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.

• 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

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 minnow trap clip at each end and one in the middle. A dendy is attached to each clip, with the middle clip also being attached to a brick anchor with subsurface float.  Beginning 2010, the set in Crystal lake is anchored with a dog tieout stake pushed into the sediment.  This is an attempt to reduce the migration of Dendies due to camper activity.
2. Unattached set with anchor and subsurface float. Shoreline sites in 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 this high use 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.

1. 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.
2. 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.
3. 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.
4. 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.
5. At each site, note on the field sheet whether all dendies were recovered.

Equipment list for fieldwork

1. 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.
2. 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.
3. 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.
4. 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.
5. 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.
6. 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.

1. 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.
2. We do not float LTER samples at this time. They are stored as picked above.