Emissions Control Project at Castle Peak Power Station “B” Units

Sediment Sampling and Testing Programme

 

1. Background Information

 

The operations of the Emissions Control Project at Castle Peak Power Station “B” Units will involve the use of reagents and the production of process by-products.  The reagents and by-product are expected to be transported via marine transport and new berthing facilities are expected to be required for the loading and unloading of these materials.

 

The existing Heavy Load Berth along the north-western waterfront of the Castle Peak Power Station will be extended to form a multi-purpose wharf and to provide the additional berthing facilities required.  Dredging will be required for the development of the new berthing facilities.  The exact extent and boundary of the dredging works is still being streamlined but the total area required to be dredged is currently estimated to be approximately 30,000 m2.  The dredged level is expected to be up to a depth of –8.2 mPD with the total dredged volume is estimated at 80,700 m3.  The preliminary proposed dredge area is presented in Sketch No. 24443/HLB/SK/007 in Annex D1a.

 

2. Sampling Arrangement

 

Vibrocore of sediment materials for testing of potential contaminants in the sediment is proposed within the proposed dredging area for the new berthing facilities ([1]).  Based on the existing sediment quality data published by EPD for the monitoring stations at Pillar Point and Urmston Road (NS3 and NS4), the sediment quality in the area is considered to be not contaminated.

 

Based on the total area expected to be dredged, vibrocore samples of sediments are proposed to be taken at three locations evenly distributed within the area to be dredged.  The proposed sampling locations are presented in Sketch No. 24443/HLB/SK/007 in Annex D1a.

 

3. Sampling

 

CAPCO’s site investigation contractor will carry out the sampling and provide all necessary equipment.  Equipment will be located onto barges and the barges will be towed to the Site prior to sampling.

 

The contractor will ensure that adequate sediment samples are collected for chemical testing as well as the next Tier of biological testing, based on the laboratory requirement.  If one vibrocore recovery is deemed not adequate for conducting all proposed laboratory testing, the contractor’s supervisor will be responsible to carry out additional sampling immediately to ensure adequate sediment samples are recovered.  Vibrocore sampling will be conducted to the end of the proposed dredging level or at refusal (ie end of sediment layer).  The vibrocores will be cut on-site at proposed sampling depths at the existing seabed surface, -0.9m, -1.9m, -2.9m and every 3m thereafter.  They will then be inventoried and logged on chain-of-custody forms as described above. 

 

All sediment and water samples will be stored at 4°C during transportation and at the laboratory prior to testing. 

 

The proposed sample container for each test is described in Annex D1b.

 

Sediment samples will be extracted in the laboratory and placed in the appropriate containers directly after the sampling.  All samples will be double-bagged and labelled internally and externally with indelible ink.   CAPCO contractor’s Standard Operating Procedure (SOP) for Extrusion & Homogenization of Sediment Samples is attached in Annex D1c.

Each sub-sample for chemical testing will be analysed for parameters as presented in Section 5 below.

 

Samples will be extracted and analysed within 14 days.  The laboratory will ensure that the chemical screening results are ready as soon as possible after the sampling finished so that a Tier III biological testing programme (where required) can be developed and commenced within 8 weeks from the date of sampling.

 

The sub-samples for biological testing will also be stored in the same manner as described above (including for ancillary parameters).  The composite samples for biological testing, where required, will comprise of composite samples prepared from up-to 5 sub-samples of the same category (ie sediment classified under ETWBTCW 34/2002 as (category M or H), which are continuous in vertical or horizontal profile.  The composite samples for biological testing will also be tested for ancillary parameters, including moisture content, grain size distribution, pH, TOC, ammonia and salinity of pore water.

 

4. Reference Sample

 

If Tier III biological testing programme is anticipated, samples for reference sediment will be taken, prior to the initiation of the biological testing programme.  The site for collecting reference sediment is in Port Shelter at PS6 (E850234, N820057).

 

5. Sediment Chemistry Tests

 

All samples will be tested for all the contaminants stated in Table 1 - Analytical Methodology in Appendix B of ETWBTCW 34/2002 and other proposed parameters including: metals (Cd, Cr, Cu, Hg, Ni, Pb, Ag, Zn), metalloid (As), organic-PAHs (low molecular weight PAHs (including Naphthalene, Acenaphtylene, Acenaphtene, Fluorene, Phenanthrene, Anthracene) and high molecular weight PAHs (including Benzo(a)anthracene, Benzo(a)pyrene, Chrysene, Dibenz(ah)anthracene, Fluoranthene, Pyrene, Benzo(b)fluoranthene, Benzo(k)fluoranthene, Indeno(1,2,3-cd)pyrene, Benzo(ghi)perylene)), PCBs (including 2,4' dichlorobiphenyl (PCB 8), 2,2',5 trichlorobiphenyl (PCB 18), 2,4,4' trichlorobiphenyl (PCB 28), 2,2',3,5' tetrachlorobiphenyl (PCB 44), 2,2',5,5' tetrachlorobiphenyl (PCB 52), 2,3',4,4' tetrachlorobiphenyl (PCB 66), 3,3',4,4' tetrachlorobiphenyl (PCB 77), 2,2',4,5,5' pentachlorobiphenyl (PCB 101), 2,3,3',4,4' pentachlorobiphenyl (PCB 105), 2,3',4,4',5 pentachlorobiphenyl (PCB 118), 3,3',4,4,5 pentachlorobiphenyl (PCB 126), 2,2',3,3',4,4' hexachlorobiphenyl (PCB 128), 2,2',3,4,4',5' hexachlorobiphenyl (PCB 138), 2,2',4,4',5,5' hexachlorobiphenyl (PCB 153), 3,3',4,4',5,5' hexachlorobiphenyl (PCB 169), 2,2',3,3',4,4',5 heptachlorobiphenyl (PCB 170), 2,2',3,4,4',5,5' heptachlorobiphenyl (PCB 180), 2,2',3,4',5,5',6 heptachlorobiphenyl (PCB 187) and Total PCBs (as sum of the 18 congenors)), chlorinated pesticides (including, Alpha-BHC, Beta BHC, Gamma BHC Delta-BHC, Heptachlor, Aldrin, Heptachlor epoxide, Endosulfan 1, p, p'-DDT, p, p'-DDD, p, p'-DDE and Endosulfan sulphate), TBT in interstitial water and other parameters relating to water quality impact assessment (particle size, redox potential, TOC, TKN, nitrate, nitrite, ammonia nitrogen, ortho-phosphate, total phosphorus).

 

Elutriate samples will be analysed for metals (Cd, Cr, Cu, Hg, Ni, Pb, Ag, Zn), metalloid (As), organic-PAHs (low molecular weight and high molecular weight PAHs), PCBs, chlorinated pesticides, TBT, and other parameters relating to water quality impact assessment (ammonia, TKN, nitrate, nitrite, ammonia nitrogen, ortho-phosphate, total phosphorus, biological and chemical oxygen demand).

 

Water samples will be taken at 3 depths, ie 1m below surface, mid-depth and 1m above the seabed level.  If the seabed level is less than 6m but more than 3m, samples will be taken at 1m below surface and mid-depth.  If the seabed level is less than 3m, samples will be taken at 1m below surface.

 

Water samples will be tested for metals, ammonia, TKN, nitrate, nitrite,

ammoniacal nitrogen, ammonia nitrogen, orthophosphate, total phosphorus,

PAHs, PCBs, chlorinated pesticides and TBT.

 

List of the instrumentation, analytical methods and reporting limit of individual parameters for sediment, elutriate, interstitial water and water samples are summarized in Annex D1d.

 

6. Quality Assurance/Quality Control

 

The laboratory should ensure that all equipment and instruments to be used for analysis meet the requirements and specifications of the reference method procedures.  The laboratory will set upper and lower control limits based on statistical analysis of historical performance data to monitor the acceptability of the QA/QC sample data.  All instruments will be calibrated prior to analysis to monitor sensitivity and precision.

 

The following QA/QC samples will be analysed.

 

·         Laboratory blanks - an analyte free matrix to which all reagents are added in the same volumes or proportions as used in the standard sample preparation to monitor contamination introduced in the laboratory (inorganics and organics).

 

·         Field blanks – a control standard solution to be used for monitoring of potential contamination of samples from the environmental suring the on-site sample handling.  A field blank shall be collected for each set of samples for analysis of organic contents (PAHs).

 

·         Batch duplicates - an intra laboratory split sample randomly selected from the sample batch to monitor method precision (intra batch) in a given sample matrix (inorganics only).  It is proposed that duplicate samples of 5% from each batch will be analysed.

 

·         Reference Materials - analysis of a material with a known concentration of contamination to determine the accuracy of results in a given matrix (inorganics only) (eg CASS 3).

 

·         Single Control Samples - a known, interference-free matrix spiked with target analytes used to monitor laboratory preparation techniques (organics only).

 

·         Duplicate Control Samples - multiple single control samples designed to monitor preparation technique reproducibility (organics only).

 

·         Matrix Spike - An intra laboratory split sample spiked with the target analytes prior to sample preparation and analysis to determine method bias in a given sample matrix (organics only).

 

A laboratory blank, a batch duplicate (5% of each batch) and a suitable reference material will be analysed with batch of samples.  For organics, a method spike will also be analysed with each batch of samples.  Each batch will contain a maximum of 20 samples.  Results of instrument calibration checks and QA/QC results will be included in each laboratory report.  Data Quality Objectives (DQOs) have been developed to address precision, accuracy and analyte recovery, as described below.

 

Precision

 

Duplicates (1 in every 10 samples) will be used to monitor the precision of the analysis.  Results will be flagged for reference when:

 

·         For all analytes, except metals, with concentration >4x Method Detection Limit (MDL), the duplicate results have more than a 20% Relative Percentage Deviation (RPD);

 

·         For metals with a concentration >4x MDL, the duplicate results have more than a 25% RPD; and

 

·         For all analytes with concentration <4x MDL, the duplicate results will be reported as analysed and no bounds will be quoted.

 

Accuracy

 

Standard and certified reference material (CRM) are used to monitor accuracy and precision within and between batches:  Results should be flagged for reference if:

 

·         The variation of the standard from its true value is more than 15% (for mercury: 20%).

 

Recovery

 

Post digest spikes are used to determine the recovery of determinants in complex sample matrices.  Results should be rejected if:

 

Spike recoveries are more than 25% from the theoretical recovery for waters, sediment and marine biota.  An exceptional case would be if the sample concentration is greater than four times the spike value, the spike may be disregarded.

 

7. Sediment Classification

 

The tested sediment samples will be classified according to their level of contamination of metals (eight priority metals, including Cd, Cr, Cu, Hg, Ni, Pb, Ag and Zn), metalloid (arsenic), organic–PAHs (low molecular and high molecular weight PAHs), organic-non-PAHs (total polychlorinated biphenyls) and organometallics (tributyltin in interstitial water) as stipulated in ETWBTCW 34/2002.  The Chemical Exceedance Levels (CEL) specified in Appendix A of ETWBTCW 34/2002 serve as criteria for determining the testing and disposal requirements of marine dredged sediments.  These include:

 

Category L:  Sediment with all contaminant levels not exceeding the Lower Chemical Exceedance Level (LCEL).  The material must be dredged, transported and disposed of in a manner, which minimizes the loss of contaminants either into solution or by resuspension.

 

Category M: Sediment with any one or more contaminant levels exceeding the Lower Chemical Exceedance Level (LCEL) and none exceeding the Upper Chemical Exceedance Level (UCEL).  The material must be dredged and transported with care, and must be effectively isolated from the environment upon final disposal unless appropriate biological tests demonstrate that the material will not adversely affect the marine environment.

 

Category H:  Sediment with any one or more contaminant levels exceeding the Upper Chemical Exceedance Level (UCEL).  The material must be dredged and transported with great care, and must be effectively isolated from the environment upon final disposal.

 

8. Necessity to Proceed to Tier III Biological Screening

 

There is no need to proceed to Tier III for Category L sediment.  However, the Tier III biological testing must be implemented for further analysis of Category M and certain Category H sediment.  For the latter, Tier III screening is only required if one or more contaminant levels exceed 10 times the LCEL.

 

9. Sediment Toxicity Testing

 

In order to determine whether sediment with contaminant concentrations exceeding LCEL and over 10 times LCEL present a toxicological risk to biota inhabiting areas adjacent to the contaminated mud disposal site during their disposal, ecotoxicological evaluations (bioassays) will be performed on these sediment samples.  The ecotoxicological testing programme featured a suite of tests that include three phylogenetically distinct species which interact with bedded sediments in different ways.  The objective of the bioassays is to determine if there are any potential risks of toxicological impacts from the sediment to the marine biota and whether there is any difference in the toxicity of the sediments samples and the reference sediment (collected from clean areas).

 

Sediment ecotoxicity testing will be conducted using three bioassays (using amphipod, polychaete and bivalve larvae) defined in the ETWBTCW34/2002.  The species used in the bioassays are listed in Table 1.  All tests will be initiated within the allowable holding period for the sediments as recommended by both international testing and programmes adopted locally (ie eight weeks) ([2]).

 

Table 1           Sediment Toxicity Test Species

Test

Species

Amphipod (Solid-phase)

Leptocheirus plumulosus

Polychaete (Solid-phase)

Neanthes arenaceodentata

Bivalve Larvae (Water-soluble phase)

Crassostrea gigas

 

10. Control Sediment

 

The control sediment will be used to evaluate background behaviour of the test organism such as mortality, behaviour and development.  The results from the control sediment will be used to assess the condition (health) of the test organisms and verify the acceptability of the sediment bioassay using pre-defined criteria (eg should > 10% mean mortality occur in the control sediment in the amphipod test then the test must be repeated as the result indicates that the batch of test organisms were in poor health and may not provide a true indication of the potential for toxicity in the Impact sediment).

 

11. Statistical Methodology and Interpretation of Test Results

 

The null hypothesis examined for this project is:

 

H0     There are no differences between toxicity of the contaminated sediments and the Reference sediments.

 

One-way ANOVA will be performed to examine any differences in test organism response when exposed to the sediment in the six treatments.  Statistically significant differences is determined at a probability, p≤0.05.

 

Amphipod Test - a biologically significant toxic response is considered to be: amphipod mortality that is significantly different (p≤0.05) between the Reference sediment and the sample, and, mean survival in the test sediment <80% of mean survival in Reference sediment ([3]).

 

Bivalve Larval Test - a biologically significant toxic response is defined as: corrected abnormality or combined mortality that is statistically different (p≤0.05) between the Reference Sediment and the sample, and, mean normality survival in the test sediment <80% of mean survival in reference sediment ([4])([5]).

 

Polychaete Test - a biologically significant toxic response is an individual growth rate that is recorded when: Mean dry weight in test sediments is significantly different (p≤0.05) from mean dry weight in Reference sediment , and, mean dry weight in test sediments <90% of mean dry weight in Reference sediment ([6])([7]).

 

12. Final Classification and Disposal

 

The final classification decision and selection of appropriate disposal options, routing and the allocation of a permit to dispose at the designated disposal site will be made by the EPD, in consultation with the Marine Fill Committee (MFC) in accordance with WBTC 12/2000 ([8]).



 

([1])  This sampling plan is based on the fact that no reclamation is required for the proposed development.

(2) ETWBTCW (2002) Works Bureau Technical Circular No. 34/2002. Management of Dredged/Excavated Sediment.

(3) Environment, Transport and Works Bureau (2002), Technical Circular (Works) No.34/2002 – Management of Dredged/Excavated Sediment, Appendix B – Test End Points and Decision Criteria do Tier III Biological Screening, Environment, Transport and Works Bureau, Technical Circular (Works) No.34/2002.

(4) Environment, Transport and Works Bureau (2002) Op cit.

(5) Normality Survival integrates the normality and survival end points, and measures survival of only the normal larvae relative to the starting number.

(6) Dry weight means total dry weight after deducing dead and missing worms.

(7) Environment, Transport and Works Bureau (2002) Op cit.

(8) Work Bureau Technical Circular No. 12/2000 - Fill Management, ETWB.