Chapter
3.1.3. Summary of the Technology-Verification Applied for CDT
3.2. Verification of the CCP-technology
3.2.1. Summary Results of the CCP in Lab-Microcosms and Field Experiments
3.2.2. Evaluation of the CPP Technology and Validation of the Verification Tool
Initial and Final Risk of the Contaminated Soil
Site Specific Environmental Risk of the Application of CCP
Risk Reduction Alternatives
Regional and Global Risk Elements in Comparison with the Technology-Alternatives
Costs-Efficiency Assessment
3.2.3. Summary of the Verification Tool Applied for Combined Chemical and Phytostabilisation
Chapter 2 DISINFECTION OF EMPTY ANIMAL HOUSES – SCIENTIFIC EVIDENCE FOR APPLIED PROCEDURES
PROCEDURES FOR CLEANING AND DISINFECTION OF ANIMAL HOUSES
FACTORS THAT INFLUENCE THE EFFECTIVENESS OF DISINFECTION
Disinfectant Types and Factors that Influence their Efficacy
General Aspects of Resistance in Micro-Organisms
Membrane-related mechanisms
Enzymatic Breakdown of Disinfectant in Cell
Stress Response Systems in Bacteria and Cross-Resistance
Types of Disinfection Tests
Disinfectant Resistance Studies in which Laboratory Conditions were Regulated
Disinfection Resistance Studies Involving Field Strains
Other Laboratory Disinfectant Studies
Chapter 3 NATURAL BACTERIAL BIOFILMS IN THE ENVIRONMENT
I. STRUCTURE AND FUNCTIONS OF NATURAL BIOFILMS
I.4. Biofilm Formation and Structure
I.4.1. Bacterial Adhesion
I.4.2. Biofilm Growth and Matrix Production
I.4.3. Biofilm Maturation
II. BIOFOULING AND BIOCORROSION
II.1. Biofilm Context and Concept in Biofouling and Biocorrosion
II.2. Biofouling and Biocorrosion Processes
II.2.1. Interface Bacterial Metabolism
II.2.2. Bacteria Respiration and Biocorrosion
II.2.3. Sulfate-Reducing Bacteria (SRB)
II.2.4. Biofilm EPS Presence is also a Promoting Biocorrosion Factor
II.3. Targets and Biofilm Prevention Strategies
II.4.1. Use of Natural Molecules with Antifouling Activity
II.4.2. Development of New Polymers for the Formulation of Paintings
III. PHOTOSYNTHETIC BIOFILMS IN THE ENVIRONMENT
III.1 Similarities and Differences between Phototrophic and Chemotrophic Biofilms
III.2. Structure and Composition of Phosynthetic Biofilms
III.2.1. Adaptations to High Light Intensities
III.2.2. Stratified Sedimentary Biofilms and Microbial Mats
III.3. Wax and Wane of Photosynthetic Biofilms
III.3.1. Photosynthetic Biofilm Development and Succession Phenomena
III.3.2. Role of Predation in Photosynthetic Biofilms
III.4. Photosynthetic Biofilms and the Geological History of Life on Earth
Chapter 4 MICROBIAL AND CHEMICAL ASSAYS TO DETERMINE THE ORIGIN OF FAECAL POLLUTION AND THE PRESENCE OF WATERBORNE PATHOGENS
METHODOLOGY FOR THE IDENTIFICATION OF THE ORIGIN OF FAECAL POLLUTION IN WATER SOURCES
Genotyping of F-RNA Phages
Gene Probes used for F-RNA Phage Genotyping
Gene Hybridisation of F-RNA Isolates
Detection of DNA:RNA Hybrids of F-RNA Phages
Faecal Sterols Used as a Tool to Trace the Origins of Faecal Pollution in Water
Cholesterol Used as a Faecal Indicator
Coprostanol Used as a Faecal Indicator
Faecal Sterol Formation and Structure
Extraction of Faecal Sterols from Water
Gas Chromatography-Mass Spectrometry used for the Detection of Faecal Sterols
Sample Collection for F-RNA Genotyping and Chemical Assays (Study 1)
Sample Collection for F-RNA Genotyping During an Intervention Study (Study 2)
Evaluation of DNA:RNA Hybridisation Techniques Using Control Phages
Genotyping of F-RNA Phages from Wastewater and River Samples
Faecal Sterol Assays on Wastewater Samples
Faecal Sterol and F-RNA Phage Genotyping Assays on Environmental Samples
Origin of Male Specific F-RNA Bacteriophage Groups in the Primary Water Sources
Origin of Male Specific F-RNA Bacteriophage Subgroups in the Stored Household Water at the Point-of-Use in the Traditional and CDC Safe Water Storage Containers in Rural Households
Summary of the Use of Male Specific F-RNA Bacteriophages Group Typing to Determine the Faecal Source Origin in Primary Water Sources and Drinking Water Stored in Traditional and CDC Safe Storage Containers in Rural Households
Chapter 5 THE EFFECTS OF FINE SCALE ENVIRONMENTAL VARIATION ON MICROBIAL COMMUNITY STRUCTURE AND FUNCTION IN AQUATIC ENVIRONMENTS
FINE SCALE VARIATION IN MICROBIAL COMMUNITIES IN THE WATER COLUMN OF AQUATIC ENVIRONMENTS
FINE SCALE VARIATION IN BIOFILMS
FINE SCALE VARIATION IN MICROBIAL COMMUNITIES IN SEDIMENTS
THE EFFECTS OF PARTICLE SIZE ON BACTERIAL COMMUNITY STRUCTURE AND ACTIVITY IN WETLAND SEDIMENTS
FINE SCALE SPATIAL VARIATION IN MICROBIAL ACTIVITY ACROSS THE SURFACE OF DECOMPOSING LEAVES
Chapter 6 CHANGES OF MARINE BACTERIAL POPULATIONS IN A SHIP’S BALLAST WATER AND SEDIMENT, AND APPLICATION OF SHOCK PRESSURES TO COMPLETE KILLING OF VIBRIO SP. CELLS ISOLATED FROM BALLAST WATER
2. CHANGES OF MARINE BACTERIAL POPULATIONS IN BALLAST WATER AND SEDIMENT OF LNG CARRIER BOUND FROM JAPAN TO QATAR FOR LOADING LNG
2.1. Navigation Route and a Ship Used for Sampling Ballast Water and Sediment
2.2. Changes in the Number of Viable Marine Bacterial Populations in Ballast Water and Sediment
2.3. Vibrio Species Isolated from Ballast Water and Sediment
3. BALLAST WATER MANAGEMENT IN ORDER TO PREVENT DIFFUSION OF NON-NATIVE SPECIES
3. 1. Treatment of Ballast Water by Chemical and Physical Approaches
3.2. Vibrio sp. September 1 and Properties of Shock Pressures
3.3. Inactivation of Vibrio sp. September 1 by Exposure to Shock Pressures
3.4. Additional Effect of Sodium Ascorbate on the Number of Colony-Forming Vibrio sp. September 1 Cells After Exposure to Shock Pressures
3.5. Observation of Morphological Changes of Cells Exposed by Shock Pressures with a Scanning Electron Microscope
Chapter 7 BIODIVERSITY AND ECOLOGY OF EUKARYOTIC ORGANISMS IN EXTREME ACIDIC ENVIRONMENTS, THE RÍO TINTO CASE
Extreme Environments and Extremophiles
Eukaryotes in Extreme Environments
3. EUKARYOTIC DIVERSITY AND ECOLOGY IN RIO TINTO
4. EXTREME ACIDIC PHOTOSYNTHETIC BIOFILMS
5. STRUCTURE OF EXTREME ACIDIC PHOTOSYNTHETIC BIOFILMS
6. EXTRACELLULAR MATRIX ASSEMBLY EXTREME ACIDIC EUKARYOTIC BIOFILMS
7. IMPLICATION OF THE EXTRACELLULAR MATRIX IN HEAVY METAL ABSORPTIONS
Chapter 8 ARE RHIZOBIUM AND SOIL ENZYME ACTIVITIES GOOD INDICATORS OF HEAVY METAL SOIL CONTAMINATION?
2. HEAVY METAL TOLERANCE OF RHIZOBIUM STRAINS ISOLATED FROM BRAÇAL MINE
3. SOIL ENZYME ACTIVITIES
Chapter 9 VIRUS-BINDING PROTEINS IN WATER ENVIRONMENTS: NATURAL LIGANDS FOR HUMAN VIRUSES
OCCURENCE, FUNCTIONS AND PROPERTIES OF VBP
THE ISOLATION OF ADENOVIRUS-BINDING PROTEIN
GENE ACQUISITION OF VIRUS-BINDING PROTEIN
FUTURE APPLICATIONS AND PERSPECTIVES OF VIRUS-BINDING PROTEIN
Chapter 10 ADVANCES IN MARINE BACTERIAL POLLUTION MONITORING
Assessment of the Microbiological Quality of Seawater: Importance of Coastal Monitoring
Why the Need for Advanced Technologies and Rapid Methods?
Escherichia coli as the Main Bacterial Indicator of Faecal Pollution
Expertise Developed at the CNR- IAMC- Messina in the Field of Rapid Methods for the Detection of Bacterial Indicators
Combined FA–Viability Staining Protocol
β-glucuronidase Activity Estimates
Combined FA–Viability Staining Protocol
β-glucuronidase Activity Estimates