The Influence of Salinity on Seagrass Growth, Survivorship, and Distribution within Biscayne Bay, Florida: Field, Experimental, and Modeling Studies
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1 Estuaries Vol. 6, No., p. 3 4 February 003 The Influence of Salinity on Seagrass Growth, Survivorship, and Distribution within Biscayne Bay, Florida: Field, Experimental, and Modeling Studies DIEGO LIRMAN* and WENDELL P. CROPPER, JR. Rosenstiel School of Marine and Atmospheric Science, University of Miami, 4600 Rickenbacker Causeway, Miami, Florida 3349 ABSTRACT: We evaluate if the distribution and abundance of Thalassia testudinum, Syringodium filiforme, and Halodule wrightii within Biscayne Bay, Florida, are influenced by salinity regimes using a combination of field surveys, salinity exposure experiments, and a seagrass simulation model. Surveys conducted in June 00 revealed that while T. testudinum is found throughout Biscayne Bay (84% of sites surveyed), S. filiforme and H. wrightii have distributions limited mainly to the Key Biscayne area. H. wrightii can also be found in areas influenced by canal discharge. The exposure of seagrasses to short-term salinity pulses (4 d, 5 45 ) within microcosms showed species-specific susceptibility to the salinity treatments. Maximum growth rates for T. testudinum were observed near oceanic salinity values (30 40 ) and lowest growth rates at extreme values (5 and 45 ). S. filiforme was the most susceptible seagrass species; maximum growth rates for this species were observed at 5 and dropped dramatically at higher and lower salinity. H. wrightii was the most tolerant, growing well at all salinity levels. Establishing the relationship between seagrass abundance and distribution and salinity is especially relevant in South Florida where freshwater deliveries into coastal bays are influenced by water management practices. The seagrass model developed by Fong and Harwell (994) and modified here to include a shortterm salinity response function suggests that freshwater inputs and associated decreases in salinity in nearshore areas influence the distribution and growth of single species as well as modify competitive interactions so that species replacements may occur. Our simulations indicate that although growth rates of T. testudinum decrease when salinity is lowered, this species can still be a dominant component of nearshore communities as confirmed by our surveys. Only when mean salinity values are drastically lowered in a hypothetical restoration scenario is H. wrightii able to outcompete T. testudinum. Introduction Seagrasses are keystone components of coastal ecosystems throughout the world, where they contribute to productivity, carbon budget, and sediment stability, as well as provide essential habitat to a large number of associated organisms (e.g., Zieman 97; Davis and Dodrill 989; Holmquist et al. 989; Walker et al. 00). The importance of seagrass beds to the health of coastal ecosystems was evidenced by the recent seagrass mass mortality within Florida Bay, U.S., where both water quality and abundance of commercial fishery stocks were greatly diminished after over 4000 ha of Thalassia testudinum were lost starting in 987 (Robblee et al. 99; Durako 994; Zieman et al. 999). Although the exact causes of this demise are still being debated, several interacting factors including elevated temperature, changes in salinity, reduced dissolved oxygen, sulfide toxicity, and disease have all been proposed as causative agents (Hall et al. 999). Many of the potential factors influencing this * Corresponding author; tele: 305/36-468; fax: 305/ ; dlirman@rsmas.miami.edu. seagrass die-off have been linked to the reduction in freshwater inputs and modification of salinity fields within the coastal lagoons of South Florida as a consequence of the water management system now in place (Smith et al. 989; Fourqurean and Robblee 999). The present hydrology of the region is managed by over,500 km of canals and other structures that control freshwater deliveries into coastal habitats (Davis and Ogden 994; Light and Dineen 994; Harwell 997; Browder and Ogden 999). In response to patterns of environmental degradation, the Comprehensive Everglades Restoration Project (CERP) was proposed to restore the lost natural hydrology (CERP 00). One of the management goals of this project is to increase freshwater inputs from upland sources to reestablish estuarine conditions along nearshore environments (Davis and Ogden 994; Browder and Wanless 00). Considering the potential impacts of these activities on the salinity fields of these coastal lagoons, we investigate how the abundance and distribution of seagrass species may be influenced by salinity using a combination of field surveys, salinity exposure experiments, and a seagrass simulation model. 003 Estuarine Research Federation 3
2 3 D. Lirman and W. P. Cropper, Jr. Previous studies that documented spatial correlations between seagrass distribution and salinity have yielded the commonly accepted conclusion that Halodule wrightii has a high tolerance for low salinities and can be dominant in nearshore areas influenced by canal discharge (Montague and Ley 993; Fong et al. 997). T. testudinum and Syringodium filiforme can also be found near canals, but growth and productivity of these species may be reduced at sites influenced by freshwater discharge (Conover 964; Lewis et al. 985; Montague 989). A limited number of experimental studies have examined the effects of salinity stress on T. testudinum, H. wrightii, and S. filiforme. McMillan and Moseley (967) showed that while salinities of can cause S. filiforme and T. testudinum to stop growing, H. wrightii can continue to grow even at 7. High tolerance of H. wrightii to a wide range of salinities (5 80 ) was also reported by McMahan (968) and McMillan (974). Within Biscayne Bay, Florida, seagrass beds composed of T. testudinum, H. wrightii, and S. filiforme cover over 70% of the bottom, providing essential habitat for numerous commercial species including tarpon, snook, bonefish, snappers, groupers, shrimp, and crabs (de Sylva 969; Thorhaug 976; Ault et al. 999a,b). Past changes in seagrass abundance and distribution in Florida Bay raise concerns that future changes in salinity within Biscayne Bay may result in similar patterns of loss. We conducted field surveys within Biscayne Bay to determine whether seagrass distribution and abundance were correlated with measured gradients in salinity. A microcosm experiment was also conducted to determine the growth response of T. testudinum, H. wrightii, and S. filiforme to prolonged exposure to different salinities (4 d, 5 45 ). The results from this experiment were incorporated into the seagrass growth model developed by Fong and Harwell (994) and Fong et al. (997) to evaluate the sensitivity of the model to the newly obtained salinity-growth functions under different simulation scenarios. These scenarios simulate the environmental conditions commonly found within different areas of Biscayne Bay, as well as potential salinity changes resulting from the Everglades Restoration activities. Materials and Methods SALINITY FIELDS WITHIN BISCAYNE BAY Salinity fields within Biscayne Bay are influenced by precipitation, freshwater inputs from land, canal, and groundwater sources, and tidal influx of oceanic water (Alleman 995; Wang et al. In press). The spatial and temporal distribution of these influences results in marked salinity fields Fig.. Map of the study area with the location of seagrass survey sites (n 6), salinity instruments (* Nearshore, * Eastern Bay), and canals draining into Biscayne Bay. The dashed lines and numbered diamonds ( 6) show the six survey strata that divided the area into three regions (Key Biscayne, Safety Valve, Central Bay) and two salinity regimes (Nearshore and Eastern Bay). with distinct characteristics. A clear salinity gradient can be found, with lower, variable salinity occurring in the western margin of the bay due to freshwater inflow from canal discharge and runoff, and higher, more stable salinities in the eastern margin, where oceanic influences prevail (Wang et al. 978, In press; Brook 98; Chin Fatt and Wang 987). SEAGRASS DISTRIBUTION The blade density of the three main seagrass species within Biscayne Bay was documented in June 00. Sampling locations (6 random points) were determined based on a stratified random sampling design modified from methods described by Ault et al. (999b). The sampling area was divided into six strata (3 geographical regions salinity regions; Fig. ). The three geographical regions, Key Biscayne, Safety Valve, and Central Bay, were sub-divided into the following two salinity regions identified based on data collected by field instruments: a Nearshore region with highly vari-
3 Salinity Effects on Seagrass Distribution 33 Fig.. daily salinity values for 998 (see Fig. for location of instruments). Nearshore areas are influenced mainly by freshwater inputs from canal, groundwater, and overland sources, whereas oceanic influences prevail along the Eastern margin of Biscayne Bay. Data provided by Biscayne National Park. Missing salinity values were estimated by linear interpolation. able and lower mean salinity (mean salinity in , SD 4.8, range 34 ) and an Eastern Bay region with more constant, oceanic salinity conditions (mean salinity 33., SD.4, range 9 39 ; Fig. ). Locations within each stratum were determined by selecting cells at random from the SEASCAPE model of Biscayne Bay that divides the bay into 70,848 square grid elements (0 0 m; Cropper et al. 00). The center coordinates for the cells chosen for each stratum were determined and a differential Global Positioning System unit was used to locate the survey point. At each location, divers surveyed four haphazardly located plots (0.5 m ). Within each plot, all the aboveground seagrass biomass was collected by clipping; the number of seagrass blades was determined by species and averaged by location (n 4). Depth at each station was obtained with a weighted line marked with 5-cm intervals. Data collected in these surveys were interpolated with ArcView s Spatial Analyst Extension using an Inverse Distance Weighted interpolation procedure with a cell size of 0 0 m. SALINITY EXPOSURE EXPERIMENTS T. testudinum, S. filiforme, and H. wrightii were collected from Key Biscayne, Florida (depth m). Rhizome sections with at least 3 intact short shoots were used as rhizomes with short shoots were found to experience high mortality in previous transplant studies (Tomasko et al. 99; Lirman unpublished data). Salinity exposure experiments were conducted at the microcosm facility at the University of Miami s Rosenstiel School of Marine and Atmospheric Science in April 000. The experimental units were 0-L aquaria filled with cm of sediments obtained from the seagrass collection site and housed in an outdoor greenhouse. Salinity for each treatment (n tanks per salinity treatment) was adjusted prior to the onset of the experiment and adjusted daily as needed. The salinity treatments used were 5,, 5, 0, 5, 30, 35 (ambient), 40, and 45. A 4-d exposure period was selected to represent the longest low-salinity peaks observed adjacent to canal outflow areas (Fig. ). The seagrass rhizomes were placed directly (i.e., without an acclimation period) into the salinity treatments to simulate the sudden drops in salinity associated with storm events or the opening of water control structures along the coast. Three rhizome sections from each species were anchored to the sediments with plastic anchors inside each aquarium. Short shoots of T. testudinum were marked for growth using the needle-punching method described by Zieman (974) and Zieman et al. (999). Production in H. wrightii and S. filiforme was estimated using the clipping method described by Dunton (990, 994). After 4 d, leaf extension rates were determined for each shoot. Linear blade growth values were averaged by shoot and rhizome for each tank. These values were averaged by treatment if no significant differences in mean growth were detected between tanks (t-tests, p 0.05). SEAGRASS MODEL We modified an existing seagrass growth model (Fong and Harwell 994; Fong et al. 997) by implementing our measured short-term salinity responses while all other model structures and parameters are held constant. The salinity-response function in the original seagrass model was derived from observational studies that correlated seagrass distribution and productivity with measured field salinity patterns. To assess the effects of replacing the original, distribution-based salinity function, our new model was run under the four environmental scenarios chosen by Fong and Harwell (994) to describe representative areas with contrasting nutrient, temperature, and light regimes (Table ). While the original model was run using a periodic function to simulate salinity patterns, the new model was run under two contrasting salinity regimes, Nearshore and Eastern Bay, using salinity values measured in the field (Fig. ). We ran a version that incorporates competition among the three seagrass species (interactive model) as well as a version restricted to a single seagrass spe-
4 34 D. Lirman and W. P. Cropper, Jr. TABLE. Parameters from original model used in the simulation scenarios described by Fong and Harwell (994). Salinity values used in the new model were obtained from field data collected from Nearshore and Eastern regions of Biscayne Bay (Fig. ). Scenario Temperature ( C) Range PO 4 Concentration ( M) Water Column Sediment Light ( E m s ) Range Comments Average bay conditions High input of freshwater and organic matter Oligotrophic conditions Enriched water column cies (single-species model) to evaluate the effects of competitive interactions. Competition effects are based on a reduction of the maximum growth rate of each species as a function of total seagrass biomass of all three species. Thalassia biomass was reduced by total seagrass biomass less than the other species (Fong and Harwell 994) leading to rapid Thalassia dominance under many conditions. The single-species model retained the biomass-dependent maximum growth reduction, but replaced the total biomass of the three seagrass species with that of only the species being simulated. Although the precise scenarios that describe future changes in freshwater delivery into Biscayne Bay have not been formulated, one such restoration scenario was simulated by decreasing salinity by 0 from measured Nearshore salinities. This extreme salinity-reduction scenario was chosen to represent the potential impacts of increased freshwater flows in the vicinity of canal outflow areas where the effects of the salinity changes would be most likely detected. The seagrass model was developed as a system of differential equations of the following form: db/dt maxg (f(s) f(t) f(l) f(n)) loss rate () where maxg is the species specific maximum daily aboveground productivity (g dry wt m d ), f(s) is a zero to one salinity scalar, f(t) is the temperature scalar, f(l) is the light scalar, and f(n) is the sediment nutrient scalar. We simulated the model using fourth order Runge-Kutta integration with a time step of 0.0 d. The salinity response function (f(s)) was implemented as a look-up table with linear interpolation that mapped daily salinity values to the daily salinity scalar value (0 ). Loss rate was simulated as a function of seagrass senescence and turnover. Driving functions for light and temperature were simulated in the model as periodic functions: Daily value (R sin(3 / ( ) DayNo/360)) () where is the average annual value for the environmental variable ( C for temperature, and mol m s of PAR for light), R is half of the annual range of the variable, and DayNo is the number of days from the start of the simulation. Results SEAGRASS SPATIAL DISTRIBUTION T. testudinum, the most abundant seagrass within Biscayne Bay, was present at 84% of the points surveyed (present in 89 of 6 points surveyed), while S. filiforme was present at % (n points) and H. wrightii at 6%. Beds containing all three seagrass species were found at 7% of sites, beds with T. testudinum and H. wrightii at 7%, and beds with T. testudinum and S. filiforme at %. Beds containing S. filiforme and H. wrightii together were not found. Monospecific beds of T. testudinum were found at 57% of sites (mean depth [ SE] [] cm), S. filiforme at % (depth 50 cm), and H. wrightii at % (mean depth 45 [3] cm). Only 3% of the sites surveyed had no seagrass biomass, and these sites were mainly within deeper dredged areas of the bay (mean depth 80 cm [SE 3]) where boat traffic is high and light penetration limited due to suspended sediments. The contours constructed based on blade density indicate that T. testudinum is found throughout Biscayne Bay, while S. filiforme and H. wrightii have more restricted distributions, being limited mainly to the Key Biscayne area (Figs. and 3). H. wrightii can be found in areas heavily influenced by canal discharge such as the Black Point and Chicken Key areas, as well as a shallow bank in the middle of the Bay (Figs. and 3). Maximum blade densities were 4,30 blades m for T. testudinum,,57 blades m for H. wrightii, and,539 blades m for S. filiforme. SALINITY EXPOSURE EXPERIMENTS Exposure of seagrasses to different salinity treatments revealed species-specific growth responses. T. testudinum exhibited peak leaf elongation rates at 40, decreasing gradually as salinity decreased, and having its lowest growth rates at the highest salinity, 45 (Fig. 4a). Maximum extension rate for a single blade was 0.3 cm d. The highest mean blade extension rates were recorded at 40
5 Salinity Effects on Seagrass Distribution 35 Fig. 3. Contour maps of seagrass blade densities within Biscayne Bay based on point surveys performed in June 00 (n 6 sites). (0.08 cm d ). extension rates at the salinity extremes were 0.03 cm d at 45 (35% of the mean rate recorded) and 0.05 cm d at 5 (63% of the mean). S. filiforme was the species most susceptible to changes in salinity (Fig. 4b). Maximum extension rate for a single blade was 0.75 cm d. The highest mean blade extension rates were recorded at 5 (0.34 cm d ) and dropped dramatically at both higher and lower salinity. leaf extension rates were 0. cm d at 45 (35% of the mean rate recorded) and 0.08 cm d at 5 (3% of the mean). Of the three species tested, H. wrightii showed the widest tolerance to changes in salinity as growth rates did not vary widely among salinity treatments (Fig. 4c). Maximum extension rate for a single blade was 0.64 cm d. The highest mean blade extension rates were recorded at 35 (0. cm d ) and lowest at 45 (0.7 cm d ) and 5 (0.7 cm d ). Blade extension rates did not fall bellow 76% of the maximum mean extension rates for any salinity treatment. SIMULATION RESULTS When the measured Eastern Bay salinity was used in the simulation models, highest biomass values were obtained for T. testudinum under Scenario, used to represent intermediate sediment nutrient concentrations, S. filiforme under Scenario 3, used to represent low-nutrient conditions, and H. wrightii under Scenario, used to represent high sediment nutrient conditions commonly found areas influenced by canal inputs (Table ). Biomass differences between the models were generally low when Eastern Bay salinity values were used (rarely exceeding %), but the simulated biomass of T. testudinum was always lower with the Fig. 4. daily leaf extension rates (cm, SE) of A) Thalassia testudinum, B) Syringodium filiforme, and C) Halodule wrightii exposed to different salinity treatments for 4 days. new model, biomass of H. wrightii was higher with the new model, especially under the interactive version, and biomass of S. filiforme was unchanged except under Scenario 3 where the new model predicted lower mean annual biomass. The largest differences in the species-specific responses were simulated when Nearshore salinity values were used (Table ). As was the case for the simulations with Eastern Bay salinity, when using Nearshore salinity, highest mean biomass values were obtained for T. testudinum under Scenario (Fig. 5), S. filiforme under Scenario 3 (Fig. 6), and H. wrightii under Scenario (Fig. 7). The mean annual biomass of T. testudinum simulated with the new model was consistently higher than in the original model under all the scenarios simulated for both the interactive (Fig. 5a) and single-species versions (Fig. 5b). The new model also
6 36 D. Lirman and W. P. Cropper, Jr. TABLE. annual aboveground biomass of seagrass species found in Biscayne Bay, Florida, simulated under different scenarios. Field salinity data are from Nearshore () and Eastern Bay () locations. Results from both the interactive model and the single-species model are presented here. The two different salinity functions are those used in the original seagrass model (Fong and Harwell 994) and the new function obtained from a microcosm experiment. Halodule wrightii Syringodium filiforme Thalassia testudinum Interactive Model Single-Species Model Interactive Model Single-Species Model Interactive Model Single-Species Model Seagrass Model Field Salinity Scenario Fig. 5. Aboveground biomass of Thalassia testudinum for Scenario (average bay conditions) using measured Nearshore salinity values for A) new and original models, single-species version, and B) new and original models, interactive version. led to less seasonal variability in the simulated T. testudinum biomass. S. filiforme reached high biomass only under the scenario representing oligotrophic conditions (Scenario 3; Table ). Increases in biomass as well as a reduction in seasonal variability were seen for S. filiforme with the new model compared with the original model for both the interactive (Fig. 6a) and single-species versions (Fig. 6b). Biomass patterns differed in magnitude and variability between the original and new models for H. wrightii. In the interactive version, mean annual biomass of H. wrightii almost disappeared in Scenarios and 3, and was lowered by 6% in Scenario 4 (Table ). In the single-species version, the new model resulted in either no change (Scenario 3) or increases in biomass (0% in Scenario and 37% in Scenario 4). Under Scenario, which represents the best growing conditions for this species under canal-influenced areas with high sediment nutrient concentrations, no differences between the models were found using the single-species version (Fig. 7a). A reduction in both the mean biomass (36% lower with the new model compared to the original) and the seasonal variability were seen when the new model was run using the interactive version (Fig. 7b). Effects of interspecific competition were ob-
7 Salinity Effects on Seagrass Distribution 37 Fig. 6. Aboveground biomass of Syringodium filiforme for Scenario 3 (oligotrophic conditions) using measured Nearshore salinity values for: A) new and original models, single-species version, and B) new and original models, interactive version. served only for H. wrightii. The biomass of H. wrightii was higher in all scenarios in the singlespecies compared to the interactive version of both models (Table ). Using the new model, mean annual biomass from the H. wrightii-only model was twice as high and less variable than H. wrightii biomass from the interactive version (Fig. 7). The simulations also indicated that H. wrightii was being suppressed by T. testudinum. With the new model, T. testudinum biomass was higher than H. wrightii biomass, as opposed to H. wrightii dominance in the original model under Scenario (Table ). When Nearshore salinity values were lowered by 0 year-round to simulate the potential impacts of the Everglades restoration project on freshwater deliveries to coastal bays of South Florida, biomass patterns of H. wrightii and T. testudinum were altered. When the interactive version of the new model was run under Scenario to simulate Nearshore conditions, mean annual biomass of T. testudinum (83gm ) exceeded that of H. wrightii (63 gm ; Fig. 8a). This pattern was reversed when salinity values were lowered by 0. In this simulated restoration scenario, the biomass of H. wrightii (95gm ) was more than double that of T. testudinum (45 g m ; Fig. 8b). Fig. 7. Aboveground biomass of Halodule wrightii for Scenario (high input of freshwater and organic matter) using measured Nearshore salinity values for: A) new and original models, single-species version, and B) new and original models, interactive version. Discussion The commonly accepted paradigm of seagrass succession and resource competition indicates that T. testudinum, the recognized competitive-dominant species, will monopolize available space and persist under low nutrient conditions when temperature and salinity exhibit restricted variability (Zieman 976, 98; Williams 987, 990; Gallegos et al. 994). S. filiforme is a dominant component of seagrass beds only in deeper areas with direct oceanic influences (Zieman et al. 989; Hall et al. 999) and possibly higher phosphorus availability (Fourqurean et al. 00). H. wrightii is often considered an early successional, pioneer species able to monopolize space only after other species have been removed by disturbance and remain dominant under high-nutrient conditions or fluctuating environments (Montague and Ley 993; Fourqurean et al. 995). The spatial distribution of seagrasses documented within Biscayne Bay was generally consistent with this paradigm and agreed with the distribution patterns documented within the neighboring Florida Bay, where T. testudinum has a wide distribution, S. filiforme dominates in deeper areas, and H. wrightii is abundant only in
8 38 D. Lirman and W. P. Cropper, Jr. Fig. 8. Aboveground biomass of Halodule wrightii and Thalassia testudinum for Scenario (high input of freshwater and organic matter) using A) Nearshore salinity values and B) salinity values from a Restoration Scenario (Nearshore salinity reduced by 0 ) simulated with the new model and the interactive version. areas with high nutrients and fluctuating salinity (Zieman et al. 999; Fourqurean et al. 00). Both nutrient availability and salinity may play a role in explaining the distribution of S. filiforme and H. wrightii in the Key Biscayne and canal discharge areas. Although nutrient concentrations were not recorded in this study, historical data (979 99) show elevated phosphorus and nitrogen levels in water samples from northern Biscayne Bay and adjacent to canal discharge sites (Alleman 995). The spatial correlation of this nutrient pattern and seagrass distribution agree with studies that have shown that S. filiforme and H. wrightii can coexist or even outcompete T. testudinum under elevated nutrient conditions (Williams 987; Fourqurean et al. 995). The distribution of S. filiforme highlights a limitation of the model which, in its present form, simulates high biomass of this species only under oligotrophic conditions. Low and variable salinity can delineate localized nearshore habitats where dense H. wrightii populations can persist over time even when surrounding areas are dominated by T. testudinum. These salinity patterns would preclude the establishment of S. filiforme based on its documented low tolerance of this species to extreme low salinity, even when the new model predicted a high biomass for S. filiforme for these areas (Scenario 3, Nearshore salinity). In this case, although salinity was lower at the Nearshore location, it never reached the extreme levels required to remove S. filiforme based on its salinity tolerance. Data from other locations as well as a hydrodynamics model of Biscayne Bay have shown that salinity can indeed reach values below near canal outflow areas (Brand 00; Wang et al. In press). The documented salinity responses of T. testudinum, S. filiforme, and H. wrightii were consistent with those reported in previous studies (McMillan and Moseley 967; McMahan 968; McMillan 974). Just as in these studies, H. wrightii showed the widest salinity tolerance while S. filiforme was the most susceptible to sudden changes in salinity, and T. testudinum showed decreased growth only at extreme values. While microcosm studies may not be fully representative of natural conditions, the leaf extension rates calculated for H. wrightii and S. filiforme during the salinity exposure experiment were within the lower range of values obtained by previous studies in the field ( cm d ; Short et al. 985; Williams 987; Dunton 990). And while mean leaf elongation rates of T. testudinum were lower within the experimental units compared to field measurements ( cm d ; Zieman 975), maximum elongation rates (0.3 cm d ) were within the observed range. The lower levels recorded may be a response of the timing of this study (April) before the reported summer peak in growth and standing stock in Biscayne Bay (Zieman 975) as well as the use of rhizome fragments. The use of short rhizome segments, the lack of an acclimation period prior to exposure, and the prolonged exposure period used (4 d), simulate rather extreme conditions that may also over-emphasize the effects of salinity changes on seagrass growth. Sudden and prolonged drops in salinity are common features of the salinity regime near canal outflow areas in coastal bays, and the response of seagrasses to these fluctuating conditions does need to be characterized. When the outcome of the original model (Fong and Harwell 994; Fong et al. 997) and that of the new version of the model were compared, only minor differences in annual biomass were obtained for the three seagrass species under the stable salinity regime found along the Eastern Bay. This indicates that when mean salinity is high and seasonal variability is limited, a salinity function derived from correlational studies of seagrass distribution is adequate to simulate seagrass biomass.
9 Salinity Effects on Seagrass Distribution 39 Caution should be exercised when using functions based on geographical distributions to model growth and competition under rapidly fluctuating environments. As is the case along the canal-influenced environment of Biscayne Bay, a salinity response determined experimentally provides a better representation of short-term seagrass growth and competition dynamics. Using a similar modeling approach, short-term salinity response functions were used by Wortmann et al. (997) to determine the potential effects of floods and dry conditions on the growth and survivorship of Zostera capensis in South Africa. An example where the new model provides a better description of the documented seagrass distribution patterns is that of T. testudinum in nearshore environments. In this case, the simulated mean annual biomass is 60% to 0% higher with the new model, which agrees with the density and biomass observed for T. testudinum in the nearshore environments of Biscayne Bay (Zieman 975; Irlandi et al. 00). The higher simulated output is due to the reduced susceptibility of T. testudinum observed in the exposure experiment compared to the previously used salinity function based on geographical distributions (Fong and Harwell 994). This shows that although growth rates of T. testudinum decrease when salinity is lowered, this species can still be a dominant component of nearshore communities. Our simulations also highlight how competitive interactions can determine seagrass community composition in variable environments. Whereas the biomass of the competitive dominant T. testudinum shows little difference between the interactive and single-species versions of the model, the growth dynamics of H. wrightii are greatly affected by competitive interactions. Although the competitive dominance of T. testudinum has been documented in studies of seagrass succession (Williams 987, 990), a change in environmental conditions can shift this dominance and allow other species to thrive. When salinity values were drastically lowered in our hypothetical restoration scenario, H. wrightii was able to outcompete T. testudinum, which is adversely affected by the lower salinities to a greater extent. Replacement of T. testudinum by H. wrightii was also observed under nutrient enriched conditions (Fourqurean et al. 995). salinity values as well as salinity fluctuations can play a role in the abundance and distribution of seagrass species in Biscayne Bay. Even if localized distribution patterns such as the high abundance of H. wrightii in canal-influenced areas may be explained on the basis of salinity regimes, salinity tolerances alone can not account for all of the observed large-scale patterns in seagrass distribution. The restricted distribution of S. filiforme and the lack of additional dense H. wrightii populations along the coastal fringe still remain unexplained by the documented or simulated environmental gradients. Data on other important factors such as sediment nutrient dynamics, light availability, seagrass recruitment and rhizome expansion, competition from seagrasses, epiphytes, and drift and rhizophytic macroalgae, are needed to fully understand and predict the large-scale distribution dynamics of SAV within Biscayne Bay. Establishing the relationship between seagrass growth, abundance, and distribution and salinity patterns is especially relevant in South Florida where freshwater deliveries into coastal bays are influenced to a large extent by water management practices. The seagrass model developed by Fong and Harwell (994) and modified here to include an experimental salinity-response function can provide an important tool within the restoration framework proposed for the Everglades landscape by providing testable hypotheses where different restoration scenarios can be tested prior to their implementation. Within this context, the simulations presented here indicate that increased freshwater inputs and associated decreases in salinity in nearshore areas can influence growth dynamics of single species as well as modify competitive interactions so that species replacements may occur. ACKNOWLEDGMENTS We would like to thank those people whose help in the field made this research possible: B. Orlando, P. Biber, L. Kaufman, T. Jones, S. Maciá, and D. Manzello. Financial support was provided by National Oceanic and Atmospheric Administration Coastal Ocean Program (#NA67RJ049) and Environmental Protection Agency STAR Program (#R ). Richard Curry, Science Director of Biscayne National Park, provided field support for this project. This manuscript was improved by the helpful suggestions provided by P. Fong, T. Chesnes, and an anonymous reviewer. LITERATURE CITED ALLEMAN, R. W An update to the surface water improvement and management plan for Biscayne Bay. South Florida Water Management District, West Palm Beach, Florida. AULT, J., G. A. DIAZ, S. G. SMITH, J. LUO, AND J. E. SERAFY. 999b. An efficient sampling survey design to estimate pink shrimp population abundance in Biscayne Bay, Florida. North American Journal of Fisheries Management 9: AULT, J., J. LUO, S. G. SMITH, J. E. SERAFY, J. D. WANG, R. HUM- STON, AND G. A. DIAZ. 999a. A spatial dynamic multistock production model. Canadian Journal of Fisheries and Aquatic Science 56:4 5. BRAND, L. E. 00. The transport of terrestrial nutrients to South Florida coastal waters, p In J. W. Porter and K. G. Porter (eds.), The Everglades, Florida Bay, and Coral Reefs of the Florida Keys. An Ecosystem Sourcebook. CRC Press, Boca Raton, Florida. BROOK, I. M. 98. The effect of freshwater canal discharge on the stability of two seagrass benthic communities in Biscayne National Park, Florida. Proceedings of the International Sym-
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WANG. 00. Sponge population dynamics in Biscayne Bay, Florida. Estuarine, Coastal and Shelf Science 53:3 3. DAVIS, G. E. AND J. W. DODRILL Recreational fishery and population dynamics of spiny lobsters, Panulirus argus, in Florida Bay, Everglades National Park, Florida. Bulletin of Marine Science 44: DAVIS, S. M. AND J. C. OGDEN Toward ecosystem restoration, p In S. M. Davis and J. C. Ogden (eds.), Everglades. The Ecosystem and its Restoration. St. Lucie Press, Delray Beach, Florida. DE SYLVA, D. P Sport fisheries, p In G. L. Voss, F. M. Bayer, C. R. Robins, M. F. Gomon, and E. T. LaRoe (eds.), The Marine Ecology of the Biscayne National Monument Miami. Institute of Marine and Atmospheric Sciences, University of Miami, Miami, Florida. DUNTON, K. H Production ecology of Ruppia maritima L. s.l. and Halodule wrightii Aschers in two subtropical estuaries. Journal of Experimental Marine Biology and Ecology 43: DUNTON, K. H Seasonal growth and biomass of the subtropical seagrass Halodule wrightii in relation to continuous measurements of underwater irradiance. Marine Biology 0: FONG, P. AND M. A. HARWELL Modeling seagrass communities in tropical and subtropical bays and estuaries: A mathematical model synthesis of current hypotheses. Bulletin of Marine Science 54: FONG, P., M. E. JACOBSON, M.C.MESCHER, D.LIRMAN, AND M. C. HARWELL Investigating the management potential of a seagrass model through sensitivity analysis and experiments. Ecological Applications 7: FOURQUREAN, J. W., M. J. DURAKO, M.O.HALL, AND L. N. HEFTY. 00. Seagrass distribution in South Florida: A multi-agency coordinated monitoring program, p In J. W. Porter and K. G. Porter (eds.), The Everglades, Florida Bay, and Coral Reefs of the Florida Keys. An Ecosystem Sourcebook. CRC Press, Boca Raton, Florida. FOURQUREAN, J. C., G. V. N. POWELL, W. J. KENWORTHY, AND J. W. ZIEMAN The effects of long-term manipulation of nutrient supply on competition between the seagrasses Thalassia testudinum and Halodule wrightii in Florida Bay. Oikos 7: FOURQUREAN, J. W. AND M. B. ROBBLEE Florida Bay: A brief history of recent ecological changes. Estuaries : GALLEGOS, M. E., M. MERINO, A. ROBRIGUEZ, N. MARBA, AND C. M. DUARTE Growth patterns and demography of pioneer Caribbean seagrasses Halodule wrightii and Syringodium filiforme. Marine Ecology Progress Series 9:99 4. HALL, M. O., M. J. DURAKO, J.W.FOURQUREAN, AND J. C. ZIEMAN Decadal changes in seagrass distribution and abundance in Florida Bay. Estuaries : HARWELL, M. A Ecosystem management of South Florida. BioScience 47: HOLMQUIST, J. G., G. V. N. POWELL, AND S. M. SOGARD Decapod and stomatopod assemblages on a system of seagrass-covered mud banks in Florida Bay. Marine Biology 0: IRLANDI, E., B. ORLANDO, S. MACIA, P. BIBER, T. JONES, L. KAUF- MAN, D. LIRMAN, AND E. PATTERSON. 00. The influence of freshwater runoff on biomass, morphometrics, and production of Thalassia testudinum. Aquatic Botany 536:. LEWIS, III, R. R., M. J. DURAKO, AND R. C. PHILLIPS Seagrass meadows in Tampa Bay A review, p. 46. In S. A. F. Treat, J. L. Simon, R. R. Lewis, III, and R. L. Whitman, Jr. (eds.), Proceedings Tampa Bay Area Scientific Information Symposium. Florida Sea Grant College Report 65. Florida Sea Grant, Gainsville, Florida. LIGHT, S.S. AND J. W. DINEEN Water control in the Everglades: A historical perspective, p In S. M. Davis and J. C. Ogden (eds.), Everglades. The Ecosystem and Its Restoration. St. Lucie Press, Delray Beach, Florida. MCMAHAN, C. A Biomass and salinity tolerance of shoalgrass and manateegrass in Lower Laguna Madre, Texas. Journal of Wildlife Management 3: MCMILLAN, C Salt tolerance of mangroves and submerged aquatic plants, p In R. J. Reimold and W. H. Queen (eds.), Ecology of Halophytes. Academic Press, York. MCMILLAN, C. AND F. N. MOSELEY Salinity tolerances of five marine spermatophytes of Redfish Bay, Texas. Ecology 48: MONTAGUE, C. L The distribution and dynamics of submerged vegetation along gradients of salinity in northeast Florida Bay. Bulletin of Marine Science 44:5. MONTAGUE, C.L.AND J. A. LEY A possible effect of salinity fluctuation on abundance of benthic vegetation and associated fauna in Northeastern Florida Bay. Estuaries 6: ROBBLEE, M. B., T. R. BARBER, P. R. CARLSON, M. J. DURAKO, J. W. FOURQUREAN, L. K. MUEHLSTEIN, D. PORTER, L. A. YARBRO, R. T. ZIEMAN, AND J. C. ZIEMAN. 99. Mass mortality of the tropical seagrass Thalassia testudinum in Florida Bay (USA). Marine Ecology Progress Series 7: SHORT, F. T., M. W. DAVIS, R.A.GIBSON, AND C. F. ZIMMERMAN Evidence of phosphorus limitation in carbonate sediments of the seagrass Syringodium filiforme. Estuarine, Coastal and Shelf Science 0: SMITH, III, T. J., J. H. HUDSON, M. B. ROBBLEE, G. V. N. POWELL, AND P. J. 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11 Salinity Effects on Seagrass Distribution 4 WANG, J. D., J. LUO, AND J. AULT. In press. Flows, salinity, and some implications on larval transport in South Biscayne Bay, Florida. Bulletin of Marine Science. WILLIAMS, S. L Competition between the seagrasses Thalassia testudinum and Syringodium filiforme in a Caribbean lagoon. Marine Ecology Progress Series 35:9 98. WILLIAMS, S. L Experimental studies of Caribbean seagrass bed development. Ecological Monographs 60: WORTMANN, J. J., W. HEARNE, AND J. B. ADAMS A mathematical model of an estuarine seagrass. Ecological Modelling 98: ZIEMAN, J. C. 97. Origin of circular beds of Thalassia (Spermatophyta: Hydrocharitaceae) in south Biscayne Bay, Florida, and their relationship to mangrove hammocks. Bulletin of Marine Science : ZIEMAN, J. C Methods for the study of the growth and production of turtle grass, Thalassia testudinum Konig. Aquaculture 4: ZIEMAN, J. C Seasonal variation of turtle grass, Thalassia testudinum König, with reference to temperature and salinity. Aquatic Botany :7 3. ZIEMAN, J. C The ecological effects of physical damage from motor boats on turtle grass beds in southern Florida. Aquatic Botany :7 39. ZIEMAN, J. C. 98. The ecology of the seagrasses of south Florida: A community profile. FWS/OBS-8/5. U.S. Fish and Wildlife Services, Office of Biological Services, Washington, D.C. ZIEMAN, J. C., J. W. FOURQUREAN, AND T. A. FRANKOVICH Seagrass die-off in Florida Bay: Long-term trends in abundance and growth of turtle grass, Thalassia testudinum. Estuaries : ZIEMAN, J. C., J. W. FOURQUREAN, AND R. L. IVERSON Distribution, abundance and productivity of seagrasses and macroalgae in Florida Bay. Bulletin of Marine Science 44:9 3. Received for consideration, October, 00 Revised, June 7, 00 Accepted for publication, July, 00
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