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Document ID ca-gcdwqgtd-2021-01-13 Title Guidelines for Canadian Drinking Water Quality: Guideline Technical Document – Cyanobacterial Toxins URL https://www.canada.ca/en/health-canada/services/publications/healthy-living/guidelines-canadian-drinking-water-quality-guideline-technical-document-cyanobacterial-toxins-document.html Jurisdiction /ca Subdomain(s) Drinking water Language en Status completed Analyzed at 2026-03-18 13:27:29.904742+00:00 Relevance Defines drinking water quality guidelines and treatment for cyanotoxins.

Q Qualitative Requirements (77)

Req ID Category Intent Legal Status Name Subdomain(s) Context Conditions Confidence
#Q001reportinghealthrecommendedInfant Formula Precautionary Notificationdrinking waterConsequently, as a precautionary measure during a bloom event, when levels of total microcystins in treated water are detected above a reference value of 0.0004 mg/L (0.4 µg/L), drinking water authorities should inform the public in the affected area that an alternate suitable source of drinking water (such as bottled water) should be used to reconstitute infant formula.During a bloom event, when levels of total microcystins in treated water are detected above a reference value of 0.0004 mg/Lhigh
#Q002monitoringtreatmentrecommendedVariant Analysis Requirementdrinking waterAnalysis should be conducted for all of the measurable microcystin variants that are both dissolved in the water and bound within the cyanobacterial cells using a laboratory validated method.high
#Q003treatmenttreatmentrecommendedIntracellular and Dissolved Microcystins Treatmentdrinking waterSimilarly, water should be treated to remove both intracellular (cell-bound) and dissolved microcystins.high
#Q004administrativeoperationalrecommendedMonitoring and Response Strategydrinking waterResponsible authorities and water supply managers should develop an appropriate monitoring, assessment and response strategy for their systems.high
#Q005monitoringhealthrecommendedRoutine Monitoring of Susceptible Suppliesdrinking waterDrinking water supplies known or suspected to be susceptible to blooms should be monitored routinely for the presence of cyanobacteria.When supplies are known or suspected to be susceptible to bloomshigh
#Q006monitoringoperationalrecommendedVisual Monitoring During Peak Seasondrinking waterWater bodies that have exhibited blooms should be visually monitored during the peak season (usually late May to early October, but this may deviate depending on local conditions).During peak seasonhigh
#Q007monitoringhealthrecommendedSampling Upon Bloom Detectiondrinking waterSamples should be collected for analysis if a bloom is detected or suspected by visual inspection, and may also be collected as part of routine surveillance.If a bloom is detected or suspected by visual inspectionhigh
#Q008monitoringoperationalrecommendedSampling During and After Collapsedrinking waterIt is recommended that authorities analyze samples during, and after the collapse of the bloom to better characterize the extent of the risk posed by the cyanobacteria (see Appendix B).During and after the collapse of a bloomhigh
#Q009monitoringoperationalrecommendedSampling Location for Source Water Bloomsdrinking waterIn the source water, if a bloom develops, it should be sampled to establish the extent of its spread and the variability in the population. Sampling from a water body should be done as close to the inlet/shore and/or the bloom formation as possible.If a bloom develops in the source waterhigh
#Q010monitoringtreatmentrecommendedRaw Water Sampling at Intakedrinking waterRaw water samples should be collected at the intake to the treatment plant prior to any pretreatment, including prechlorination or filtration to determine the concentration of microcystins entering the treatment plant.high
#Q011monitoringtreatmentrecommendedTreated Water Sampling Locationdrinking waterTreated samples should be taken at the treated water tap of the treatment plant after the final treatment step.high
#Q012monitoringhealthrecommendedToxin Analysis Conditiondrinking waterToxin analysis should be performed on the raw and treated water supply if the responsible authority determines that the drinking water intake is vulnerable to contamination by a cyanobacterial bloom.If the responsible authority determines that the drinking water intake is vulnerable to contamination by a cyanobacterial bloomhigh
#Q013administrativereportingrecommendedConfirming Lab Methodology for Total Microcystinsdrinking waterUtilities should confirm the sample processing and analytical methods used by the laboratory to ensure that total microcystins (as defined above) are being measured.high
#Q014monitoringreportingrecommendedPhysicochemical Method Recommendation for Detected Microcystinsdrinking waterIt is recommended that when microcystins are detected in source or drinking water using ELISA or PPIA, a portion of subsequent samples should be analyzed using a physico-chemical method (i.e., LC-MS/MS) so that the predominant variants in a bloom can be identified and quantified and potential low level microcystin concentrations can be measured.When microcystins are detected in source or drinking water using ELISA or PPIAhigh
#Q015reportinghealthrecommendedNotification of Communities for MAC Exceedancedrinking waterIf results for treated water exceed the MAC, the sampling authority should follow standard protocol for notifying communities and other appropriate authorities and agencies.If results for treated water exceed the MAChigh
#Q016reportinghealthrecommendedNotification of Dialysis Providersdrinking waterDialysis treatment providers at all levels (e.g., large facilities/hospitals, small community facilities, mobile units, providers for independent/home dialysis) should also be notified, especially if it is a first-time occurrence for blooms on this supply.If results for treated water exceed the MAChigh
#Q017prohibitionhealthmandatoryProhibition of Contaminated Water for Dialysisdrinking waterDialysis with water contaminated with cyanobacterial toxins presents severe health risks and must be avoided.When water is contaminated with cyanobacterial toxinshigh
#Q018reportinghealthrecommendedDo Not Consume Advisory for Small Systemsdrinking waterFor small systems that lack the necessary knowledge or treatment capabilities, the use of a do not consume advisory should be considered.For small systems that lack necessary knowledge or treatment capabilitieshigh
#Q019corrective_actionoperationalrecommendedActions for Treated Water MAC Exceedancedrinking waterIf results for treated water exceed the MAC, the responsible authorities should consider the following actions: resample the treated water supply (confirmation sample) and perform additional toxin analysis; initiate risk assessment consultation and decision-making; and review possible treatment adjustments and strategy for continued monitoring of the treated water supply.If results for treated water exceed the MAChigh
#Q020corrective_actionhealthrecommendedActions for Confirmation Sample MAC Exceedancedrinking waterIf results of the confirmation sample exceed the MAC, the responsible authorities should consider the following actions: notify communities and other appropriate authorities; issue a do not consume advisory; [...] consider treatment improvements, intake adjustments or use of an alternative supply as part of ongoing consultation and decision-making; communicate that the addition of algicides may be harmful, as this would release toxins from the cells, making them more difficult to remove; and continue monitoring the raw water and treated water supply.If results of the confirmation sample exceed the MAChigh
#Q021prohibitionhealthrecommendedProhibition of Boil Water Advisoriesdrinking waterBoil water advisories should not be issued as a response to the detection of microcystins in water supplies;In response to the detection of microcystinshigh
#Q022reportingoperationalrecommendedReporting When Confirmation Sample Passes MACdrinking waterIf results of the confirmation sample do not exceed the MAC, results should be sent to the communities and other appropriate authorities and agencies. Authorities and water providers should continue to visually monitor the source water for intensification of the existing bloom or bloom recurrence...If results of the confirmation sample do not exceed the MAChigh
#Q023monitoringhealthrecommendedVisual Monitoring for Residential/Private Suppliesdrinking waterThe recommended approach for residential scale and private supplies is for owners or authorities to visually monitor the source waters during the peak season for evidence of increasing cyanobacterial cell density or bloom development.During the peak seasonhigh
#Q024reportinghealthrecommendedPrivate Supply Notificationdrinking waterOwners of residential scale and private drinking water systems who suspect that their water has been contaminated with cyanobacteria should consult their local health authority as to whether a concern exists and what actions should be taken.When owners suspect their water has been contaminated with cyanobacteriahigh
#Q025treatmenthealthrecommendedConsultation Before Residential Treatment System Installationdrinking waterIt is recommended that a qualified person be consulted prior to selecting and installing a residential scale treatment system.Prior to selecting and installing a residential scale treatment systemhigh
#Q026monitoringreportingrecommendedUse of Accredited Laboratory for Analysisdrinking waterFor these reasons, microcystin analyses should be conducted by an accredited laboratory and/or water utilities should discuss in detail the methodology and quality assurance/quality control (QA/QC) of the laboratory selected to conduct the analyses.high
#Q027monitoringoperationalrecommendedAmber Glass Bottles for Sample Collectiondrinking waterIn general, samples for microcystin analysis should be collected in amber glass bottles as microcystins have been shown to sorb to polypropylenehigh
#Q028monitoringoperationalrecommendedSample Preparation for Dissolved and Total Microcystinsdrinking waterWhen treatment is needed for removal of microcystins, utilities also need to have an understanding of the amounts that are present in both the intracellular and dissolved (extracellular) forms. ... In this case, two samples should be taken, with one processed for total microcystin analysis and the other filtered in the laboratory or field and then analyzed for dissolved microcystins (extracellular).When treatment is needed for removal of microcystinshigh
#Q029monitoringoperationalrecommendedFiltration to Minimize Cell Damagedrinking waterSamples should be carefully filtered to minimize cell damage so that the microcystin concentration in the filtrate is representative of the dissolved fraction.When filtering samples for dissolved microcystins analysishigh
#Q030monitoringoperationalrecommendedTreatment Plant Analysis Certificationdrinking waterIn cases where utilities choose to perform analyses at the treatment plant, it is recommended that the analyses be conducted by a well-trained technician or analyst and that duplicate samples be sent periodically to an accredited laboratory to confirm the on-site analyses.When utilities choose to perform analyses at the treatment planthigh
#Q031administrativehealthrecommendedConsultation Prior to Intervention Measuresdrinking waterBefore implementing any intervention measure in a water supply, the appropriate authorities should be consulted to determine if permits or approvals are required.Before implementing any intervention measurehigh
#Q032operationaltreatmentrecommendedSludge Isolation During Bloomdrinking waterTherefore, during a cyanobacterial bloom, sludge and sludge supernatant should be isolated from the water treatment plant and supernatant should not be returned to the inlet of the plant.During a cyanobacterial bloomhigh
#Q033operationaltreatmentrecommendedFilter-to-Waste Proceduredrinking waterAdditionally, backwash water from the filters may contain cyanobacterial cells and/or dissolved microcystins; hence, filter-to-waste should be practised to prevent the reintroduction of cells and toxins into the treatment train.During periods of high algal concentrationshigh
#Q034treatmentoperationalmandatoryTreatment Optimization and Monitoringdrinking waterUtilities need to ensure that the treatment processes in place have been optimized for removal of both cyanobacterial cells and dissolved microcystins and that the appropriate monitoring is being conducted to ensure that adequate removal is occurring at each step in the treatment process.high
#Q035monitoringoperationalmandatoryCell Lysis During Analysisdrinking waterit is important that analysis of treated water include cell lysis so that the total microcystin concentration is determined.high
#Q036designtreatmentrecommendedPoint of Entry Filtration Installationdrinking waterThe first step should be the installation of a filtration system at the point of entry (POE) to the home to reduce the number of cyanobacterial cells that are present in water used for bathing and washing dishes. This POE filtration system should also be installed upstream of any disinfection that may already be present in the home treatment system (e.g., UV or chlorination).When an individual household treats surface water containing a cyanobacterial bloomhigh
#Q037designtreatmentrecommendedPoint of Use Activated Carbon and RO Filtrationdrinking waterThe final filtration step should be a filter system installed at the point of use (POU) of drinking water—for example, before the kitchen faucet. This POU filtration system should include an activated carbon filter followed by an RO filter.When an individual household treats surface water containing a cyanobacterial bloomhigh
#Q038treatmenthealthrecommendedResidential Treatment Device Certificationdrinking waterHealth Canada does not recommend specific brands of drinking water treatment devices, but it strongly recommends that consumers use devices that have been certified by an accredited certification body as meeting the appropriate NSF International (NSF)/American National Standards Institute (ANSI) drinking water treatment unit standards.When consumers select drinking water treatment deviceshigh
#Q039monitoringhealthrecommendedResidential Periodic Testingdrinking waterperiodic testing should be conducted by an accredited laboratory on both the water entering the home and the finished water (at the POU) to verify that the treatment devices are effective. Consumers should request that the laboratory analyze for total microcystins, which includes both the microcystins that are within the cells of the cyanobacteria and the dissolved microcystins in the water.For residential treatment systemshigh
#Q040operationaltreatmentrecommendedMaintenance of Residential Treatment Systemsdrinking waterconsumers should verify its expected longevity and replace the medium and service the system when required, as per the manufacturer's recommendations.For activated carbon and RO systemshigh
#Q041administrativeoperationalrecommendedCyanobacterial Bloom Action Plandrinking wateran action plan should be established or updated prior to bloom season for systems using a surface water source that is or may be vulnerable to cyanobacterial blooms.For systems using a surface water source vulnerable to bloomshigh
#Q042operationaloperationalrecommendedMonitor Training for Bloom Identificationdrinking waterAs accumulations of algae and pollen can be mistaken for cyanobacterial blooms, monitors should receive appropriate training to correctly identify blooms.high
#Q043monitoringreportingrecommendedFinished Water Sampling Collectiondrinking waterThe water provider or authorities should collect samples of finished water in the treatment plant, after the water has undergone the final treatment step and prior to its entry into the distribution system. Samples should be collected, stored and transported following instructions from the analytical laboratory.If signs of a bloom are detectedhigh
#Q044monitoringoperationalrecommendedSample Storage and Transportdrinking waterIn general, samples should be clearly labelled and kept cool (not frozen) and in the dark (e.g., in coolers) after collection and during transport.high
#Q045corrective_actionhealthrecommendedDo Not Consume Advisory and Alternativesdrinking waterThe lead authority should issue a “Do not consume” advisory and notify communities and other appropriate agencies or authorities. If possible, an alternate source of drinking water (such as bottled water) should be identified. Dialysis treatment providers or units in the community should also be notified.If total microcystin levels are confirmed to be above the guideline of 1.5 µg/Lhigh
#Q046monitoringhealthrecommendedResampling Following Advisorydrinking waterAuthorities and water providers should continue to resample and analyse the treated water until the concentration of total microcystins is confirmed to be at or below 1.5 µg/L.When an advisory is issuedhigh
#Q047monitoringreportingrecommendedTreated Water Analytical Method Selectiondrinking waterIn general, laboratory enzyme-linked immunosorbent assay (ELISA), protein phosphatase inhibition assays (PPIA) or a physicochemical method such as liquid chromatography with tandem mass spectrometry (LC-MS/MS) should be used to measure total microcystins in treated water.high
#Q048monitoringreportingguidanceAdda-specific ELISA Considerationdrinking waterAuthorities may also wish to consider use of an Adda-specific ELISA system as this type of ELISA has been shown to provide a good representation of total microcystinshigh
#Q049administrativeoperationalrecommendedResponse Consultation Requirementdrinking waterThe degree of response to the presence of total microcystins should be discussed with the appropriate authorities (e.g., for system ownership, regulation and health) and will depend on a risk-based assessment of the significance and extent of the problem, taking into account the history and variability of the quality of the raw water supply and the documented effectiveness of the treatment process.high
#Q050monitoringoperationalrecommendedLaboratory Coordination for Samplingdrinking waterUtilities should obtain specific instructions from the laboratory on sample collection, preservation and shipping.high
#Q051administrativereportingrecommendedLaboratory Preparation Method Validationdrinking waterit is important for responsible authorities to ensure that laboratories are validating the methods chosen for sample preparation.high
#Q052operationaltreatmentrecommendedAlgicide Use Discouragementdrinking waterthe use of algicides to control blooms in drinking water source waters is discouraged.high
#Q053administrativeoperationalrecommendedImplementation Guidance Sourcedrinking waterSpecific guidance related to the implementation of drinking water guidelines should be obtained from the appropriate drinking water authority in the affected jurisdictionhigh
#Q054monitoringoperationalrecommendedSite-Specific Monitoring Program Developmentdrinking waterBecause the distribution of cyanobacteria affects the risk assessment, monitoring programs will be dependent on site-specific considerations and should be developed on a case-by-case basis.high
#Q055monitoringoperationalrecommendedSampling Frequency Determination Factorsdrinking waterIn order to determine an appropriate sampling frequency, the following factors should be considered: past frequency of occurrence of blooms and cyanotoxins in the water source or nearby water bodies; characteristics of the water body (size, depth, current/flow, thermal stratification) and changes in these characteristics (e.g., prolonged periods of stagnation or decreased water levels); distribution of cyanobacteria, particularly under bloom conditions, which is often patchy and variable over time during the day; source water quality (nutrient levels, turbidity, clarity); seasonal and weather influences (inside/outside peak bloom season, temperature, prevailing wind strength and direction, rainfall) and changes to these influences; noted changes (increases/decreases) in monitoring program elements (cell counts, pigments, such as phycocyanin and chlorophyll-a, toxins); and adequacy of treatment and capacity of the treatment plant to deal with cyanotoxins.high
#Q056monitoringoperationalmandatoryFinished Water Sample Quenchingdrinking waterStudies have shown that certain microcystins are destroyed in the presence of chlorine and the use of quenchers is needed. However, care must be taken when adding quenchers to samples as Froscio et al. (2010) found that sodium thiosulphate, sodium sulfite and taurine all affected analysis using ELISA, whereas ascorbic acid did not affect the assay results.When analyzing finished drinking water containing disinfectantshigh
#Q057administrativereportingmandatoryAuthority Proficiency in Analytical Method Limitationsdrinking waterit is important for responsible authorities to have an understanding of the cross-reactivity, sensitivity, matrix interferences, detection limits and reporting format of the type of ELISA system being used so that the limitations of the analytical results can be considered in the decision-making process.When using ELISA methods for routine analysishigh
#Q058treatmenttreatmentrecommendedPre-change Coagulation Optimizationdrinking waterit is recommended that the existing coagulation/flocculation processes be optimized before considering a change in coagulants during a cyanobacterial bloom (Newcombe et al., 2010).During a cyanobacterial bloom before changing coagulantshigh
#Q059monitoringtreatmentmandatoryBromate Potential Characterizationdrinking waterUtilities should also be aware that the use of ozone may result in the formation of bromate and other DBPs. As such, characterization of the source water needs to be undertaken to ascertain the potential for bromate formation (Health Canada, 1998).When using ozone for microcystin oxidationhigh
#Q060reportinghealthrecommendedInfant Formula Advisory Durationdrinking waterThe advice for bottle-fed infants should continue until microcystin levels are below 0.4 µg/L. ... authorities should continue to advise parents of infants of the approach to take when reconstituting infant formula, until microcystins are no longer detected in the treated water.When total microcystins are detected in treated water above the reference value for infantshigh
#Q061monitoringoperationalrecommendedRaw Water Measurement Requirements during Responsedrinking waterWater providers or utilities should also collect raw water samples at this time to measure microcystins and cell counts and identify cyanobacteria species.When signs of a bloom are detected and finished water samples are collectedhigh
#Q062reportingreportingmandatoryTimely Detection Reportingdrinking waterWhen microcystins are detected in the treated water, it is important to ensure that appropriate agencies and contact people (identified in the action plan) are informed in a timely manner.When microcystins are detected in treated waterhigh
#Q063monitoringoperationalrecommendedPre-installation Water Testing for Private Systemsdrinking waterGenerally, before a treatment system is installed, the water should be tested to determine general water chemistry and to provide an estimate of the concentration of the contaminant to be removed.Before a residential treatment system is installedhigh
#Q064corrective_actionoperationalrecommendedTreatment Adjustment Actiondrinking waterWhere feasible, appropriate actions should be taken to reduce microcystin levels in the treated water.When microcystins are detected in the treated waterhigh
#Q065treatmentoperationalmandatoryFlocculation Mixing and Speed Optimizationdrinking waterSufficient mixing must be provided at the point of chemical addition to ensure rapid contact, and an appropriate mixing speed must be determined to optimize the flocculation process (Newcombe, 2009).When removing cyanobacterial cells using coagulation and flocculationhigh
#Q066monitoringoperationalmandatoryStaggered Sampling for Performance Assessmentdrinking waterIf treatment performance is being assessed, then samples of raw and treated water need to be staggered to account for the residence time of water in the treatment plant.If treatment performance is being assessedhigh
#Q067designtreatmentrecommendedRO Activated Carbon Filter Componentdrinking waterRO systems should include an activated carbon filter within the unit, or a separate activated carbon device can be purchased and installed before (upstream of) the RO unit.For residential-scale RO systemshigh
#Q068monitoringreportingrecommendedMethod Comparison Conversion Requirementdrinking waterDirect comparison of ELISA and LC-MS/MS results are not recommended without a conversion of the LC-MS/MS data based on the cross-reactivity of the detected variants before summing the concentration of all of the variants (Loftin et al., 2008).When comparing ELISA and LC-MS/MS resultshigh
#Q069monitoringoperationalrecommendedVisual Monitoring Timing Considerationdrinking waterWhen planning visual monitoring, it is important to consider that cyanobacteria may be mixed back into the water column during the day.high
#Q070treatmentoperationalrecommendedCoagulant and pH Optimization Jar Testingdrinking waterOperational procedure for optimizing cyanobacterial cell removal in conventional treatment plants using coagulation and flocculation.When removing cyanobacterial cells using coagulation and flocculationhigh
#Q071administrativeoperationalrecommendedEarly Analytical Laboratory Coordinationdrinking waterIt is recommended that water providers establish early contact with the analytical laboratory as part of the action plan in order to minimize the time required for sample analysis and management response.As part of the action plan implementationhigh
#Q072operationaltreatmentrecommendedFrequent Filter Backwashing for Cell Breakthrough Preventiondrinking waterFrequent backwashing has been recommended to minimize the risk of breakthrough of cells into filtered water (Newcombe, 2009).During periods of high algal concentrationshigh
#Q073administrativehealthmandatoryNatural Health Product Microcystin Tolerance LimitsotherIn Canada, licensing of natural health products that contain cyanobacteria must adhere to a finished product tolerance limit of 0.02 µg MC-LR/kg body weight (bw) per day or a raw material tolerance limit of 1 part per million (ppm) (Health Canada, 2015).For licensing of natural health products containing cyanobacteriahigh
#Q074treatmentoperationalrecommendedJar Testing for Coagulation Optimizationdrinking waterThe appropriate coagulant and coagulation pH should be determined through jar testing, and tests should be carried out on waters with high algal concentrations to maximize cell removal.When removing cyanobacterial cells using coagulation and flocculationhigh
#Q075administrativeoperationalrecommendedAction Plan Elementsdrinking waterThe action plan should: describe the sampling strategy (parameters, frequency, timing, locations) to be followed for the duration of the bloom with respect to both routine sampling and resampling when microcystins are detected; identify the analytical laboratory or laboratories that can do microcystin analysis; ensure that agreement(s) and protocol(s) are in place with lab(s) for receiving and processing samples in a timely manner, and for communicating results from the lab to the appropriate contact people; outline individual responsibilities for how samples will be collected and delivered to the laboratory; specify the method(s) of microcystin detection/analysis that can be used; identify the appropriate contact people to receive the results from the lab and who they must notify if microcystins are detected; identify which authority or authorities are responsible to decide further notifications and actions; identify which authority will take the lead role in notifying communities and other appropriate agencies or authorities; set out a communications plan describing the circumstances and target groups for notifications, including when an advisory is issued or rescinded; include sample communications products, such as messages, Qs &As and press releases, to deal with different situations (e.g., microcystins level above guideline, microcystins detected below guideline level but still of concern for infants) and to provide clear guidance to the public; and identify any corrective actions (e.g., treatment adjustments) and the triggers for such actions.For systems using a surface water source vulnerable to bloomshigh
#Q076administrativeoperationalmandatoryLocal Trigger Decision Authoritydrinking waterAny decisions concerning triggers for possible action based on cell counts or biovolume values are made at the local or provincial/territorial levels, taking into account site-specific knowledge.When establishing triggers for action based on cell counts or biovolumehigh
#Q077monitoringoperationalguidanceAntimicrobial Preservative and Storagedrinking waterThe addition of an antimicrobial preservative may be necessary, along with storage of samples in dark cold conditions.When preserving raw and finished drinking water sampleshigh

P Quantitative Requirements (60)

Req ID Category Intent Legal Status Name Subdomain(s) Limit Type Limit Value Context Conditions Confidence
#P001chemicalhealthmandatorytotal microcystinsdrinking waterMAC0.0015 mg/LA seasonal maximum acceptable concentration (MAC) of 0.0015 mg/L (1.5 µg/L) is established for total microcystins in drinking water.seasonalhigh
#P002chemicalhealthmandatorytotal microcystinsdrinking waterMAC1.5 µg/LA seasonal maximum acceptable concentration (MAC) of 0.0015 mg/L (1.5 µg/L) is established for total microcystins in drinking water.seasonalhigh
#P003chemicalhealthrecommendedtotal microcystinsdrinking waterunknown0.0004 mg/Las a precautionary measure during a bloom event, when levels of total microcystins in treated water are detected above a reference value of 0.0004 mg/L (0.4 µg/L), drinking water authorities should inform the public in the affected area that an alternate suitable source of drinking water (such as bottled water) should be used to reconstitute infant formula.during a bloom event for reconstituting infant formulahigh
#P004chemicalhealthrecommendedtotal microcystinsdrinking waterunknown0.4 µg/Las a precautionary measure during a bloom event, when levels of total microcystins in treated water are detected above a reference value of 0.0004 mg/L (0.4 µg/L), drinking water authorities should inform the public in the affected area that an alternate suitable source of drinking water (such as bottled water) should be used to reconstitute infant formula.during a bloom event for reconstituting infant formulahigh
#P005chemicalhealthguidelinetotal microcystin-LRdrinking waterunknown0.001 mg/LThe World Health Organization has established a provisional guideline value of 0.001 mg/L for total microcystin-LR.International considerations (WHO)high
#P006chemicalhealthguidelinetotal microcystinsdrinking waterunknown0.0013 mg/LThe Australian National Health and Medical Research Council established a guideline of 0.0013 mg/L for total microcystins in drinking waterInternational considerations (Australia)high
#P007chemicalhealthguidelinemicrocystinsdrinking waterunknown0.0003 mg/LThe U.S. EPA has established short-term drinking water health advisories: For children less than six years old, the health advisories are 0.0003 mg/L for microcystinsFor children less than six years old (US EPA)high
#P008chemicalhealthguidelinecylindrospermopsindrinking waterunknown0.0007 mg/LThe U.S. EPA has established short-term drinking water health advisories: For children less than six years old... 0.0007 mg/L for cylindrospermopsin.For children less than six years old (US EPA)high
#P009chemicalhealthguidelinemicrocystinsdrinking waterunknown0.0016 mg/LFor the rest of the population, health advisories of 0.0016 mg/L for microcystins... were established.For the rest of the population (US EPA)high
#P010chemicalhealthguidelinecylindrospermopsindrinking waterunknown0.003 mg/LFor the rest of the population, health advisories of... 0.003 mg/L for cylindrospermopsin were established.For the rest of the population (US EPA)high
#P011chemicalhealthmandatoryMC-LRotherunknown0.02 µg/kg bw per dayIn Canada, licensing of natural health products that contain cyanobacteria must adhere to a finished product tolerance limit of 0.02 µg MC-LR/kg body weight (bw) per daynatural health productshigh
#P012chemicalhealthmandatoryMC-LRotherunknown1 ppmor a raw material tolerance limit of 1 part per million (ppm)natural health products raw materialhigh
#P013chemicaltreatmentmandatorymicrocystinsdrinking waterrequirement0.0003 mg/LProtocol P477 requires testing of a device for the reduction of 0.004 mg/L of microcystins in the influent water down to 0.0003 mg/L in the treated water (NSF International, 2015).NSF/ANSI Protocol P477 testinghigh
#P014chemicalhealthguidelinetotal microcystinsdrinking watertreatment_goal0.056 µg/kg bw per dayA tolerable daily intake (TDI) from this study can be derived as follows: The TDI for microcystins is approximately 0.056 micrograms per kilogram body weight per day.based on liver toxicity in rats (Heinze, 1999)high
#P015chemicalhealthguidelinetotal microcystinsdrinking watertreatment_goal2 µg/LThe HBV for total microcystins is 2 micrograms per litre (rounded).Health-based value (HBV)high
#P016chemicalhealthmandatorymicrocystinsdrinking waterMAC1 µg/LThe state of Ohio has established a maximum contaminant level of 1 µg/L for microcystinsOhio drinking water regulationshigh
#P017chemicalhealthguidelineanatoxin-adrinking waterMAC3 µg/Lthe state of Oregon has established limits of 3 µg/L for anatoxin-aOregon state limitshigh
#P018chemicalhealthguidelinecylindrospermopsindrinking waterMAC1 µg/LOregon has established limits of... 1 µg/L for cylindrospermopsinOregon state limitshigh
#P019chemicalhealthguidelinesaxitoxindrinking waterMAC3 µg/LOregon has established limits of... 3 µg/L for saxitoxinOregon state limitshigh
#P020chemicalhealthguidelinemicrocystinsdrinking waterMAC1 µg/LNew Zealand has established provisional maximum acceptable values of 1 µg/L for microcystins (as MC-LRequiv)New Zealand provisional maximum acceptable valueshigh
#P021chemicalhealthguidelineanatoxin-adrinking waterMAC6 µg/LNew Zealand has established provisional maximum acceptable values of... 6 µg/L for anatoxin-aNew Zealand provisional maximum acceptable valueshigh
#P022chemicalhealthguidelineanatoxin-a(s)drinking waterunknown1 µg/LNew Zealand has established provisional maximum acceptable values of 1 µg/L for anatoxin-a(s)New Zealand provisional maximum acceptable valueshigh
#P023chemicalhealthguidelinehomoanatoxin-adrinking waterunknown2 µg/LNew Zealand has established provisional maximum acceptable values of 2 µg/L for homoanatoxin-aNew Zealand provisional maximum acceptable valueshigh
#P024chemicalhealthguidelinenodularindrinking waterunknown1 µg/LNew Zealand has established provisional maximum acceptable values of 1 µg/L for nodularinNew Zealand provisional maximum acceptable valueshigh
#P025chemicalhealthguidelinesaxitoxinsdrinking waterunknown3 µg/LNon-regulatory health advisory levels of 1 μg/L and 3 μg/L were developed for cylindrospermopsin and saxitoxins, respectively.Australian National Health and Medical Research Council (NHMRC) advisoryhigh
#P026chemicaltreatmentrecommendedmicrocystins (ELISA detection limit)drinking waterrequirement<= 0.05 µg/LWhen the potential presence of low levels (<0.4 µg/L) of microcystins needs to be determined, enhanced-sensitivity ELISA methods with detection limits equal to or below 0.05 µg/L may be necessary.for determining potential presence of low levels (<0.4 µg/L)high
#P027chemicalhealthguidelineSaxitoxin (New Zealand)drinking waterMAC3 µg/LNew Zealand has established provisional maximum acceptable values of ... 3 µg/L for saxitoxin (as equivalents) (Chorus, 2012).New Zealand provisional maximum acceptable valueshigh
#P028chemicalhealthguidelineCylindrospermopsin (New Zealand)drinking waterMAC1 µg/LNew Zealand has established provisional maximum acceptable values of ... 1 µg/L for cylindrospermopsinNew Zealand provisional maximum acceptable valueshigh
#P029chemicalhealthguidanceCylindrospermopsin (Australia Advisory)drinking waterunknown1 µg/LNon-regulatory health advisory levels of 1 μg/L and 3 μg/L were developed for cylindrospermopsin and saxitoxins, respectively [by NHMRC].Australian NHMRC non-regulatory health advisoryhigh
#P030chemicaltreatmentguidelineMicrocystins (influent test concentration)drinking waterrequirement0.004 mg/LProtocol P477 requires testing of a device for the reduction of 0.004 mg/L of microcystins in the influent waterNSF/ANSI Protocol P477 testing specificationhigh
#P031operationaloperationalrecommendedFree chlorine residual (operational)drinking waterOG0.5–1.5 mg/Lmicrocystins are efficiently oxidized if pH is maintained below 8, the chlorine dose is greater than 3 mg/L and 0.5–1.5 mg/L of free chlorine residual is present after 30 minutes of contact timefor efficient oxidation of microcystinshigh
#P032operationaloperationalrecommendedChlorine dose (operational)drinking waterOG> 3 mg/Lmicrocystins are efficiently oxidized if pH is maintained below 8, the chlorine dose is greater than 3 mg/L and 0.5–1.5 mg/L of free chlorine residual is present after 30 minutes of contact timefor efficient oxidation of microcystinshigh
#P033operationaltreatmentrecommendedPAC dose (general recommendation)drinking waterOG20 mg/LNewcombe et al. (2009) made a general recommendation that a PAC dose of 20 mg/L and a contact time of at least 45 minutes should be considered for removal of most dissolved microcystinsfor removal of dissolved microcystinshigh
#P034operationaltreatmentrecommendedPAC contact time (general recommendation)drinking waterOG>= 45 minutesNewcombe et al. (2009) made a general recommendation that a PAC dose of 20 mg/L and a contact time of at least 45 minutes should be consideredfor removal of dissolved microcystinshigh
#P035designoperationalguidanceWater intake depthdrinking waterunknown>= 6 mAn intake located at least 6 m below the water surface is less likely to be affected by cyanobacteria present in the water body.to minimize intake of cyanobacteria during bloomshigh
#P036operationaltreatmentguidancepH (for efficient chlorine oxidation of microcystins)drinking waterOG< 8 pH unitsmicrocystins are efficiently oxidized if pH is maintained below 8, the chlorine dose is greater than 3 mg/L and 0.5–1.5 mg/L of free chlorine residual is present after 30 minutes of contact timefor efficient chlorine oxidation of microcystinshigh
#P037operationaltreatmentguidanceChlorine contact time (for microcystin oxidation)drinking waterOG30 minutesmicrocystins are efficiently oxidized if pH is maintained below 8, the chlorine dose is greater than 3 mg/L and 0.5–1.5 mg/L of free chlorine residual is present after 30 minutes of contact timefor efficient chlorine oxidation of microcystinshigh
#P038operationaltreatmentguidanceChlorine CT (for microcystin oxidation)drinking waterOG15–25 mg·min/LFor waters with a DOC of 5 mg/L and a microcystin concentration of 5 µg/L or less, CT values between 15 and 25 mg·min/L should be sufficient to achieve a treated water concentration below 1.0 µg/L.for waters with DOC of 5 mg/L and microcystin <= 5 µg/Lhigh
#P039operationalaestheticguidancePotassium permanganate discoloration thresholddrinking waterAO0.05 mg/LTreatment plants considering potassium permanganate for oxidation of microcystins should be aware that permanganate can discolour water when it is present at concentrations in excess of 0.05 mg/L.to avoid consumer complaints due to water discolorationhigh
#P040operationaltreatmentguidancePAC dose (for cylindrospermopsin removal)drinking waterOG33 mg/LThe results demonstrated that to remove 5 µg/L of cylindrospermopsin to less than 1 µg/L, a PAC dose of 33 mg/L and a contact time of 30 minutes would be required.to remove 5 µg/L of cylindrospermopsin to < 1 µg/Lhigh
#P041operationaltreatmentguidancePAC contact time (for cylindrospermopsin removal)drinking waterOG30 minutesThe results demonstrated that to remove 5 µg/L of cylindrospermopsin to less than 1 µg/L, a PAC dose of 33 mg/L and a contact time of 30 minutes would be required.to remove 5 µg/L of cylindrospermopsin to < 1 µg/Lhigh
#P042operationaltreatmentguidanceFree chlorine residual (for cylindrospermopsin removal)drinking waterOG0.5 mg/LRodriguez et al. (2007a) found that maintaining a chlorine residual of 0.5 mg/L with a 30-minute reaction time could completely degrade 60 µg/L of cylindrospermopsin.to degrade 60 µg/L of cylindrospermopsinhigh
#P043operationaltreatmentguidanceChlorine contact time (for cylindrospermopsin removal)drinking waterOG30 minutesRodriguez et al. (2007a) found that maintaining a chlorine residual of 0.5 mg/L with a 30-minute reaction time could completely degrade 60 µg/L of cylindrospermopsin.to degrade 60 µg/L of cylindrospermopsinhigh
#P044designtreatmentguidanceResidential filter pore sizedrinking waterOG<= 1 µmBased on the size of cyanobacteria, a filter with an absolute pore size of 1 µm or less will likely remove most cells, but this will depend on the type of cyanobacteria present in the water.residential-scale point of entry (POE) filtrationhigh
#P045chemicalhealthmandatorymicrocystins (Ohio MCL)drinking waterMAC1 µg/LThe state of Ohio has established a maximum contaminant level of 1 µg/L for microcystinsOhio drinking water regulationshigh
#P046chemicalhealthguidelineanatoxin-a (Oregon limit)drinking waterMAC3 µg/Lthe state of Oregon has established limits of 3 µg/L for anatoxin-aOregon state limitshigh
#P047chemicalhealthguidelinecylindrospermopsin (Oregon limit)drinking waterMAC1 µg/LOregon has established limits of... 1 µg/L for cylindrospermopsinOregon state limitshigh
#P048chemicalhealthguidelinesaxitoxin (Oregon limit)drinking waterMAC3 µg/LOregon has established limits of... 3 µg/L for saxitoxinOregon state limitshigh
#P049chemicalhealthguidancesaxitoxins (Australia Advisory)drinking waterunknown3 µg/LNon-regulatory health advisory levels of 1 μg/L and 3 μg/L were developed for cylindrospermopsin and saxitoxins, respectively [by NHMRC].Australian NHMRC non-regulatory health advisoryhigh
#P050chemicalhealthmandatorymicrocystins (international standards)drinking waterMAC1 µg/LBrazil, France and Spain, have also established drinking water standards of 1 µg/L, however, for all microcystinsstandards in Brazil, France, and Spainhigh
#P051designtreatmentguidanceGAC empty bed contact time (EBCT)drinking waterOG> 10 minutesAlvarez et al. (2010) demonstrated that, in most cases, the EBCT for GAC filter adsorbers needs to be greater than ten minutes to achieve adequate MC-LR removalfor adequate MC-LR removal in GAC filter adsorbershigh
#P052chemicalhealthguidelinetotal microcystins (HBV)drinking watertreatment_goal0.002 mg/LAn HBV of 0.002 mg/L (2 µg/L) can be calculated using Heinze (1999).Health-based value (HBV)high
#P053chemicalhealthguidelinemicrocystins (Oregon limit)drinking waterMAC1–12 µg/Lthe state of Oregon has established limits of 3 µg/L for anatoxin-a, 1 µg/L for cylindrospermopsin, 1–12 µg/L (indicated as “to be determined”) for microcystins and 3 µg/L for saxitoxin.Oregon state limits; range indicated as to be determinedhigh
#P054chemicalhealthguidancetotal microcystins (Do Not Consume trigger)drinking waterMAC> 1.5 µg/LIf the resample confirms a concentration of total microcystins above the guideline of 1.5 µg/L, proceed to Box 9... issue a “Do not consume” advisory.Confirmed treated water concentration exceeding guidelinehigh
#P055chemicalhealthrecommendedtotal microcystins (Infant formula advice trigger)drinking waterunknown> 0.4 µg/Las a precautionary approach where microcystins are detected in treated water above the reference value for infants of 0.4 µg/L, drinking water authorities should consider informing the public... that an alternate suitable source of drinking water... should be used to reconstitute infant formula.Treated water detection above infant reference valuehigh
#P056operationaloperationalguidanceVisual monitoring intervaldrinking waterrequirement1–2 weeksThe approach would require visual monitoring for evidence of bloom formation at regular intervals (one or two weeks).During peak bloom season or susceptibilityhigh
#P057chemicaltreatmentrecommendedmicrocystins (Analytical protocol threshold)drinking waterrequirement> 0.15 µg/LELISA or PPIA could be used for the initial screening of samples, followed by HPLC-PDA or LC-MS/MS analysis on samples above the detection limit (approximately > 0.15 µg/L).Trigger for secondary physicochemical analysis after initial screeninghigh
#P058chemicalhealthguidelinemicrocystins (US EPA child HA)drinking waterunknown0.0003 mg/LFor children less than six years old, the health advisories are 0.0003 mg/L for microcystins and 0.0007 mg/L for cylindrospermopsin.Children less than six years old (US EPA)high
#P059chemicalhealthguidelinecylindrospermopsin (US EPA child HA)drinking waterunknown0.0007 mg/LFor children less than six years old, the health advisories are 0.0003 mg/L for microcystins and 0.0007 mg/L for cylindrospermopsin.Children less than six years old (US EPA)high
#P060chemicalhealthmandatorymicrocystins (International Standards - Singapore/Uruguay)drinking waterMAC1 µg/LDrinking water standards for MC-LR ... have been set by other international jurisdictions, including the Czech Republic, Singapore and Uruguay ... 1 µg/LStandards for microcystin-LRhigh

D Definitions (135)

Req ID Category Name Context Confidence
#D001Total microcystinsTotal microcystins is the sum of the measurable microcystin variants that are both dissolved in the water (extracellular) and bound within the cyanobacterial cells (intracellular).high
#D002ALPalkaline phosphatasehigh
#D003ALS-PDCamyotrophic lateral sclerosis/parkinsonism-dementia complexhigh
#D004ALTalanine aminotransferasehigh
#D005ANSIAmerican National Standards Institutehigh
#D006AOPadvanced oxidation processhigh
#D007APCIatmospheric pressure chemical ionizationhigh
#D008ASTaspartate aminotransferasehigh
#D009BMAAbeta-methylamino-L-alaninehigh
#D010bwbody weighthigh
#D011CIconfidence intervalhigh
#D012CTconcentration x timehigh
#D013CYPcytochrome P450high
#D014DAFdissolved air flotationhigh
#D015DBPdisinfection by-producthigh
#D016DMBAdimethylbenzanthracenehigh
#D017DMSOdimethyl sulphoxidehigh
#D018DNAdeoxyribonucleic acidhigh
#D019DOCdissolved organic carbonhigh
#D020EBCTempty bed contact timehigh
#D021ELISAenzyme-linked immunosorbent assayhigh
#D022EPAEnvironmental Protection Agency (U.S.)high
#D023equivequivalentshigh
#D024ERKextracellular signal-regulated protein kinasehigh
#D025ESIelectrospray ionizationhigh
#D026FSHfollicle stimulating hormonehigh
#D027GACgranular activated carbonhigh
#D028GCgas chromatographyhigh
#D029GDgestation dayhigh
#D030GGTgamma-glutamyltransferasehigh
#D031GnRHgonadotropin-releasing hormonehigh
#D032GSHglutathionehigh
#D033GSTglutathione S-transferasehigh
#D034HAAhaloacetic acidhigh
#D035HBVhealth-based valuehigh
#D036HPLChigh-performance liquid chromatographyhigh
#D037HUHazen unithigh
#D038IC50median inhibitory concentrationhigh
#D039ISOInternational Organization for Standardizationhigh
#D040LCliquid chromatographyhigh
#D041LCATlecithin-cholesterol acyltransferasehigh
#D042LD50median lethal dosehigh
#D043LDHlactate dehydrogenasehigh
#D044LDTDlaser diode thermal desorptionhigh
#D045LHluteinizing hormonehigh
#D046LOAELlowest-observed-adverse-effect levelhigh
#D047LOQlimit of quantificationhigh
#D048Mmoles per litre (molar)high
#D049MACmaximum acceptable concentrationhigh
#D050MALDImatrix-assisted laser desorption/ionizationhigh
#D051MAPKmitogen-activated protein kinasehigh
#D052MCmicrocystin variant (e.g., MC-LR, MC-LA, MC-YA, MC-RR, MC-YR)high
#D053MDLmethod detection limithigh
#D054MFmicrofiltrationhigh
#D055MMPmatrix metalloproteinasehigh
#D056MMPB2-methyl-3-methoxy-4-phenylbutyric acidhigh
#D057MRLminimum reporting levelhigh
#D058mRNAmessenger ribonucleic acidhigh
#D059MS/MStandem mass spectrometryhigh
#D060MTDmaximum tolerated dosehigh
#D061MWCOmolecular weight cut-offhigh
#D062NFnanofiltrationhigh
#D063NOAELno-observed-adverse-effect levelhigh
#D064NOMnatural organic matterhigh
#D065NSFNSF Internationalhigh
#D066NTUnephelometric turbidity unithigh
#D067OATPorganic anion-transporter polypeptidehigh
#D068ORodds ratiohigh
#D069PACpowdered activated carbonhigh
#D070PCRpolymerase chain reactionhigh
#D071PNDpostnatal dayhigh
#D072POEpoint of entryhigh
#D073POUpoint of usehigh
#D074PP1protein phosphatase 1high
#D075PP1cprotein phosphatase 1chigh
#D076PP2Aprotein phosphatase 2Ahigh
#D077PPIAprotein phosphatase inhibition assayhigh
#D078ppmpart per millionhigh
#D079QAquality assurancehigh
#D080QCquality controlhigh
#D081PDAphotodiode arrayhigh
#D082PQLpractical quantitation levelhigh
#D083RNAribonucleic acidhigh
#D084ROreverse osmosishigh
#D085ROSreactive oxygen specieshigh
#D086S99000 x g supernatant fraction from rat liver homogenatehigh
#D087SCCStandards Council of Canadahigh
#D088SPEsolid-phase extractionhigh
#D089SRRstandardized rate ratiohigh
#D090TDItolerable daily intakehigh
#D091TEFtoxicity equivalency factorhigh
#D092THMtrihalomethanehigh
#D093THPTamm-Horsfal proteinhigh
#D094TOCtotal organic carbonhigh
#D095TOFtime of flighthigh
#D096TPAO-tetradecanoylphorbol 13-acetatehigh
#D097UFultrafiltrationhigh
#D098UPLCultra-high-performance liquid chromatographyhigh
#D099UVultraviolethigh
#D100Visvisiblehigh
#D101cyanobacterial bloomlarge accumulation of cells recognized by the colouration from their pigmentshigh
#D102planktonic cyanobacteriathose that live freely in the water columnhigh
#D103Benthic cyanobacteriathose that grow on bottom surfaceshigh
#D104Adda groupunique amino acid side chainhigh
#D105alkaloidsa broad group of low to moderate molecular weight (< 1000 Da) compounds that contain ring structures and at least one carbon–nitrogen bondhigh
#D106akinetesresting stages that can provide protection for the organism in unfavourable temperatureshigh
#D107biovolume estimatescalculated by obtaining reference values for cell volume for each of the species present and multiplying these by the corresponding cell numbers present as determined from cell countshigh
#D108LOQ / MRLindicate the lowest concentration of an analyte that can be determined with an acceptable level of accuracy and precisionhigh
#D109MDLrepresent the minimum concentration of an analyte that can be measured and reported with confidence that the concentration is greater than zerohigh
#D110acanthocytesabnormal red blood cells characterized by a spiked external membranehigh
#D111cyanobacteriabacteria that have features in common with algae (they obtain energy through photosynthesis and are of similar size)high
#D112hepatotoxinsliver toxinshigh
#D113neurotoxinsnervous system toxinshigh
#D114dermatotoxinsskin toxinshigh
#D115irritant toxinstoxins that affect the skin and mucous membraneshigh
#D116Saxitoxinsa group of related toxins that include saxitoxin, neosaxitoxin, the gonyautoxins and C-toxinshigh
#D117Cylindrospermopsina toxic alkaloid with a molecular weight of approximately 400 Da and a tricyclic ring structure as one of its identifying featureshigh
#D118Lipopolysaccharides (LPSs)complex molecules having toxic properties that are integral to the cell wall of all Gram-negative bacteria, including cyanobacteriahigh
#D119lag periods in microcystin biodegradationthe time between when microorganisms encounter the toxin and when breakdown beginshigh
#D120Microcystinshepatotoxins that are generally regarded as the most important of the freshwater cyanotoxins owing to their stability and resilience to biological and chemical breakdown, their widespread occurrence and their potential to reach high concentrations in blooms and scums; functionally, they are inhibitors of the enzyme protein phosphatase, acting by disrupting the balance of phosphorylation and dephosphorylation in the structures that give liver cells their shape.high
#D121anatoxinsneurotoxins that interfere with the activity of the nerve transmitter acetylcholine. This, in turn, affects the functioning of the nervous system by disrupting communication between nerves and muscle cells.high
#D122ALS-PDCneurodegenerative disease with symptoms similar to Parkinson's disease and Alzheimer's disease.high
#D123phycocyaninthe most common photosynthetic accessory pigment to chlorophyll, and the most specific pigment present in cyanobacteria cellshigh
#D124matrix effectsion suppression or enhancement effects that can be difficult to control in field sampleshigh
#D125THPTamm-Horsfal protein, the predominant mammalian protein in urine.high
#D126Intervention measuresactions intended to destroy an active bloomhigh
#D127Sonicationthe use of ultrasonic sound waves to disrupt cyanobacterial cellshigh
#D128Lyngbyatoxinsdermatotoxins produced by the benthic marine cyanobacteria Lyngbya majusculahigh
#D129Aplysiatoxinsanother category of dermatatoxins produced by some types of cyanobacteriahigh
#D1302-MIB2-methyl isoborneolhigh
#D131MERISMedium Resolution Imaging Spectrometerhigh
#D132LCMRLlowest concentration MRLhigh
#D133MALDI-TOF-MSmatrix-assisted laser desorption/ionization time-of-flight mass spectrometryhigh
#D134LDTD-APCI-MS/MSlaser diode thermal desorption–atmospheric pressure chemical ionization interface coupled to tandem mass spectrometryhigh
#D135JNKc-Jun N-terminal protein kinasehigh