Methods in Stream Ecology :Volume 2: Ecosystem Function ( 3 )

Publication subTitle :Volume 2: Ecosystem Function

Publication series :3

Author: Lamberti   Gary;Hauer   F. Richard  

Publisher: Elsevier Science‎

Publication year: 2017

E-ISBN: 9780128132692

P-ISBN(Paperback): 9780128130476

Subject: Q142 abiotic and biotic environmental relationship

Keyword: 环境科学、安全科学,生态学(生物生态学),普通生物学,植物学

Language: ENG

Access to resources Favorite

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Description

Methods in Stream Ecology: Volume 2: Ecosystem Structure, Third Edition, provides a complete series of field and laboratory protocols in stream ecology that are ideal for teaching or conducting research. This new two-part edition is updated to reflect recent advances in the technology associated with ecological assessment of streams, including remote sensing. Volume two covers community interactions, ecosystem processes and ecosystem quality.

With a student-friendly price, this new edition is key for all students and researchers in stream and freshwater ecology, freshwater biology, marine ecology and river ecology. This book is also supportive as a supplementary text for courses in watershed ecology/science, hydrology, fluvial geomorphology and landscape ecology.

Methods in Stream Ecology, 3rd Edition, Volume 1: Ecosystem Structure, is also available now!
  • Provides a variety of exercises in each chapter
  • Includes detailed instructions, illustrations, formulae and data sheets for in-field research for students
  • Presents taxonomic keys to common stream invertebrates and algae
  • Includes website with tables and a links written by leading experts in stream ecology

Chapter

23.2.2 General Procedures

23.2.2.1 Influence of Urbanization on Food Webs

23.2.2.2 Gradients in δ13C and δ15N in Basal Resources

23.2.2.3 Use of δD in Stream Food Web Studies

23.2.2.4 Use of Mixing Models to Quantify Food Web Transfers

23.3 SPECIFIC METHODS

23.3.1 Basic Method: Comparison of Stream Food Webs Using Stable Isotopes of C and N

23.3.1.1 Site Selection

23.3.2 Advanced Method 1: Tracing Use of a Novel Terrestrial Particulate Organic Matter Source in a Stream Food Web

23.3.3 Advanced Method 2: Tracing Spatial Variation in Diet Sources for Food Webs

23.3.4 Advanced Method 3: Tracing Shifts in Basal Resources of Stream Food Webs Using δD

23.3.5 Data Analysis

23.4 QUESTIONS

23.5 MATERIALS AND SUPPLIES

REFERENCES

24 - Dissolved Organic Matter

24.1 INTRODUCTION

24.2 GENERAL DESIGN

24.2.1 Site Selection and Study Design

24.2.2 Sample Collection and Analysis

24.3 SPECIFIC METHODS

24.3.1 Basic Method 1: A Stream and Its Multiple Sources of Dissolved Organic Matter

24.3.2 Advanced Method 1: Heterotrophic Activity of Dissolved Organic Matter

24.3.2.1 Dark Incubation to Assess Bioavailability

24.3.2.2 Data Analysis

24.3.3 Advanced Method 2: Enzymatic Characterization of the Dissolved Organic Matter Demand

24.3.3.1 Enzyme Collection

24.3.3.2 Enzyme Activity Measurement

24.3.3.3 Data Analysis

24.3.4 Advanced Method 3: Fluorescent Analysis of Dissolved Organic Matter Composition

24.3.4.1 Data Analysis

24.3.5 Advanced Method 4: Limitations to Degradation

24.3.5.1 Nutrients

24.3.5.2 Photolysis/Photobleaching

24.3.6 Advanced Method 5: Sorption of Dissolved Organic Matter in Soils

24.4 QUESTIONS

24.5 MATERIALS AND SUPPLIES

REFERENCES

APPENDIX 24.1

APPENDIX 24.2

25 - Transport and Storage of Fine Particulate Organic Matter

25.1 INTRODUCTION

25.2 GENERAL DESIGN

25.2.1 Seston

25.2.2 Fine Benthic Organic Matter

25.2.3 Linkages

25.2.4 Site Selection

25.2.4.1 Seston

25.2.4.1 Fine Benthic Organic Matter

25.2.4.2 Linkages

25.3 SPECIFIC METHODS

25.3.1 Basic Method 1: Seston Concentration

25.3.1.1 Protocol for Seston Sampling in Streams and Small Rivers

25.3.1.2 Protocol for Seston Sampling in Large Rivers

25.3.1.3 Standard Processing Protocols

25.3.1.4 Particle Size Separation Protocols

25.3.1.5 Optional Experiment A: Seston Export

25.3.1.6 Optional Experiment B: Seston Sampling During Storms

25.3.2 Basic Method 2: Fine Benthic Organic Matter

25.3.2.1 Protocols for Field Collection of Fine Benthic Organic Matter

25.3.2.2 Fine Benthic Organic Matter Processing Protocols

25.3.3 Advanced Method 1: Linkages of Sestonic Fine Particulate Organic Matter to the Biota

25.3.3.1 Field Release and Larval Collection

25.3.3.2 Laboratory Analysis

25.4 QUESTIONS

25.4.1 Seston

25.4.2 Fine Benthic Organic Matter

25.4.3 Linkages of Sestonic Fine Particulate Organic Matter to the Biota

25.5 MATERIALS AND SUPPLIES

REFERENCES

26 - Coarse Particulate Organic Matter: Storage, Transport, and Retention

26.1 INTRODUCTION

26.2 GENERAL DESIGN

26.2.1 Site Selection

26.2.2 Basic Methods

26.2.3 Advanced Methods

26.3 SPECIFIC METHODS

26.3.1 Basic Method 1: Coarse Particulate Organic Matter Storage and Measurement

26.3.1.1 Field Measurements

26.3.1.2 Laboratory Processing

26.3.1.3 Data Analysis

26.3.2 Basic Method 2: Coarse Particulate Organic Matter Transport and Retention

26.3.2.1 Laboratory Preparation

26.3.2.2 Field Physical Measurements

26.3.2.3 Field Coarse Particulate Organic Matter Releases

26.3.2.4 Data Analysis

26.3.2.5 Option to Basic Method 2: Single-Particle Releases

26.3.3 Advanced Method 1: Enhancement of Stream Retentive Capacity

26.3.3.1 Laboratory Preparation

26.3.3.2 Field Measurements-Deployment of Retention Devices

26.3.3.3 Field Measurements-Related Ecosystem Measurements

26.3.4 Advanced Method 2: Measurement of Organic Carbon Spiraling

26.3.4.1 Site Selection

26.3.4.2 Field Measurements-Transported Organic Carbon

26.3.4.3 Field Measurements-Benthic Organic Carbon

26.3.4.4 Field Measurements-Organic Carbon Turnover

26.3.4.5 Field Measurements-Physical Characteristics of the Stream

26.3.4.6 Laboratory Processing

26.3.4 7 Data Analysis

26.4 QUESTIONS

26.5 MATERIALS AND SUPPLIES

ACKNOWLEDGMENTS

REFERENCES

27 - Leaf-Litter Breakdown

27.1 INTRODUCTION

27.2 GENERAL DESIGN

27.2.1 Site Selection

27.3 SPECIFIC METHODS

27.3.1 General Protocol for Leaf-Litter Breakdown Experiments

27.3.2 Basic Method 1: Leaf Breakdown for One or More Leaf Species

27.3.3 Basic Method 2: Effects of Spatially Varying Stream Features on Leaf Breakdown Rates

27.3.4 Advanced Method 1: Effects of Anthropogenic Activities on Leaf Breakdown Rates

27.3.5 Advanced Method 2: Assessing Relationships Among Leaf Breakdown Rates and Shredders

27.3.6 Advanced Method 3: Assessing Microbial Activity During the Litter-Breakdown Process

27.3.7 Field Protocol

27.3.8 Data Analysis

27.4 QUESTIONS

27.5 MATERIALS AND SUPPLIES

REFERENCES

28 - Riparian Processes and Interactions

28.1 INTRODUCTION

28.2 GENERAL DESIGN

28.2.1 Quantifying Riparian Vegetation Communities

28.2.2 Attenuation of Solar Radiation-Shading

28.2.3 Input and Decomposition of Coarse Organic Matter

28.2.4 Transfer of Dissolved Organic Matter and Nutrients

28.2.5 Remote Sensing of the Riparian Zone

28.3 SPECIFIC METHODS

28.3.1 Site Selection

28.3.2 Basic Method 1: Quantifying Riparian Vegetation Communities

28.3.2.1 Point-Centered Quarter Method

28.3.3 Basic Method 2: Attenuation of Solar Radiation-Shading

28.3.3.1 Pyranometer or Quantum Sensor

28.3.3.2 Spherical Densiometer Measurements

28.3.3.3 Hemispherical Photo Measurements

28.3.4 Basic Method 3: Input and Decomposition of Coarse Particulate Organic Matter

28.3.4.1 Leaf Litter Traps

28.3.4.2 Measurement of Coarse Particulate Organic Matter Decomposition Rates

28.3.4.3 Assessment of Detritivore Standing Crops

28.3.5 Advanced Method 1: Transfer of Dissolved Organic Matter and Nutrients from the Riparius to the Stream

28.3.5.1 General Measures of Dissolved Organic Matter and Nutrient Transfer

28.3.5.2 Nitrogen Mineralization Potential

28.3.5.3 Stable Isotope Analysis

28.3.6 Advanced Method 2: Remote Sensing of the Riparian Zone

28.3.6.1 Satellite Imagery

28.3.6.2 Airborne-Based Imagery

28.3.6.3 Light Detection and Ranging

28.3.6.4 Classification of Vegetation and Riparian Patches

28.4 QUESTIONS

28.5 MATERIALS AND SUPPLIES

REFERENCES

29 - Dynamics of Wood

29.1 INTRODUCTION

29.1.1 Dynamics of Wood in Streams

29.1.1.1 Storage

29.1.1.2 Breakdown and Decomposition

29.1.1.3 Input

29.1.1.4 Transport

29.1.2 Models of Wood Dynamics

29.1.3 Humans and the Dynamics of Wood

29.2 GENERAL DESIGN

29.2.1 Site Selection

29.2.2 Marking Techniques for Repeated Surveys

29.3 SPECIFIC METHODS

29.3.1 Basic Method 1: Estimation of Standing Stocks of Wood

29.3.1.1 Data Analysis

29.3.2 Basic Method 2: Line-Intersect Estimation of Large Wood

29.3.3 Basic Method 3: Long-Term Wood Retention and Transport

29.3.4 Advanced Method 1: Modeling Wood Accumulation

29.3.5 Advanced Method 2: Modeling Effects of Timber Harvest on Wood Accumulation

29.3.6 Advanced Method 3: Modeling Wood Abundance in a River Network

29.4 QUESTIONS

29.5 MATERIALS AND SUPPLIES

REFERENCES

E - Ecosystem Processes

30 - Conservative and Reactive Solute Dynamics

30.1 INTRODUCTION

30.1.1 Conservative Solute Dynamics

30.1.2 Reactive Solute Dynamics

30.2 GENERAL DESIGN

30.2.1 Site Selection

30.2.2 Tracer Selection

30.2.3 Release Techniques

30.2.4 Data Analyses

30.3 SPECIFIC METHODS

30.3.1 Basic Method: Dynamics of Conservative Solutes

30.3.1.1 Laboratory Preparation

30.3.1.2 Field Preparation-Prerelease

30.3.1.3 Field Procedure-Pulse Release

30.3.1.4 Field Procedure-Constant-Rate Release

30.3.1.5 After the Release

30.3.1.6 Estimating Discharge

30.3.1.7 Estimating Other Hydraulic Parameters

30.3.1.8 Transient Storage

30.3.2 Advanced Method: Reactive (Nonconservative) Solute Dynamics

30.4 QUESTIONS

30.5 MATERIALS AND SUPPLIES

ACKNOWLEDGMENTS

REFERENCES

31 - Nutrient Limitation and Uptake

31.1 INTRODUCTION

31.1.1 Elevated Nutrient Loading to Streams

31.1.2 Capacity for Nutrient Retention in the Landscape

31.1.3 Overview of Chapter

31.2 GENERAL DESIGN

31.2.1 Index of Limitation: Nutrient Diffusing Substrata

31.2.2 Short-Term Nutrient Addition

31.2.3 Short-Term 15N Tracer Release

31.3 SPECIFIC METHODS

31.3.1 Basic Method: Nutrient Diffusing Substrata

31.3.1.1 Laboratory Procedures

General Laboratory Protocol

Agar Preparation (see Table 31.2)

Pouring Agar Solution

Attaching Cups to L-Bars and Storage

31.3.1.2 Field Procedures

Placement of Nutrient Diffusing Substrata in Stream (Fig. 31.3)

Retrieval From Stream

31.3.1.3 Metabolism Incubation of Discs

31.3.1.4 Chlorophyll a and Ash-Free Dry Mass Analysis on Discs

31.3.1.5 Modifications and Enhancements

31.3.2 Advanced Method 1: Short-Term Nutrient Release

31.3.2.1 General Preparations

Site Selection and Solute Decisions

Calculating the Amount of Salt to Be Added to the Carboy (see Table 31.3)

Laboratory Preparations for the Field

31.3.2.2 Field Procedures

Before Turning on the Dripper

Preparing Injectate

Adding Injectate to Stream and Sampling at Plateau

31.3.2.3 Laboratory Procedures

Analysis of Water Samples

Calculating Nutrient Uptake Length (Sw)

31.3.2.4 Modifications and Enhancements

31.3.3 Advanced Method 2: Short-Term 15N Stable Isotope Tracer Addition

31.3.3.1 General Preparations

Isotope Purchase and Site Selection

Presampling and Preliminary Information for Calculations

31.3.3.2 Field Procedures

Before Turning on the Dripper

Carboy Preparation

Adding Injectate to Stream and Sampling at Plateau

31.3.3.3 Laboratory Procedures

Sample Processing for Selected Rapid-Turnover Compartment (e.g., Filamentous Green Algae)

31.3.3.4 Potential Modifications to Protocols

31.3.3.5 Calculation of 15N Uptake Length

31.3.3.6 Modifications and Enhancements

31.4 QUESTIONS

31.4.1 Basic Method: Nutrient Diffusing Substrata

31.4.2 Advanced Method 1: Short-Term Nitrogen Release

31.4.3 Advanced Method 2: Short-Term 15N Tracer Release

31.5 MATERIALS AND SUPPLIES

31.5.1 Basic Method

31.5.2 Advanced Method 1

31.5.3 Advanced Method 2

REFERENCES

32 - Nitrogen Transformations

32.1 INTRODUCTION

32.1.1 Nitrogen Fluxes

32.1.2 Small-Scale Assays for Fluxes

32.2 GENERAL DESIGN

32.2.1 Basic Method 1: Denitrification-Determining Unamended Denitrification and Denitrification Enzyme Activity Rates

32.2.2 Basic Method 2: Nitrification-Determining Gross and Net Nitrification Rates

32.2.3 Basic Method 3: Nitrogen Fixation

32.2.4 Advanced Methods: Isotopes for Flux Rate Measurement

32.3 SPECIFIC METHODS

32.3.1 Basic Method 1: Denitrification

32.3.1.1 General Preparation

32.3.1.2 Denitrification Rate Procedures (Laboratory)

Incubation Vessel Setup

Incubation, Sampling, and Analyses

Calculation of Denitrification Rate

Tips and Notes

32.3.2 Basic Method 2: Nitrification

32.3.2.1 Gross Nitrification Procedure

Day 0 Flask Setup

Day 3 Laboratory Procedures

Calculation of Nitrification Rate

Tips and Notes

32.3.2.2 Net Nitrification Procedure

Day 0 Flask Setup

Day 3 Laboratory Analyses

Calculation of Nitrification Rate

Tips and Notes

32.3.3 Basic Method 3: Nitrogen Fixation

32.3.3.1 General Preparation

Gas Chromatograph Configuration

Site Selection, Preparation, and Incubation Decisions

32.3.3.2 Field Procedures

Setting up a Run

Initializing the Assay

Terminating the Assay

32.3.3.3 Laboratory Procedures

Analysis of Headspace Samples via Gas Chromatography

Calculating N2 Fixation Rates (Based on Capone, 1993)

Tips and Notes

32.3.4 Advanced Method 1: Using 15N to Measure DNRA

32.3.4.1 General Preparation

Analytical Considerations (Prepare ﹥1Month Prior to Experiment)

32.3.4.2 Field Procedures

32.3.4.3 Laboratory Procedures

Adding 15N to Incubations

Calculating DNRA Rates

Tips and Notes

32.3.5 Advanced Method 2: Using MIMS to Measure Net N2 Flux

32.3.5.1 Assay Procedure

32.3.5.2 Running MIMS Samples

32.3.5.3 Calculations (Adapted From Kana et al., 1998)

32.4 QUESTIONS

32.4.1 Denitrification

32.4.2 Nitrification

32.4.3 Nitrogen Fixation

32.4.4 DNRA and N2 Flux

32.5 MATERIALS AND SUPPLIES

32.5.1 Denitrification

32.5.2 Nitrification

32.5.3 Nitrogen Fixation

32.5.4 Dissimilatory Nitrate Reduction to Ammonia

32.5.5 N2 Flux

REFERENCES

33 - Phosphorus Limitation, Uptake, and Turnover in Benthic Stream Algae

33.1 INTRODUCTION

33.1.1 Assessment of P Limitation

33.1.2 P Uptake Rates

33.1.3 P Turnover Rates

33.1.4 Overview of Chapter

33.2 GENERAL DESIGN

33.2.1 Basic Method 1: Phosphatase Activity

33.2.2 Basic Method 2: Chemical Composition (C:P Ratio in Algal Tissue)

33.2.3 Basic Method 3: Net Nutrient Uptake-Stable Phosphorus

33.2.4 Advanced Method 1: Gross Nutrient Uptake (Phosphorus Radiotracer)

33.2.5 Advanced Method 2: Phosphorus Turnover

33.3 SPECIFIC METHODS

33.3.1 Basic Method 1: Phosphatase Activity

33.3.1.1 Preparation Protocol

33.3.1.2 Field Collection Protocol

33.3.1.3 Laboratory Protocol

33.3.1.4 Data Analysis

33.3.2 Basic Method 2: Chemical Composition

33.3.2.1 Preparation Protocol

33.3.2.2 Field Collection Protocol

33.3.2.3 Laboratory Protocol

33.3.2.4 Data Analysis

33.3.3 Basic Method 3: Net Nutrient Uptake (Stable Phosphorus)

33.3.3.1 Preparation Protocol

33.3.3.2 Field Collection Protocol

33.3.3.3 Laboratory Protocol

33.3.3.4 Soluble Reactive Phosphorus Analysis (Adapted From APHA et al., 1995)

33.3.3.5 Data Analysis

33.3.4 Advanced Method 1: Gross Nutrient Uptake (Phosphorus Radiotracer)

33.3.4.1 Preparation Protocol

33.3.4.2 Field Collection Protocol

33.3.4.3 Laboratory Protocol

33.3.4.4 Data Analysis

33.3.5 Advanced Method 2: Phosphorus Turnover

33.3.5.1 Preparation Protocol

33.3.5.2 Field Placement and Collection (Option 1)

33.3.5.3 Chamber/Aquarium Placement and Collection (Option 2)

33.3.5.4 Laboratory Protocol (Applicable for Both Options 1 and 2)

33.3.5.5 Data Analysis

33.4 QUESTIONS

33.4.1 Limitation: Phosphatase Activity

33.4.2 Limitation: Chemical Composition

33.4.3 Net Uptake: Stable Phosphorus

33.4.4 Total Uptake: Radiolabeled Phosphorus

33.4.5 Turnover

33.5 MATERIALS AND SUPPLIES

ACKNOWLEDGMENTS

REFERENCES

34 - Stream Metabolism

34.1 INTRODUCTION

34.2 GENERAL DESIGN

34.2.1 Basic Method: Stream Metabolism

34.2.1.1 Site Selection and Data Collection

34.2.2 The Fundamental Metabolism Equation

34.2.3 Air-Water Gas Exchange

34.2.4 Advanced Analyses: Inverse Modeling of Ecosystem Metabolism

34.3 SPECIFIC METHODS

34.3.1 Basic Method: Stream Metabolism

34.3.1.1 In the Field: Site Parameters and Diel O2 Data

34.3.1.2 In the Field: Gas Exchange From Tracer Additions

34.3.1.3 In the Laboratory: Gas Exchange From Tracer Additions

34.3.1.4 On the Computer: Gas Exchange From O2 Data

34.3.1.5 On the Computer: Estimating Metabolism

Direct Calculation

34.3.1.6 Advanced Method: Metabolism Modeling

Inverse Modeling

34.4 QUESTIONS

34.5 MATERIALS AND SUPPLIES

ACKNOWLEDGMENTS

REFERENCES

35 - Secondary Production and Quantitative Food Webs

35.1 INTRODUCTION

35.1.1 Biomass Turnover and the P/B Concept

35.1.2 Utility of Secondary Production in Ecosystem Studies

35.2 GENERAL DESIGN

35.2.1 Population Density

35.2.2 Population Size Structure

35.2.3 Individual and Population Biomass

35.3 SPECIFIC METHODS

35.3.1 Cohort Techniques

35.3.2 Noncohort Techniques: Size-Frequency Method

35.3.3 Noncohort Techniques: Instantaneous Growth Rate Method

35.3.4 ``Shortcut'' Approaches

35.3.5 Statistical Approaches

35.3.6 Quantification of Food Webs

35.4 QUESTIONS

35.5 MATERIALS AND SUPPLIES

REFERENCES

36 - Elemental Content of Stream Biota

36.1 INTRODUCTION

36.2 GENERAL DESIGN

36.2.1 Site Selection

36.2.2 Elemental Composition of Food Web Compartments

36.2.3 Measuring Nutrient Release Rates of Stream Biota

36.2.4 Estimating Threshold Elemental Ratios for Stream Invertebrates

36.3 SPECIFIC METHODS

36.3.1 Basic Method 1: Estimating C, N, and P Content of Food Web Compartments

36.3.1.1 Protocol for Field Collection

36.3.1.2 Protocol for Laboratory Preparation

36.3.1.3 Sample Analysis11Wear personal protective equipment (PPE), including lab coat, eyewear, and gloves, whenever conducting lab ...

36.3.1.4 Data Analysis and Assessment of Consumer-Resource Imbalances

36.3.2 Basic Method 2: Measuring Organismal Nutrient Release Rates

36.3.2.1 Field Protocol

36.3.2.2 Laboratory Protocol: Excretion

36.3.2.3 Laboratory Protocol: Egestion

36.3.2.4 Calculations

36.3.3 Advanced Method 1: Measuring C, N, and P Content in a Single Sample With the ``One-Vial Technique''

36.3.3.1 Preparation

36.3.3.2 Recrystallize the Potassium Persulfate (24h Before Analysis)

36.3.3.3 Digestion

36.3.3.4 Carbon Analysis

36.3.3.5 Nitrogen and Phosphorus Analysis

36.3.4 Advanced Method 2: Evaluating the Relative Importance of Animal Excretion at the Ecosystem Scale

36.3.4.1 Metrics of Relative Ecosystem-Level Importance of Animal Excretion

36.3.5 Advanced Method 3: Accounting for the Effects of Fasting and Stress on Organismal Excretion Rates

36.3.5.1 Calculations

36.3.6 Advanced Method 4: Estimating Threshold Elemental Ratios

36.3.6.1 Periphyton Incubation

36.3.6.2 Growth Experiment

Preparation

36.3.6.3 Experimental Procedure

36.3.6.4 Data Analysis

36.4 QUESTIONS

36.5 MATERIALS AND SUPPLIES

ACKNOWLEDGMENTS

REFERENCES

F - Ecosystem Assessment

37 - Ecological Assessment With Benthic Algae

37.1 INTRODUCTION

37.2 GENERAL DESIGN

37.2.1 Ecological Assessment

37.2.2 Project Plan

37.2.3 Sampling Plan

37.2.3.1 Site Selection

37.2.3.2 Field Sampling and Laboratory Assays

37.2.4 Data Analysis Plan

37.2.4.1 Objective A

37.2.4.2 Objective B

37.2.4.3 Objective C

37.3 SPECIFIC EXERCISES

37.3.1 Basic Exercise 1: Rapid Periphyton Survey

37.3.1.1 Field Assessment

37.3.2 Basic Exercise 2: Genus-Level Periphyton Assays and Index of Biotic Condition

37.3.2.1 Collecting Periphyton Samples

37.3.2.2 Subsampling for Different Assays

37.3.2.3 Identifying Diatom Genera and Counting Cells

37.3.2.4 Calculating Diatom Metrics

37.3.3 Advanced Exercise 1: Identification and Counting of All Algae (Optional)

37.3.3.1 Calculating Algal Metrics

37.3.4 Advanced Exercise 2: Species Autecologies and Inferring Environmental Condition (Optional)

37.3.4.1 Calculating an Environmental Optimum for a Species

37.3.4.2 Calculate Inferred Total Phosphorus Concentration for a Stream

37.3.5 Advanced Exercise 3: Biomass Assays (Optional)

37.3.6 Advanced Exercise 4: Analysis and Interpretation of Data

37.3.6.1 Determine Expected Conditions

37.3.6.2 Assess Stream Conditions for Targeted Streams

37.3.6.3 Assess Stream Conditions for the Region

37.3.6.4 Diagnose Likely Causes of Impairment

37.4 QUESTIONS

37.5 MATERIALS AND SUPPLIES

REFERENCES

38 - Macroinvertebrates as Biotic Indicators of Environmental Quality

38.1 INTRODUCTION

38.1.1 Evaluating Stressors

38.1.2 Advanced Approaches to the Identification of Macroinvertebrates

38.1.2.1 Genetic Approach

38.1.2.2 Species Traits Approach

38.1.3 Volunteer (Citizen-Based) Assessments

38.2 GENERAL DESIGN

38.2.1 Analytical Approaches

38.2.1.1 Multimetric Approach

38.2.1.2 Multivariate Approaches

38.2.2 Habitat Assessment

38.3 SPECIFIC METHODS

38.3.1 Basic Method: Assessment of Two Sites

38.3.1.1 Site Selection

38.3.1.2 Physical Habitat Description

38.3.1.3 Macroinvertebrate Field Collection Option

38.3.1.4 Macroinvertebrate Laboratory-Only Option

38.3.1.5 Data Analyses

38.3.2 Advanced Method: Assessment of Multiple Sites

38.3.2.1 Site Selection

38.3.2.2 Macroinvertebrate Collections

38.3.2.3 Habitat Assessment

38.3.2.4 Subsampling, Sorting, and Identification

38.3.2.5 Calculate Metrics

38.3.2.6 Comparison of Replicate Samples

38.3.2.7 Generate Ordination Scores

38.3.2.8 Correlations

38.4 QUESTIONS

38.4.1 General Questions for Both Basic and Advanced Methods

38.4.2 Questions for Basic Method

38.4.3 Questions for Advanced Method

38.5 MATERIALS AND SUPPLIES

ACKNOWLEDGMENTS

REFERENCES

39 - Environmental Quality Assessment Using Stream Fishes

39.1 INTRODUCTION

39.1.1 A Brief History of the Index of Biotic Integrity

39.1.2 Patterns in ``Noise'' Versus ``Signal''

39.1.3 Motivation and Regionalization

39.2 GENERAL DESIGN

39.2.1 Family of Indices

39.2.2 Regional Calibration

39.2.3 Major Assumptions

39.2.4 Establishment of Baseline Considerations

39.2.5 Metric Selection and Replacement

39.2.5.1 Range Test

39.2.5.2 Signal-to-Noise

39.2.5.3 Correlation With Natural Gradients

39.2.5.4 Responsiveness Test

39.2.5.5 Redundancy Test

39.2.5.6 Range Test for Metric Values

39.2.5.7 Metric Scoring

39.2.6 Additional Considerations

39.3 SPECIFIC METHODS

39.3.1 Basic Method: Application of the Index of Biotic Integrity to a Reference Site and an Impacted Site

39.3.1.1 Field Methods

39.3.1.2 Data Analysis

39.3.2 Advanced Method: Calibration and Testing a Stream Fish Index of Biotic Integrity

39.3.2.1 Field Methods

39.3.2.2 Data Analysis

39.4 QUESTIONS

39.4.1 General Questions

39.4.2 Questions for Basic Method

39.4.3 Questions for Advanced Method

39.5 MATERIALS AND SUPPLIES

REFERENCES

APPENDIX 39.1

40 - Establishing Cause-Effect Relationships in Multistressor Environments

40.1 INTRODUCTION

40.1.1 Linking Field Biomonitoring to In Situ Bioassay Experiments

40.1.2 Artificial Stream Approaches

40.2 GENERAL DESIGN

40.2.1 Site Selection

40.2.2 General Procedures

40.3 SPECIFIC METHODS

40.3.1 Basic Method: Retrospective Ecological Risk Assessment of an Effluent Discharge

40.3.1.1 Site Characterization

40.3.1.2 Field Assessment of Ecological Effects

40.3.1.3 Laboratory Methods

40.3.1.4 Data Analysis

40.3.2 Advanced Method 1: Determining Nutrient Limitation Using Nutrient Diffusing Substrate Bioassays

40.3.3 Advanced Method 2: In Situ Determination of Sublethal Effects of the Effluent

40.3.4 Advanced Method 3: Separating Nutrient and Contaminant Effects on Benthic Food Webs

40.4 QUESTIONS

40.4.1 Basic Method: Retrospective Ecological Risk Assessment of an Effluent Discharge

40.4.2 Advanced Method 1: Determining Nutrient Limitation Using Nutrient Diffusing Substrate Bioassays

40.4.3 Advanced Method 2: In Situ Determination of Sublethal Effects of the Effluent

40.4.4 Advanced Method 3: Separating Nutrient and Contaminant Effects on Benthic Food Webs

40.5 MATERIALS AND SUPPLIES

ACKNOWLEDGMENTS

REFERENCES

Glossary

Index

A

B

C

D

E

F

G

H

I

K

L

M

N

O

P

Q

R

S

T

U

V

W

Back Cover

The users who browse this book also browse