ISBN-13: 9780470659854 / Angielski / Twarda / 2014 / 392 str.
ISBN-13: 9780470659854 / Angielski / Twarda / 2014 / 392 str.
Biofouling Methods provides a "cook book" for both established workers and those new to the field. The methods included in this important new book range from tried and tested techniques to those at the cutting edge, encompassing the full diversity of this multidisciplinary field. The book covers methods for microbial and macrofouling, coatings and biocides, and ranges from methods for fundamental studies to methods relevant for industrial applications. There is an emphasis on answering questions and each chapter provides technical methods and problem-solving hints and tips. Bringing together a wealth of international contributions and edited by three internationally known and respected experts in the subject Biofouling Methods is the essential methodology reference in the field for all those working in the antifouling industry including those involved in formulation of antifouling products such as paints and other coatings. Aquatic biologists, ecologists, environmental scientists and lawyers, marine engineers, aquaculture personnel, chemists, and medical researchers will all find much of interest within this book. All universities and research establishments where these subjects are studied and taught should have copies of this important work on their shelves.
Biofouling Methods is a comprehensive collection of tried and trusted methods and practical information for those working in or entering the biofouling field. This book contains three broad sections; Microbial Methods, Macrofouling Methods and Coating and Biocide Methods.
List of Contributors xii
Introduction xvi
Guide to Methods xviii
Part I Methods for Microfouling 1
Part Editor: Sergey Dobretsov
1 Microscopy of biofilms 3
Section 1 Traditional light and epifluorescent microscopy 4
Sergey Dobretsov and Raeid M.M. Abed
1.1 Introduction 4
1.2 Determination of bacterial abundance 8
1.3 Catalyzed reporter deposition fluorescent in situ hybridization (CARD–FISH) 9
1.4 Suggestions, with examples, for data analysis and presentation 12
Acknowledgements 13
References 13
Section 2 Confocal laser scanning microscopy 15
Koty Sharp
1.5 Introduction 15
1.6 Materials, equipment, and method 18
1.7 Image acquisition 21
1.8 Presentation 21
1.9 Troubleshooting hints and tips 21
1.10 Notes 23
References 23
Section 3 Electron microscopy 26
Omar Skalli, Lou G. Boykins, and Lewis Coons
1.11 Introduction 26
1.12 Transmission electron microscopy (TEM) 27
1.13 Scanning electron microscopy (SEM) 35
References 40
2 Traditional and bulk methods for biofilms 44
Section 1 Traditional microbiological methods 45
Hans–Uwe Dahms
2.1 Introduction 45
2.2 Enrichment culture, isolation of microbes 45
2.3 Counting methods 48
2.4 Troubleshooting hints and tips 49
References 50
Section 2 Bulk methods 52
Sergey Dobretsov
2.5 Introduction 52
2.6 Measurement of biofilm thickness 53
2.7 Biofilm dry weight determination 54
2.8 Biofilm ATP content 55
2.9 Troubleshooting hints and tips 56
Acknowledgements 57
References 57
3 Biocide testing against microbes 58
Section 1 Testing biocides in solution: flow cytometry for planktonic stages 59
Tristan Biggs, Tom Vance, and Glen Tarran
3.1 Introduction 59
3.2 Method introductions 60
3.3 Pros and cons 66
3.4 Materials and equipment 67
3.5 Methods 68
3.6 Troubleshooting hints and tips 70
3.7 Suggestions 71
References 72
Section 2 Biocide testing using single and multispecies biofilms 76
Torben Lund Skovhus
3.8 Introduction 76
3.9 Questions to answer when applying biocides 76
3.10 Laboratory methods for testing biocide effect 78
3.11 Field methods for testing biocide effect 81
3.12 Troubleshooting hints and tips 83
Acknowledgements 84
References 84
4 Molecular methods for biofilms 87
Section 1 Isolation of nucleic acids 88
Isabel Ferrera and Vanessa Balagué
4.1 Introduction 88
4.2 Materials 89
4.3 Isolation of DNA from a biofilm 90
4.4 Troubleshooting hints and tips 91
References 91
Section 2 PCR and DNA sequencing 93
Christian R. Voolstra, Manuel Aranda, and Till Bayer
4.5 PCR and DNA sequencing: General introduction 93
4.6 PCR 93
4.7 Microbial marker genes 16S 94
4.8 DNA sequencing 95
4.9 454 16S amplicon pyrotag sequencing 95
4.10 Protocol 1: DNA extraction using the Qiagen DNeasy Plant Mini Kit 96
4.11 Protocol 2: Full–length 16S PCR using the Qiagen Multiplex Kit 98
4.12 Protocol 3: Analysis of full–length 16S genes 100
4.13 Protocol 4: 16S amplicon PCR for 454 sequencing using the Qiagen Multiplex Kit 102
4.14 Protocol 5: Trimming and filtering of 454 16S pyrotag sequencing 106
4.15 Protocol 6: Taxon–based analyses 108
4.16 Protocol 7: Phylogeny–based analyses 109
References 111
Section 3 Community comparison by genetic fingerprinting techniques 114
Raeid M.M. Abed and Sergey Dobretsov
4.17 Introduction 114
4.18 History and principles of the methods 115
4.19 Advantages and limitations of fingerprinting techniques 116
4.20 Materials and equipment 116
4.21 Suggestions for data analysis and presentation 121
4.22 Troubleshooting hints and tips 121
Acknowledgements 122
References 122
Section 4 Metagenomics 125
Sarah M. Owens, Jared Wilkening, Jennifer L. Fessle, and Jack A. Gilbert
4.23 Introduction and brief summary of methods 125
4.24 Overview of metagenomics methods 125
4.25 Method introduction 126
4.26 Overview of DNA handling for BAC library construction 127
4.27 BAC and Fosmid library construction 127
4.28 Library handling, archiving, and databasing 128
4.29 Facilitating library screening 128
4.30 Time frame considerations 129
4.31 Materials and equipment 129
4.32 Detailed methods: DNA handling and BAC library construction 130
4.33 Troubleshooting tips 131
4.34 Suggestions for data analysis 132
4.35 Suggestions for presentation of data 134
Acknowledgements 135
References 135
5 Methods for biofilm constituents and turnover 138
Section 1 Destructive and nondestructive methods 139
Arnaud Bridier, Florence Dubois–Brissonnet, and Romain Briandet
5.1 Introduction 139
5.2 Pros and cons of destructive and nondestructive M–LSM methods for biofilm analysis 140
5.3 Materials and equipment required for M–LSM 140
5.4 Example of questions than can be answered with the method 140
5.5 Suggestions for data analysis and presentation 148
References 149
Section 2 Biofilm formation and quorum sensing bioassays 153
Clayton E. Cox, William J. Zaragoza, Cory J. Krediet, and Max Teplitski
5.6 Introduction 153
5.7 Materials and equipment 157
5.8 Methods 157
Acknowledgements 165
References 165
6 Sampling and experiments with biofilms in the environment 168
Section 1 Field trials with biofilms 169
Jeremy C. Thomason
6.1 Introduction 169
6.2 Materials and equipment 170
6.3 Method 170
6.4 Troubleshooting hints and tips 171
6.5 Suggestions for data analysis and presentation 172
References 173
Section 2 Sampling from large structures such as ballast tanks 175
Robert L. Forsberg, Anne E. Meyer, and Robert E. Baier
6.6 Introduction 175
6.7 Materials and equipment 178
6.8 Troubleshooting hints and tips 180
6.9 Analytical methods 180
6.10 Suggestions for data analysis and presentation 182
References 182
Section 3 Sampling from living organisms 184
Christina A. Kellogg
6.11 Introduction 184
6.12 Historical background 185
6.13 Advantages and limitations of collection techniques 185
6.14 Protocols 186
6.15 Suggestions for data analysis 187
6.16 Troubleshooting hints and tips 187
Acknowledgment 188
References 188
Section 4 Optical methods in the field 190
Richard J. Murphy
6.17 Introduction 190
6.18 Examples of the use of optical methods 191
6.19 Spectral characteristics of biofilms 192
6.20 The use of chlorophyll–a as an index of biomass of biofilm 193
6.21 Multi–versus hyperspectral measurements (CIR imagery versus field spectrometry) 194
6.22 Calibration of data to reflectance 195
6.23 Suggestions for data analysis and presentation 195
6.24 Methods 197
6.25 Troubleshooting hints and tips 201
References 202
7 Laboratory experiments and cultures 204
Section 1 Static, constant depth and/or flow cells 205
Robert L. Forsberg, Anne E. Meyer, and Robert E. Baier
7.1 Introduction 205
7.2 Portable Biofouling Unit 207
7.3 Pros and cons of the method 207
7.4 Materials and equipment 208
7.5 Suggestions for data analysis 209
7.6 Benchmark bacteria and biofilm characterization 210
7.7 Troubleshooting hints and tips 212
References 212
Section 2 Mixed population fermentor 214
Jennifer Longyear
7.8 Introduction 214
7.9 Pros and cons 215
7.10 Fermentor 215
7.11 Mixed species microfouling culture 215
7.12 Utilizing the fermentor test section 218
7.13 Troubleshooting, hints and tips 218
References 219
Part II Methods for Macrofouling, Coatings and Biocides 221
Part Editors: Jeremy C. Thomason, David N. Williams.
8 Measuring larval availability, supply and behavior 223
Section 1 Larval availability and supply 224
Sarah Dudas and Joe Tyburczy
8.1 Introduction to measuring larval availability and supply 224
8.2 Measuring settlement and recruitment 235
References 238
Section 2 Larval behavior 241
Jeremy C. Thomason
8.3 Introduction 241
8.4 Method for tracking larvae 242
8.5 Troubleshooting hints and tips 245
8.6 Suggestions for data analysis and presentation 246
References 249
9 Assessing macrofouling 251
Section 1: Assessing fouling assemblages 252
João Canning–Clode and Heather Sugden
9.1 Introduction 252
9.2 A note on taxonomy 253
9.3 Field methods 253
9.4 Digital methods 258
9.5 Functional groups 261
9.6 Predicting total richness: from the known to the unknown 264
References 267
Section 2 Assessment of in–service vessels for biosecurity risk 271
Francisco Sylvester and Oliver Floerl
9.7 Introduction 271
9.8 Surveys of vessel hulls 272
9.9 Sample and data analysis 277
Acknowledgements 279
References 279
Section 3 Experiments on a global scale 281
Mark Lenz
9.10 Experiments in ecology: the need for scaling up 281
9.11 GAME a program for modular experimental research in marine ecology 281
9.12 Marine macrofouling communities as model systems 282
9.13 Chronology of a GAME project 283
Acknowledgements 289
References 289
10 Efficacy testing of nonbiocidal and fouling–release coatings 291
Maureen E. Callow, James A. Callow, Sheelagh Conlan, Anthony S. Clare, and Shane Stafslien
10.1 Introduction 291
10.2 Test organisms 293
10.3 Test samples 294
10.4 Antifouling settlement assays 295
10.5 Fouling–release assays 299
10.6 Adhesion assays for high–throughput screening 304
10.7 Apparatus 310
Acknowledgements 313
References 314
11 Contact angle measurements 317
Section 1 Surface characterization by contact angle measurements 318
Doris M. Fopp–Spori
11.1 Introduction 318
11.2 Liquids in contact with solids 318
11.3 Reproducible contact angle measurements 320
11.4 Surface energy calculations 323
References 324
Section 2 Underwater contact angle measurement by the captive bubble method 326
Pierre Martin–Tanchereau
11.5 Introduction 326
11.6 Materials and requirements 327
11.7 Method 329
11.8 Surface energy 330
Acknowledgements 330
References 331
12 Efficacy testing of biocides and biocidal coatings 332
Christine Bressy, Jean–François Briand, Chantal Compère, and Karine Réhel
12.1 Introduction 332
12.2 Laboratory assays for biocides 333
12.3 Field test methodology for biocidal coatings 337
References 343
13 Commercialization 346
Section 1 Processing a new marine biocide from innovation through regulatory approvals towards commercialization 347
Lena Lindblat
13.1 Introduction 347
13.2 Basics about the regulatory landscape from the academic perspective 349
13.3 Risk, risk assessment and risk management 349
13.4 Future directions 353
13.5 Conclusions 355
References 356
Section 2 From laboratory to ship: pragmatic development of fouling control coatings in industry 358
Richie Ramsden and Jennifer Longyear
13.6 Introduction 358
13.7 Laboratory coating development 358
13.8 Laboratory bioassay screening 359
13.9 Fitness for purpose (FFP) testing 360
13.10 Field antifouling performance testing 361
13.11 Test patch and vessel trials 363
13.12 Performance monitoring 364
13.13 Summary 365
References 365
Index 366
Dr. Sergey Dobretsov has worked for more than 20 years on biofouling, is widely published, and is the co–inventor on four international antifouling patents. He trained as a biologist in St Petersburg State University, Russia, and has worked in leading biofouling research centers in Russia, Hong Kong, Germany, and the USA. He is currently an Assistant Professor at Sultan Qaboos University, Oman. He is on the editorial boards of the journals Marine Ecology Progress Series and Biofouling.
Dr. David N. Williams is the RD&I Director for AkzoNobel Marine & Protective Coatings. Based in the North East of England he originally trained as a chemist at Durham University and at Lausanne University, Switzerland. His specific expertise is in the area of nonbiocidal antifouling technologies and he is the co–inventor on a number of patents on silicone foul–release coatings and applications.
Dr. Jeremy C. Thomason is a marine biologist, a former academic at a British University and Royal Society Industrial Research Fellow, and now runs a scientific and technical consultancy, Ecoteknica, from the Yucatán, México. He has worked in the field of biofouling for more than 20 years, is co–inventor on several patents, and is a co–editor of the book Biofouling also published by Wiley Blackwell in 2010.
Biofouling Methods provides a cook book for both established workers and those new to the field. The methods included in this important new book range from tried and tested techniques to those at the cutting edge, encompassing the full diversity of this multidisciplinary field.
The book covers methods for microbial and macrofouling, coatings and biocides, and ranges from methods for fundamental studies to methods relevant for industrial applications. There is an emphasis on answering questions and each chapter provides technical methods and problem–solving hints and tips.
Bringing together a wealth of international contributions and edited by three internationally known and respected experts in the subject, Biofouling Methods is the essential methodology reference in the field for all those working in the antifouling industry, including those involved in formulation of antifouling products such as paints and other coatings. Aquatic biologists, ecologists, environmental scientists and lawyers, marine engineers, aquaculture personnel, chemists, and medical researchers will all find much of interest within this book. All universities and research establishments where these subjects are studied and taught should have copies of this important work on their shelves.
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