To sample riffle or run/glide habitats, hold the net perpendicular to the bottom downstream <strong>of</strong> thearea being sampled, so that the current carries material into the net. Remove any rocks thatblock close contact between the net and the substrate, so that all organisms dislodged from thebenthos will be carried into the net and not be lost underneath the net’s edge. Use your fingers ora s<strong>of</strong>t brush to gently rub the rocks while holding them in front <strong>of</strong> the net to remove and collectany attached organisms. Then, stir and disturb the sediment in a 0.16 m 2 (1.7 ft 2 ) sampling areain front (upstream) <strong>of</strong> the net mouth for 1-2 minutes using hands, boots, or a small three-prongedgarden trowel. Small cobble and rocks in the sampling area should be picked up and rubbed orbrushed gently while held in the current to dislodge any attached organisms. To sample pools,stir the sediment in the same way and sweep the net upwards from the top <strong>of</strong> the substratethrough the water column to collect dislodged material. Root wads can be sampled by holdingthe net underneath and kicking or shaking the root wad to dislodge organisms while sweepingthe material into the net. Large pieces <strong>of</strong> woody debris can be sampled in the same manner, orexamined visually and attached organisms rinsed <strong>of</strong>f or picked <strong>of</strong>f using entomological forcepsor tweezers.A stream reach may have are<strong>as</strong> that are wetted but lack sufficient depth to allow the use <strong>of</strong> akicknet or Surber sampler. In these c<strong>as</strong>es, a modified bucket sampling technique should be used(see also Fritz et al., 2006). Remove larger rocks and cobble in the designated 0.16 m 2 samplingarea and gently rub and rinse any attached material into a 5 gallon pl<strong>as</strong>tic bucket. Use a smallhand trowel to stir the remaining sediment in the sampling area for 1-2 minutes, and collect thesuspended material by simultaneously sweeping a small hand net or aquarium net through thewater column.Once a sample h<strong>as</strong> been collected, w<strong>as</strong>h the material in the into a 5 gallon pl<strong>as</strong>tic bucket. Largepieces <strong>of</strong> debris caught in the net (stones, pieces <strong>of</strong> wood, large intact leaves) can be gentlyrubbed using fingers or a small s<strong>of</strong>t brush and rinsed into the bucket to dislodge attachedorganisms, and then discarded. If the net contains an excessive amount <strong>of</strong> sand or silt, whichmay occur when sampling in are<strong>as</strong> with s<strong>of</strong>t substrates, this can be reduced if needed by gentlyswirling and rinsing down the outside <strong>of</strong> the net bag in the stream. Once all the sample materialh<strong>as</strong> been rinsed into the bucket, it is poured through a 500 μm sieve to collect and concentratethe organisms; additional water may be poured over the sieve to rinse the sample further.Examine the bucket to ensure that no organisms are left behind; snails and leeches <strong>of</strong>ten attach tothe sides <strong>of</strong> the bucket, and heavier organisms such <strong>as</strong> fingernail clams, mollusks, and largecaddisflies may remain in sediment left at the bottom <strong>of</strong> the bucket. Invertebrates can be pickeddirectly from the sieve using entomological forceps or tweezers, but it is preferable to rinse thesieved material into shallow white pl<strong>as</strong>tic trays (using a w<strong>as</strong>h bottle) for picking. This willfacilitate picking, <strong>as</strong> the small size and cryptic coloration <strong>of</strong> many aquatic invertebrates makesthem difficult to see when they are not in motion, and organisms are more visible whenswimming against a light background.If any further sample identification is to be performed later or if voucher specimens are desired,invertebrates can be preserved in pl<strong>as</strong>tic Nalgene jars containing 95% ethanol. Sample volumeand any <strong>as</strong>sociated organic material (i.e. algae, leaf debris) should comprise no more than onehalfto two-thirds <strong>of</strong> the sample jar volume to ensure adequate sample preservation (i.e. greater<strong>Macroinvertebrates</strong> <strong>as</strong> indicators <strong>of</strong> stream flow duration,The Xerces Society for Invertebrate Conservation20
amount <strong>of</strong> organic material = smaller sample volume per jar); use multiple jars if needed, andlabel each with stream name, reach location, habitat type in pencil on waterpro<strong>of</strong> paper.To ensure that each subsequent sample set taken in a different reach is not “contaminated” byinvertebrates from the previous site, rinse all equipment thoroughly between each samplingevent. Examine the net closely after rinsing and use forceps or fingers to remove any organismsstill clinging to it.Dry channelOur recommendation when <strong>as</strong>sessing a “dry” stream channel is that the reach should first bescouted to <strong>as</strong>certain whether it is completely dry, or if are<strong>as</strong> <strong>of</strong> standing water such <strong>as</strong> smallpools or seeps that can be sampled for aquatic invertebrates still remain. Are<strong>as</strong> with standingwater can be sampled <strong>as</strong> described above; the sampling effort should also include searching inare<strong>as</strong> <strong>of</strong> likely refuge such <strong>as</strong> underneath rocks, in leaf packs, or in are<strong>as</strong> <strong>of</strong> moist substrate.Scoring would be done <strong>as</strong> described above.If the channel completely lacks standing water, a twenty-minute search effort should be made inwhich are<strong>as</strong> <strong>of</strong> likely refuge such <strong>as</strong> underneath rocks, in leaf packs, in are<strong>as</strong> <strong>of</strong> moist substrate,etc. are investigated. If NO aquatic organisms, c<strong>as</strong>es, shells, or exuviae are found, thenmacroinvertebrates should be omitted completely from the <strong>as</strong>sessment process. Any liveinvertebrates that are unequivocally aquatic forms may be scored; omit any terrestrial organisms,<strong>as</strong> these will rapidly invade a dry channel. If no aquatic invertebrates are found, but a searchreveals caddisfly fly c<strong>as</strong>ings, aquatic invertebrate exuviae (i.e. dragonfly exuviae), or musselshells, this should be noted and scored <strong>as</strong> an indicator <strong>of</strong> intermittent flow. This can be arevealing process if sufficient time is taken to adequately search, <strong>as</strong> the presence <strong>of</strong> caddisflyc<strong>as</strong>es in a dry channel or a fishfly larva hiding beneath a rock, for example, would be a strongerindicator <strong>of</strong> more recent flow and thus an intermittent stream.The decision to retain macroinvertebrates in the <strong>as</strong>sessment metric when the stream channel isdry will depend in part on the amount <strong>of</strong> time and effort that practitioners are willing to spendsearching and sampling. Searching for invertebrates with adaptations to resist or avoiddesiccation in dry or nearly dry streams will require alternative sampling methods. Individualsmay burrow into the hyporheic zone, undergo egg or larval diapause in moist sheltered habitatsin the stream bed or edge, or diapause <strong>as</strong> adults in nearby terrestrial habitat. Invertebratesampling during dry periods therefore requires a greater degree <strong>of</strong> effort, <strong>as</strong> stream reaches mustbe scanned for any remaining small seeps or pools <strong>as</strong> well <strong>as</strong> are<strong>as</strong> that might harbor aestivatingor diapausing life stages, such <strong>as</strong> the underside <strong>of</strong> rocks and branches or the moist substrate <strong>of</strong>the hyporheic zone.Identification <strong>of</strong> invertebrate taxa will also become more problematic, <strong>as</strong> many invertebrates indry stream beds are terrestrial, and a practitioner without the necessary entomological expertiseidentifying organisms in the field may not be able to differentiate between some aquatic andterrestrial invertebrates. Less error would be incurred by treating the invertebrate metric similarto the fish metric and omitting it entirely from the <strong>as</strong>sessment process if the stream channel iscompletely dry. It is anticipated that the redundancy in the other metrics would provide an<strong>as</strong>sessment that would be sufficiently robust even in the absence <strong>of</strong> macroinvertebrate data.<strong>Macroinvertebrates</strong> <strong>as</strong> indicators <strong>of</strong> stream flow duration,The Xerces Society for Invertebrate Conservation21
- Page 1 and 2: Using Aquatic Macroinvertebratesas
- Page 3 and 4: GoalsThe goal of this project is to
- Page 5 and 6: supported different macroinvertebra
- Page 7 and 8: that some studies have found simila
- Page 9 and 10: DispersalAdult invertebrates with s
- Page 11 and 12: majority of all caddisflies collect
- Page 13 and 14: North CarolinaAquatic macroinverteb
- Page 15 and 16: Amphipoda), water mites (subclass H
- Page 17 and 18: ScoringThe current Oregon Draft Str
- Page 22 and 23: However, the degree of dryness in b
- Page 24 and 25: Boulton A.J. & Lake P.S. 1992b. Ben
- Page 26 and 27: Li, J., Herlihy, A., Gerth, W., Kau
- Page 28 and 29: Williams, D. D., 1996. Environmenta
- Page 30 and 31: shelter and to filter organic parti
- Page 32 and 33: • Dytiscidae (predaceous diving b