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Indicator 2.2.4
Requirement
The UoC shall ensure that the site has a low risk of negative impact on sensitive habitats, as determined through the ERA (see Indicator 2.1.1).
How Do I Interpret This Requirement?
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The Environmental Risk Assessment (ERA) will determine whether there are sensitive habitats within the vicinity of the site and the risk drivers that increase the likelihood of negative impacts on any sensitive habitats.
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The ERA will determine whether the risk of negative impacts on the identified sensitive habitats is minimal.
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Appendix 3.3 outlines the risk factors that shall be considered as a minimum when conducting the ERA.
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Appendix 3.3 also outlines the types of sensitive habitats that shall be considered as a minimum.
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Other types of sensitive habitats may be identified in the ERA.
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Evidence of Implementation
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An ERA report has been completed, which assesses the risk of negative impacts on any relevant sensitive habitats.
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The ERA report demonstrates whether the risk of negative impacts on sensitive habitats is ‘low’.
Auditors Should Confirm
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An ERA has been completed, which includes at a minimum the risk factors outlined in Appendix 3.3.
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The ERA determined whether sensitive habitats are located within the vicinity of the site.
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If sensitive habitats were identified, the ERA determined whether the risk of negative impacts on the sensitive habitats is minimal.
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Useful Resources
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GIS portal: GIS portal – ASC International (asc-aqua.org)
Indicator 2.2.3
Requirement
The UoC shall preserve any critical habitat identified within the site.
How Do I Interpret This Requirement?
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In accordance with Indicator 2.2.2, the ERA report will identify whether critical habitats are located within the boundaries of the site.
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The size and biodiversity characteristics of critical habitats should either remain the same since the ERA was conducted or have increased/improved.
Evidence of Implementation
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The ERA report has identified the presence of critical habitats within the boundaries of the site.
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Documented measures and outcomes, which demonstrate critical habitats have been preserved, and that their size and biodiversity has not decreased.
Auditors Should Confirm
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Whether critical habitats have been identified in the ERA report.
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If critical habitats are present, evidence has been provided to demonstrate measures to preserve the documented critical habitats.
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Outputs of preservation measures should also be available where appropriate.
Useful Resources
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GIS portal: GIS portal – ASC International (asc-aqua.org)
Indicator 2.2.2
Requirement
The UoC shall ensure that the site has a low risk of negative impact on critical habitats, as determined through the ERA (see Indicator 2.1.1).
How Do I Interpret This Requirement?
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The Environmental Risk Assessment (ERA) will determine whether there are critical habitats within the vicinity of the site and the risk drivers that increase the likelihood of negative impacts on any critical habitats.
Evidence of Implementation
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An ERA report has been completed, which assesses the risk of negative impacts on any relevant critical habitats.
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The ERA report demonstrates whether the risk of negative impacts on critical habitats is ‘low’.
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In cases where the risk level is not ‘low’, the ERA report identifies the risk drivers.
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In cases where the risk level is ‘medium’ or ‘high’, the site demonstrates the actions taken to reduce the risk level to ‘low’.
Auditors Should Confirm
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Whether there are critical habitats in the vicinity of the site. If so, evidence has been provided in the ERA that the risk of negative impacts on the critical habitats is minimal.
Indicator 2.2.1
Requirement
The UoC shall1818An exemption applies for the following species groups: tilapia, pangasius, bivalve and abalone. ensure that the site is not located in Protected Areas (PA). An exception applies where conditional siting is allowed according to Appendix 4.
How Do I Interpret This Requirement?
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Conditional allowances to the siting in Protected Areas (PA) have been taken from the ASC species standards while work is ongoing to develop updated conditional allowances.
Evidence of Implementation
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Whether the site is in a PA and if so, provide evidence that the PA meets the conditional allowances specified in Appendix 4. This includes the demonstration of the Protected Areas Management Plan.
Auditors Should Confirm
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Whether the site is in a PA. If so, evidence has been provided to demonstrate that the site meets the conditional allowances in Appendix 4 (4.2).
Useful Resources
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Protected Planet: World Database on Protected Areas (WDPA): Explore the World’s Protected Areas.
Indicator 2.1.2
Requirement
The UoC shall ensure that the ERA (see Indicator 2.1.1) is conducted by a person with the necessary competencies, experience and training that is appropriate to the size and complexity of the site. For larger, more complex sites, an independent person shall conduct the ERA. This person shall: a. have an academic background in Biology, Ecology, Environmental Science, or an equivalent field of study; and b. have a minimum of 5 years of experience in conducting ERA, including survey design, data collection, data analysis and interpretation. In cases where legal requirements are defined, the UoC shall ensure that the person conducting the ERA complies with these requirements.
How Do I Interpret This Requirement?
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An independent person is required to conduct the ERA for larger, more complex sites. However, small-scale or extensive aquaculture sites are not expected to contract an independent person to conduct the ERA.
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To demonstrate competence, personnel conducting the ERA for small-scale or extensive aquaculture sites should be able to:
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Analyse environmental risks.
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Conduct data analysis.
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Record, review and authorise the release of results.
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Contribute to or produce reports that can clearly and concisely follow the method outlined in Appendix 3.1.
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Have undergone training, or have experience, relating to ERAs.
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Evidence of Implementation
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Documents outlining the person conducting the ERA has experience and competences that are relevant to the size and complexity of the site.
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For larger, more complex sites, documents outlining the qualifications and experience of the independent person conducting the ERA.
Auditors Should Confirm
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Evidence and documents have been presented to demonstrate the person conducting the ERA has the necessary experience, competencies and qualifications.
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Auditor discretion is permitted to determine whether the experience, competences and qualifications are suitable for the size of the site.
Indicator 2.1.1
Requirement
The UoC shall conduct an Environmental Risk Assessment (ERA) per site, following the method outlined in Appendix 3 (3.3).
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Indicator 1.4.7
Requirement
The UoC shall report to ASC the production volumes and sales/dispatch volumes of ASC certified and non-certified products originating from each site, and submit specified traceability data (when requested), according to ASC data submission procedures.
No additional guidance is provided for this indicator.
Indicator 1.4.6
Requirement
The UoC shall disclose to buyers of their ASC certified product, upon request, a list of all veterinary therapeutants applied to the product.
No additional guidance is provided for this indicator.
Indicator 1.4.5
Requirement
The UoC shall not sell or dispatch the following as ASC certified: a. crustaceans treated with antibiotics at the UoC, or b. any product treated with antimicrobials listed as Critically Important Antimicrobials for Human Medicine by the World Health Organisation (WHO), at any stage in the lifecycle of the product.
How Do I Interpret This Requirement?
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This requirement addresses situations where a product may conform to the Standard, however it cannot be sold or dispatched as ASC certified.
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The UoC should:
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Maintain detailed records of any antibiotic treatments applied prior to the UoC (see Indicator 1.5.2).
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Implement a process to ensure that the product under 1.4.5(a) or (b) is not sold or dispatched as ASC certified.
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Evidence of Implementation
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Records:
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antibiotic treatments, including those applied prior to the UoC.
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Auditors Should Confirm
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UoC’s process to ensure that the product under 1.4.5(a) or (b) is not sold or dispatched as ASC certified.
Indicator 1.4.4
Requirement
Indicator applicability: every UoC using compound feed The UoC shall disclose to all buyers of their ASC certified product when a product’s feed contains >0.9%77European Council. (2003). Regulation (EC) No 1830/2003 concerning the traceability and labelling of genetically modified organisms and the traceability of food and feed products produced from genetically modified organisms and amending Directive 2001/18/EC. European Parliament, Council of the European Union. Genetically Modified Organisms (GMO) or macro ingredients produced from GMO.
How Do I Interpret This Requirement?
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The required disclosure is to the UoC’s buyers of ASC certified products.
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A public disclosure is possible but not required.
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The UoC shall ensure buyers are informed when a product’s feed contains or is produced from GMO.
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Disclosure may be provided to buyers individually or collectively.
Evidence of Implementation
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Records:
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disclosure to buyers.
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Auditors Should Confirm
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Evidence of disclosure to buyers.
