Workshop on Testing of Ballast Water Treatment Systems: General Guidelines and Stepwise Strategy Toward Shipboard Testing Invasion Vectors June 14-15, 2005 Portland, OR Why Hold a Workshop? Audit of the four large-scale shipboard tests of ballast water treatments in the US found that “the experimental designs and analyses had fundamental problems whose extent and gravity undermined any conclusions that could be drawn about the treatment performance of any of the BWT systems” (US Coast Guard, 2004) Problems with: Experimental design Use of controls Replication Type and methods of measurement of dependent variables Quality control Participants Kate Murphy, SERC and Univ. New South Wales Jeff Cordell, UW Russ Herwig, UW Fred Dobbs, Old Dominion University Nick Welschmeyer, Moss Landing Marine Lab Edward Lemieux, Naval Research Lab, Key West Brian Howes, Univ. Massachusetts Jose Matheikal, IMO Whitman Miller, SERC Michael Holmes, National Univ. Singapore Bill Stubblefield, Parametrix Bob Gensemer, Parametrix Greg Ruiz, SERC Mark Sytsma, PSU Consideration of Scale in BW Treatment Testing Shipboard Testing: Merits & Tradeoffs Lab Mesocosm Ship Control of Environmental Conditions Control of Biotic Content Ease of Replication Time to Results Cost / Effort Logistical Constraints Control of Treatment (dose-response) Scale Appropriate Results Real-World Variation (ship x voyage x source envt. x biota) Scale-independent Experimental Design Control Treatments Allows evaluation under temporal and spatial changes that occur in BW tanks Controls need to be identical to treatment tanks except for application of treatment Control and treatment should be concurrently or use appropriate experimental designs (blocking) Measure initial and final state of dependent and independent (treatment characteristics during experiment) variables Treatment dose may change over time Concentration x exposure time may influence treatment efficacy Measure environmental conditions that may influence efficacy Temperature, DOC, , salinity, pH, turbidity, biomass, etc. Replicate treatments and controls The Problem with Factorial Designs and Replication Salinity High ------ Low 2 Temperature High ------ Low 2 Turbidity High ------ Low 2 Biomass High ------ Low 2 Tank Size/Complexity Large ---- Small 2 Bioregion Type Temperate – Tropical 2 Organic Carbon High -------Low 2 ___________________________________________________ Number of Treatment Combinations = 27 = 128 (Reps) x 3 = 384! The Way Things Should Happen According to Russ Herwig IDEA Perform Search of Literature Perform Benchtop Experiments (milliliters to liter) Microcosm Experiments (liters) Mescocosm Experiments (100's of liters) Shipboard or Testbed Experiments (100's of cubic meters) The Way Things Have Been Done According to Russ Herwig IDEA Shipboard Experiments Perform Benchtop Experiments Microcosm Experiments Mescocosm Experiments Recommended Approach Laboratory-scale experiments – Rigorously and quantitatively define the response of organisms to treatment – < ~ 5 L experimental units – Purpose is to define the “dose” required for desired result under a range of environmental conditions – Use appropriate replication and controls Recommended Approach Microcosm-scale experiments – Test for conformity with results in more complex and realistic, “tank-like” conditions – ~10 – ~500 L experimental units – Purpose is to confirm performance at larger sace and engineering design to allow refinement of system – Test at limits to performance (fewer replicates possible) Recommended Approach Full-scale test-bed experiments – Test for meeting performance standards – BW tank volumes and complexity (100s of tons and realistic flow rates) – Purpose is to demonstrate consistent and predictable performance at full scale under realistic tank conditions – Tests consider spatial and structural variation in tanks and sampling issues NRL Test-bed Facility – Key West Seawater Intakes Pump Room ETV Ballast Water Treatment Facility Microscopy Biochemistry Lab NRL Test-bed Facility – Key West L From Seawater Source V I T L pH Dechlor Tank F DC Cl ECG-1 Frequency Drive F P Cl F RPM kWh V-6 P F TB T pH V-39 V-7 V-38 V-36 TB P V-1 V-2 V-5 V-37 S-1 V-3 V-4 V DC ECG-2 I V-8 DP Discharge Tank 104,000 gals V-35 V-9 V-34 Seawater (SW) Manifold Feed P F P F P F P V-10 P S-9 V-11 V-52 E To Ambient P V-12 Transfer Pump Skid Ballast Water Supply Manifold RPM kWh P Ballast Water (BW) Feed Manifold Frequency Drive V-29 *See Notes* V-19 P V-17 T V-13 P TB Cond T L pH Cl DO pH E P-8 6"x4" P F S-5x P S-6x Tx V-30 V-21 V-32 V-33 V-14 S-4 P RPM P kWh V-15 V-31 Frequency Drive P T L pH V-20 V-16 V-18 Large P-9 6"x4" Test Ballast Tank 101,400 gals Abbreviations T V-40 V-42 V-44 V-46 V-48 Control Test Tank 40,000 gals - V-41 V-43 V-45 V-47 Sensors Temperature Biospecies Culturing Tanks Temperature - Pressure out) Flow Rate Flow, - Tank Level Conductivity Cond - Turbidity - Conductivity Dissolved - V - I - RPM Salinity Oxygen Chlorine kWh P-11 - P TB E (2" diameter) Technology (in/out), pH Evaluation Pressure (in/ (in/out) (in/out) (in/out) (in/out) Transmissivity Elapsed Volume Time Per Redox (in/out) Free Kilowatt-hours of Operation Used/Left Injection Revolutions Rate Potential & Filter Total Oxidant Load/Changeout Particle S-7 F diameter) (1" Man-hours Voltage Amperage - Power, Turbidity Minute L P for - Concentration F Parameters L TB (6" Piping P Cl V-49 for Piping Diameter Piping diameter) Diameter F DO V-22 Diameter Medium Small Counting V-50 S-8 pH To Ambient V-51 E V-P 21 3-P4 TOM / MM Slurry V-24 To Ambient V-25 S-2 T L DO Cond pH S-3 F P TB pH TITLE Aquatic V-26 Biospecies V-27 V-28 P-10 DRAWN Nusiance Species (ANS) Facility - Key Piping & Instrumentation Diagram Pre-Ballast Treatment Plan BY NRL West, DATE Code 6136 08/25/2003 Scale: N/A FL NRL Described “Observer Effect” in BW Testing Sampling causes mortality Avoid Sampling Problems: Collect everything Sampling Mortality Method I: 50% mortality Method I: 45% mortality Method III: 3% mortality Recommended Approach Shipboard Evaluation – Test for performance when integrated on a ship – Purpose is to demonstrate acceptable performance under real operating conditions – Tests include robustness and performance over time, maintenance, etc. Challenges Test organisms Surrogate species Culturable Within species variation in tolerance Multiple geographic regions for source populations Life stage Cysts Habitat occupied Planktonic Epibenthic Infaunal Sessile Challenges How to measure viability Poke test Vegetative or resting stages Vital stains Metabolic activity Habitat occupied Planktonic Epibenthic Infaunal Sessile Challenges Residual toxicity FIFRA CWA NPDES requirment Challenges Selecting Vessels and Routes Many different types of ships with differing ballasting requirements 1,132 Mean TBOB Mean Discharge 1,170 1,386 508 553 Pa s se n ge r bo r th e om C lC er a en G O ar go o oR R ed ec ifi ai ne r ns p U C on t r 40 144 er 307 ee f 151 R 9 Bu lk e nk er 45,000 40,000 35,000 30,000 25,000 20,000 15,000 10,000 5,000 0 Ta Volume (MT) Mean Capacity Challenges Ship’s Objectives Scientific Objectives Safety of crew, passengers and cargo Scientifically rigorous experiments Compliance with regulations Risk analysis / scenario testing Non-interference with commercial objectives Representative sampling Easy implementation Replication Economical Interpretability & clarity of diagnosis Limited scope and timeframe Efficiency and economy Unequivocal & timely outcomes Transferable protocols Feasibility Cooperation Communication Expense A Phased Approach to Shipboard Testing Recommended Experimental Phase (1-2 yrs) Sampling in control and treatment tanks to determine if the treatment system: Is robust in a ship environment Provides expected efficacy Two tests/season (FWSS=8 tests per yr)) under a range of Monitoring Phase (5 yrs) All tanks experience treatment Quarterly monitoring of biological efficacy in a “core” tank and a rotating series of other tanks upon ballasting and prior to discharge Compliance Phase (< 5 yrs) Environmental conditions Organism density and community composition Engineering performance monitoring on all voyages using parameters developed in smaller scale studies and during Experimental Phase Biological monitoring 2x/yr to establish longevity of treatment efficacy as in Monitoring Phase Approach similar to USCG STEP Program but with a more explicit description of testing protocols and challenges to the system to assure adequate system performance Status Draft report sent to workshop participants Comments requested by 8 April 2006 Revised draft by May 1 The End