Notes
Slide Show
Outline
1
Field Training for Non-Wadeable
Streams and Rivers
Part 1.
  • From Dave Peck April 2003
  • (EMAP Western Pilot Study)


  • With CPCB modifications 17 August 2007
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SITE SELECTION
  • YEAR 1 = 5 random sites chosen by EPA
  • YEAR 2 = 30 random sites chosen by EPA
  •                         5 reference sites chosen by CPCB


  • Office evaluation
    • Maps & permission
    • No sites in Missouri R. floodplain
    • No more than 3 sites per tributary


  • Reconnaissance if possible
    • Access & hazards


  • Go through list of PRIMARY sites first.
  • If you can’t sample a site, replace it with the next site on the ALTERNATE list



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SAFETY
    • Updated tetanus shots
    • CPR and 1st aid training


    • WEAR LIFEJACKETS in BOATS


    • Sunscreen, water, food, etc.
    • Water quality may pose a hazard at some sites (Wash often, use sanitizer)


    • Comfortable with site conditions and access
    • Wide range of sites (urban, canals to wilderness )-- need to be prepared for all kinds of different safety situations
    • Electrofishing– using powerful generators, dealing with water in raft at times

4
Data Recording (Table 2-3)
  • Data Forms
    • Will be only record of your visit
      • “If you don’t write it down, it never happened.”
    • No doodling!!
    • Make copies, but send originals
    • Stream ID and visit (date) must be correct on all forms for a site
    • Check forms before you leave the site


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A “Good” Data Form
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Not-Too Bad, but…
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Not-so Hot #1
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Not-so-Hot #2
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Not-So-Hot #3
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Not-So-Hot #4
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Not-So-Hot #5
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Not-So-Hot #6
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GENERAL SEQUENCE OF ACTIVITIES
  • Sampling conducted during one pass downstream through the sampling reach
    • Fish raft – samples along shoreline, stops to process fish at each transect.  Alternate banks every 2 transects.
    • Habitat raft - samples down channel, then stops at each transect for nearshore and riparian measurements.  One bank entire reach (Fig. 6-1).
    • GPS reading taken at each transect.
  • Some duties (e.g., collection of benthos and periphyton samples) can be done by either raft (said EPA)
    • But probably better for fish raft b/c of switching banks?
  • At last transect K
    • Water chemistry samples & in situ measurements, mid-channel
    • Qualitative assessment forms (e.g., Channel Constraint, Visual Assessment, RBP Habitat)
  • Samples processed at take-out point
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FIND THE X-SITE
  • PROBABILITY SAMPLING
    • Systematic randomized sample of stream network from 1:100,000 scale USGS topo maps (perennial “blue line” streams)
    • Design is optimized to estimate condition of the population expressed as stream length
    • Very important to go to randomly selected  (X-site) site on map; no alternatives
    • But can slide reach around X
  • FINDING THE X-SITE
    • Non-wadeable sites:  located on map prior to sampling, sampling reach is estimated based on x-site, location of put-in and take-out points
    • Goal is to be within 100 m; 0.25 inches on 7.5” map = 150 m = 0.1 miles
    • In the field, use all available means to confirm you are at the correct river
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INITIAL SITE ACTIVITIES
  • Site Verification
    • Sampleable
      • Wadeable
      • Boatable
      • Partial:  Sampled by wading or by boat
      • Interrupted flow
      • Altered:  stream different than map depiction
        • Make sketches on form
    • Non-Sampleable (Permanent)
      • Dry when visited (100 %)
      • Dry- not visited (e.g., During recon or when calling for access permission)
        • Still need to complete a verification form for these sites
      • Wetland (no defined channel)
      • Map error--No Channel or Water Body Present
      • Impounded
      • Other (e.g., pipeline or underground flow)
        • Non target Canal: Must meet both criteria
          • No natural channel
          • Only purpose is to move water
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INITIAL SITE ACTIVITIES (cont.)
  • Site Verification (Continued)
    • No Access
      • Permission Denied
      • Permanently Inaccessible
      • Temporarily Inaccessible (fire, weather, floods, need permission)
        • Can be re-scheduled for following year
        • Still need to complete a verification form for these sites
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SAMPLING CONSIDERATIONS
  • Sampling Atypical Flow Conditions
    • Do not sample if flow seems atypical due to recent precipitation (Table 4-2)
      • Classify as “Temporarily Inaccessible” on Verification Form
    • Partially Boatable sites (Table 4-1)
      • Do what can be done SAFELY
    • Interrupted flow (enduring pools)
      • Do not sample if excessive dragging of rafts will be required
        • Classify as “Temporarily Non-sampleable—Not Boatable” on Verification Form
      • If sampled by raft, collect all indicators if possible
  • Access Permission/Public Relations
    • Always ask for permission on site
      •  land owner may not have told renters
    • Act professionally
    • Good P.R. goes a long way
  • Safety
    • Don’t sample during storm events if water is very turbid/high.  Flash floods?
    • Think safety first; driving is biggest hazard

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VERIFICATION FORM
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BASE SITE ACTIVITIES (Section 3)
  • Before sampling
    • Site dossiers
    • Check equipment (pre-label and package chemistry sample containers)
      • If used
        • Conductivity meter needs to be checked periodically (but not before every site) if you are doing field measurements
        • QC check solution
          • Low conductivity (Dilute phosphate buffer), approx. 75 microSiemens/cm at 25 degrees C.
          • Medium/high conductivity:  (Potassium chloride), approx 700 or 1400 microSiemens/cm at 25 degrees C.
        • Check temperature probe on oxygen meter periodically using a thermometer
    • CHECKLISTS!!!!
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REACH
  • Determined ahead of time from map measurements
  • A is upstream, K is downstream


  • This is different than the manual:
  • 40 x mean wetted width (at the point of entry)
  • Minimum reach length = 150 m; Maximum 1000 m


  • Can slide reach as long as X is still within reach
  • X is the site coordinates


  • Main channel between transects
    • 10 habitat, substrate, backwater measurements
    • 20 snags, Thalweg measurements
  • At transects (switch shores every other transect: odd # sites begin on the left, even # sites begin on the right)
    • Habitat
    • Bugs
    • Periphyton



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REACH (cont.)
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SLIDING THE REACH
  • Barriers in reach
    • Ponds, lakes, reservoirs
    • Stream order (100,000 map) changes (confluences)
    • Impassable physical barriers (cliffs, dams)
    • Access denials
  • Keep constant reach length, slide reach to avoid barrier, X-site must be in reach
    • Do Not slide for bridges, rip-rap, pipes
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WATER CHEMISTRY (Section 5)
  • Collect a water sample at last transect (K) in mid-channel or flowing section of stream (or another transect if necessary)


  • EPA will tell us what they want, but here’s the former method:
    • One 4 L cubitainer: major anions/cations, total nutrients, DOC, TSS, acid-base chemistry
    • Two, 60 mL sealed syringes (protect from CO2 exposure):
      • Dissolved inorganic carbon (DIC)
      • pH
  • Avoid contamination
    • Rinse container and lid 3x
    • Do not inflate cubitainers by mouth
    • Avoid food, insect repellent, sunscreen before collecting sample
    • Fill syringes to 60cc, no bubbles in syringe, don't label over graduations
    • Exclude all air from cubitainers, tape lids
  • Keep cold and dark on ice, ship next day if possible
    • If not, ship as soon as you can
    • Use ice substitute packs instead of ice to ship if possible
    • LOTS OF ICE (Total wt. of cooler should be 40-50 lbs.)
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WATER CHEMISTRY (Section 5), cont’d
  • In situ meter reading of air and water temperature,dissolved oxygen (DO),conductivity, turbidity, salinity at same place
    • Record on both EPA and CPCB forms







  • Phytoplankton
    • 50 ml
    • Filter!
    • Return to Lim.


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SAMPLE COLLECTION FORM
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PERIPHYTON (Section 7)
  • NOT the EPA method in the Peck et al. manual
  • CPCB 5 vial method
  • Every other transect (A, C, E, G, I), proper bank
  • CPCB form


  • Label vials
    • Site number
    • Vial number (1 through 5)
    • Date

  • Use deliminator
  • Hard substrate - Upper surface scrubbed & aspirated
  • Soft substrate - Top 0.5 cm aspirated


  • Filter!


  • Keep on ice, in dark


  • Return to Lim


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CPCB SAMPLE COLLECTION FORM
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MACROINVERTEBRATES (Section 9)
  • Each transect, proper bank
  • 1 D-frame kick net sample - 500 micrometer mesh
  • At appropriate bank
    • Away from river margin, but
    • Depth <1 m

  • Sample area = 1 net width wide, 1 net width long
  • Place heavy mussels and snails in net
  • Scrub large rocks into net, then remove from quadrant
  • 30 second kick


  • Note habitat and substrate
  • Composite all 11 samples from a site
  • Label
  • Preserve in formalin


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MACROINVERTEBRATES (Cont.)
  • Kick net sampling (Table 9-1)
    • Riffle/run sampling (enough flow to extend net)
      • Examine and scrub rocks and larger substrates within 1 ft2 quadrant first, then place them outside of quadrat.
      • Kick remaining finer substrate (top layer only) in quadrat for 30 seconds
        • Stand at side of net, not upstream
      • Only check one substrate type per sample
      • Also indicate microhabitat type at sampling point

    • Pool sampling (not enough flow to extend net)
      • Examine and scrub rocks and larger substrates within 1 ft2 quadrant first, then place them outside of quadrant.
      • Stir up top sediments within quadrant, sweep net through cloud for 30 seconds
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MACROINVERTEBRATES (Cont’d)
  • Processing (Table 9-2)
    • Don’t label jars until you’ve collected the sample!
    • Remove as much material as possible before preserving (coarse and fine)
      • Do not fill jar more than 1/4 full of residue
    • Fill to top with preservative (no headspace) to cushion specimens
    • After adding preservative, gently rotate the jar to horizontal position to mix to minimize damage to specimens
      • Don’t invert, agitate, or swirl
    • Complete label for inside of jar (water-resistant paper)
    • Make sure info on label and form match (e.g., no. jars)
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SAMPLE COLLECTION FORM
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AQUATIC VERTEBRATES (Section 10)
  • NOT amphibians and crayfish


  • Electrofishing - primary sampling technique
    • If conductivity > 1700 us/cm, use GPP 5 unit
    • 1 pass through reach along banks, with effort allocated among entire reach length (45 min for small streams, 3 hr for large, wide streams)
      • Areas between transects (“sub-reaches”) used to spread effort throughout reach, and to keep track of where species were collected
      • Alternate banks every 2 sub-reaches
    • On larger streams, may take > 1 day to completely sample reach

  • Electrofishing swath
    • 3 – 4 m wide
    • At oar’s length from shore
    • Near cover
    • Depths < 3 meters wherever possible.



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AQUATIC VERTEBRATES (cont.)

  • Sein each transect as last resort
    • Kick seining or sweep hauls
    • Multiple short hauls preferred over long ones to minimize mortality

  • Need to keep track of sites not fished and why, and how much of reach was sampled effectively
    • Header section of collection form


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AQUATIC VERTEBRATES (cont.)
  • ID and tally
    • Keep “species” bagged separately
      • OK to use more than one tag for species to avoid opening and closing bags as you progress through reach
    • Voucher specimens:
      • Listed species;  photograph, then release
      • Large or easy to ID:  Keep 1-2 specimens, or photograph if too large or game species
      • Smaller or hard to ID will have been brought back to lab:    Preserve up to 20 adults
        • Need to be able to correct counts for misidentifications
  • GOOD CLEAR PHOTOS ARE CRITICAL
      • Must be able to confirm ID from photo
  • Make sure vouchers are properly preserved!
      • Don’t pack fish in bags; use > 1 bag/tag if necessary
  • Fill in every sub-reach where species is collected
      • We won’t compute Jaccard coefficient
  • Record any specimens with anomalies (not type), and mortality from collecting or handling
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VOUCHER PHOTOGRAPHS
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VERTEBRATE COLLECTION FORM
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FISH TISSUE CONTAMINANTS (Section 11)
  • Used as “Sampling device” to get some idea of long-term exposure of stream to toxics
  • Vouchers come before tissue.
  • Two types of samples
    • Big  > 120 mm total length
      • Up to 3 individuals of 3 different species
        • Piscivores >> Invertivores >> Omnivores
      • Up to 9 different samples
      • Each species gets own ID number
    • Small  < 100 mm total length
      • Similar sized individuals; 400 g wet wt. (approx 14-16 oz.) “Pop can”
      • One ID number for all
  • If tissue samples are too large for a clear zip-lock bag, place in a garbage bag and put a second label on the outside of the garbage bag
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VERTEBRATE COLLECTION FORM (p. 2)
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Visual Assessments
  • Done at end of day (or on the way to hotel)
  • Visual Assessment
    • Place to note things you can’t on other forms
    • Watershed disturbance:
      • Consider “catchment” (watershed upstream of Transect K)
      • Include any observations driving to and from site
    • Site Characteristics:
      • 200m circle about X-site for site characteristics
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TRACKING FORMS
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BACK AT KBS
  • Take care of samples the day you return!


  • Chemistry samples for USEPA
    • Chain-of-custody
    • Seal coolers
    • Store in walk-in cooler
    • Take to EPA the next day


  • Periphyton & phytoplankton samples for Lim
    • Chain-of custody
    • Small cool in walk-in-cooler
    • Leave a note for her


  • Fish and bugs
    • Track on sign-in sheet in tile room
    • Let lab person know samples have arrived


  • Fish tissue to ???
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BACK AT KBS (cont.)
  • The next day review field sheets
    • Missing info
    • Clean up handwriting
    • Photocopy & put in order


  • Clean equipment
    • Hose outside
    • Clean up vehicles and boats


  • FIX anything needing fixing


  • Gas receipts to Josh
  • Travel forms
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Habitat Methods
  • These are in the other presentations.