical quality monitoring can usually be taken from the sample points used for microbiological monitoring. Since physical and chemical quality monitoring requires many fewer samples in a given period, a decision must be made on whether to rotate sampling around all the sample points within a zone (providing an indication of performance across the zone) or to use only one or two fixed sample points (providing an opportunity to plot trends).

For chemical characteristics that are more stable and unaffected by the distribution system, sampling can occur at the entry point to the distribution system. For some characteristics that change across the distribution system e.g. trihalomethanes (THMs), additional monitoring from specific areas may be required to ensure the data collected are representative of all water supplied.

Operational monitoring such as chlorine residual monitoring is typically also carried out concurrently at these sample points, as well as at other strategic locations within the distribution system, such as entry points (e.g. outlets of service reservoirs/tanks), trunk mains, and dead ends.

Figure 9.3 provides an illustration of sampling locations within a typical distribution system and shows how operational monitoring and drinking water quality monitoring are integrated.

Figure 9.3 Example of sample locations in a typical distribution system

Microbial quality – sampling frequency

Routine monitoring for specific microbial pathogens is not recommended as it is usually complex, expensive and time-consuming, and may fail to detect their presence. Rather, the recommendation is to monitor for the microbial indicator bacterium E. coli as a marker for the presence of faecal contamination and the possible presence of microbial pathogens (see fact sheets on microbial indicators). Whilst there are limitations to the use of E. coli as an indicator of faecal contamination of water supplies (e.g. Cryptosporidium oocysts may survive chlorine disinfection and may be present in the absence of E. coli), it is currently the best verification indicator available for faecally related microbial quality.

The recommended minimum monitoring frequency for E. coli, based on World Health Organization recommendations (WHO 2008), is detailed in Table 9.4. Samples should be collected at points within the distribution system that are representative of the quality of water supplied to consumers.

Table 9.4 Recommended minimum frequency of E. coli monitoring


Samples that are representative of the quality of water supplied to consumers should be collected and analysed for E. coli at the following minimum frequency:

Population in monitoring zone
Minimum number of samples

>100,000

Six samples per week per monitoring zone, plus one additional sample per month per monitoring zone for each 10,000 above 100,000

5,000–100,000

One sample per week per monitoring zone plus one additional sample per month per monitoring zone for each 5,000 above 5,000

1,000–5,000

One sample per week per monitoring zone (52 samples per year)

<1000

One sample per week per monitoring zone (52 samples per year). Where the water supply in this category is remote, the recommended sampling frequency needs to be balanced against the logistics of collecting the samples, the risk profile for the supply, and the risk mitigation processes that are operating on the supply. With remote water supply systems, regular physical inspections and operational monitoring are more beneficial to ensuring water quality than infrequent E. coli sampling.

Sampling frequency should be increased at times of flooding or emergency operations and following repair work or interruptions to supply.


The frequency of sampling should be increased during any significant environmental events or emergency operations, or following interruptions of supply or repair work. More frequent sampling should also occur at sample points where previous results have indicated potential problems. Operational monitoring such as disinfectant residuals, temperature and turbidity are often taken concurrently with E.coli to provide complementary evidence of system status and enhance interpretation of data.

The results of the E. coli monitoring program will not prevent unsafe water being supplied to consumers, and drinking water quality monitoring should not be substituted for or used in place of a well-constructed operational monitoring program. For systems serving small communities, regular physical inspections of the water supply system, and the monitoring of critical processes and activities, such as chlorination, yield more information than infrequent sampling (see Chapter 4).

Drinking water quality (non-microbial) – sampling frequency

Monitoring requirements for non-microbial characteristics will vary for each water supply system, depending on the key characteristics identified through water supply system analysis and risk assessment. In general, characteristics that pose a high level of risk require more frequent monitoring, while those posing a low risk require less monitoring. The closer the mean value of a characteristic is to the guideline value, and/or the greater its variability, the more frequent the monitoring needs to be. Those characteristics that are deemed, on the basis of a thorough analysis of the catchment and water supply system, unlikely to be present will typically require very infrequent monitoring, or no monitoring at all.

Table 9.5 provides a generic guide to monitoring frequency for drinking water quality characteristics. Monitoring frequencies and characteristics for individual systems should be adjusted as needed, based on the ongoing review of the water supply system and risk assessment.

Table 9.5 Generic frequencies for monitoring non-microbial drinking water quality as supplied to the consumer

Frequency of sampling - Weekly
Frequency of sampling - Monthly
Frequency of sampling - Quarterly
Frequency of sampling - Annually+
Comments

Physical characteristics

pH

Temperature

Total dissolved solids¹

Colour

Turbidity

Dissolved oxygen

Hardness²

Taste and odour

¹ If reverse osmosis used, or there are known salinity issues, otherwise quarterly

² If water is treated for hardness

Water treatment related chemicals (if used)

Fluoride¹

Aluminium²

Chlorine

Copper (seasonal)

Any related organic contaminants, e.g. acrylamide, carbon tetrachloride, epichlorohydrin

¹ Will not require frequent monitoring if fluoridation is not carried out or if naturally occurring fluoride is either absent or at a level below the level for optimal fluoridation.

² Aluminium not likely to be present if no alum-based coagulant is used.

Disinfection byproducts (DBPs)

Trihalomethanes (THMs)Ā¹š„’Ā²

Ammonia, nitrite, nitrate²

Bromate, formaldehyde³

Chlorite⁓

¹ Where chlorine or chloramine are used.

² Where chloramine is used.

³ Where ozone is used.

⁓ Where chlorine dioxide or liquid chlorine is used.

If detected at elevated concentrations, close to, or above guideline values, additional related DBPs should also be analysed.

Inorganics

Iron

Manganese

Arsenic, nitrate, fluoride, selenium, lead, mercury¹

Ammonia, cadmium, chromium, nickel, zinc, copper, hydrogen sulfide

Tin, silver beryllium, uranium, iodide, molybdenum, boron, barium

¹ Priority contaminants: quarterly sampling for groundwater sources, more frequent monitoring when detected at elevated concentrations; otherwise sampling reduced to annually, seasonally or event-related (e.g. storm events, reservoir turnover events).

Pesticides and organic toxicants

If detected or potential presence

If not detected

Monthly or quarterly sampling for pesticides/organic toxicants previously (or potentially) detected; seasonally annually, or event-related (e.g. storm events, spills) for other pesticides/organic toxicants.

Radiological

Radionuclides

New supplies should be assessed quarterly for one year, then every 2 years (groundwater) or 5 years (surface water). Increase frequency to quarterly if guideline screening levels exceeded.

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Last updated 8 months ago