Journal of Water Resource and Protection, 2013, 5, 732-742 http://dx.doi.org/10.4236/jwarp.2013.57074 Published Online July 2013 (http://www.scirp.org/journal/jwarp) Changes in Diatom Biodiversity in Lake Sinclair, Baldwin County, Georgia, USA Marká E. Smith*, Kalina M. Manoylov Department of Biological and Environmental Sciences, Georgia College and State University, Milledgeville, USA Email: *marka.smith@tn.gov Received April 29, 2013; revised May 28, 2013; accepted June 22, 2013 Copyright © 2013 Marká E. Smith, Kalina M. Manoylov. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. ABSTRACT The effects of increased water temperature on algal community composition were investigated in Lake Sinclair, Bald- win County, Georgia, USA. The lake received waste cooling water from a coal burning power plant. Discharges of re- cycled lake water were, on average, 15˚C ± 1.5˚C (and up to 23˚C) warmer than typical ambient temperatures. Seasonal changes in algal composition were observed, and the warmer sample site had a greater diversity of diatom species year round independent of changes in temperature. Thermal pollution created a high percent dissimilarity between diatoms at the warmer site and the remainder of the lake. Species turnover observed in natural samples was not detected for the warmer site. Anthropogenic thermal pollution was implicated as the factor inducing changes in the natural algal com- munity composition, which may impact other trophic levels and ultimately the overall ecology of Lake Sinclair. Keywords: Diatoms; Heated Water; Southern Lakes; Thermal Pollution 1. Introduction Thermal pollution is the degradation of water quality by any process that changes the ambient water temperature. Persistent differences in ambient water temperature may result in eutrophication, loss of ecosystem processes such as biological productivity and lake metabolism, con- taminant toxicity, and loss of aquatic biodiversity [1]. It has been reported that cooling systems from coal burning power plants have no harmful effects on a system as a whole [2]. However, effects of thermal pollution in aqua- tic systems are greatly influenced by industry, agriculture, and urban habitats [1,3-9]. Effect of thermal pollution on algae has not been addressed in Georgia, but in a sou- thwestern lake thermal loading depressed primary pro- duction of phytoplankton [10]. Lake Sinclair, in Central Georgia, is a manmade lake owned by Georgia Power. Water from the lake is used to cool the turbines of a coal burning Power plant. About a billion gallons of water per day is extracted from the lake, and when pumped back into the lake it is intended to be within a few degrees of the ambient temperature [11]. The effects of thermal pollution have been documented previously [12], and it was reported that approximately 3% of the lake was di- rectly impacted by water that was too warm when it was released. Cooling towers are supposed to decrease water tem- perature to ambient temperatures before being released, reducing the impact of thermal pollution on the sur- rounding system [13]. In 2002, Georgia Power finished installing a cooling tower to comply with Georgia Envi- ronmental Protection Division’s (GA EPD) [14] regula- tion to control effluent water temperature. The other condition required for compliance is that at no time is the temperature of the receiving waters to be increased by more than 15˚C above intake temperature or the lake’s natural temperature gradient. The installation was done in response to a number of fish kills in the 1990’s in Beaverdam Creek [15]. Past research on Lake Sinclair is limited, with little to no research on potential thermal pollution and its effects on primary producers. The State of Georgia has continuously monitored temperature data from DNR/EPD/Watershed Protection Branch since 2009. Three sites that the State monitored on Lake Sinclair provided additional temperature information in this study for the baseline conditions within the lake. Diatoms (Bacillariophyta) are often reported as the dominant group in lake communities [16] and are known to show definitive responses to different stressors and environmental conditions [17-21]. Their rapid cell cycles have been used to infer changes in composition due to *Corresponding author. C opyright © 2013 SciRes. JWARP
M. E. SMITH, K. M. MANOYLOV 733 anthropogenic influences from days to weeks [22,23]. Diatoms are able to recolonize bare surfaces as primary colonizers in approximately 14 days [24]. They have also been used extensively to directly infer climate variables, such as temperature [25,26], but never as a model to un- derstand thermal pollution within the same aquatic habi- tat. Diatoms are particularly useful for assessing envi- ronmental change because of their fast response rate and potential presence in sedimentary records, which means they can be used to compare past with present communi- ties. Diatoms were used to detect shifts due to global warming when there were changes of only a few degrees centigrade [1], and the community composition shifted to species that preferred longer growing seasons with less ice cover [27-29]. A shift from primarily benthic diatoms to planktonic species has also been suggested as a sign that warming is occurring [30-37]. Visible changes in community dominance of diatoms followed by satellite imagery showed the effects of thermal pollution on shal- low estuaries [38], and as little as 1˚C temperature in- crease changed the dominant species composition in the local area. Species richness, diversity, and evenness are routinely used to assess community change and. In the case of cli- mate, warmer temperatures have been found to favor higher biological production [39]. High species richness is a measure of high biotic integrity, because of the vari- ety of habitats present and the ability of taxa to adapt to the available niches [40]. Much research on algae has addressed the relationship between species richness and nutrient concentrations [41,42]. High nutrient concentra- tions can lead to toxic blooms [43]. However, many habitats may be naturally stressed by low nutrients, low light, low temperature or other factors [18]. A slight in- crease in nutrient enrichment has been shown to trigger an increase in algal species richness in headwater and naturally unproductive, nutrient poor streams [44]. Tem- perature changes may have a similar effect [45]. However, information from stressor specific monitor- ing is generally lacking. Little is known about the eco- logical impacts of thermal pollution on primary produc- ers within the same lake. In an attempt to determine the nature and magnitude of environmental changes in a lake impacted by anthropogenic temperature increase, two sites on Lake Sinclair were systematically monitored and diatom species composition was analyzed to assess re- sponse to temperature differences. It can be expected that some algal species differ at the two sites because they have different tolerances to temperature. The goals of this study were to: 1) understand the biological impacts of thermal pollution in Lake Sinclair; 2) evaluate the changes in primary producer community structure and function due to changes in temperature; and 3) assess the potential of change in diatom community structure as an indicator of thermal pollution. 2. Materials and Methods 2.1. Study Area: Lake Sinclair, from the Oconee River Watershed Lake Sinclair is located in central Georgia on the Oconee River watershed (33˚10′49.06″N, 83˚17′28.70″W). It stret- ches through three counties including Baldwin, Hancock, and Putnam. The Oconee River is the main source of water for this reservoir and supplies 70% of the lake’s water. The lake is also fed by waters from the Apalachee River and several small creeks in the area [46]. The re- gion is characterized by a warm and humid, temperate climate. The average annual temperature is about 15.6˚C. Runoff is not generally significant. The Oconee River basin contains parts of the Pied- mont and Coastal Plain physiographic provinces, which extend throughout the southeastern United States. Lake Sinclair sits on the Piedmont region. Predominant soil types are sandy loam clay to fine sandy loam [13]. Lake Sinclair is a manmade lake created in 1953. It is the second largest reservoir in Georgia (surface area 62 km²) and has a maximum depth of 27 m. Lake Sinclair and Lake Oconee are considered oligotrophic lakes, with deep nutrient poor lake basins with sandy or rocky bot- toms, and scarce bottom vegetation. Georgia Power, a Southern Company, owns the lake and uses it as a reser- voir to cool the turbines in their coal burning plant. In addition, the lake area is used for residential housing and recreation. In the counties surrounding the lake, there is a population of about 150,000. The counties that surround Lake Sinclair remain heavily forested by oak/pine forests with little agriculture and industry [13]. The agriculture and housing developments on water bodies above Lake Sinclair have little to no influence on the streams and lakes themselves [47]. 2.2. Sampling Site Locations Prior to this study, non-significant differences in diatom community composition from Lake Sinclair were re- ported in 22 sites [47,48]. For the current study, two sites on Lake Sinclair were chosen for comparison of the temperature effects. One in the immediate “warmer” area of the power plant (where discharge from the cooling tower occurs), and the other was approximately 1.7 km to the south representing ambient temperatures, “the cooler or cold site”. The cold and warm locations were sampled for seven months. There were a total of 15 samples taken from each sample site. Sampling methods followed Standard protocols [49,50]. Once collected, the samples were transported to the laboratory in a cooler with ice and immediately preserved. Algal samples were pre- served with 3% formaldehyde for later processing and Copyright © 2013 SciRes. JWARP
M. E. SMITH, K. M. MANOYLOV 734 identification [50]. Algal samples were collected approximately every 14 days from August 2008 to February 2009, along with triplicate measures of water temperature, pH, and con- ductivity with YSI 556 MPS instrument. Turbidity was measured using a LaMotte® Portable Turbidity meter. Turbidity was measured as having sediment or foreign particles stirred up or suspended, muddy. Based on the GA EPD requirement for small differences in natural habitats due to human activities, temperature differences between the two sites were categorized as 1 = small dif- ferences from 1˚C to 10˚C, 2 = medium differences from 11˚C to 20˚C, and 3 = high differences more than 20˚C. After classification, 4 sampling events fell into the first category, 5 fell into the second category, and 6 fell into the third category for a total of 15 sampling events. A Secchi disc (Carolina biological Inc.) was used to evalu- ate the depth of the photic zone. Water for nutrients analyses was collected in 125 ml acid washed bottles and sent to the University of Georgia Marine Extension Ser- vice and University of Georgia commercial chemical ana- lyses lab in Athens, Georgia. Water samples were ana- lyzed for nutrients including Ammonium, Nitrate/Nitrite, Total Nitrogen, and total Phosphorus. Three further sam- ples were taken for nutrient analysis and compared to Georgia’s DNR data, but there were no significant dif- ferences in nutrient concentrations. Lab analysis of algal diatom assemblage composition was performed using cleaned (digested) samples pre- served on permanent slides [50]. The samples were cleaned of organic matter in 50% nitric acid for 2 hours. Then less than one gram of potassium dichromate was added to them as a catalyzer, heated for approximately 5 minutes and left to cool for 30 minutes. Permanent dia- tom slides were prepared by acid cleaning, to increase the clarity of observing diatoms [51], and then mounted in Naphrax resin (RI 1.74, Northern Biological Supplies L., Ipswich, UK). Taxa that appeared as auxospores or single broken valves without the central area were not included in the analyses. At least 300 valves were counted from each sample using the 1000x objective lens on an Aus JenaLumar scope (AUSJena Germany). Diatoms were identified to the lowest taxonomic unit using standard identification keys and following standard procedures for diatom iden- tifications [51-56]. 2.3. Diatom Indices Presence or absence and species numbers were recorded at the cold site and the warm site. Species richness de- scribes the number of species in a habitat. Species even- ness [57] represents the relative abundance of species in a community (if one taxon dominates the community and there are many rare taxa, evenness will be close to 0). Species diversity is a measure of diversity that increases with either species richness or species evenness. The Shannon diversity index considers species richness and proportion of species in a site [58]. Lastly, 2 other meas- ures were utilized to compare the sites. Similarity rich- ness Index (S = 2C/A + B) and % Dissimilarity index (%D = 100 minus Σ min relative abundance of “C”), where C is the number of common species between the two sites, A is the number of species in one site, B is the number of species in the other site and “C” is relative abundance of common taxon that appeared in both sites; the smaller of the 2 relative abundances is summed for the index [59]. Similarity varies from 0 to 1, high Simi- larity is expected at 0.7 and above. Dissimilarity values vary from 0 to 100% with values close to 0 indicating identical communities and more than 50% indicating very different diatom communities [60]. 2.4. Statistical Analyses To test if the number of rare taxa were significantly dif- ferent between natural and high temperature impacted sites, sites were compared with t tests as α = 0.05 and significance was considered. If the assumptions for t test were not met (e.g., normality, equal variance) and if transformation did not help, the Mann Whitney non pa- rametric test was used. Descriptive statistics, Pearson correlations, and regression analyses were conducted to analyze environmental variability and relationships be- tween variables. Linear regression predicted patterns of community indices in the warm and cold environments. Statistical analyses were performed with SYSTAT® 13 [61]. 3. Results 3.1. Physical Parameters Temperatures at the cold site ranged from 10˚C to 31.5˚C (mean 20.6˚C) and at the warm site from 29˚C to 35˚C (mean 32.5˚C). The seasonal temperatures at the cold site were normal for the lake but the warm site, which re- ceived the cooling water discharge, showed little varia- tion throughout the study. Temperature differences be- tween the two sites diverged the most during the winter season, while summer months temperature values over- lapped. Dissolved oxygen concentrations at both sites were similar, with 4.2 mg/L at the warm site and 4.7 mg/L at the cold site, with the highest levels in winter, and de- clining in the summer months. There was no statistical difference between the dissolved oxygen at each site over each sampling event. Average pH within the study area was 7.04 ± 0.22 with values ranging from 6.82 to 7.26. Secchi depth averaged 0.85 ± 0.50 m for the study area. Conductivity averaged 66 ± 6.24 µS/cm for the study Copyright © 2013 SciRes. JWARP
M. E. SMITH, K. M. MANOYLOV Copyright © 2013 SciRes. JWARP 735 area. Turbidity in the study area averaged 14.32 NTU. 3.2. Nutrient Analyses Water samples for nutrient analysis were taken three times during this research, at the beginning the middle and the end. The average concentrations of ammonia was 0.23 ± 0.04 mg/L, of nitrate was 0.17 ± 0.01 mg/L, and total nitrogen 0.20 ± 0.18 mg/L. There was no statistical difference between the nitrogen, ammonium, and total phosphorus at each site over each sampling event. 3.3. Diatom Enumeration There were a total of 131 diatom species observed from the two sites at Lake Sinclair. Only 10 were considered common species with relative abundance of >25% (Ta- bles 1 and 2). Rare species made up approximately 90% of the species documented during the study. Different rare species were observed at both sites. Planktonic and benthic diatoms were observed throughout the study. Variation among total species richness remained low for the duration of the study. The highest species richness in the cold site occurred during the summer months with a total of 37 species observed, which corresponded to the highest Shannon diversity value. The warm sites highest species richness occurred during the summer as well with 39 different species observed. This number correlated with the highest Shannon diversity value for the warm Table 1. Species that appeared in 25% or more relative abundanc e in cold habitat in Lake Sinclair, GA. Date Diatom Species % RA 2008/10/27 Achnanthidium minutissimum (Kützing) Czarnecki 0.310 2008/11/1 Achnanthidium minutissimum (Kützing) Czarnecki 0.307 2008/12/5 Aulacoseira ambigua (Grunow in Van Heurck) Simonsen 0.310 2008/12/5 Discostella stelligera (Cleve et Grunow in Cleve) Houk et Klee 0.273 2009/1/16 Achnanthidium minutissimum (Kützing) Czarnecki 0.578 2009/1/16 Aulacoseira granulata (Ehrenberg) Simonsen 0.278 2009/1/25 Achnanthidium minutissimum (Kützing) Czarnecki 0.430 2009/2/11 Melosira varians Agardh 0.331 Table 2. Species that appeared in 25% or more relative abundanc e in warm habitat in Lake Sinclair, GA. Date Diatom Species % RA 2008/9/3 Fragilaria capucina Desmazières var. mesolepta (Rabenhorst) Rabenhorst 0.276 2008/10/3 Achnanthidium catenatum (Bily et Marvan) Lange-Bertalot 0.313 2008/10/3 Achnanthidium minutissimum (Kützing) Czarnecki 0.280 2008/10/10 Achnanthidium catenatum (Bily et Marvan) Lange-Bertalot 0.247 2008/10/10 Achnanthidium minutissimum (Kützing) Czarnecki 0.440 2008/10/17 Achnanthidium minutissimum (Kützing) Czarnecki 0.273 2008/11/1 Encyonema silesiacum (Bleisch in Rabenhorst) Mann in Round 0.253 2008/11/7 Nitzschia filiformis var. conferta (Richter) Lange-Bertalot in Lange-Bertalot and Krammer 0.248 2008/11/17 Aulacoseira ambigua (Grunow in Van Heurck) Simonsen 0.277 2008/12/5 Aulacoseira granulata (Ehrenberg) Simonsen 0.333 2009/1/16 Aulacoseira granulata (Ehrenberg) Simonsen 0.291 2009/1/16 Thalassiosira pseudonana Hasle et Heimdal 0.258 2009/1/25 Achnanthidium minutissimum (Kützing) Czarnecki 0.333 2009/2/11 Achnanthidium catenatum (Bily et Marvan) Lange-Bertalot 0.424 2009/2/11 Achnanthidium minutissimum (Kützing) Czarnecki 0.435
M. E. SMITH, K. M. MANOYLOV 736 water site as well. There were 100 species recorded at the cold site. The average number of species was 23 ± 1.90, ranging from 13 to 37 species. The highest species richness and even- ness observed in the cold samples occurred during warmer calendar months, when not a single taxon ap- peared with more than 25% relative abundance (Table 1). There were a total of 103 diatom species documented at the warm site. The average number of species was 23 ± 1.87, ranging from13 to 39 species. The cold water community was dominated by Ach- nanthidium minutissimum (Kützing) Czarnecki (Table 1), with secondary abundances of other pennate genera in- cluding Nitzschia, Aulocoseria, Melosira, Synedra, and Cymbella. For the warm site, the subdominant genera like Aulacoseira and Cymbella were at much greater abundances than in cold water. Cocconeis pediculus Ehrenberg, Martyana martyi (Héribaud) Round, and Ca- loneis schumanniana (Grunow in Van Heurck) Cleve, were found only at the warm site (Table 2). Adlafia minuscula (Grunow) Lange Bertalot, Amphipleura pellu- cida (Kützing) Kützing, Diadesmis contenta (Grunow ex Van Heurck) Mann in Round, Crawford and Mann, Fal- lacia tenera (Hustedt in Schmidt) Mann in Round, Craw- ford and Mann, Stephanodiscus minutulus (Kützing) Cleve et Möller, and Tabularia fasciculata (Agardh) Williams et Round were only present in the cold site. Warm water community composition remained consis- tent with the cold site throughout the year. However, as the study progressed over time, the dominant species shifted as the temperature changed in the cold sites more than in the warm sites. The Shannon diversity values for the cold site ranged from 1.26 to 3.02. The warm sites values were compara- ble, ranging from 1.73 to 3.10. When temperature dif- ferences were small between the two sites, there were no significant differences in values of the average Shannon diversity. With a change in the seasons, the Shannon di- versity values at both warm and cold site’ varied signifi- cantly, showing an increase, on average, in the cold site and a decrease in the average warm sites value. During the winter months at the cold sites, the Shannon diversity value decreased further while the warmer site stayed at about the same. Evenness for the warm site ranged from 0.68 in October to 0.85 in August. The cold site had a low evenness of 0.45 in February and a high evenness of 0.87 in November. Similarity calculated with presence of common taxa at both sites was very low and reached close to 50% only in September (Table 3). Similarity based on species rich- ness related common species between the two sites with the total number of species in both areas. Dissimilarity measured with minimum relative abundance of a com- mon taxon for the two locations was very high for all pairs (Table 3), dissimilarity decreased below 50% only during one warmer calendar month. Average richness similarity during winter months similarly was 0.08 to 0.43, dissimilarity based on species identity and relative abundance was high throughout the sampling season. Temperature explained one third to 50 % of the varia- tion only for the cold or natural habitats (Table 4). The Shannon diversity within the cold sites increased signifi- cantly with temperature changes (Linear regression, y = 0.007x + 2.143, R² = 0.54, p = 0.002). The Species rich- ness for the cold site increased with increase in tempera- ture (Linear regression, y = 0.77x + 6.838, R² = 0.37, p = 0016). The Evenness for the cold site significantly in- creased with temperature too (Linear regression, y = 0.013x + 0.511, R² = 0.52, p = 0.002). No significant changes between the communities attributed and tem- perature were documented for the warm site. 3.4. Representative Diatom Species Evaluations (from the Taxonomic Literature) Cocconeis pediculus Ehrenberg, is described as having a valve that is strongly arched, broadly ellipitical. Interca- lary band occasionally seen. Raphe valve with narrow, linear axial area terminating in a small semicircular clear space near the valve extremities. Centrals are small, cir- Table 3. Species richness similarity and % abundance dis- similarity of diatom community composition in warm and cold sites within Lake Sinclair system for each sampling date. Date Species Similarity Abundance % Dissimilarity 2008/8/27 0.1967 67 2008/9/3 0.2040 65 2008/9/12 0.4535 49 2008/9/26 0.5160 63 2008/10/3 0.4895 59 2008/10/10 0.3179 76 2008/10/17 0.3806 55 2008/10/27 0.4829 68 2008/11/1 0.1733 74 2008/11/7 0.1113 73 2008/11/17 0.1942 63 2008/12/5 0.2767 58 2009/1/16 0.3244 72 2009/1/25 0.4394 74 2009/2/11 0.0870 62 Copyright © 2013 SciRes. JWARP
M. E. SMITH, K. M. MANOYLOV 737 Table 4. Mean, Standard Deviation, Regression equations, R², and p-values for cold and warm sites within Lake Sinclair. Group Variable N Mean Std. Dev. Regression equation R² p-value Shannon 15 2.43 0.506 y = 2.143 + 0.007x 0.54 0.002 Species Richness 15 23.133 7.347 y = 6.838 + 0.776x 0.37 0.016 Cold Eveness 15 0.777 0.101 y = 0.511 + 0.013x 0.52 0.002 Shannon 15 2.346 0.433 y = 1.076 + 0.064x 0.01 ns Species Richness 15 22.667 7.355 y = 21.1 + 0.0056x 0.002 ns Warm Eveness 15 0.76 0.09 y = 0.699 + 0.002x 0.02 ns cular to somewhat irregular. Raphe filiform, proximal ends close, extending into the central area; distal ends straight, terminating at the small semicircular space near the valve extremities. Striae curved-radiate, finely but distinctly punctuate. Striae not extending completely to the valve margin, but interrupted by a narrow, clear mar- ginal area which is continuous around the valve much as rim. Pseudoraphe valve with very narrow, linear pseu- doraphe. Central area lacking. Striae also curved radiate, faintly etched as a shallow trough, with distantly placed conspicuous puncta. Puncta arranged in longitudinally undulating rows. Straie, about 20 in 10 µ along the axial area, 16 - 17 in 10 µ near the margins (RV); 18 in 10 µ along the axial area, 15 - 16 in 10 µ near the margins (PRV). Length, 11 µ - 30 µ. Breadth, 6 µ - 20 µ. The range of this diatom has been reported in the South East- ern United States. This species is a widespread species; epiphytic on many aquatic plants and other objects, but not often found in large numbers. Considered by some as resistant to moderate amounts of organic pollution; alka- liphil, and salt “indifferent”. The measured specimens from our samples fell within the range of the given de- scription. Achnanthidium minutissimum (Kützing) Czarnecki (Figure 1(7)) is described as having a valve linearel- lipitical with obtusely rounded subrostrate to capitate ends. Raphe valve with narrow, linear axial area and narrow, somewhat irregularly shaped, central area occu- pying up to about one-half the total width of the valve in the middle portion. Raphe filiform; proximal raphe ends close, distal ends curving subtlety in the same direction. Striae slightly to moderately radiate, becoming more numerous towards the ends. One or two shorter striae on either side of the central area sometimes spaced slightly farther apart than the reaming straie. Pseudoraphe valve with narrow, linear axial area, slightly broadened in the middle portion of the valve or with an occasional short- ened stria at the center, but with no distinct central area as such. Striae character and direction as on the raphe valve. Striae, 30 - 32 in 10 µ at the center, becoming 36 - 38 in 10 µ near the ends (both valves). Length, 5 µ - 40 µ. Breadth, 2 µ - 4 µ. This species has been reported in the South Eastern United States. This species is described as a very widespread taxon to be found throughout the country, Eurytropic, Euryők. Found at very wide range of pH about 6.5 - 9.0. Oligohalobe, probably “indifferent”. The measurements in our study were in the range of the given description. Fragilaria capucina Desmazières var. mesolepta (Ra- benhorst) Rabenhorst (Figure 2(2)) is described as hav- ing a valve linear to linear-lanceolate, constricted at the rectangularly shaped central area. Apices somewhat at- tenuated, rostrate. Pseudoraphe very narrow. Central area somewhat variable, may be longer than broad or broader than long. Striae parallel, 15 - 18 in 10 µ. Length, 30 µ - 35 µ. Breadth in narrowest portion of the middle of the valve, 2 µ - 4 µ. This taxon is distinguished from other verities of this species by the constriction in the middle portion of the valve. This species has been reported in the South Eastern United States, and occurs in fresh water, slightly alkaline; sometimes found in slightly brakish (4) (3) (2) (1) (5) (6) (7) (8) (9) Figure 1. Warm water pennate araphid, monoraphid and biraphid diatom taxa, (1 - 2) Fragilaria bidens Heiberg, (3) Fragilaria sp., (4) Staurosirella sp. (5) Gomphonema sp., 6. Gomphonema gracile Ehrenberg, (7) Achnanthidium minu- tissimum (Kützing) Czarnecki, (8) Planothidium sp. (9) En- cyonopsis microcephala (Grunow) Krammer. Scale bar is 10 µm. Copyright © 2013 SciRes. JWARP
M. E. SMITH, K. M. MANOYLOV 738 water. The specimens in our samples were not the same size as the description given. Encyonema silesiacum (Bleisch in Rabenhorst) Mann in Round, Crawford and Mann (Figure 3(7)) is described as having valves that are strongly dorsi-ventral with rounded, undifferentiated apices. The dorsal margin is strongly convex; the ventral margin is more or less straight. The straie are parallel to slightly radiate. Axial area is narrow linear, with slightly expanded central area. Raphe is filiform and more or less straight. Proximal raphe fissures are small pores; distal raphe fissures are strongly deflected towards the ventral surface and ex- tended along the valve margin. The isolated pore (stigma) at the end of the central straie may or may not be dis- cerned with LM. Areolae open externally as slits. Encyo- nema silesiacum has fewer areolae/10 µm. Length 7 µm - 23 µm (Encyonema silesiacum usually larger). Width is 4 µm - 7 µm with a straie density of 15 - 18/10 µm. This species was restricted to more eutrophic locali- ties with higher pH and was never dominant in Lake Sin- clair samples. The sizes of our specimens of this species were not the same as the description given. (2) Aulacoseira ambigua (Grunow in Van Heurck) Si- monsen (Figure 4(2)) is described as having cells that are cylindrical with a mantle height to valve diameter often between 1.5 and 3. The valve face is usually unor- namented. Straie on the mantle composed of relatively (1) (2) (4) (5) (6) (3) Figure 2. Cold water Pennate araphid diatom taxa, (1) Synedra ulna cf. Var ramesi, (2) Fragilaria capucina Desma- zières var. mesolepta (Rabenhorst) Rabenhorst, (3) Tabu- laria fasciculata (Agardh) Williams et Round, (4) Fragilaria bidens Heiberg, (5) Pseudostaurosira brevistriata (Grunow in Van Heurck) Williams et Round, (6) Martyana martyi (Héri- baud) Round. Scale bar is 10 µm. (4) (5) (8) (9) (3) (1) (7) (6) Figure 3. Cold water Pennate biraphid diatom taxa, (1) Bra- chysira vitrea (Grunow) Ross in Hartley, (2) Diadesmis con- tenta (Grunow ex Van Heurck) Mann in Round, Crawford and Mann, (3) Encyonema minutum (Hilse in Rabenhorst) Mann in Round, Crawford and Mann, (4) Encyonema sile- siacum (Bleisch in Rabenhorst) Mann in Round, (5) Navi- cula notha Wallace, (6) Gomphonema gracile Ehrenberg, (7) Nitzschia filiformis var. conferta (Richter) Lange-Bertalot in Lange-Bertalot and Krammer, (8) Fallacia tenera (Hustedt in Schmidt et al.) Mann in Round, Crawford and Mann, (9) Geissleria decussis (Østrup) Lange-Bertalot et Metzeltin. Scale bar is 10 µm. (1) (4) (7) (5) (6) (8) (3) (2) spines are short, and triangular, fork or heart-shaped. Figure 4. Warm water Centric diatom taxa, (1) Aulacoseira alpigena (Grunow in Van Heurck) Krammer, (2) Aulaco- seira ambigua (Grunow in Van Heurck, (3 - 7) Aulacoseira granulata (Ehrenberg) Simonsen, (8) Melos ira var ia ns Agardh; scale bar 10 µm. large, circular areolae that spiral to the right. Since each mantle costae terminates with a spine on the valve face, the density of spines equals the density of straie. Linking Copyright © 2013 SciRes. JWARP
M. E. SMITH, K. M. MANOYLOV 739 Although rare, separating spines are longer, pointed, and also terminate the ends of each mantle costae. Cells have a well-defined collum, the height of which is quite stable, and a thick hollow Ringleiste that forms a characteristic indentation when cells are viewed at mid-focus. The height is 5 µm - 13 µm with a diameter of 4 µm - 17 µm. This taxon is reported to be observed in slightly acidic to slightly alkaline, and mesotrophic conditions. This is a planktonic species that dominated in 6% of our commu- nities. The specimens observed fell within the range of the given description. 4. Discussion d evidence for a shift from benthic to ance of diatom species was expected to be m oal of assessing and managing aquatic ec s excellent indi- ca rst taxonomic evaluation of diatoms from La 5. Acknowledgements gia’s Environmental Protec- REFERENCES [1] S. Kaushal, G. Pace, M. Sides, D. and ct of Strip-Cutting on There was limite planktonic diatoms as Lake Sinclair is very turbid with a shallow photic zone as compared to arctic lakes where most of the temperature relationships have been reported [27-29]. During the warmer months of the study when there was less than 10˚C temperature difference, diver- sity values and richness were close in value. When the seasons changed, there was a statistically significant dif- ference between the sites that triggered on average 65% dissimilarity. Within the median increase in temperature differences (still less than 20˚C), cold sites were more diverse. Diatom species composition, richness, and abun- dance of naturally occurring species in Lake Sinclair were significantly changed in parts of the lake with con- stant high temperature. The expected decrease in native taxa richness, because these taxa are less competitive in higher temperature, was strongly suggested and observed. Competitive exclusion for other limiting resources, in- creased predation, or alteration of other abiotic factors through indirect effects of temperature (e.g., dissolved oxygen concentration, microbial interaction, or habitat structure) may all be influencing diatom community cha- racteristics. The abund ore sensitive to environmental changes than presence/ absence of taxa, because taxa were expected to change their reproductive rate before being totally lost from a habitat. Taxonomic evaluation of diatoms from natural conditions in either low nutrients [62] or as evaluated in this study, low temperature, present a valuable resource for evaluation of changes due to human activities. Ideally, reference conditions are developed according to the cen- tral tendency and variability of natural or minimally dis- turbed systems. The ultimate g Str osystems is to restore these ecosystems to natural con- ditions, which will not be possible for Lake Sinclair. The suite of community assessment presented here (such as native conditions, diatom richness, relative abundance, and species characteristics) should be monitored along the temperature gradients in the future. Diatoms have long been regarded a tors of environmental change in aquatic systems, re- sponding with quantifiable trends over relatively short time periods. The warmer sample site was anticipated to promote a greater diversity of species. As our results de- monstrated, constant high temperature supported higher biodiversity and prevented natural competitive processes to take place as in the rest of the lake. Winter differences in temperature were above regulation (GA EPD), and significantly changed the community structure of the primary producers. Anthropogenic thermal pollution is implicated here as a factor inducing changes in the natu- ral diatom community composition, which may impact other trophic levels and ultimately the overall ecology of Lake Sinclair. This is the fi ke Sinclair, and the observed (diatom dominated pri- mary producers community) was due to changes in tem- perature. The highest similarity values occurred when temperature corresponded to high summer air tempera- ture. Warmer water supported more algal species and higher algal density. Inversely it was observed that as the temperature dropped, similarity decreased and varied with season. The temperature in the lake is affected by recycled water that is released by the power plant daily. Diatoms are an effective source for determining tem- perature changes over a relatively short period of time and good indicators of impairment. We would like to thank Geor tion Division and Georgia’s Department of Natural Re- sources for the additional data. Likens, N. Jaworski, M. Seekell, K. Belt, D. Secor and R. Wingate, “Rising Streams and River Temperatures in the United States,” Ecology and Environment, Vol. 9, 2010, pp. 461-466. [2] C. D. Becker, C. E. Cushing, K. L. Gore, K. S. Baker D. H. McKenzie, “Synthesis and Analysis of Ecological Information from Cooling Impoundments,” Study Site Histories and Data Synopsis, Technical Report: EPRRI- EA-1054. Vol. 2, 1979, pp. 1-291. [3] M. Burton and E. Likens, “Effe eam Temperatures in Hubbard Brook Experimental Forest, New Hampshire,” BioScience, Vol. 23, 1973, pp. 433-35. doi:10.2307/1296545 [4] S. Kaushal, M. Groffman, G. Likens, et al., “Increased Salinization of Fresh Water in the Northeastern US,” Pro- ceedings of the National Academy of Sciences of the United States of America, Vol. 102, No. 38, 2005, pp. 13517-13520. doi:10.1073/pnas.0506414102 [5] S. Kaushal, M. Groffman, E. Band, et al., “Interaction Copyright © 2013 SciRes. JWARP
M. E. SMITH, K. M. MANOYLOV 740 between Urbanization and Climate Variability Amplifies Watershed Nitrate Export in Maryland,” Environmental Science and Technology, Vol. 42, No. 16, 2008, pp. 5872- 5878. doi:10.1021/es800264f [6] T. Kinouchi, “Impact of Long Term Water and Energy Consumption in Tokyo on Wastewater Effluent: Implica- tions for Thermal Degradation of Urban Streams,” Hydro- logical Process, Vol. 21, No. 9, 2007, pp. 1207-1216. doi:10.1002/hyp.6680 [7] K. Nelson and A. Palmer, “Predicting Stream Tempera- tures in Urbanization and Climate Change: Implications for Stream Biota,” Journal of American Water Resources Association, Vol. 43, No. 2, 2007, pp. 440-452. doi:10.1111/j.1752-1688.2007.00034.x [8] W. Webb and F. Nobilis, “Longterm Changes in River Temperature and the Influence of Climatic and Hydro- logic Factors,” Hydrological Sciences Journal, Vol. 52, No. 1, 2007, pp. 74-85. doi:10.1623/hysj.52.1.74 [9] N. D. Weston, J. T. Hollibaugh and S. B. Joye, “Popula .066 - tion Growth Away from the Coastal Zone: Thirty Years of Land Use Change and Nutrient Export in the Altamaha River, Ga,” Science of the Total Environment, Vol. 407, No. 10, 2009, pp. 3347-3356. doi:10.1016/j.scitotenv.2008.12 se of Thermal Pollu-[10] T. J. Stuart and J. A. Stanford, “A Ca tion Limited Primary Productivity in a Southwestern USA. Reservoir,” Hydrobiologia, Vol. 58, No. 3, 1978, pp. 199-211. doi:10.1007/BF02346956 [11] S. Barczak and R. Kilpatrick, “Energy Impacts on Geor- d Power Plant Cooling Systems: Policy Al- gia’s Water Resources,” Proceedings of the 2003 Georgia Water Resources Conference, Athens, 20-21 April 2003. [12] US EPA, “Report on Sinclair Lake Baldwin, Hancock an Putnam Counties Georgia EPA Region IV Working Paper No. 294,” US Environmental Protection Agency National Eutrophication Survey Working Paper Series, Vol. 294, 1972, pp. 1-66. [13] J. Z. Reynolds, “ ternatives,” Science, Vol. 207, No. 4429, 1980, pp. 367- 372. doi:10.1126/science.207.4429.367 [14] Georgia Department of Natural Resources Environmental B. Evans, “Thermal Load, Dissolved Ox vancedCooling/PresentationsDay1/6_E on to Algal Ecology in cological Implications .x Protection Division, “Water Quality in Georgia,” Atlanta, 1996-1997. [15] T. Cheek andy- gen, and Assimilative Capacity; Is 316(a) Becoming Ir- relevant,” 1998. http://Epridocs/Ad PRI-Cheek%20&%20Evans.pdf [16] R. J. Stevenson, “An Introducti Freshwater Benthic Habitat,” In: R. J. Stevenson, M. L. Bothwell and R. L. Lowe, Eds., Algal Ecology, Academic Press, San Diego, 1996, pp. 3-30. [17] C. Hudon and P. Legendre, “The E of Growth Forms in Epibenthic Diatoms,” Journal of Phycology, Vol. 23, 1987, pp. 17-46. doi:10.1111/j.1529-8817.1987.tb02529 sity-Dependen rns, “The Evolution of Life Histories,” Oxford oylov, P. Parker, P. Lar- [18] K. Manoylov and R. Stevenson, “Dent Algal Growth along N and P Nutrient Gradients in Artifi- cial Streams,” Advances in Phycological Studies, 2006, pp. 333-352. [19] S. C. Stea University Press, Oxford, 1992. [20] J. Stevenson, Y. Pan, K. M. Man sen and T. Herlihy, “Development of Diatom Indicators of Ecological Condition for Streams of the Western US,” Journal of the North American Benthological Society, Vol. 27, No. 4, 2008, pp. 1000-1016. doi:10.1899/08-040.1 [21] B. Van De Vijver and I. Beyerns, “Biogeography and Ecology of Freshwater Diatoms in Subantartica: A Re- view,” Journal of Biogeography, Vol. 26, No. 5, 1999, pp. 993-1000. doi:10.1046/j.1365-2699.1999.00358.x [22] G. Kelly and A. Whitton, “The Trophic Diatom Index: A New Index for Monitoring Eutrophication in Rivers,” Journal of Applied Phycology, Vol. 7, No. 4, 1995, pp. 433-444. doi:10.1007/BF00003802 [23] B. Hill, J. Stevenson, Y. Pan, T. Herlihy and R. K. John- son, “Comparison of Correlations between Environmental Characteristics and Stream Diatom Assemblages Charac- terized at Genus and Species Levels,” Journal of the North American Benthological Society, Vol. 20, No. 2, 2001, pp. 299-310. doi:10.2307/1468324 [24] R. J. Stevenson, C. G. Peterson, D. B. Kirschtel, C. C. King and N. C. Tuchman, “Succession and Ecological Strategies of Benthic Diatoms (Bacillariophyceae): Den- sity-Dependent Growth and Effects of Nutrients and Shading,” Journal of Phycology, Vol. 27, 1991, pp. 59-69. doi:10.1111/j.0022-3646.1991.00059.x [25] R. Pienitz, J. Smol and H. Birks, “Assessment of Fresh- water Diatoms as Quantitative Indicators of Past Climatic Change in the Yukon and Northwest Territories, Canada,” Journal of Paleolimnology, Vol. 13, No. 1, 1995, pp. 21- 49. doi:10.1007/BF00678109 [26] J. Smol, A. Wolfe, J. Birks, M. Douglas, V. Jones, A. Kprjhola, R. Pienitz, et al., “Climate-Driven Regime Shifts in the Biological Communities of Artic Lakes,” PNAS, Vol. 102, No. 12, 2005, pp. 4397-4402. doi:10.1073/pnas.0500245102 [27] J. Smol, “The Power of the Past: Using Sediments to Track the Effects of Multiple Stressors on Lake Eco- systems,” Freshwater Biology, Vol. 55, 2010, pp. 43-59. doi:10.1111/j.1365-2427.2009.02373.x [28] J. P. Smol, A. P. Wolfe, H. J. B. Birks, M. S. V. Douglas, V. J. Jones, A. Kprjhola, R. Pienitz, K. Ruhland, S. So- rvari, D. Antoniades, S. Brooks, M. Fallu, M. Hughes, B. Keatley, T. Laing, N. Michelutti, L. Nazarova, S. Nyman, A. Paterson, B. Perren, R. Quinlan, M. Rautio, E. Talbot, S. Siitonen, N. Solovieva and J. Weckstrom, “Climate- Driven Regime Shifts in the Biological Communities of Artic Lakes,” PNAS, Vol. 102, No. 12, 2005, pp. 4397- 4402. doi:10.1073/pnas.0500245102 [29] J. Smol and M. Douglas, “Crossing the Final Ecological Threshold in High Arctic Ponds,” PNAS, Vol. 104, No. 30, 2007, pp. 12395-12397. doi:10.1073/pnas.0702777104 [30] J. Alefs and J. Muller, “Differences in the Eutrophication Dynamics of Ammersee and Starnberger, Reflected by the Diatom Succession in Varve-Dated Sediments,” Journal of Paleolimnology, Vol. 21, No. 4, 1999, pp. 395-407. doi:10.1023/A:1008098118867 Copyright © 2013 SciRes. JWARP
M. E. SMITH, K. M. MANOYLOV 741 [31] J. Catalan, S. Pla, M. Rierradevall, et al., “Lake Redo Ecosystem Response to an Increasing Warming in the Pyrenees during the Twentieth Century,” Journal of Pa- leolimnology, Vol. 28, No. 1, 2002, pp. 129-145. doi:10.1023/A:1020380104031 [32] S. Fritz, J. Kingston and D. Engstrom, “Quantitattive Trophic Reconstruction from Sedimentary Diatom As- semblages: A Cautionary Tale,” Freshwater Biology, Vol. 30, No. 1, 1993, pp. 1-23. doi:10.1111/j.1365-2427.1993.tb00784.x [33] M. Harris, B. Cumming and J. Smol, “Assessment of Recent Environmental Changes in New Brunswick (Ca- nada) Lakes Based on Paleolimnological Shifts in Diatom Species Assemblages,” Canadian Journal of Botany, Vol. 84, No. 1, 2006, pp. 151-163. doi:10.1139/b05-157 [34] A. Marchetto, A. Lami, S. Musazzi, J. Massaferro, L. Langone and P. Guilizzoni, “Lake Maggiore (N. Italy) Trophic History: Fossil Diatom, Plant Pigments, and Lim- nological Data,” Quaternary International, Vol. 113, No. 1, 2004, pp. 97-110. doi:10.1016/S1040-6182(03)00082-X [35] K. Ruhland, A. Paterson and J. Smol, “Hemispheric-Scale Paleolimnologica Korhola and R. Thompson, “Lake Diatom Patterns of Climate-Related Shifts in Planktonic Diatoms from North America and European Lakes,” Global Change Biology, Vol. 14, 2008, pp. 2740-2754. [36] K. Ruhland, A. Priesnitz and J. Smol, “l Evidence from Diatoms for Recent Environmental Chan- ges in 50 Lakes Across the Canadian Artic Treeline,” Arc- tic, Antarctic, and Alpine Research, Vol. 35, No. 1, 2003, pp. 110-123. [37] S. Sorvari, A. Response to Recent Artic Warming in Finnish Lapland,” Global Change Biology, Vol. 8, No. 2, 2002, pp. 171-181. doi:10.1046/j.1365-2486.2002.00463.x [38] T. Ingleton and A. McMinn, “Thermal Plume Effects: A Multi-Disciplinary Approach for Assessingeffects of Thermal Pollution on Estuaries Using Benthic Diatoms and Satellite Imagery,” Estuarine, Coastal and Shelf Sci- ence. Vol. 99, 2012, pp. 132-144. doi:10.1016/j.ecss.2011.12.024 [39] R. Ricklefs and D. Schluter, “Species Diversity in Eco- lov, “Ecological Strategies of Benthic Dia- licatio logical Communities,” University of Chicago press, Chi- cago, 1993. [40] K. M. Manoy toms for Nutrient Competition,” Ph.D. Dissertation, Mi- chigan State University, East Lansing, 2005. [41] J. Smol and E. Stoermer, “The Diatoms: Appns for the Environmental and Earth Sciences,” 2nd Edition, Cambridge University Press, Cambridge, 2010. doi:10.1017/CBO9780511763175 [42] B. J. Cardinale, D. M. Bennett, C. E. Nelson and K. Gross, “Does Productivity Drive Diversity or Vice versa? A Test of the Multivariate Productivity-Diversity Hypothesis in Streams,” Ecology, Vol. 90, No. 5, 2009, pp.1227-1241. doi:10.1890/08-1038.1 [43] J. D. Wehr and R. G. Sheath, “Freshwater Algae of North ntis and S. Tralles, “Benchmark Biol- yton Responses to Temperature . L. Steiner, D. M. Endale, et al., “The Re- America Ecology and Classification,” Academic Press, San Diego, 2003. [44] L. Bahls, R. Buka ogy of Montana Reference Streams,” Water Quality Bu- reau, Department of Health and Environmental Sciences, Helena, Montana, 1992. [45] D. M. DeNicola, “Periph at Different Ecological Levels,” Algal Ecology: Freshwa- ter Benthic Ecosystems. Academic Press, New York, 1996, pp. 150-176. [46] D. S. Fisher, J lationship of Land use Practices to Surface Water Quality in the Upper Oconee Watershed of Georgia,” Forest Eco- logy and Management, Vol. 128, No. 1-2, 2000, pp. 39-48. doi:10.1016/S0378-1127(99)00270-4 [47] D. S. Bachoon, T. W. Nichols, K. M. Manoylov and D. R. .x Oetter, “Assessment of Faecal Pollution and Relative Alga Abundances in Lakes Oconee and Sinclair, Georgia, USA,” Lakes and Reservoirs: Research and Management, Vol. 14, No. 2, 2009, pp. 139-149. doi:10.1111/j.1440-1770.2009.00396 anoylov, “Re- ard Methods for Examination of Water and riphyton Protocols,” eimer, “The Diatoms of the United mer and H. Lange-Bertalot, “Bacillariophyceae. eae. alot, “Bacillariophyceae. alot, “Bacillariophyceae. [48] K. Geyer, M. Weilbacher and K. M. M sponse of Algal Community to Anthropogenically-in- duced Temperature Differences in Lake Sinclair, Baldwin County,” Georgia College and State University, Milled- geville, 2009. [49] APHA, “Stand Wastewater,” Washington DC, American Public Health Association, Washingotn DC, 1998. [50] R. J. Stevenson and L. L. Bahls., “Pe In: M. T. Barbour, J. Gerritsen and B. D. Snyder, Eds., Rapid Bioassessment Protocols for Use in Wadeable Streams and Rivers: Periphyton, Benthic Macroinverte- brates, and Fish, 2nd Edition. EPA 841-B-99-002 United States Environmental Protection Agency, Washington, 1999, pp. 6-1 to 6-22. [51] R. Patrick and C. W. R States,” Vol. 1. Monographs of the Academy of Natural Sciences of Philadelphia, Vol. 1, No. 13, 1966, pp. 1-688. [52] R. Patrick and C. W. Reimer, “The Diatoms of the United States. Vol. 2, Part 1,” Monographs of the Academy of Natural Sciences of Philadelphia, Vol. 2, No. 13, 1975, pp. 1-213. [53] K. Kram 1. Teil: Naviculaceae,” In: H. Ettl, J. Gerloff, H. Heynig, and D. Mollenhauer, Eds., Süsswasserflora von Mitte- leuropa, Gustav Fisher Verlag, Jena, 1986, pp.1-876. [54] K. Krammer and H. Lange-Bertalot, “Bacillariophyc 2. Teil: Bacillariaceae, Epithemiaceae, Surirellaceae,” In: H. Ettl, H. Gerloff, H. Heynig and D. Mollenhauer, Eds., Süsswasserflora von Mitteleuropa, Gustav Fisher Verlag, Stuttgart, 1988, pp. 1-596. [55] K. Krammer and H. Lange-Bert 3. Teil: Centrales, Fragilariaceae, Eunotiaceae,” In: H. Ettl, J. Gerloff, H. Heynig and D. Mollenhauer, Eds., Süsswasserflora von Mitteleuropa, Gustav Fisher Verlag, Stuttgart, 1991, pp. 1-576. [56] K. Krammer and H. Lange-Bert 4. Teil: Achnanthaceae. Kritische Ergänzungen zu Navi- cula (Lineolatae) und Gomphonema,” In: H. Ettl, G. Gärtner, J. Gerloff, H. Heynig and D. Mollenhauer, Eds., Süsswasserflora von Mitteleuropa, Gustav Fisher Verlag, Copyright © 2013 SciRes. JWARP
M. E. SMITH, K. M. MANOYLOV Copyright © 2013 SciRes. JWARP 742 tion to Mathematical Ecology,” thematical Theo- n, C. Ter Brakk and O. Van Tongeren, “Data Stuttgart, 1991, pp.1-437. [57] E. C. Pielou, “An Introduc John Wiley and Sons, New York, 1969. [58] C. E. Shannon and W. Weaver, “The Ma ry of Communication,” University of Illinois Press, Urba- na, 1963. [59] R. Jongma Analysis in Community and Landscape Ecology,” Cam- bridge University Press. Cambridge, 1995. doi:10.1017/CBO9780511525575 [60] D. F. Charles, C. Knowles and R. S. Davis, “Protocols for the Analysis of Algal Samples Collected as Part of the U. S. Geological Survey National Water-Quality Assessment Program. Report No. 02-06,” The Academy of Natural Sciences of Philadelphia, Patrick Center for Environ- mental Research-Phycology Section, Philadelphia, 2002. www.acnatsci.org [61] L. Wilkinson, “Systat: The System for Statistics,” Evans- , “Cymbella excisa Kütz. ton Illinois, 1989, 822 pages. [62] K. Manoylov and R. Stevenson in Different Nutrient Conditions,” Proceedings of the 17th International Diatom Symposium, Ottawa, 25-31 August 2004, pp. 31-45.
|