US Long-Term Ecological Research Network

Cascade Project at North Temperate Lakes LTER Phosphorus, Chlorophyll, DOC, Color, and pH for Twenty UNDERC Lakes 1995 - 2003

Abstract
Data on total phosphorous, chlorophyll a, dissolved organic carbon, water color, and pH for a set of lakes located at the University of Notre Dame Environmental Research Center (UNDERC). Surface water samples were collected monthly from May through August either from shore with a telescoping pole or from a boat. Twenty lakes were sampled from 1995-2000. Fifteen of these lakes were sampled from 2001-2003.
Contact
Dataset ID
361
Date Range
-
Methods
Methods are described in Pace and Cole 2002 (https://doi.org/10.4319/lo.2002.47.2.0333). Surface water samples for the analysis of pH, dissolved organic carbon (DOC), chlorophyll a , total phosphorus color were collected by dipping a sample bottle. The total phosphorus (TP) samples were stored in a separate acid-washed bottle. Samples were collected monthly from May through August from a set of 20 lakes for the years 1995-2000. A subset of fifteen lakes were sampled in the same way from 2001-2003. Samples were stored in a cooler and returned the lab for processing within a few hours.
Version Number
3

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

Cascade Project at North Temperate Lakes LTER Core Data Nutrients 1991 - 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. The 1991-1999 chemistry data was 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. Nutrient samples were sent to the Cary Institute of Ecosystem Studies for analysis beginning in 2000. The Kjeldahl method for measuring nitrogen is not used at IES, and so measurements reported from 2000 onwards are Total Nitrogen.
Core Areas
Dataset ID
351
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

Cascade Project at North Temperate Lakes LTER Core Data Carbon 1984 - 2016

Abstract
Data on dissolved organic and inorganic carbon, particulate organic matter, partial pressure of CO2 and absorbance at 440nm. Samples were collected with a Van Dorn sampler. Organic carbon and absorbance samples were collected from the epilimnion, metalimnion, and hypolimnion. Inorganic samples were collected at depths corresponding to 100%, 50%, 25%, 10%, 5%, and 1% of surface irradiance, as well as one sample from the hypolimnion. Samples for the partial pressure of CO2 were collected from two meters above the lake surface (air) and just below the lake surface (water). Sampling frequency: varies; number of sites: 14
Core Areas
Dataset ID
350
Date Range
-
Methods
Detailed field and laboratory protocols can be found in the Cascade Methods Manual, found here: https://cascade.limnology.wisc.edu/public/public_files/methods/CascadeManual1998.pdf
POC, PON and DOC: 1. 100 - 300 ml (Typically ~200mL for PML, 150 metalimnion and 75 – 100 for the hypolimnion) of lake water from each depth was filtered through 153 um mesh to remove large zooplankton. Water was then filtered through a precombusted 25mm GF/F filter (0.7 um pore size) at less than 200 mm Hg pressure. Filters were placed in drying oven at 60 C to dry for at least 48 hours. 20mL of filtered water was stored in a scintillation vial and acidified with 200uL of 2N H2SO4 for DOC analysis. Blank samples for POC and DOC were prepared with deionized water to control for contamination. All samples were sent to the Cary Institute of Ecosystem Studies for analysis.

Version Number
24

Cascade project at North Temperate Lakes LTER - High-resolution spatial analysis of CASCADE lakes during experimental nutrient enrichment 2015 - 2016

Abstract
This dataset contains high-resolution spatio-temporal water quality data from two experimental lakes during a whole-ecosystem experiment. Through gradual nutrient addition, we induced a cyanobacteria bloom in an experimental lake (Peter Lake) while leaving a nearby reference lake (Paul Lake) as a control. Peter and Paul Lakes (Gogebic county, MI USA), were sampled using the FLAMe platform (Crawford et al. 2015) multiple times during the summers of 2015 and 2016. In 2015 nutrient additions to Peter Lake began on 1 June, and ceased on 29 June, Paul Lake was left unmanipulated. In 2016 no nutrients were added to either lake. Measurements were taken using a YSI EXO2 probe and a Garmin echoMap 50s. Sensor- data were collected continuously at 1 Hz and linked via timestamp to create spatially explicit data for each lake.

Crawford, J. T., L. C. Loken, N. J. Casson, C. Smith, A. G. Stone, and L. A. Winslow. 2015. High-speed limnology: Using advanced sensors to investigate spatial variability in biogeochemistry and hydrology. Environmental Science & Technology 49:442–450.
Contact
Dataset ID
343
Date Range
-
Maintenance
complete
Methods
In two consecutive years, we measured lake-wide spatial patterning of cyanobacteria using the FLAMe platform (Crawford et al. 2015). To evaluate early warning indicators of a critical transition, in the first year we induced a cyanobacteria bloom through nutrient addition in an experimental lake while using a nearby unmanipulated lake as a reference ecosystem (Pace et al. 2017). During the second year, both lakes were left unmanipulated. Proposed detection methods for early warning indicators were compared between the manipulated and reference lakes to test for their ability to accurately detect statistical signals before the cyanobacteria bloom developed.
Peter and Paul Lakes are small, oligotrophic lakes (Peter: 2.5 ha, 6 m, 19.6 m and Paul: 1.7 ha, 3.9 m, 15 m, for surface area, mean, and max depth respectively) located in the Northern Highlands Lake District in the Upper Peninsula of Michigan, USA (89°32’ W, 46°13’ N). These lakes have similar physical and chemical properties and are connected via a culvert with Paul Lake being upstream. Both lakes stratify soon after ice-off and remain stratified usually into November (for extensive lake descriptions, see Carpenter and Kitchell, 1993).
In the first year, Peter Lake was fertilized daily starting on 1 June 2015 (DOY 152) with a nutrient addition of 20 mg N m-2 d-1 and 3 mg P m-2 d-1 (molar N:P of 15:1) through the addition of H3PO4 and NH4NO3 until 29 June (day of year, DOY 180). The decision to stop nutrient additions required meeting four predefined criteria based on temporal changes in phycocyanin and chlorophyll concentrations indicative of early warning behavior of a critical transition to a persistent cyanobacteria bloom state. (Pace et al. 2017). Nutrients uniformly mix within 1-2 days after fertilization based on prior studies (Cole and Pace 1998). No nutrient additions were made to Paul Lake. In the second year (2016), neither lake received nutrient additions.
We mapped the surface water characteristics of both experimental lakes to identify changes in the spatial dynamics of cyanobacteria. In 2015, mapping occurred weekly from 4 June to 15 August (11 sample weeks). In 2016, when neither lake was fertilized, the lakes were mapped three times in early to mid-summer. In both years, mapping occurred between the hours of 07:00 to 12:00 (before the daily nutrient addition). We rotated the order that we sampled the lakes to avoid potential biases due to differences in time of day. Each individual lake sampling event was completed in approximately one hour.
The FLAMe platform maps the spatial pattern of water characteristics. A boat-mounted sampling system continuously pumps surface water from the lake to a series of sensors while geo-referencing each measurement (complete description of the FLAMe platform in Crawford et al. 2015). For this study, the FLAMe was mounted on a small flat-bottomed boat propelled by an electric motor and was outfitted with a YSI EXO2™ multi-parameter sonde (YSI, Yellow Springs, OH, USA). We focused for this study on measures of phycocyanin (a pigment unique to cyanobacteria) and temperature. Phycocyanin florescence was measured using the optical EXO™ Total Algae PC Smart Sensor. The Total Algae PC Smart Sensor was calibrated with a rhodamine solution based on the manufacturer’s recommendations. Phycocyanin concentrations are reported as ug/L; however, these concentrations should be considered as relative because we did not calibrate the sensor to actual phycocyanin nor blue-green algae concentrations. Geographic positions were measured using a Garmin echoMAP™ 50s. Sensor- data were collected continuously at 1 Hz and linked via timestamp to create spatially explicit data for each lake. Each sampling produced approximately 3500 measurements in the manipulated lake and 2000 in the reference lake. The measurements were distributed by following a gridded pattern across the entire lake surface to characterize spatial patterns over the extent of the lake.
Version Number
15

North Temperate Lakes LTER Long-term winter chemical limnology and days since ice-on for primary study lakes 1983 - 2014

Abstract
This data set integrates long-term data sets on winter nutrient chemistry with ice phenology (number of days since ice-on), focusing on the subset of measurements taken during ice cover. Parameters characterizing limnology of 5 primary lakes (Allequash, Big Muskellunge, Crystal, Sparkling, and Trout lakes, are measured at one station in the deepest part of each lake at the surface, middle, and deep (~1 meter above bottom). These parameters include nitrate-N, ammonium-N, total dissolved phosphorus, dissolved inorganic carbon, water temperature, dissolved oxygen, and pH. Water temperature and dissolved oxygen values are the zonal averages from more complete depth profiles. Sampling Frequency: every 6 weeks during ice-covered season for the northern lakes. Number of sites: 5
Dataset ID
341
Date Range
-
Maintenance
completed
Methods
This is a compilation of three data sets

North Temperate Lakes LTER: Chemical Limnology of Primary Study Lakes: Nutrients, pH and Carbon 1981 - current
https://lter.limnology.wisc.edu/dataset/north-temperate-lakes-lter-chemical-limnology-primary-study-lakes-nutrients-ph-and-carbon-19

North Temperate Lakes LTER: Physical Limnology of Primary Study Lakes 1981 - current
https://lter.limnology.wisc.edu/dataset/north-temperate-lakes-lter-physical-limnology-primary-study-lakes-1981-current

North Temperate Lakes LTER: Ice Duration - Trout Lake Area 1981 - current
https://lter.limnology.wisc.edu/dataset/north-temperate-lakes-lter-ice-duration-trout-lake-area-1981-current
Version Number
6

Lake Mendota Carbon and Greenhouse Gas Measurements at North Temperate Lakes LTER 2016

Abstract
This original dataset contains carbon and greenhouse gas (GHG) data collected in Lake Mendota during the summer of 2016. Data were collected between 15 April 2016 and 14 November 2016 on both Lake Mendota and its surrounding streams—four major inflows and the primary outflow of Lake Mendota. The dataset is comprised of four linked tables, corresponding to carbon and GHG measurements on Lake Mendota (lake_weekly_carbon_ghg), weekly physico-chemical sonde casts on Lake Mendota (lake_weekly_ysi), ebullition rate estimates on Lake Mendota (lake_weekly_ebullition), and carbon and physico-chemical data from the four major inflows and primary outflow of Lake Mendota (stream_weekly_carbon_ysi). These data were used to explore the relationship between organic carbon dynamics and greenhouse gas production on a eutrophic lake. From these data, it is possible to estimate daily oxygen, methane, and carbon dioxide flux on Lake Mendota during the study time period. Additional methods and applications of this data can be found in J.A. Harts Masters Thesis, University of Wisconsin-Madison Center for Limnology, May 2017.
Core Areas
Dataset ID
339
Date Range
-
Methods
lake_weekly_carbon_ghg.csv
Carbon Sample Analysis: Weekly observational data were collected on Lake Mendota between 15 April 2016 and 14 November 2016. All lake samples collected from the deep hole were taken at five discrete depths (3, 10, 12, 14, and 20 m), intended to span the seasonal thermocline. All lakes samples collected in littoral zones (Point, Ubay, and Yahara) were taken at two discrete depths (0.1 and 2 m). Two liters of water were collected at each sampling location and depth using a Van Dorn sampler for measurement of particulate organic carbon (POC), dissolved organic carbon (DOC), and dissolved inorganic carbon (DIC). Between 1200 mL and 1800 mL of water was passed through a ProWeigh 47 mm filter (Environmental Express, Charleston, SC, USA) depending on how quickly water became impassable. POC was estimated by performing loss on ignition on the filter. The difference in mass before and after combustion at 500°C was multiplied by 0.484 to account for the OC fraction of organic matter (Thomas et al. 2005). Filtrate was analyzed for DOC and DIC on a Shimadzu TOC-V-csh Total Organic Carbon Analyzer (Shimadzu Scientific Instruments, Kyoto, Japan), where organic carbon is measured by combustion and inorganic carbon after phosphoric acid digestion.
Dissolved Gas Analysis: Water samples for dissolved methane (CH4) and carbon dioxide (CO2) were collected at each depth in the lake using a Van Dorn sampler and stored in 30-mL serum vials. Serum vials were overfilled and capped in the field with a rubber septa and aluminum cap. Care was taken to ensure that no bubbles were present in the sample. Serum vials were then stored on ice until they could be placed in the refrigerator. Within 24 hours of collection, samples received a 3 mL N2 gas headspace, were shaken vigorously, and left to equilibrate at room temperature. Headspace CH4 and CO2 was analyzed on a Varian 3800 gas chromatograph, and headspace-water CH4 and CO2 partitioning was accounted for using Henrys Law.
Version Number
20

Spatial variability in water chemistry of four Wisconsin aquatic ecosystems - High speed limnology Environmental Science and Technology datasets

Abstract
Advanced sensor technology is widely used in aquatic monitoring and research. Most applications focus on temporal variability, whereas spatial variability has been challenging to document. We assess the capability of water chemistry sensors embedded in a high-speed water intake system to document spatial variability. We developed a new sensor platform to continuously samples surface water at a range of speeds (0 to > 45 km hr-1) resulting in high-density, meso-scale spatial data. Here, we archive data associated with an Environmental Science and Technology publication. Data include a single spatial survey of the following aquatic ecosystems: Lake Mendota, Allequash Creek, Pool 8 of the Upper Mississippi River, and Trout Bog. Data have been provided in three formats (raw, hydraulic-corrected, and tau-corrected).
Dataset ID
337
Date Range
-
Maintenance
completed
Methods
The Fast Limnology Automated Measurement (FLAMe) platform is a novel flow-through system designed to sample inland waters at both low- (0 to appr. 10 km hr-1) and high-speeds (10 to greater than 45 km hr-1) described in Crawford et al. (2015). The FLAMe consists of three components: an intake manifold that attaches to the stern of a boat; a sensor and control box that contains hoses, valves, a circulation pump and sensor cradles; and a battery bank to power the electrical components. The boat-mounted intake manifold serves multiple purposes. First, sensors are mounted inside the boat, protecting them from potential damage. Second, the intake system creates a constant, bubble-free water flow, thus preventing any issues for optical sensors due to cavitation. Finally, to analyze dissolved gases, a constant water source is needed on board. Water flow via both the slow- and high-speed intakes is regulated by the onboard impeller pump, allowing for seamless switching between slow- and high-speed operations. Any number of sensors could be integrated into the platform with simple modifications, and can be combined with common limnological instruments such as acoustic depth-finders. In our example applications we used a YSI EXO2 multiparameter sonde (EXO2; Yellow Springs, OH, USA), and a Satlantic SUNA V2 optical nitrate (NO3) sensor (Halifax, NS, Canada), both integrated into the control box plumbing with flow-through cells available from the manufacturer. Additionally, a Los Gatos Research ultraportable greenhouse gas analyzer (UGGA) (cavity enhanced absorption spectrometer; Mountain View, CA, USA) was used to measure dry mole fraction of carbon dioxide (CO2) and methane (CH4) dissolved in surface water by equilibrating water with a small headspace using a sprayer-type equilibration system that has previously been shown to have fast response times relative to other designs16 (Figure S1). Both the EXO2 and the UGGA are capable of logging data at 1 Hz. Because the SUNA was operated out of the water and on a boat during warm periods, data were collected less frequently (appr. 0.1 Hz) to minimize lamp-on time and avoid the lamp temperature cutoff of 35° C. The EXO2 sonde uses a combination of electrical and optical sensors for: specific conductivity, water temperature, pH, dissolved oxygen, turbidity, fluorescent dissolved organic matter (fDOM), chlorophyll-a fluorescenece, and phycocyanin fluorescence. The SUNA instrument measures NO3 using in situ ultraviolet spectroscopy between 190-370 nm, has a detection range of 0.3-3000 microM NO3, and a precision of 2 microM NO3. The UGGA has a reported precision of 1 ppb (by volume). In order to translate time-series data from the instruments into spatial data, we also logged latitude and longitude at 1 Hz with a global positioning system (GPS) with the Wide Area Augmentation System (WAAS) functionality enabled allowing for less than 3 m accuracy for 95percent of measured coordinates. Synchronized time-stamps from the EXO2, UGGA, SUNA, and GPS were used to combine data streams into a single spatially-referenced dataset.
We ran a simple set of experiments to determine the residence time of the system and the overall response time of the EXO2 and UGGA sensors integrated into the platform. After determining first-order response characteristics of each sensor, we applied an ordinary differential equation method to correct the raw data for significant changes in water input resulting in higher accuracy spatial data (see Crawford et al. 2015).
Sensor response experiments
We conducted a series of sensor response experiments on Lake Mendota on August 1, 2014. The goal was to understand the potential lags and minimum response times for the EXO2 and UGGA sensors integrated into the FLAMe platform. These data were then used to develop correction procedures for higher accuracy spatial datasets. To test sensor responses to step-changes in water chemistry, we mixed a 40 L tracer solution into a plastic carboy that was connected to the reservoir port on the FLAMe. The reservoir was mixed with 50 mL of rhodamine WT to test the phytoplankton fluorescence sensors, 6 mL of quinine sulfate solution in acid buffer (100 QSE) to test the fDOM sensor, 14 g of KCl to test the conductivity sensor, and appr. 2 kg of ice to reduce the temperature of the solution relative to lake water. The mixture volume was increased to 40 L using tap water. We did not modify the CO2 concentration or pH in the carboy as we found the municipal water source to have greater than ambient lake CO2 (4300 vs. 290 microatm, respectively) and lower pH (7.5 vs 8.3, respectively). At the beginning of the experiments, we allowed lake water to circulate through the system for appr. 10 minutes. We then switched to the tracer solution for a period of five minutes, followed by five minutes of lake water, then back to the tracer solution for an additional five minutes.
Using the step-change experiment data, we determined each sensors hydraulic time constant (Hr) and parameter time constant (taus). The sensor-specific Hr is a function of system water residence time and sensor position/shielding within the system. Taus is the time required for a 63 percent response to a step-change input. Hr was calculated based on the plateau experiments and was indicated by the first observation with a non-zero rate of change. The CO2 and CH4 sensors had a much greater Hr than the EXO2 sensors because water must travel further through the system before equilibrating with the gas solution being pumped to the UGGA. Using these Hr values, we offset response variables thus removing the hydraulic lag. This correction does not account for sensor-specific response patterns (tau s). The EXO2 sensors have manufacturer-reported taus values between 2-5 s, but these values are not appropriate to apply to the FLAMe system because they do not include system hydraulic lag and mixing. In order to match sensor readings with spatial information, we first applied Hr values from each sensor output according to equation 2. This step aligns the time at which each sensor begins responding to the changing water, and accounts for the physical distance the water must travel before being sensed
In order to match individual sensor response characteristics and to obtain more accurate spatial data, we then applied sensor-specific corrections using Equation 3 (Fofonoff et al., 1974).
We first smoothed the raw data using a running mean of 3 observations in order to reduce inherent noise of the 1 Hz data. We then calculated dX/dt using a 3-point moving window around Xc. Equation 3 should ideally lead to a step response to a step-change input. We note that this is the same strategy used to correct oceanographic conductivity and temperature instruments (see Fozdar et al., 1985). Overall, the taus-corrected data show good responses to step-change inputs and indicate that this is a useful technique for generating higher accuracy spatial data. We include three types of data for each variable including: raw (e.g., TempC), the hydraulic lag corrected (e.g., TempC_hydro) and the taus-corrected data (e.g., TempC_tau). Note that not all sensors were used in each survey and not all sensors have each type of correction. This data was from our preliminary FLAMe sampling campaigns and future studies will include additional sensor outputs and corrections.
We used the FLAMe throughout the summer of 2014 on four distinct aquatic ecosystems including: a small dystrophic lake, a stream/lake complex, a medium-sized eutrophic lake, and a managed reach of the Upper Mississippi River. Each of these applications demonstrates the spatial variability of surface water chemistry and the flexibility of FLAMe for limnological research.
References
Crawford JT, Loken LC, Casson NJ, Smith C, Stone AG, and Winslow LA (2015) High-speed limnology: Using advanced sensors to investigate spatial variability in biogeochemistry and hydrology. Environmental Science and Technology 49:442-450.
Fozdar FM, Parker GJ, and Imberger J (1985) Matching temperature and conductivity sensor response characteristics. Journal of Physical Oceanography 15:1557-1569.
Version Number
14

Satellite derived secchi disk depth and other lake and landscape characteristics in Wisconsin, USA, 1991 - 2012

Abstract
This data supports the following publication: Rose, K.C., S.R. Greb, M. Diebel, and M.G. Turner. Annual precipitation as a regulator of spatial and temporal drivers of lake water clarity. Ecological Applications. The data uses satellite remotely sensed estimates of Secchi disk depth (Landsat imagery), landscape features, and lake characteristics to understand how and why lakes vary and respond to different drivers through time and space. The data were produced by the authors and their collaborators, as acknowledged in the manuscript. The Secchi disk depth data span the time period 1991-2012.
Contact
Dataset ID
331
Date Range
-
Methods
The complete methods for this manuscript are described in the manuscript: Rose, K.C., S.R. Greb, M. Diebel, and M.G. Turner. Annual precipitation as a regulator of spatial and temporal drivers of lake water clarity. Ecological Applications.
NTL Keyword
Version Number
16

CLA Yahara Lakes Citizen Offshore Water Quality Monitoring 2016 - 2017

Abstract
In 2013, Clean Lakes Alliance (CLA) launched a Citizen Water Quality Monitoring pilot. Objectives included evaluating and tracking nearshore water quality conditions on all five Yahara lakes: Lakes Mendota, Monona, Waubesa, Kegonsa and Wingra. In 2016, in order to fully understand the interaction between the offshore and nearshore
environment, CLA volunteers will begin sampling the deepest point (deep hole) of all Yahara lakes. The offshore monitoring program will focus on two components: water clarity sampling and dissolved oxygen and temperature measurement. Data from the offshore monitoring program will be compared to data from the nearshore program.
Contact
Creator
Dataset ID
330
Date Range
-
Methods
On Lakes Mendota, Monona, Waubesa, Kegonsa and Wingra, volunteers will use a Secchi disk to measure water clarity, and a digital handheld thermometer to measure air and surface water temperatures once per week on Thursday mornings . Secchi depth monitoring will take place at the deepest point of each lake. On Lakes Monona and Waubesa, concurrent with Secchi sampling, volunteers will use a YSI 550A multiprobe meter to measure dissolved oxygen and temperature at multiple depths. All volunteers are trained by Clean Lakes Alliance staff.
Version Number
2
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