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PFAS in Biota: risk context & robust analytical solutions

Published: January 2026
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EnviroMail_30_Europe_PFAS in Biota: Risk Context & Robust Analytical Solutions

 

Analyzing biota as indicators of environmental pollution is a core practice known as biomonitoring (or bioindication). This approach assesses environmental quality (air, water, soil) by evaluating the responses of living organisms (bioindicators) to pollutant-driven changes. Given the persistence and bioaccumulative potential of PFAS, fish and shellfish are key targets for such studies, serving as bioaccumulators whose tissue concentrations reflect an integrated measure of PFAS contamination in the environment.

 

How PFAS Contaminate Biota

Water and Soil Contamination:
PFAS are released into the environment from various sources, including industrial facilities, landfills, and firefighting foams. Short chain PFAS are highly mobile and persist in surface water and groundwater, whereas many long chain PFAS sorb to organic matter and accumulate in sediments.

Bioaccumulation in the Aquatic Food Chain:
Aquatic organisms such as fish and shellfish absorb PFAS from the water and contaminated food sources, accumulating them in their tissues. This accumulation is often magnified along the food chain (biomagnification), particularly for long chain PFAS (e.g., PFOS) in predatory fish.

Contamination of Terrestrial Animals:
In affected areas, animals are exposed through drinking water, feed, and soil or dust. PFAS bind to proteins and accumulate primarily in the blood and liver. Transfer to animal derived products (e.g., milk and eggs) may occur.

Crop Contamination:
Plants grown in contaminated soil or irrigated with contaminated water can absorb PFAS. Uptake rates vary; shorter chain PFAS are generally taken up more readily by roots, facilitating their entry into the terrestrial food chain.

Additional Pathways and Considerations:
PFAS precursors can transform into persistent perfluoroalkyl acids (PFAAs), such as PFOS and PFOA, increasing body burdens in biota over time. Sediments and benthic organisms represent key exposure pathways in aquatic systems. Atmospheric transport and deposition contribute to soil and water contamination; additionally, land application of biosolids and the use of contaminated irrigation water can introduce PFAS into agricultural systems.
 

Impact on Biota

Accumulation Over Time:
Because of their chemical stability and slow elimination, 
many long chain PFAS persist in organisms, and their concentrations can increase over time. They bind to proteins and tend to accumulate in the blood and liver, as well as in eggs. Biomagnification can occur at higher trophic levels.

Potential Health Effects:
PFAS exposure in wildlife is associated with immune suppression; endocrine and thyroid disruption; altered lipid metabolism and liver toxicity; and developmental and reproductive effects (e.g., reduced hatching success). With respect to cancer, the International Agency for Research on Cancer (IARC) classifies PFOA as carcinogenic to humans (Group 1) and PFOS as possibly carcinogenic to humans (Group 2B).

Maternal Transfer and Life Stage Sensitivity:
PFAS can be transferred from adults to offspring through eggs and lactation, making early life stages particularly vulnerable.
 

Current and Future EU Legislation

Under Directive 2013/39/EU, only PFOS is listed as a priority substance in the aquatic environment, with a biota (fish) Environmental Quality Standard (EQS) of 9.1 μg/kg wet weight. However, food safety standards have tightened significantly. Since 2023, Regulation (EU) 2023/915 has set maximum levels for the sum of four PFAS (PFOA, PFOS, PFNA, and PFHxS) in various foodstuffs, including fish (muscle meat), where the limit is generally 2.0 μg/kg. 

Looking ahead, the EU is moving toward a group based approach to environmental protection. A proposed amendment to the Water Framework Directive would expand monitoring to PFAS as a group. This shift reflects EFSA’s latest scientific findings on the bioaccumulation and combined toxicity of these “forever chemicals.” It marks a transition from regulating individual substances to managing the entire chemical class, to ensure a high level of protection for both human health and aquatic ecosystems.
 

Monitoring and Biomagnification Patterns

Wild fish and invertebrates across the EU have measurable PFAS body burdens (PFOS and PFCAs) in the tens to low hundreds of μg/kg (wet weight). Marine top predators often exhibit elevated PFOS levels relative to biota EQS values. Biomagnification patterns vary among compounds, but several long chain PFAS bioaccumulate.
 

Analytical Methods

ALS Laboratories uses ISO/IEC 17025 accredited LC–MS/MS method to determine PFAS in biota, which serve as critical indicators of environmental contamination. This method have been rigorously validated across a wide range of matrices, including fish and other seafood (bivalves, crustaceans, cephalopods), meat, eggs, milk, and various plant tissues.

Sample Logistics and Handling:
To preserve analyte integrity and prevent biological degradation, strict transport protocols are followed. Samples 
should be shipped via overnight courier. If shipped frozen, they must be transported in a way that ensures they remain frozen throughout transit.

Sample Weight:
Although the laboratory can process as little as 10 g, we recommend submitting 50 g of sample to ensure 
representativeness. To obtain a stable, uniform test portion, samples are freeze-dried (lyophilized) and then thoroughly homogenized. This process stabilizes the matrix and preconcentrates analytes, enabling trace-level detection.

Extraction and Analysis:
The analytical workflow uses a modified QuEChERS 
extraction to ensure efficient analyte recovery, followed by a solid phase extraction (SPE) cleanup to remove matrix interferences. Final separation and detection are performed on state of the art UHPLC–MS/MS instrumentation (ExionLC™ coupled to a SCIEX QTRAP® 6500).

Quantitation:
The concentration of each PFAS is determined by internal standard calibration. Response ratios are related to the 
concentration ratios of the native analytes and their corresponding isotopically labeled internal standards, providing robust correction for potential matrix effects and ensuring high accuracy and precision.
 

References:

List of Target PFAS
LOQ: Limit of Quantification (μg/kg)
 

Parameter

Abbreviation

Limit of quantification (µg/kg)

PERFLUOROALKYL CARBOXYLIC ACIDS

 

 

Perfluorobutanoic acid

PFBA

1

Perfluoropentanoic acid

PFPeA

0.1

Perfluorohexanoic acid

PFHxA

0.1

Perfluoroheptanoic acid

PFHpA

0.1

Perfluorooctanoic acid

PFOA

0.1

Perfluorononanoic acid

PFNA

0.1

Perfluorodecanoic acid

PFDA

0.1

Perfluoroundecanoic acid

PFUnDA

0.1

Perfluorododecanoic acid

PFDoDA

0.1

Perfluorotridecanoic acid

PFTrDA

0.1

Perfluorotetradecanoic acid

PFTeDA

0.1

Perfluorohexadecanoic acid

PFHxDA

0.1

PERFLUOROALKANE SULFONIC ACIDS

 

 

Perfluorobutane sulfonic acid

PFBS

0.1

Perfluoropentane sulfonic acid

PFPeS

0.1

Perfluorohexane sulfonic acid

PFHxS

0.1

Perfluoroheptane sulfonic acid

PFHpS

0.1

Perfluorooctane sulfonic acid

PFOS

0.1

Perfluorononane sulfonic acid

PFNS

0.1

Perfluorodecane sulfonic acid

PFDS

0.1

Perfluoroundecane sulfonic acid

PFUnDS

0.1

Perfluorododecane sulfonic acid

PFDoDS

0.1

Perfluorotridecane sulfonic acid

PFTrDS

0.1

PERFLUOROALKYL SULFONAMIDES

 

 

Perfluorooctane sulfonamide

PFOSA

0.1

FLUOROTELOMER SULFONIC ACIDS

 

 

4:2 Fluorotelomer sulfonic acid

4:2 FTS

0.1

6:2 Fluorotelomer sulfonic acid

6:2 FTS

0.1

8:2 Fluorotelomer sulfonic acid

8:2 FTS

0.1

OTHER PFAS

 

 

2,3,3,3‑Tetrafluoro‑2‑(heptafluoropropoxy)‑propanoic acid

HFPO-DA (GenX)

0.1

7H‑Perfluoroheptanoic acid

HPFHpA

0.1

Perfluoro-3,7-dimethyloctanoic acid

P37DMOA

0.1