Appendix 8 – Methods for measuring water quality
This Appendix details the methods for all water quality measurements and calculations as required in Criterion 2.6. Some calculations are only required for certain waterbody types as classified in Indicator 2.6.4, while others are applicable across all waterbodies.
|
Section |
Waterbody Type Applicability |
|---|---|
|
8.1 Introduction |
|
|
8.2 Total Nitrogen (TN) and Total Phosphorous (TP) load |
A, B and C |
|
8.3 Percentage of fines in feed |
A, B and C |
|
8.4 Receiving waterbody classification |
A, B and C |
|
8.5 Waterbody Unit of Management |
A |
|
8.6 Components of a Water Quality Monitoring Network |
A |
|
8.7 Site level monitoring and baseline characterisation |
A |
|
8.8 Point source effluent measurement |
B |
|
8.9 Effluent flow contribution |
B |
|
8.10 Dissolved oxygen measurement |
A, B and C |
|
8.11 Water quality analytical methods |
A, B and C |
8.1 Introduction
The water quality monitoring methods are based on the type of waterbody in which a site is situated and the type of effluent discharge from the culture system.
The first sections of the Appendix, sections 8.2 to 8.4, apply to all waterbody types and culture systems. They include methods to calculate nutrient releases, fines in feed and how to classify the type of receiving waterbody.
The methods in sections 8.5 to 8.7 outline the steps to determine the Waterbody Unit of Management, form a collaborative network with other aquaculture sites, how to conduct a 24-month water quality monitoring survey and characterise the baseline of the waterbody. These sections apply to sites located in waterbodies that are the most sensitive to nutrient loading, based on the classification outlined in section 8.4.
Calculations can be made using the ASC Water Quality Calculator provided by ASC.
For culture systems with point source discharges, methods outlined in sections 8.8 to 8.10 determine the steps to measure nutrients in effluent waters, calculate the effluent flow contribution to the receiving waterbody and monitor dissolved oxygen.
ASC has benchmarked the ASC Farm Standard methods for water quality against applicable regulatory requirements. Outcomes of the benchmark are available via the ASC Programme Centre.
8.2 Total Nitrogen and Total Phosphorous load (Indicators 2.6.1 and 2.6.2)
To calculate Total Nitrogen (TN) and Total Phosphorous (TP) load per tonne of production, one of the four following formulas shall be used per site:
-
Formula 1: shall apply to sites in Type A, B and C waterbodies releasing diffuse source effluents.
-
Formula 2: shall apply to pond-based sites with point-source effluents discharging directly (i.e. without treatment) to Type A or B waterbodies. This formula requires knowledge of the effluent volume.
-
Formula 3: shall apply to pond-based sites that have some form of effluent treatment. Sites shall control and measure nutrient levels and volumes of effluents entering Type A or B waterbodies. This formula requires estimation of daily water exchange to determine the effluent volume and is most suitable for earthen pond-sites with < 10% daily water exchange.
-
Formula 4: shall apply to some land-based sites discharging to Type B or C waterbodies that do not need to record effluent water quality.
Unless otherwise stated, all values shall apply over the previous 12-month period. Net production volume shall be calculated using the following formula:
Formula 1:
TN load shall be calculated using the following formula:
-
TN release (kg) shall be the difference between the TN added to the system in feed (TN feed (kg)) and the TN in animals. It is calculated as follows:
-
TN in feed shall be equal to the mass of feed used (tonnes, dry weight) multiplied by the feed TN content:
-
The mass of TN in animals shall be calculated as follows:
-
TP load shall be calculated using the following formula:
-
TP release (kg) shall be the difference between the TP added to the system in feed (TP feed (kg)) and the TP in animals. It shall be calculated as follows:
TP in feed shall be equal to the mass of feed used (tonnes, dry weight) multiplied by the feed TP content:
-
The mass of TP in animals shall be calculated as follows:
Formula 2:
TN load shall be calculated using the following formula:
-
Where TN out (kg) and TN in (kg) shall be the mass of TN in effluent and influent water respectively.
-
TN out shall be calculated from the mean TN concentration in effluent, [TN] effluent (mg/L, which is equal to g/m3), effluent volume (m3), and a scaling factor of 0.001:
-
TN in shall be calculated from mean TN concentration in influent, [TN] influent (mg/L, which is equal to g/m3), influent volume (m3), and a scaling factor of 0.001:
-
TP load shall be calculated as follows:
-
Where TP out (kg) and TP in (kg) shall be the mass of TP in effluent and influent water respectively.
-
TP out shall be calculated from mean TP concentration in effluent, [TP] effluent (µg/L, which is equal to mg/m3), effluent volume (m3), and a scaling factor of 0.000001:
-
TP in shall be calculated from mean TP concentration in influent, [TP] influent (µg/L, which is equal to mg/m3), influent volume (m3), and a scaling factor of 0.000001:
Formula 3:
The average daily water exchange rate (%/day x 0.01), multiplied by the total pond volume, multiplied by the numbers of days in a year shall give a proxy for the daily effluent volume and influent volume respectively. This formula assumes the influent volume equals the effluent volume.
Annual TN load shall be calculated using the following formula:
-
Days (n) shall be the number of days during the previous 12 months in which ponds were operational. If the ponds were in continuous operation, the daily value (above) shall be multiplied by 365 to obtain the TN load over a 12-month period.
-
[TN]effluent and [TN]influent shall be the mean TN concentrations in effluent and influent respectively.
-
Volumepond shall be the average water volume of all ponds at the site over the 12-month period on days in which ponds were operational.
-
Daily water exchange shall be the percentage of the total pond volume of all ponds in production at the site that is renewed each day divided by 100. For example, if daily 10% of the total pond volume at the site is renewed, then the daily water exchange is 10/100 = 0.1
Daily Total P load shall be calculated using the following formula:
-
Days (n) shall be the number of days during the previous 12 months in which ponds were operational.
-
If the ponds were in continuous operation, the daily value (above) shall be multiplied by 365 to obtain the TP load over a 12-month period.
-
-
[TP]effluent and [TP]influent shall be the mean of the TP concentrations in effluent and influent respectively.
-
Volumepond shall be the average water volume of all ponds at the site over the 12-month period on days in which ponds were operational.
-
Daily water exchange shall be the percentage of the total pond volume of all ponds in production at the site that is renewed each day divided by 100. For example, if daily 10% of the total pond volume at the site is renewed, then the daily water exchange is 10/100 = 0.1
-
Formula 4:
Nutrient loads shall be calculated using the following formula:
-
TN input (kg) shall be the TN input from feed and fertiliser combined over the preceding 12 months. e.g. if a feed contains 5% TN and 100kg is used, then the TN input is 5kg.
-
TP input (kg) shall be the TP input from feed and fertiliser combined over the preceding 12 months.
8.3 Percentage of fines in feed (Indicator 2.6.3)
The site shall determine the percentage of fines in feed using one of the two methods outlined below. Testing shall take place either on-site (Appendix 8 (8.3.1)) after feed has been delivered to the site, or by the feed manufacturer prior to the feed arriving on-site (Appendix 8 (8.3.2)).
8.3.1 On-site testing
This method shall be used when the percentage of fines is determined on-site. The method encompasses the sampling and testing of feed and the calculation of fines. The determination of fines shall be conducted when the feed is delivered to site.
Feed sampling
The steps to conduct the sampling of feed lots per site are as follows:
-
A minimum of six samples shall be taken from the lot, evenly distributed throughout the lot.
-
Each sample shall have a mass of 500g.
-
A pooled sample shall be created from the six individual samples (i.e. total of 3kg based on six samples of 500g).
-
The pooled sample shall be reduced to one sample for testing of 500g.
Feed testing
Feed testing can be conducted by either a manual test or by using a sifting machine. The sample of fines shall be sieved with a sieve of a maximum sieve opening of:
-
1mm when the feed diameter is ≤5mm; or
-
2.36mm when the feed diameter is >5mm.
Manual feed testing
The steps to conduct the testing are as follows:
-
The sieve shall be placed on top of the fines accumulation box. The type of sieve (based on the maximum sieve opening) shall be determined based on the feed diameter.
-
The sieve shall be placed on the balance and tared.
-
The sample shall be weighed on the sieve, note the weight (m0).
-
The feed shall be sieved smoothly and carefully for about 30 seconds.
-
The lid shall be removed and the fines remaining in the accumulation box shall be weighed.
-
A brush shall be used to remove all the feed particles from the sieves.
-
The feed particles that have passed through the sieve are called fines (md).
-
If the feed is fatty, or if the fines that have passed through the sieve are unevenly distributed, the test shall be replicated.
Sifting machine feed testing
The steps to conduct testing with a sifting machine are as follows:
-
The sieve shall be placed on top of the fines accumulation box. The type of sieve (based on the maximum sieve opening) shall be determined based on the feed diameter.
-
The sieve shall be placed on the balance and tared.
-
The analysis sample shall be weighed on the sieve, note the weight (m0).
-
The sieve shall be placed on the sifting machine and then the cover shall be closed properly.
-
The sifting machine shall run 2 x 1 minute.
-
The lid shall be removed and the fines remaining in the accumulation box shall be weighed.
-
The feed particles that have passed through the sieve are called fines (md).
-
If the feed is fatty, or if the fines that have passed through the sieve are unevenly distributed, the test shall be replicated.
Calculations – both methods:
The following equation shall be used to calculate the percentage of fines in the feed sampled: fines percentage (%) = (md/m0) x 100.
-
m0 = weight of feed before sieving.
-
md = weight of fines that has passed through all sieves.
8.3.2 Feed manufacturer testing
If fines testing is conducted by the feed manufacturer, results shall demonstrate a <0.25% difference between manufacturer-tested fines content and on-site tested fines content. Either the manual feed testing or sifting machine feed testing method shall be used to determine on-site fines content.
The requirements for feed manufacturer testing are as follows:
-
One full year of quarterly on-site tests shall be collected, with resulting values <1% fines and a difference between manufacturer and on-site testing <0.25% fines content.
-
If this is achieved, on-site sampling shall be conducted at least once per year to validate the quarterly test results received by the manufacturer.
-
On-site sampling shall revert to every quarter for another year (12 months) if at least one of the following applies:
-
On-site sampling results show a >0.25% difference in fines compared to the results from the manufacturer; or
-
There is a change in feed supplier; or
-
There is a substantial change to transport, handling or storage of feed.
-
8.4 Receiving Waterbody classification (Indicator 2.6.4)
The site shall classify the Receiving Waterbody (RW) according to Table 1 based on:
-
The default waterbody type, or
-
The result of the Hydraulic Retention Time (HRT), flow rate and Total Suspended Solids (TSS) calculations (Appendix 8 (8.4.1)). These classification parameters determine the sensitivity of a waterbody to nutrient loading.
Table 1. Overview of the Receiving Waterbody types and thresholds for the classification parameters.
|
Receiving Waterbody Type |
Default Waterbody Type |
Hydraulic retention time (HRT) and flow rate/total suspended solids (TSS) thresholds |
|---|---|---|
|
Type A |
Default for enclosed freshwater and semi-enclosed marine/brackish waterbodies unless Type C requirements are met |
HRT ≥5 days |
|
Type B |
Default for confined or linear waterbodies not classified as Type A and unless Type C requirements are met |
HRT <5 days |
|
Type C |
Default for channelised waterbodies, exposed near-shore and offshore marine/brackish waterbodies Flow rate and TSS are used to distinguish between Types B and C freshwater and brackish systems only |
HRT <5 days Flow rate is >1000m3/s, or TSS is >20mg/L at low flow |
8.4.1 Hydraulic Retention Time (HRT)
HRT shall be calculated using the following formula, where HRT is used to classify the RW (according to Table 1):
-
Q (m3/s) = the steady state (long-term) average flow rate through the waterbody outflow.
-
A (km2) = the surface area of the waterbody.
-
z̄ (m) = the mean depth of the waterbody.
8.4.1.1 Flow rate calculation
Flow rate data is required to calculate the HRT of the RW. The method to calculate flow rate is based on the characteristics of the waterbody:
Marine waterbodies:
-
Flow rate shall be calculated as the mean current speed (flow velocity (m/s)) through the waterbody outflow, multiplied by the cross-sectional area (m2) of the waterbody outflow.
Freshwater and brackish waterbodies:
-
Four (quarterly) measurements shall be taken upstream from the outflow point in a calendar year.
-
Measurements shall be taken during periods of medium and low tidal flow.
-
Low flow shall be determined as the lowest of the four flow measurements taken in a calendar year.
-
Flow rate (Q) (m3/s) shall be calculated as the mean current speed (flow velocity (m/s)) multiplied by the cross-sectional area (m2) at a location immediately upstream from the outflow point.
8.4.1.2 Determination of total suspended solids (TSS) at low flow
Flow rate and TSS calculations are used to distinguish between Type B and C freshwater and brackish waterbodies only (TSS is >20mg/L at low flow, according to Table 1). The following method shall be used to determine TSS:
-
Samples shall be collected during periods of medium and low flow (and can be the same time as flow rate data is collected).
-
Samples shall be collected at approximately 0.5m from the surface.
-
Samples shall be analysed according to the analytical methods in Appendix 8 (8.11).
8.5 Waterbody Unit of Management (WUM) (Indicator 2.6.5)
A Waterbody Unit of Management (WUM) is the geographic or spatial scope of the waterbody. The WUM shall be defined per site and include information on aquaculture sites discharging effluents in the waterbody.
Using one of the following methods, the site shall demonstrate that a WUM has been created per site:
-
Where a WUM has not been defined, the site shall define a new WUM136136The site can submit information to the ASC Water Quality Advisory Committee (WQAC) to resolve issues with defining the spatial scope of the WUM. More information on the process can be found here.; or,
-
Evidence of an existing defined WUM shall be presented; or,
-
Evidence that a WUM has been defined by a national or regional regulatory body for the jurisdiction in which a site is located shall be presented.
A map shall be created or presented for the WUM which indicates the following characteristics:
-
The spatial boundaries of the WUM. Semi-enclosed waterbodies (for example a bay) within a larger waterbody shall equate to the WUM by default.
-
The distribution of all operational aquaculture sites releasing effluents into the WUM, including cages and any land-based sites, further differentiating ASC-certified sites, non-certified sites belonging to ASC Certificate Holders, ASC applicants and non-certified sites.
-
Any sites discharging effluents to a river or channel flowing into a Type A waterbody located <1km upstream of the river/channel mouth.
-
Any zones identified for future aquaculture farming expansion.
-
The location of the sampling sites for the members of the Water Quality Monitoring Network, according to the method outlined in Appendix 8 (8.7).
-
The map shall be accompanied by a written rationale explaining the basis for the boundary setting. The map shall be revised on an annual basis (if required) to reflect any changes in these characteristics.
8.6 Components of a Water Quality Monitoring Network (Indicator 2.6.7)
The intent of the Water Quality Monitoring Network (WQMN) is to establish a mechanism for collaboration and the sharing of information between aquaculture sites in Type A waterbodies. This will provide the foundation for an Area Management Agreement (AMA) in a future version of the ASC Farm Standard.
Based on the WUM characterised according to the method outlined in Appendix 8 (8.5), the site shall establish, join a WQMN or present evidence of an area-based approach to manage water quality at a national level.
The steps to establish a WQMN per site are as follows:
-
Outreach shall be conducted to ASC-certified sites and non-certified sites belonging to ASC Certificate Holders within the defined WUM. This will determine the members of the WQMN.
-
A Terms of Reference (ToR) document shall be developed, outlining how the members will meet the objectives of the WQMN regarding the sharing of water quality data.
-
A focal point shall be appointed to coordinate data sharing and collective agreement of the ToR of the WQMN.
-
Where a WQMN has been established in the WUM, the site shall join the WQMN and agree to the ToR and meet the objectives of the WQMN.
If water quality is managed using an area-based approach by the national or regional regulatory body in which a site is located, the site shall present evidence demonstrating that the area-based approach meets the requirements of the WQMN, as outlined in Appendix 8 (8.6.1).
8.6.1 WQMN Requirements
The requirements of the WQMN are as follows:
-
Members shall agree upon, and define the boundaries of, the WUM.
-
Data sharing shall take place between members. This shall include:
-
The locations of the water quality monitoring site locations for the site level monitoring survey, according to the method outlined in Appendix 8 (8.7); and
-
The results of the monitoring surveys and baseline characterisations to determine the baseline for the waterbody, according to the method outlined in Appendix 8 (8.7); and
-
Results of the BOD calculations per site, according to the method outlined in Appendix 8 (8.7.3); and
-
Information relating to scenarios indicating excessive nutrient loading, as outlined in Indicator 2.6.12, if one of these scenarios has been determined.
-
8.7 Site level monitoring survey and baseline characterisation(Indicators 2.6.8 to 2.6.12)
The site level monitoring survey outlines a method to collect data to establish the trophic status and baseline characterisation of Type A waterbodies.
8.7.1 Site level monitoring survey
The steps to conduct the monitoring survey per site are as follows:
-
At the initial audit, 24 months of baseline data shall be presented if available.
-
Where 24 months of baseline data is not available, 12 months of baseline shall be presented.
-
If no baseline data is available, a sampling plan shall be presented which outlines the method to initially collect 12 months, and subsequently, 24 months of baseline data.
-
-
The following parameters shall be monitored: dissolved oxygen (DO) concentration and percent saturation, Secchi disk (SD) depth, Chlorophyll-a (Chl-a), Total Nitrogen (TN) and Total Phosphorus (TP) nutrient concentrations.
-
Sampling shall be conducted at two locations as follows:
-
A ‘downstream, near-field’ impacted location: immediately downstream of the site. This shall be the same location for each sampling event.
-
An ‘upstream, far-field’ non-impacted reference location: at a minimum 500m upstream from the site. This shall be the same location for each sampling event.
-
The sampling locations shall be identified with GPS coordinates on the map of the WUM.
-
-
Sampling shall be repeated quarterly over a 12-month period to capture seasonal variations.
-
Water quality samples shall be collected at each sample location at 0.5-1.0m depth below the water surface.
-
Samples of TN concentration, TP concentration, TSS (where applicable) and Chl-a shall be collected and analysed, according to the methods outlined in Appendix 8 (8.11).
-
SD depth and the depth of thresholds at which DO=4mg/L (‘zone of oxygen depletion’) and DO=2mg/L (‘zone of anoxia’) shall be measured.
-
DO measurements shall take place with a calibrated temperature compensated probe with suitably extended cable length.
-
If a DO threshold is not reached at either 50m depth or 1m off the bottom, this shall be recorded as the depth of DO depletion.
-
8.7.2 Trophic status
The steps to determine trophic status are as follows:
-
The results of the 24-month site level monitoring survey shall be submitted per site to ASC, in accordance with the ASC Data Submission Procedure.
-
The ASC Water Quality Calculator will use the submitted data to determine the baseline trophic status at the two sampling locations (see Appendix 8 (8.7.1)) and for each of the four classification parameters137137SD should only be used where the TSI is <40, indicative of oligotrophic conditions, as it becomes progressively less reliable as a trophic status indicator above this level. (see Table 2).
-
After the initial baseline trophic status has been determined, quarterly monitoring data shall be submitted to MyASC, in accordance with the ASC Data Submission Procedure.
-
The ASC Water Quality Calculator will determine whether there has been a change in trophic status compared to the baseline trophic status of the RW (at either of the two sampling locations in Appendix 8 (8.7.1)).
Table 2. The Trophic Status Index (TSI) for four classification parameters: Secchi depth (SD), total phosphorous (TP) concentration, total nitrogen (TN) concentration and Chlorophyll-a (Chl-a).
|
TSI |
Status |
SD (m) |
[TP] (µg/L) |
[TN] (mg/L) |
[Chl] (µg/L) |
|---|---|---|---|---|---|
|
<30 |
Ultra-oligotrophic |
≥8 |
<6 |
<0.18 |
<0.9 |
|
≥30-<40 |
Oligotrophic |
≥4 – <8 |
≥6 – <12 |
≥0.18 – <0.37 |
≥0.9 – <2.6 |
|
≥40-<50 |
Mesotrophic |
≥2 – <4 |
≥12 – <24 |
≥0.37 – <0.73 |
≥2.6 – <7.3 |
|
≥50-<60 |
Eutrophic |
≥1 – <2 |
≥24 – <48 |
≥0.73 – <1.46 |
≥7.3 – <20 |
|
≥60 |
Hyper- eutrophic |
<1 |
≥48 |
≥1.46 |
≥20 |
8.7.3 Biological oxygen demand (BOD) calculation
BOD shall be calculated per site per closed calendar year, based on:
-
Feed properties: (Total Nitrogen (TN) and Total Carbon (TC) content); and,
-
Feed use; and,
-
Fertiliser properties (TN and TC content) (where applicable);
-
Fertiliser use (where applicable);
-
Production volume; and,
-
Animal properties (Nitrogen (N) and Carbon (C) content).
BOD shall be calculated according to the following formula:
-
TN in feed (kg) = Feed use (tonnes/year) x TN content feed (%) x 10
-
Where TN content feed (%) shall be the TN in the feed (value between 0-100)
-
-
TC in feed (kg) = Feed use (tonnes/year) x TC content feed (%) x 10
-
Where Total Carbon (TC) content feed (%) shall be the TC in the feed (value between 0-100)
-
-
TN in fertiliser (kg) = Fertiliser use (tonnes/year) x TN content fertiliser (%) x 10
-
Where TN content fertiliser (%) shall be the TN in the fertiliser (value between 0-100)
-
-
TC in fertiliser (kg) = fertiliser use (tonnes/year) x TC content fertiliser (%) x 10
-
Where Total Carbon (TC) content fertiliser (%) shall be the TC in the fertiliser (value between 0-100)
-
-
TN in animals (kg) = (Net production volume (tonnes/year) x TN content animals (%) x 10
-
Where TN content animals (%) shall be the crude TN content at harvest of the whole animal (not only edible part) as a percentage of the wet weight (value between 0-100)
-
-
TC in animals (kg) = Net production volume (tonnes/year) x TC content animals (%) x 10
-
Where TC content animals (%) shall be the crude, TC content at harvest of the whole animal (not only edible part) as a percentage of the wet weight (value between 0-100).
-
Net production volume (tonnes/year) = the increase in biomass in the indicated calendar year at the site, including known removed volume (e.g. mortalities).
-
Feed use (tonnes/year) = the feed used at the site in the indicated calendar year.
-
Fertiliser use (tonnes/year) = the fertiliser used at the site in the indicated calendar year.
-
8.7.4 Baseline characterisation
The results of the site level monitoring survey shall be used to characterise the baseline of the RW per site. The steps to characterise the baseline are as follows:
-
The ASC Water Quality Calculator data submission shall be completed in MyASC per site with the following information, in accordance with the ASC Data Submission Procedure:
-
The results of the site level monitoring survey; and,
-
The results of measurements used to calculate the HRT for the RW (Appendix 8 (8.4)):
-
Flow rate (Q; m3/s); and,
-
Surface area of the RW (A; km2); and,
-
Mean depth (z̄; m).
-
-
Nutrient settling velocity (m/yr). A value of 8.91m/yr138138Harrison, J.A., Maranger, R.J., Alexander, R.B. et al. The regional and global significance of nitrogen removal in lakes and reservoirs. Biogeochemistry 93, 143–157 (2009). https://doi.org/10.1007/s10533-008-9272-x shall be reported if the site has not determined settling velocity; and,
-
The number of (i) adverse turnover events and (ii) harmful algal blooms recorded over the last 10 years; and,
-
Data to calculate BOD, according to the method outlined in Appendix 8 (8.7.3).
-
The submitted data will be used by the ASC Water Quality Calculator to characterise the baseline of the RW.
-
-
The site shall obtain the baseline of the RW based on the results from the ASC Water Quality Calculator. The baseline will determine:
-
The limiting nutrient(s): N-, P- or co-limited, of the RW; and,
-
The TSI, according to Table 2 in Appendix 8 (8.7.2); and,
-
The result of the BOD calculation.
-
-
Ongoing quarterly monitoring data shall be submitted to ASC in MyASC, in accordance with the ASC Data Submission Procedure.
-
The ASC Water Quality Calculator will determine whether there has been a change in the status of the limiting nutrients, TSI and/or BOD compared to the baseline characterisation.
8.8 Point source effluent measurement (Indicators 2.6.15 to 2.6.17)
The steps to conduct sampling of point source effluents are as follows:
-
Quarterly samples of TN, TP and TSS concentrations shall be taken per site upstream from the inflow point or at the inflow point, and in any effluent water from the outflow point.
-
Samples shall be taken per site at 0.5-1.0m depth below the water surface.
-
Samples of TN, TP and TSS shall be collected and analysed according to the methods outlined in Appendix 8 (8.11).
8.9 Effluent flow contribution (Indicator 2.6.16)
The steps to determine the effluent flow contribution to the RW for sites discharging point-source effluents are as follows:
-
Quarterly measurements of flow rate shall be taken at the inflow point and/or upstream from the inflow point and in the effluent water at the outflow point. This will determine the contribution of the effluent water to the natural flow of the waterbody.
-
Measurements shall be taken during periods of medium and low flow, with measurements taken at low flow used to determine the flow contribution.
-
Low flow shall be determined as the lowest of the quarterly flow measurements taken in a calendar year.
Alternative methods to determine flow rate shall be permitted if data is available from the point-source discharge or culture treatment system.
8.10 Dissolved oxygen measurement (Indicators 2.6.18 to 2.6.21)
Measurements of DO are used to determine whether limits on DO concentration (mg/L) and percent saturation (%) are met.
8.10.1 Diffuse-source effluent release measurements
One of the following methods shall be used to conduct sampling of DO at 5m depth per site:
Method 1
-
DO, temperature and salinity (where relevant) shall be measured twice daily.
-
GPS coordinates and the altitude of the sampling location shall be recorded.
-
Weekly DO concentrations shall be calculated based on the mean of all measurements made during the week.
Method 2
DO shall be measured by conducting continuous monitoring using an electronic probe and recorder, with a 15-minute sampling frequency for at least one week.
Method 3
DO shall be measured at a ‘downstream, near-field’ impacted location immediately downstream of the site, and at an ‘upstream, far-field’ non-impacted reference location at a minimum 500m upstream from the site.
8.10.2 Point-source effluent release DO measurements
One of the following methods shall be used to conduct sampling of DO at 0.5m depth per site:
Method 1
DO concentration (mg/L) shall be recorded at sampling locations immediately downstream from the outflow point where mixing is complete. The steps to conduct sampling of DO per site are as follows:
-
DO, temperature and salinity (where relevant) shall be measured twice daily.
-
In tidal systems, measurements shall be conducted at times which correspond with high and low tides.
Method 2
DO shall be measured by conducting continuous monitoring using an electronic probe and recorder, with a 15-minute sampling frequency for at least one week.
Method 3
DO shall be measured at a ‘downstream, near-field’ impacted location: immediately downstream of the site, and at an ‘upstream, far-field’ non-impacted reference location at a minimum 500m upstream from the site.
8.10.3 Daily diurnal dissolved oxygen fluctuation
Daily diurnal dissolved oxygen (DDDO) fluctuation shall be calculated according to the following formula:
8.11 Water quality analytical methods (Indicators 2.6.8 to 2.6.11, 2.6.16 and 2.6.18)
Total Phosphorus (TP):
TP shall be measured in unfiltered 500ml samples collected in clear plastic bottles. These shall be placed on ice in a cooler and analysed within 48 hours.
A VanDorn, Kemmerer or Ruttner type sampler shall be used to collect water for field or laboratory analysis. Samples of TP shall be collected using one of the following methods:
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ISO 6878:2004 Water quality – Determination of phosphorus – Ammonium molybdate spectrometric method.
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ISO 15681-2:2018 Water quality – Determination of orthophosphate and total phosphorus contents by flow analysis (FIA and CFA) – Part 2: Method by continuous flow analysis (CFA).
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4500-P PHOSPHORUS: Standard Methods for the Examination of Water and Wastewater. Standard Methods Committee of the American Public Health Association, American Water Works Association, and Water Environment Federation. Accessed November 22, 2023: https://www.standardmethods.org/doi/10.2105/SMWW.2882.093
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United States Environmental Protection Agency: Method 365.3: Phosphorous, All Forms (Colorimetric, Ascorbic Acid, Two Reagent). Accessed June 12, 2026: https://www.epa.gov/sites/default/files/2015-08/documents/method_365-3_1978.pdf
Total Nitrogen (TN):
TN shall be measured in unfiltered 500ml samples collected in clear plastic bottles. These shall be placed on ice in a cooler and analysed within 48 hours.
A VanDorn, Kemmerer or Ruttner type sampler shall be used to collect water for field or laboratory analysis. Samples of TN shall be collected using one of the following methods:
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ISO 11905-1:1997. Water quality – Determination of nitrogen – Part 1: Method using oxidative digestion with peroxodisulfate.
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ISO 29441:2010. Water quality – Determination of total nitrogen after UV digestion – Method using flow analysis (CFA and FIA) and spectrometric detection.
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4500-N NITROGEN. Standard Methods for the Examination of Water and Wastewater. Standard Methods Committee of the American Public Health Association, American Water Works Association, and Water Environment Federation. Accessed November 22, 2023: https://www.standardmethods.org/doi/10.2105/SMWW.2882.086
Total Suspended Solids (TSS):
TSS shall be measured in unfiltered 500ml samples collected in clear plastic bottles. These shall be placed on ice in a cooler and analysed within 48 hours.
A VanDorn, Kemmerer or Ruttner type sampler shall be used to collect water for field or laboratory analysis. Samples of TSS shall be analysed using one of the following methods:
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ISO 11923:1997. Water quality – Determination of suspended solids by filtration through glass-fibre filters.
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United States Environmental Protection Agency: Method 160.2. Accessed June 12, 2026: https://www.uvm.edu/bwrl/lab_docs/protocols/106.2_TSS_by_gravimetry_(EPA_1971).pdf
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2540 SOLIDS. Standard Methods Committee of the American Public Health Association, American Water Works Association, and Water Environment Federation. Accessed November 22, 2023: https://www.standardmethods.org/doi/abs/10.2105/SMWW.2882.030?role=tab
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A method equivalent to 2540 SOLIDS.
Chlorophyll-a (chl-a) sensor:
Chl-a shall be measured in-situ using an electronic sensor and calibrated to manufacturer’s instructions according to the following method:
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Chl-a shall be measured using ethanol extraction followed by spectrophotometric measurement at wavelengths 665 and 750nm (using accredited methods), or measured in-situ using a field spectrofluorometer. The spectrofluorometer shall be calibrated according to the following method:
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Measurement range: 0 – 199µg/L chlorophyll-a.
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Resolution: 0.1µg/L chlorophyll-a.
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Accuracy: +/- 2% of reading.
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Dissolved Oxygen (DO) sensor:
DO shall be measured in-situ using an electronic sensor and calibrated to manufacturer’s instructions. The sensor shall record both percentage saturation and temperature corrected/compensated concentrations. The sensor shall be calibrated according to the following method:
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DO139139Correction factors are available here: ‘Dissolved oxygen solubility tables, accessed November 22, 2023: https://water.usgs.gov/water-resources/software/DOTABLES/ readings shall be corrected for altitude and salinity where sites are located above sea level and/or discharge to brackish receiving waters.
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Range (Polarographic DO): 0.00 to 20.00mg/L
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% Saturation Range (Polarographic DO): 0.0 to 200.0% saturation
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Resolution (Polarographic DO): 0.01, 0.1mg/L
