Temperature Inverted Haloclines Provide Winter Warm-Water Refugia for Manatees in Southwest Florida
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- Stith, B.M., Reid, J.P., Langtimm, C.A. et al. Estuaries and Coasts (2011) 34: 106. doi:10.1007/s12237-010-9286-1
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Florida manatees (Trichechus manatus latirostris) overwintering in the Ten Thousand Islands and western Everglades have no access to power plants or major artesian springs that provide warm-water refugia in other parts of Florida. Instead, hundreds of manatees aggregate at artificial canals, basins, and natural deep water sites that act as passive thermal refugia (PTR). Monitoring at two canal sites revealed temperature inverted haloclines, which provided warm salty bottom layers that generally remained above temperatures considered adverse for manatees. At the largest PTR, the warmer bottom layer disappeared unless significant salt stratification was maintained by upstream freshwater inflow over a persistent tidal wedge. A detailed three-dimensional hydrology model showed that salinity stratification inhibited vertical convection induced by atmospheric cooling. Management or creation of temperature inverted haloclines may be a feasible and desirable option for resource managers to provide passive thermal refugia for manatees and other temperature sensitive aquatic species.
KeywordsThermal inversion Halocline Stratification Passive thermal refugia Picayune Strand restoration Everglades restoration Aerial survey Satellite telemetry Climate change Aquatic species
The distribution of aquatic organisms frequently is limited by seasonal temperature extremes, and many species depend on thermal refugia to survive in key portions of their range (Matthews 1998). The Florida manatee (Trichechus manatus latirostris) is a federally and state-listed endangered species (U.S. Fish and Wildlife Service 2001) that has a limited tolerance for the cold water temperatures that occur regularly in the subtropical climates of Florida and the southeastern USA. During severe winter periods, manatees are restricted to peninsular Florida and must take refuge in warm-water sites to survive adverse winter temperatures (Lefebvre et al. 1989). This tropical-derived species has unusually low-heat production capacity and high-thermal conductance that limits its ability to thermoregulate in cold water (Irvine 1983). Manatees can suffer acute mortality during severe cold fronts, and die-offs have been documented in Florida as far south as Miami and Flamingo (Moore 1951; Hartman 1979). Even winters without extreme cold events can produce pathological features in manatees described as “cold stress syndrome” (Bossart et al. 2003), which may affect fecundity and long-term survival. When water temperatures fall below 20°C, they seek out warm water (Hartman 1979; Shane 1984). Captive manatees feed erratically in 15–20°C water, may refuse to eat at 15–18°C (Campbell and Irvine 1981), and after 2 or 3 days begin to show signs of shivering, anorexia, and changes in behavior (Bossart 2001). General agreement exists among these studies that temperatures falling below a threshold of 20°C become increasingly stressful for manatees (Laist and Reynolds 2005a).
In northern coastal Florida, harsh water temperatures occur throughout much of the winter, and manatees congregate in warm-water refugia at large artesian springs and discharge outlets at power plants (Laist and Reynolds 2005a). Coastal south Florida has few such sources of warm water, and manatees are commonly seen taking shelter in natural deep water areas and manmade canals and basins (Laist and Reynolds 2005a). Because these sites have no major source of warm-water influx, they are generally known as passive thermal refuges (PTRs). PTRs may become increasingly important for manatees in the near future due to power plant shutdowns or failing springs (U.S. Fish and Wildlife Service 2001). Loss of warm-water sites has been identified as a major threat to manatee population recovery (U.S. Fish and Wildlife Service 2001; Runge et al. 2007). Surprisingly little is known about PTRs used by manatees, and understanding those in South Florida may be especially important since they may provide inadequate protection for manatees during severe winters (Laist and Reynolds 2005a, b).
This research is part of an ongoing U.S. Geological Survey (USGS) effort to predict hydrologic changes associated with the PSRP and model potential manatee response to these changes (Swain and Decker 2009; Langtimm et al. 2009). Our primary objective was to provide a better understanding of the hydrodynamics of PTRs in the study area. We used data from aerial surveys to identify key manatee aggregation sites and satellite telemetry data to analyze movement patterns in response to changing water temperatures. We monitored vertical temperature and salinity at the two largest PTRs and compared the temporal variation in winter water temperatures among different regional types of water bodies also frequented by manatees. The empirical data showed that PTRs provided unusually warm bottom temperatures during cold periods, leading us to hypothesize salinity stratification as a mechanism for maintaining otherwise unstable temperature inversions. We calculated water densities for our surface and bottom measurements to test whether salinity stratification could establish stable density distributions that would support temperature inversions. We used a complex three-dimensional hydrology model of POI to test whether the proposed mechanism of salinity stratification could produce the patterns in water temperatures observed in this major PTR.
Materials and Methods
The study area encompasses the southern coastal region of Collier County, FL, USA centering on the Ten Thousand Islands (TTI) region, extending from the northwest portion of Everglades National Park westward to Marco Island (Fig. 1). The extent of the study area was dictated in part by manatee movements documented for radio-tagged individuals for this research. This area is a shallow, subtropical estuarine system consisting of tidally influenced rivers which discharge into inland bays enclosed by numerous mangrove islands. The coastal margin is fronted by shallow flats of the Gulf of Mexico. Tidal range is classified as microtidal (<1 m; Browder et al. 1986). Public-owned areas used by manatees include the Ten Thousand Islands National Wildlife Refuge, Everglades National Park, Rookery Bay National Estuarine Research Reserve, Collier-Seminole State Park, Fakahatchee Strand Preserve State Park, and Big Cypress National Preserve.
Two PTRs in the central portion of the study area were a special focus of this research: POI, at the north end of the Faka Union canal, and Big Cypress National Preserve (BCNP) headquarters (Fig. 1), which consists of canals that receive freshwater inflow from the upstream Big Cypress basin, and tidal inflow downstream from Halfway Creek. The area around POI is heavily influenced by the 77-km Faka Union canal system which was completed in 1971 to drain a failed real estate development, now slated for restoration (U.S. Army Corp of Engineers and South Florida Water Management District 2004; Swain and Decker 2009). The canal system intercepts sheet flow and rapidly diverts large water volumes as point discharge out the Faka Union Canal and into the Gulf of Mexico. Weirs were built to prevent over drainage during the dry season, but the canals have resulted in a general lowering of the water table, reduced groundwater seepage, and a shortened hydro-period (U.S. Army Corp of Engineers and South Florida Water Management District 2004). The southernmost weir restricts tidal incursion to the lower 7 km of the Faka Union canal (except during extreme tides or storm events).
Manatee Habitat Use
To identify areas of heavy use by manatees during winter, synoptic aerial survey data (Ackerman 1995) were obtained for the study region from 1991 to 2007 (FWRI 2009; four incomplete surveys were deleted). These surveys were flown as part of a statewide program using a standardized protocol and flight line that includes all of the major river systems, inland bays, and shallow Gulf shoals in the study area.
The aerial survey point data were overlaid with the habitat patches, and the results were summarized by zone and major winter aggregation sites. The summary data provide minimum counts of animals at surveyed sites, and underestimate the true population size by an unknown amount.
Winter telemetry data were available for 22 manatees captured and tagged at POI between 2001 and 2006 and provided data at a finer temporal and spatial resolution than aerial surveys. Data were obtained from floating Argos platform transmitter terminals (PTT; Telonics, Inc.) or GPS units (Lotek Wireless, Inc. or Telonics, Inc.) attached to manatees by flexible tethers to standardized peduncle belts (Reid et al. 1995). Argos location fixes were calculated from transmissions received by polar-orbiting satellites during four programmed duty cycles daily, potentially providing four standard quality locations per day. GPS location data were collected at time intervals ranging from 15 to 60 min.
Telemetry data were reduced to winter months only (November through March). Locational accuracy for the Argos data has a known variability, and only the two most accurate location classes (LC3, LC2) were kept: Service Argos, Inc. (1996) estimates that 68% of locations should lay within 150 m for LC3 and within 350 m for LC2. Data were further reduced to one location class per programmed duty cycle (Deutsch et al. 2003). The GPS data were subsampled to one location per 6-h interval approximating the Argos satellite fix intervals, and all winter location data from both tag types were merged for analysis.
GIS overlay procedures (ArcGIS identity function, E.S.R.I. 1997) were used to assign telemetry locations to one of the four habitat zones, river systems or canals, bays, inter-island corridors, and offshore (Fig. 2). We interpolated hourly Gulf temperatures to match date and time for each telemetry fix. The proportional manatee use of each habitat zone at different Gulf temperatures was calculated at 1°C intervals from 14°C to 27°C.
To investigate whether tagged manatees showed preferential use of different habitat zones based on water temperature, we calculated kernel density surfaces for each animal–winter combination using Gulf temperature to segregate the telemetry locations into three Gulf temperature bins: less than 18°C, 18°C to less than 20°C, and 20°C or above. We used the Home Range Extension for ArcView (Rodgers and Carr 1998) with a fixed kernel (500 m) for the utilization distribution (Worton 1989) and least square cross validation for the smoothing parameter (Silverman 1986). We summed the resulting surface grid files for all animals tracked for each threshold temperature bin, treating each animal–winter–temperature bin combination as a single sample. Maps were displayed using the 50th and tenth percentile contour levels to show moderately and heavily used areas.
Hydrodynamic Thermal Properties
Collection of Environmental Data
To investigate differences in thermal properties among the different water bodies frequented by manatees, data on water and air temperature, rainfall, salinity, flow, and stage in different habitat zones around the study area were obtained from permanent or temporary monitoring stations from several agencies (see Acknowledgments). Near-bottom temperatures were measured at all stations; surface temperatures were only available for the PTRs at POI and BCNP.
The PTRs were continuously monitored by USGS during four winters to characterize the vertical temperature regime. Temperature dataloggers (HOBO Water Temp v2 and Tidbit, Onset Computer Co., Pocasset, MA, USA) at near-surface and near-bottom depths recorded temperatures at 15 min intervals during two winters (2004/2005–2005/2006). These temperature-only probes were replaced by four YSI 600 XLM water quality sondes (YSI Incorporated, 1700 Brannum Lane, Yellow Springs, OH 45387-1107; www.ysi.com). Two probes were deployed at each site, within 15 cm of surface using a floating mount, and within 15 cm of the bottom. Date/time, temperature, conductance, and salinity (calculated using temperature and conductance) were logged every 30 min in subsequent winters (2006/2007–2007/2008).
Comparison of Thermal Properties of Gulf, Bay, and PTR Water Bodies
Hourly temperature data for seven site-depth locations (Fig. 1; POI top/bottom, BCNP top/bottom, Faka Union Bay, Fakahatchee Bay, Naples) representing key water bodies (PTR top/bottom, bay, and Gulf) for four winters (2004/2005–2007/2008) were analyzed to test for differences in water temperature as they related to temperature thresholds. We used the Kruskal–Wallis test followed by the Nemenyi–Damico–Wolfe–Dunn test (joint ranking; Hollander and Wolfe 1999) as implemented in the COIN library in R (Hothorn et al. 2008). To reduce the influence of warm periods on the results, the data were filtered to include only those periods when one or more sites fell below the 20°C manatee temperature threshold. This truncation resulted in strongly left-skewed distributions. Data were further filtered to obtain equal sample sizes among sites by rejecting any date–time where data were missing for one or more stations. To compare annual variation in winter water temperatures among the seven site-depth locations, we calculated the number of hourly readings at 1°C increments to provide an index of exposure time to different temperatures.
Analysis of Temperature and Salinity Profiles at the PTRs
To portray relationships among temperature and salinity, data for the two PTRs were plotted in vertical panels for the 2 years with salinity data. Mean daily discharge over the Faka Union weir also was plotted for POI (data were unavailable for BCNP).
Vertical Density Profiles at the PTRs
We calculated in-situ densities for surface and bottom layers at POI using the “International Equation of State of Water” (Fofonoff and Millard 1983) based on temperature, salinity, and pressure. These density calculations were used to examine whether density gradients associated with salinity stratification could offset opposing density gradients associated with temperature inversions. Changes in density result in fall turnover in lakes due to surface-water cooling (Reid and Wood 1976), and density gradients are commonly used to index the role of stratification in resisting turnover (Dyer 1997). For each bottom-surface measurement, we calculated and plotted the vertical difference in temperature and salinity for each paired sample. We overlaid this plot with a contoured surface of density differences to show the relationship between the vertical differences in density associated with vertical differences in salinity and temperature. The contoured surface of vertical density differences was generated as a least squares trend surface (six degree polynomial) using the “MASS” library in R (Venables and Ripley 2002).
Correlation analyses were conducted for data at POI to examine relationships among three key factors: (1) temperature difference (bottom–surface), (2) salinity difference (bottom–surface), and (3) freshwater discharge at the POI weir. The data were filtered to periods when the surface temperature fell below the threshold values of 18°C or 20°C.
Numerical Hydrology Modeling
To examine whether mechanisms associated with salinity and temperature stratification identified by analysis of the monitoring data could produce the observed patterns in water temperatures, we simulated conditions at POI with and without salinity stratification using a three-dimensional hydrodynamic model application of the Environmental Fluid Dynamics Code (EFDC) from the Virginia Institute of Marine Science (Hamrick 1992; U.S. Environmental Protection Agency 2002). This application of the EFDC model at POI is part of a larger project to investigate different restoration scenarios; here, we were only interested in comparing the POI system in the presence or absence of salt stratification. Because the physics-based EFDC application simulates the transport of variable density fluid in three dimensions, and explicitly models temperature and salinity, we viewed the model as an independent means of evaluating the patterns and mechanisms identified from the monitoring data at POI.
General model input parameters, such as cell friction, heat transfer and evaporation coefficients, and vertical and horizontal diffusion, were initially determined from standard values and previous EFDC model applications and then adjusted for better model fit. The model requires extensive atmospheric data, including rain volumes, wind speed and direction, solar radiation, and air temperature, which was obtained from the Florida Automated Weather Network. Five vertical layers were used for the majority of testing and calibration and gave adequate representation of the vertical stratification of salinity and temperature.
Two simulations were run with and without the density effects of salinity variations over a 242-day time period (1 September 2004 to 30 April 2005). The salinity stratification used was relatively small compared to observed conditions, with the surface and bottom layers differing by about 8 psu. More recent periods could not be simulated due to the unavailability of key field measurements more recent than 2005.
Manatee Aerial Surveys
Synoptic survey mean minimum counts (1991–2007) at the major passive thermal refugia (PTRs) in the study area
Port of the Islands
Synoptic survey mean minimum counts (1991–2007) within regional landscape zones
Temperature Comparisons Among Water Bodies
The PTR bottom temperatures were significantly warmer than any other water bodies. Kruskal–Wallis comparison of temperatures below the 20°C threshold at the seven site-depth localities for the four winters showed significant differences (Χ2 = 12,723.46; p < 0.0001). Ranking the median temperature values showed that the bottom layers at the PTRs were the warmest among sites (BCNP = 25.73°C; POI = 22.26°C), followed by the two PTR surface layers (BCNP surface = 20.45°C; POI surface = 20.38°C), Fakahatchee Bay (20.0°C), Faka Union Bay (19.30°C), and the Gulf (18.21°C). Post hoc comparisons showed that only the two PTR surface layers were not significantly different.
When the dataset was reduced to days when no salinity stratification was present at POI, post-hoc comparisons from the Kruskal–Wallis test showed that the surface and bottom layers no longer differed from each other, but were still warmer than the two nearby bays.
Temperature Inversions and Stratification
A source of bottom heat at POI is strongly indicated by day-long or longer periods when the bottom layer was warming while the surface layer was rapidly cooling (e.g., arrows in Fig. 7). The source of this heat was unknown, but could be due to factors such as groundwater influx, conductive subsurface heat flux, or heat generated by microbial activity. We currently lack data to evaluate these possible heat sources.
Density Relationships Associated with Stratification
Density calculations showed that the density gradient developed a more stable distribution (bottom denser than surface) as salinity differences increased, even during severe cold periods when the surface temperature was much colder than the bottom (over 8°C; Fig. 9). Salinity had a stronger influence on density than temperature across the observed range, and relatively small haloclines provided larger density differences that offset those resulting from strong temperature inversions. When density differences were close to zero (Fig. 9), temperature and salinity gradients were weak or absent, indicating a well-mixed water column associated with rapid turnover.
For manatees, the primary attraction of the two largest PTRs was warm-water temperatures maintained in the bottom layers during the coldest periods. Bottom temperatures at nearby inland bays, nearshore Gulf, and surface layers at the PTRs, regularly fell below temperatures suitable for manatees. These temperature patterns account for the aerial survey results which showed a majority of the individuals counted were aggregated at a single PTR (POI), while the next three largest aggregations occurred at similar inland sites, all artificial canals or basins. The telemetry data showed that manatees preferentially moved into these PTRs as the water temperatures fell below 20°C on their primary foraging areas in the shallow Gulf. Manatees regularly exploited the thermal inversions at PTRs by bottom-resting (pers. obs.), a behavior observed at other warm-water sites (Edwards et al. 2007).
Salinity stratification played an unexpectedly important role at the PTRs, explaining how warmer water persisted in the bottom layer, even when the surface water became much colder and turnover of the system might be expected. Thorough turnover and mixing did occur at POI, but only when salinity stratification was absent (Fig. 9). The relationship between temperature inversion and salinity stratification was readily identified in comparisons of the densities of the surface and bottom under different conditions. Buoyancy differences between strata suppress vertical flux of heat, substances and momentum (Kimmerer 2004), and the stability of stratified water bodies is proportional to the size of the vertical density differences between strata (Dyer 1997; Mann and Lazer 2006). During cold periods at POI, the warmer bottom layer was considerably denser than the cooler surface water, but only when there was a significant salinity gradient. Haloclines maintained a stable density gradient despite the temperature inversion, thus preventing vertical mixing. This finding was supported by the POI three-dimensional model, which showed that convective turnover rapidly cooled the bottom in the absence of salinity stratification. Within the typical range of salinity and temperature gradients observed at POI, salinity had a much greater impact on density than temperature, enabling haloclines to offset the potentially unstable density differences caused by temperature inversions (Fig. 9). Other things being equal, these density relationships show how temperature inverted haloclines can have stable density gradients that are resistant to vertical mixing.
The formation and maintenance of salinity stratification at POI during winter was strongly correlated with the amount of upstream freshwater discharged over the southern Faka Union weir (Fig. 10). Freshwater inflow is a key determinant of stratification in many estuarine systems (Ibanez et al. 1997; Dyer 1997) and appears to be important at POI. Under low or no-flow conditions, the stratification decreased fairly rapidly over time as the surface salinity approached the higher values of the bottom layer (Fig. 7). Tidal movement, direct bay connection, and high salinities suggest the bottom layer functions as a tidal wedge which entrains and mixes with the overlying freshwater, making the PTRs analogous to “salt-wedge estuaries” (Ibanez et al. 1997) or highly stratified systems (Dyer 1997). In such systems, an “estuarine circulation” pattern is established where the lighter freshwater layer flows seaward above a saltwater layer which is propagated upstream by tidal forcing (Kurup et al. 1998). Under such conditions, salinity stratification typically increases as freshwater discharge increases (Xu et al. 2008). At high levels of freshwater discharge tidal salinities can be eliminated (Hamilton et al. 2001). During the wet season, the entire Faka Union canal system has been observed to be oligohaline (Surge and Lohmann 2002). Nonetheless, bottom salinities at the PTRs remained high during all observed winters and were unaffected by discharge from a large storm event (Fig. 7; February 2008). At POI, the strong correlation between winter discharge and salinity stratification (Fig. 10) indicates that haloclines break down without adequate levels of freshwater discharge.
Several other mechanisms also can disrupt haloclines and impact temperature inversions in PTRs. Wind and wave action can create strong mixing effects, especially in open water bodies, but these factors are reduced in narrow estuaries or canals with limited fetch (Hamilton et al. 2001; Shafland 1995). Tides can disrupt stratification (Dyer 1997), but flushing within canals is reduced with increased depth, increased length, and bathymetry features (U.S. Environmental Protection Agency 1975; Luther et al. 2004). Localized stratification behind sills and in holes can be especially resistant to flushing (Kurup and Hamilton 2002; Luther et al. 2004), and even where bottom topography is smooth, stratification can persist in the face of large tides (Dyer 1997).
Groundwater discharge in rivers or estuaries can disrupt or maintain stratification, depending on salinity differences between the groundwater and receiving water body (Linderfelt and Turner 2001). Data on groundwater discharge at POI and BCNP were unavailable; however, the canals north of the weir at POI are thought to be deep enough to penetrate the surficial aquifer system and provide some connectivity (U.S. Army Corp of Engineers and South Florida Water Management District 2004). Canal systems in South Florida are known to act as conduits for tidal saltwater intrusion (Fitterman and Deszcz-Pan 2001; Price and Swart 2006), and aquifer discharge can act to recirculate intruded saltwater (Smith and Turner 2001). However, if groundwater discharge occurred at POI, the high bottom salinity measured during all winters indicate that the discharge did not disrupt the halocline. Although we lack data on groundwater exchange or other processes that might provide a source of heat, our analysis indicates that convective turnover eliminates any bottom warmth unless salinity stratification is present.
The temperature and salinity dynamics at these PTRs differ somewhat from the only other detailed study of a manatee PTR—the Matlacha Isles canal system (Barton 2006)—some 80 km north of Marco Island. No significant influx of freshwater was found at the surface or bottom, and opportunistic salinity sampling showed little or no stratification. The Matlacha PTR had warmer bottom temperatures than other nearby water bodies, but bottom temperatures fell below 18°C during multiple cold periods. Barton (2006) concluded that the warmer temperatures may be due to heat retention associated with two traits: deeper canals and lower tidal flushing. POI and BCNP are similar to Matlacha in having deep canals (2–4 m range) and relatively low tidal range compared to canal depth that can reduce tidal flushing (Dyer 1997). Greater canal depth also contributes to heat retention, since narrow canal width and relatively greater depths result in smaller surface-to-volume ratios, reducing heat loss compared to more open water bodies. This geometric relationship may explain why both POI surface and bottom layers were warmer than nearby bay waters, even when haloclines were absent. Nonetheless, the monitoring data and three-dimensional modeling clearly showed that salinity stratification dominated the warm-water dynamics at POI.
These relationships between temperature inversion, haloclines, and freshwater discharge have implications for potential impacts of the Picayune Strand Restoration on the warm-water characteristics at POI. The PSRP is expected to significantly reduce the discharge of freshwater into POI during the winter dry season (U.S. Army Corp of Engineers and South Florida Water Management District 2004; Swain and Decker 2009). Restoration will plug or fill most of the canals north of POI, redistribute much of the freshwater over a broader area via spreader canals, and establish sheet flow that will eventually discharge into other drainages in addition to POI. The slower drainage associated with sheet flow should raise water tables and allow more groundwater seepage, resulting in a prolonged hydro-period extending well into the dry season (U.S. Army Corp of Engineers and South Florida Water Management District 2004). Restoring predrainage conditions could improve freshwater flow at minor manatee aggregation sites that may function as natural PTRs. Possible examples include a scoured channel at the Fakahatchee River and deeper river sections in the southern Everglades (Stith et al. 2006). We suspect that natural PTRs may have been much more prevalent in South Florida prior to drainage projects, which reduced sheetflow during winter months. Restoring sheetflow could increase stratification at natural sites, improving winter conditions for manatees. However, reduction in freshwater discharge to POI could alter salinity stratification at this major warm-water refuge, degrading winter conditions for manatees. A comprehensive USGS effort based on the three-dimensional POI and two-dimensional regional hydrology models is underway (Swain and colleagues) to model potential impacts and address some of these issues.
If planned restoration would negatively impact POI for manatees, management options could be developed based on this study and additional modeling efforts. The mechanisms that maintain warmer water at PTRs seem amenable to artificially managing conditions or even engineering new PTRs. A major management objective might be to maintain sufficient levels of salinity stratification to support temperature inversions during winter. Discharging sufficient volumes of fresh or brackish water at the surface over tidal water may quickly establish a barrier to vertical mixing, providing a “blanket” effect (as well as drinking water for manatees). Limiting surface discharge to brief periods prior to advancing cold fronts might suffice if water scarcity is an issue. Increasing basin or canal depths can reduce tidal flushing and mixing and can increase thermal inertia. Creating an uneven bottom with deeper holes may provide pockets that resist tidal mixing and establish better connection with warm groundwater. The canal bathymetry at POI has some deeper pockets where manatees appear to aggregate more densely (pers. obs.). Creating conditions that favor stratification might conflict with managing water quality in canal systems experiencing hypoxia and eutrophication (U.S. Environmental Protection Agency 1975; Luther et al. 2004), although such problems typically do not arise during the winter. Additional monitoring and modeling are needed to further evaluate warm-water dynamics at POI and other PTRs.
Our results suggest that the PTRs we monitored can provide adequate warm water for manatees during typical winters when significant salinity stratification is present. Without salinity stratification, even typical winter conditions resulted in adversely cold water temperatures at POI. Under severe cold, stronger vertical mixing would be expected, and lack of salinity stratification at POI would likely result in severe temperatures throughout the water column. POI may be unsuitable as a warm-water refuge under these conditions. Further modeling efforts also might suggest how to design a PTR pilot study and could ultimately lead to a PTR management system that uses weather forecasts and real-time monitoring of salinity and temperature stratification to maximize thermal protection for manatees while efficiently managing freshwater discharge.
Understanding and managing the hydrodynamics of thermal refugia for aquatic organisms is becoming increasingly important for preserving endangered species (Schaefer et al. 2003; Torgersen et al. 1999) and limiting the spread of invasive species (Trexler et al. 2000). Here, we addressed warm-water refugia for a cold-intolerant species, but similarly cold-water refugia can be important to heat sensitive species that seek out cool bottom waters in the face of increased water temperatures associated with factors such as climate change, thermal effluent, and dam construction. Cool bottom waters have been observed at PTRs during summer, and salinity stratification may further enhance the stability of summer thermoclines. In the face of global climate change and rising sea levels, passive thermal refugia could provide vulnerable populations with respites during periods of extreme temperatures, possibly giving them time to respond and adapt to climate change effects (Baron et al. 2008). Determining effective ways to manage haloclines and thermoclines could prove to be an important option for resource managers by providing critical warm- or cold-water refugia for a wide variety of temperature sensitive aquatic species.
We wish to thank the following agencies for hydrology or environmental data: South Florida Water Management District, Rookery Bay National Estuarine Research Reserve, National Oceanic and Atmospheric Administration, Everglades National Park, Big Cypress National Preserve, Ten Thousand Islands National Wildlife Refuge, Florida Automated Weather Network of the University of Florida Institute of Food and Agriculture Extension, and United States Geological Survey. We thank the Fish and Wildlife Research Institute division of the Florida Fish and Wildlife Conservation Commission for synoptic aerial survey data. We thank Susan Butler and Dean Easton for their help with data acquisition and Andrea Bowling for manuscript proofing. Partial funding was provided by the following USGS programs: Place-Based Studies (PBS), Priority Ecosystems Science (PES), and Critical Ecosystem Studies Initiative (CESI). Use of trade or product names does not imply endorsement by the U.S. Government. The findings and conclusions in this article are those of the authors and do not necessarily represent the views of the U.S. Fish and Wildlife Service.
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