Abbreviations / Glossary
- ADI
- Acceptable daily intake. Estimated daily amount that can be taken into the body without any detrimental health effects occurring, based on available scientific information. May also be referred to as a reference dose (RfD). Applies to food additives and veterinary drug residues
- Acceptable risk level
- Regulatory-defined acceptable level of increased risk associated with exposure to contaminants
- Background exposure
- Exposure to contaminants from background sources including food, water and air
- BaP
- Benzo(a)pyrene
- BCF
- Bio-concentration factor
- BMDx
- Benchmark dose – the lowest dose, as estimated from an appropriate model, at which a given (x) excess tumour incidence occurs; used for oral exposure data
- BMDLx
- Benchmark-dose lower bound – the lower confidence limit of the estimated benchmark dose (BMD), provides an upper-bound estimate of the slope factor; used for oral exposure data
- Carcinogenic potency
- Estimates of the potency of non-threshold contaminants, may be expressed as a slope factor (risk/mg/kg bw day) or risk specific dose (mg/kg bw day) or similar
- CCA
- Chromated copper arsenate
- CLMG
- Contaminated land management guideline
- EFSA
- European Food Safety Authority
- FAO
- Food and Agriculture Organization
- Genotoxic
- Direct or indirect damage to the DNA molecule – may lead to mutations or cancer
- HAIL
- Hazardous Activities and Industries List. A list of industries and activities considered likely to manufactured, stored or used hazardous substances. List may be used as a trigger for investigating a site, and identifying possible contaminants. The full list is attached in Appendix 4.
- Index dose
- Estimated daily amount that can be taken into the body without exceeding an acceptable risk level for a non- threshold contaminant based on available scientific information. Also referred to as the risk-specific dose
- JECFA
- Joint FAO/WHO Expert Committee on Food Additives
- JMPR
- Joint FAO/WHO Meeting on Pesticide Residues
- LOAEL
- Lowest observable adverse effects level
- MfE
- Ministry for the Environment (NZ)
- NES
- National environmental standard – a regulation under the Resource Management Act 1991
- NHMRC
- National Health and Medical Research Council (Australia)
- NOAEL
- No observable adverse effect level
- Non-threshold contaminant
- Contaminant for which toxic effects are considered to occur at any level of exposure
- PAH
- Polycyclic aromatic hydrocarbon
- PCP
- Pentachlorophenol
- PEFs
- Potency equivalence factors
- PHARMAC
- Pharmaceutical Management Agency of New Zealand
- PTWI
- Provisional tolerable weekly intake
- Permitted
- The activity does not require resource consent under the RMA provided the standards, terms or conditions specified are complied with
- Phytotoxic
- Concentration at which contaminants are toxic to plants
- PTWI
- Provisional tolerable weekly intake
- QALY
- Quality adjusted life years
- RfC
- Reference concentration – an estimate (with uncertainty spanning perhaps an order of magnitude) of a continuous inhalation exposure to the human population (including sensitive subgroups) that is likely to be without an appreciable risk of deleterious effects during a lifetime. It can be derived from a NOAEL, LOAEL, or benchmark concentration, with uncertainty factors generally applied to reflect limitations of the data used. Generally used in the US EPA’s non-cancer health assessments
- RfD
- Reference dose – an estimate (with uncertainty spanning perhaps an order of magnitude) of a daily oral exposure to the human population (including sensitive subgroups) that is likely to be without an appreciable risk of deleterious effects during a lifetime. It can be derived from a NOAEL, LOAEL, or benchmark concentration, with uncertainty factors generally applied to reflect limitations of the data used. Generally used in US EPA’s non-cancer health assessments – analogous to the tolerable daily intake
- RHS
- Reference health standard – any value set by a regulatory or advisory body that provides an estimated daily (sometimes weekly or monthly) amount of a substance that can be taken into the body without either any or an unacceptable additional risk of detrimental health effects occurring (based on available scientific information), eg, tolerable daily intake, reference dose, drinking water standard
- Restricted discretionary
- A resource consent is required under the RMA. The consent authority may decline the consent, or grant it subject to conditions, but only on matters to which it has restricted its discretion.
- RIA
- Regulatory impact assessment
- Risk-specific dose
- Estimated daily amount that can be taken into the body without exceeding an acceptable risk level for a non- threshold contaminant based on available scientific information – also referred to as an index dose
- RMA
- Resource Management Act 1991
- SGVs(health)
- Soil guideline values for human health as defined in section 8 and table 3 of this document.
- SSGV
- Site-specific soil guideline value
- Slope factor
- Plausible upper-bound estimate of the probability of an individual developing cancer as a result of a lifetime of exposure to a particular level of a potential carcinogen
- TDI
- Tolerable daily intake. Estimated daily amount that can be taken into the body without any detrimental health effects occurring based on available scientific information. May also be referred to as a reference dose
- TEFs
- Toxicity equivalence factors
- TEQ
- Total toxic equivalent value
- Threshold contaminant
- Contaminant for which toxic effects are considered to occur if exposure exceeds a threshold concentration
- WHO
- World Health Organization
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