Benthic Macroinvertebrate Sampling
Dendies should be placed in the LTER
lakes during the last week or immediately following the last week of the LTER
fish sampling, and left in the lakes for approximately four weeks. Most of the dendies are set at fyke net sites so that both fish and macroinvertebrate
data are collected there, as dendies can provide an indication of the species
and biomass available as fish prey. Fish
sampling and macrophyte sampling must be finished
before dendies are set because their work disturbs the dendy sites.
Dendies were set in all the LTER
lakes through 1989, and in 1992 and 1993.
Only Trout, Crystal and Sparkling lakes were
sampled in 1990, 1991, and 1994 to present.
Assembly
Parts needed for one dendy sampler:
Six wide-meshed 3"
x 3" vexar mesh squares
Four narrow-meshed
3" x 3" vexar mesh squares
Two 3" x 3"
tempered hardboards
One 'choreboy'
plastic scrubbing puff
One 5 inch long,
1/4" diameter eyebolt with nut
Construct the dendy sampler by
pushing the eyebolt through the center hole of each piece with the pieces
fitting tightly on the bolt so the dendy cannot become compressed. The individual pieces are layered onto the
bolt in this order: hardboard, five vexar meshes
alternating wide with narrow, choreboy, five vexar meshes alternating wide with narrow, hardboard,
nut. Fold the choreboy
into three or four layers, with the most frayed end on the inside. The eyebolt should have a nylon string loop
tied to it. Dendies should be assembled
at the lab before going out to set them.
Placement in Lakes
A "dendy set" consists of
three dendy samplers from one lake site.
In each set, the middle dendy is designated 'Dendy B' and the end
dendies as dendies 'A' and 'C'. Dendy
sets are placed in the lakes in one of three configurations.
1.
Attached set with anchor and subsurface float.
Most shoreline sites (also called fyke net sites) are set this way. Each set consists of a 6 meter line with a
fishing snap swivel at each end and one in the middle. A dendy is attached to each snap swivel, with
the middle snap swivel also being attached to a brick anchor and subsurface
float.
2.
Unattached set with anchor and subsurface float.
Shoreline sites on Crystal and Sparkling Lakes are set this way. The individual dendies are not attached
together. Each dendy has its own anchor,
but only the middle dendy has a float.
Setting the dendies as unattached sets reduces disturbance and loss of
samplers to the curious public on these high use lakes. CR
shoreline dendies may be set without floats to reduce the high loss of samplers
from this lake.
3.
Attached set with surface float and no anchor.
Deep hole sites (also called gill net sites) and all
bog sites are set this way. Dendies are
connected with a 6 meter line as for the shoreline sets, but are not
anchored. The three dendies sink at a
more equal rate if one of them is not weighted, hopefully coming to rest apart
from one another rather than clumped together.
Also, an anchor may pull the dendies into the bottom sediments.
Shoreline
sets are placed parallel to shore in about one meter of water. The floats are 250ml or 500ml plastic bottles
partially filled with water so that they remain submerged.
They
should be attached directly to the brick anchors rather than to the dendy or
they will pull the dendy off the lake bottom.
Floats should be labeled with 'Trout Lake Station' and our phone
number. Sets are assembled in the boat
and simply tossed over the side at the site.
They should be set so that the dendies are spread out the length of the
attachment line rather than clumped together.
The samplers do not have to be upright.
Retrieval
Dendy sets remain in the lakes for
about four weeks. Select a calm day for
retrieval as the dendies and subsurface floats are very hard to see if there
are even moderate waves on the lake.
Two people make up the retrieval
crew: a 'boat person' and a snorkeler. Anchor the boat near the middle dendy, but
collect dendies A and C before dendy B.
Lying on your belly on the lake bottom, quickly place a dendy in its
labeled freezer container, cover with lid, and return it to the boat
person. Disturb it as little as possible
before getting it contained, and be careful not to drag the other dendies when
returning with it to the boat.
Due to physical limitations, the
deep sites (and bog sites if sampled) are retrieved without snorkeling. Slowly pull the dendies up until they are
within reach of the boat person. Place
the container in the lake beneath the dendy and lift the dendy from the water
with the container.
Unclip the line from the dendy,
replace the container lid with a mesh panel lid, and drain the lake water from
the container. Rinse the mesh lid into
the container with 95% ethanol, filling the container about half full with EtOH. Cover the container,
tilting and swirling it to immerse all the invertebrates in ethanol.
At each site, note on the field
sheet whether all dendies were recovered.
Inventory needed TR CR SP Total
dendies 21 15 15 51
brick anchors 6 12 12 30
6-meter lines 7 1 1 9
floats 7
1 5 13
Equipment list for fieldwork
Setting: dendies, lines, floats, brick anchors
Extras of
all parts
Maps, data
sheets, pencils, sharpee, string, scissors, duct tape
Retrieval: dendy containers w/ lids, big gray transport tubs
Mesh
strainer lids, 95% EtOH in gallon jugs, EtOH wash bottle
Foam board
to wrap lines on
Maps and
data sheets, pencils, sharpee, labeling tape,
scissors
Anchor for
boat, snorkeling gear (plenty of weight)
Hook to
retrieve dendies set or moved into too deep water
Processing
Dendies should be processed as soon
as possible after collection to avoid desiccation due to evaporation of the
ethanol. The freezer container lids do
not fit tightly enough to allow long term storage in these containers. Do not allow the samples to freeze; store
them in the garage storage room or the gear room if freezing nights are a
possibility.
Assemble the Dandy Dendy
Concentrator (DDC) so the stopper can be removed without crushing any organisms
and the drain will flow into the sink.
Rinse the DDC thoroughly with tap water.
Make sure the stopper is in place, and place a clean beaker or 60 ml
sample jar under the insect spout to catch any leaks.
Rinse the freezer container lid into
the DDC with tap water. Transfer the
dendy from the freezer container to a clean two-gallon bucket. The ethanol left in the freezer container can
be poured into the DDC now or later. If
there is a lot of particulate matter in the ethanol, wait till later to avoid
clogging the mesh. Disassemble the dendy
over the bucket, rinsing the vexar mesh squares,
hardboards, and eyebolt into the bucket under running tap water. Place the mesh, hardboards, and eyebolt into
a sample tray or dishpan. Leave the choreboy in the bucket to soak.
Using a fine tipped forceps, pick
all matter from the mesh pieces, hardboards, and eyebolt, placing it into the
DDC. Pick everything even if you don't
know what it is, or are sure it's not animal. Rinse all dendy parts again
into the bucket, scraping the hardboard with a razor blade under running
water. When everything but the choreboy has been picked clean and rinsed, remove the choreboy from the bucket and pour the rinse water through
the DDC. Place the bucket below the tap
and gently unfold the choreboy. Rinse thoroughly under running tap water,
turning the choreboy inside out if the organisms
don't rinse clean initially. Pick the choreboy clean with forceps. Pour the rinse water through the DDC and
rinse the bucket, sample tray ,and freezer container into the DDC.
Wash down the sides of the DDC with tap
water. If there is a large amount of
material in the DDC, use the forceps to gently transfer some of it to the
sample jar. Use 70% ethanol to rinse the
rest of the material into the sample jar.
Rinse the DDC stopper and drain spout thoroughly. Label the sample jar in pencil with lake,
dendy site number and letter, date set and date retrieved. Also record this information on a lab form
and place it in the Dendy 3-ring binder.
Fill the sample jar to the neck with 70% ethanol and cap tightly. Store all dendy samples from the same year
together in a cardboard record storage box labeled with 'Dendy' and collection
year. Transfer the sample box to the
Zoology museum in Madison.
Leave all dendy components out to
dry, then store in plastic storage boxes.
Hardboard pieces need to dry for a long time before storage to ensure
they are dry throughout. Store the choreboys in a large plastic bag.
Note: To make 4L of 70% EtOH,
mix 2950 ml 95%EtOH with 1050ml water.
Floating
The next step in the process would be to separate the
plant material from the animal material.
This is done by placing the picked material in a pan with a solution of
sugar water, in which the animals will float and can be skimmed off the top for
identification. Details of this
procedure can be found in Anderson, R.O.
A Modified Flotation Technique for Sorting Bottom Fauna Samples. Limnology and Oceanography. Vol. 4, pp. 223-225.
We do not float LTER samples at this
time. They are stored as picked above.
(reviewed 2/05 pkm)