US Long-Term Ecological Research Network

Cascade Project at North Temperate Lakes LTER Core Data Physical and Chemical Limnology 1984 - 2016

Abstract
Physical and chemical variables are measured at one central station near the deepest point of each lake. In most cases these measurements are made in the morning (0800 to 0900). Vertical profiles are taken at varied depth intervals. Chemical measurements are sometimes made in a pooled mixed layer sample (PML); sometimes in the epilimnion, metalimnion, and hypolimnion; and sometimes in vertical profiles. In the latter case, depths for sampling usually correspond to the surface plus depths of 50percent, 25percent, 10percent, 5percent and 1percent of surface irradiance.
Dataset ID
352
Date Range
-
Methods
Methods for 1984-1990 were described by Carpenter and Kitchell (1993) and methods for 1991-1997 were described by Carpenter et al. (2001).
Version Number
14

LTREB Chemical and Physical Limnology at Lake Myvatn 2012-current

Abstract
These data are part of a long-term monitoring program at station 33 in the central part of Myvatn that represents the dominant habitat, with benthos consisting of diatomaceous ooze. The program was designed to characterize import benthis and pelagic variables across years as midge populations varied in abundance. Starting in 2012 samples were taken at roughly weekly inervals during June, July, and August, which corresponds to the summer generation of the dominant midge, Tanytarsus gracilentus.
Creator
Dataset ID
287
Date Range
-
Maintenance
Ongoing
Metadata Provider
Methods
Water Profile1. Take Light, DO, pH, Temp profile every 0.5mUse YSI DO probe, pH meter, and Li Cor light meter. Take the light profile from the sunny side of the boat.2. Take Secchi depthLower Secchi disk slowly until you can never see clear boundaries between white and black quarters, record this distance to the surface of the water as lower Secchi disk observation. Then pull the Secchi up until you can always see clear boundaries between white and black quarters, record this distance to the surface as the upper Secchi observation.Benthic Net Primary Production1. Measure light, temperature, percentDO, DO, and pH at 0.5m intervals at the sampling location.2. Take 10 clean/undisturbed cores. Try to get a uniform distance between the sediment and top of tube, so the cores have the same volume of water. Cover in boat with tarp to exclude light.3. Collect water from the shore of the boat and measure temp, percentDO, and DO. Save in bucket.4. Measure light intensity at 0 (out) and 0.5m depth where the cores will be incubated.5. Set up HOBO light recorder on the incubator.6. For each tube, take initial temp, percentDO, and DO. Before taking DO measurement, move the DO probe up and down three times to ensure no DO gradient (but do not disturb sediment). Add, slowly and without bubbling, 10 to 20mL of water (just the amount needed) to the core from bucket (number 3) to ensure no air space, and replace the stopper. Measure the distance from sediment to bottom of stopper to the nearest 0.5cm (column_depth).7. Place cores 1, 3, 5, and 7 in dark chambers (opaque tubes), so there are 4 dark and 6 light treatments.8. Incubate the cores using the metal structure at saturation light intensity if possible (300 mol per meter squared per second at 0.5m depth) for about 3h.9. Before taking DO measurement, move the DO probe up and down three times to ensure no DO gradient (but do not disturb sediment), and then measure percentDO, DO, and temperature in each core.Light controlsOnce a month (June, July, August), on a sunny day, incubate 10 cores for 3h with different light intensities to determine primary productivity under different light intensities and different temperatures. It would be best to do this the day after routine sampling (i.e., when retrieving the benthic sampler) so that the results can be compared to those from the routine sampling. Different light levels are obtained using white mesh bags around the core tubes.Core 1 and 6, lightCore 2 and 7, 2xCore 3 and 8, 4xCore 4 and 9, 8xCore 5 and 10, darkIMPORTANT: After the incubations, measure light intensity inside a core tube covered for the different treatments. This is done by removing the light meter from the metal holder and placing it facing up in a core using zip ties and a blue stopper at the bottom. Then place treatment bags over the top and measure light when holding the core at the level they reach in the incubator; use the marking on the light meter cord to make sure this is standardized for all measurements. This should be done 8 times total (each bag plus twice without bags).Light saturationOnce a month in the summer of 2013, we conducted sediment core incubations with varying amounts of shade cloth applied to the cores. Sediment cores received 0, 2, 4, 8, or 15 layers of shade cloth, with two cores in each treatment. All cores were then incubated in the lake over the same 3hr period at a depth of 0.5m.Sediment Dry Weight and Weight on Combustion1. Remove 0.75cm of sediment from a core into a plastic deli container. This should be done on a fresh core. This is the same sample that is used for chl analysis.2. Subsample 5 to 10mL sediment solution and place in a pre-weighed tin tray in oven at 60C for at least 12 hours. When dry, weigh for dry weight.In 2014, the method for sampling benthic chlorophyll changed. Sediment Dry Weight measurements were taken from these samples as well. Below is the pertinent section from the methods protocols. Processing after the collection of the sample was not changed.Take sediment samples from the 5 cores collected for sediment characteristics. Take 4 syringes of sediment with 10mL syringe (15.3 mm diameter). Take 4-5cm of sediment. Then, remove bottom 2cm and place top 2cm in the film canister.3. Combust at 550C for 4.5 hours. Weigh tray.4. If not analyzing combusted samples immediately, place in drying oven before weighing.
Version Number
15

North Temperate Lakes LTER: Light Extinction - Trout Lake Area 1981 - current

Abstract
A light (PAR) extinction coefficient is calculated for the water column for the seven northern study lakes (Allequash, Big Muskellunge, Crystal, Sparkling, and Trout lakes, unnamed lakes 27-02 [Crystal Bog] and 12-15 [Trout Bog]). The fraction of surface light is computed at 0.25-m to 1-m depth intervals depending on the lake. The light (PAR) extinction coefficient is calculated by regressing ln(fraction of light(z)) on depth z. Sampling Frequency: fortnightly during ice-free season - every 6 weeks during ice-covered season Number of sites: 7
Dataset ID
259
Date Range
-
LTER Keywords
Maintenance
ongoing
Metadata Provider
Methods
Light (PAR) extinction coefficient is calculated by linearly regressing ln (FRLIGHT (z)) on depth z where the intercept is not constrained. FRLIGHT(z) = LIGHT(z) or DECK(z) where LIGHT(z) is light measured at depth z and DECK(z) is light measured on deck (above water) at the same time. For open water light profiles, the surface light measurement (depth z = 0) is excluded from the regression. For winter light profiles taken beneath the ice, the first light data are taken at the bottom of the ice cover and are included in the regression. The depth of uppermost light value is equal to the depth of the ice adjusted by the water level in the sample hole, i.e., the depth below the surface of the water. The water level can be at, above or below the surface of the ice. If the water level was not recorded, it is assumed to be 0.0 and the calculated light extinction coefficient is flagged. If ice thickness was not recorded, a light extinction coefficient is not calculated. For light data collected prior to March, 2007, light values less than 3.0 (micromolesPerMeterSquaredPerSec) are excluded. For light data collected starting in March 2007, light values less than 1.0 (micromolesPerMeterSquaredPerSec) are excluded. Except for bog lakes before August 1989, a light extinction coefficient is not calculated if there are less than three FRLIGHT values to be regressed. For bog lakes before August 1989, a light extinction coefficient is calculated if there are least two FRLIGHT values to be regressed. In these cases, the light extinction coefficient is flagged as non-standard. FRLIGHT values should be monotonically decreasing with depth. For light profiles where this is not true, a light extinction coefficient is not calculated. For samples for which light data at depth are present, but the corresponding deck light are missing, a light extinction coefficient is calculated by regressing ln (LIGHT (z)) on depth z. Note that if actual deck light had remained constant during the recording of the light profile, the resulting light extinction coefficient is the same as from regressing ln(FRLIGHT(z)). In these cases, the light extinction coefficient is flagged as non-standard.
Short Name
NTLPH08
Version Number
16

Cascade Project at North Temperate Lakes LTER: Physical and Chemical Limnology 1984 - 2007

Abstract
Physical and chemical variables are measured at one central station near the deepest point of each lake. In most cases these measurements are made in the morning (0800 to 0900). Vertical profiles are taken at varied depth intervals. Chemical measurements are sometimes made in a pooled mixed layer sample (PML); sometimes in the epilimnion, metalimnion, and hypolimnion; and sometimes in vertical profiles. In the latter case, depths for sampling usually correspond to the surface plus depths of 50percent, 25percent, 10percent, 5percent and 1percent of surface irradiance.The 1991-1995 chemistry data obtained from the Lachat auto-analyzer. Like the process data, there are up to seven samples per sampling date due to Van Dorn collections across a depth interval according to percent irradiance. Voichick and LeBouton (1994) describe the autoanalyzer procedures in detail.Methods for 1984-1990 were described by Carpenter and Kitchell (1993) and methods for 1991-1997 were described by Carpenter et al. (2001).Carpenter, S.R. and J.F. Kitchell (eds.). 1993. The Trophic Cascade in Lakes. Cambridge University Press, Cambridge, England.Carpenter, S.R., J.J. Cole, J.R. Hodgson, J.F. Kitchell, M.L. Pace,D. Bade, K.L. Cottingham, T.E. Essington, J.N. Houser and D.E. Schindler. 2001. Trophic cascades, nutrients and lake productivity: whole-lake experiments. Ecological Monographs 71: 163-186.Number of sites: 8
Dataset ID
71
Date Range
-
LTER Keywords
Maintenance
completed
Metadata Provider
Methods
The 1991-1995 chemistry data obtained from the Lachat auto-analyzer. Like the process data, there are up to seven samples per sampling date due to Van Dorn collections across a depth interval according to percent irradiance. Voichick and LeBouton (1994) describe the autoanalyzer procedures in detail.Methods for 1984-1990 were described by Carpenter and Kitchell (1993) and methods for 1991-1997 were described by Carpenter et al. (2001).Carpenter, S.R. and J.F. Kitchell (eds.). 1993. The Trophic Cascade in Lakes. Cambridge University Press, Cambridge, England.Carpenter, S.R., J.J. Cole, J.R. Hodgson, J.F. Kitchell, M.L. Pace,D. Bade, K.L. Cottingham, T.E. Essington, J.N. Houser and D.E. Schindler. 2001. Trophic cascades, nutrients and lake productivity: whole-lake experiments. Ecological Monographs 71: 163-186.Number of sites: 8
Short Name
CPHYS1
Version Number
4
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