Skip to main content

Advertisement

Log in

Mercury accumulation in largemouth bass (Micropterus salmoides Lacépède) within marsh ecosystems of the Florida Everglades, USA

  • Published:
Ecotoxicology Aims and scope Submit manuscript

Abstract

This study evaluates factors, particularly water quality related, that may influence mercury (Hg) bioaccumulation in largemouth bass (LMB, Micropterus salmoides Lacépède) within the Everglades marshes of South Florida. The investigation is an empirical analysis of ambient data from both long-term fish monitoring and marsh water quality monitoring sites across the Everglades Protection Area. Previous Hg studies of Everglade’s marsh biota have focused on the role that sulfate plays in Hg bioaccumulation. While sulfate can be important under some environmental conditions, this empirical analysis in Everglades marshes showed that sulfate has little association with Hg concentrations in LMB. It is suggested that other water quality variables including water pH, alkalinity and specific conductance may have as much or more influence in the accumulation of Hg in LMB. Furthermore, tissue Hg concentration normalized to body-weight and age-specific growth rates were significantly correlated with Water Conservation Area (WCA)-1, WCA-2 and Everglades National Park (ENP) but not WCA-3. However, body condition was correlated negatively with Hg concentration only within WCA-2, WCA-3 and ENP; the relationship was not significant within WCA-1. This disparity between Hg concentration and body condition could be attributed to ecological effects including water quality and quantity conditions within each compartment of the system that are significant driving forces for biota abundance, trophic structure and distribution within the Everglades ecosystem. While water quality and quantity are important, trophic position of LMB has the potential to influence Hg accumulation dynamics. In spite of documented biogeochemical linkages to Hg accumulation, this empirical analysis did not demonstrate enough quantitative interaction to be useful for Hg management in the Everglades ecosystem.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5

Similar content being viewed by others

References

  • Abtew W, Cadavid L, Ciuca V (2013) Chapter 2: South Florida hydrology and water management. In: 2013 South Florida environmental report—volume I, South Florida Water Management District, West Palm Beach

  • Axelrad DM, Pollman CD, Gu B, Lange T (2013) Chapter 3B: mercury and sulfur environmental assessment for the Everglades. In: 2013 South Florida environmental report—volume I, South Florida Water Management District, West Palm Beach

  • Bae HS, Dierberg FE, Ogram A (2014) Syntrophs dominate sequences associated with the mercury methylating gene hgcA in the water conservation areas of the Florida Everglades. Appl Environ Microbiol. doi:10.1128/AEM.01666-14

    Google Scholar 

  • Bancroft GT, Hoffman W, Sawicki RJ, Ogden JC (1992) The importance of the water conservation areas in the Everglades to the endangered wood stork (Mycteria americana). Conserv Biol 6:392–398

    Article  Google Scholar 

  • Bettoli PW, Maceina MJ, Noble RL, Betsill RK (1992) Piscivory in largemouth bass as a function of aquatic vegetation abundance. North Amer J Fish Manag 12:509–516

    Article  Google Scholar 

  • Bodaly RA, Rudd JWM, Fudge RJP, Kelly CA (1993) Mercury concentrations in fish related to size of remote Canadian shield lakes. Can J Fish Aquat Sci 50:980–987

    Article  CAS  Google Scholar 

  • Brandt SB, Kirsch J (1993) Spatially explicit models of striped bass growth potential in Chesapeake Bay. Trans Am Fish Soc 122:845–886

    Article  Google Scholar 

  • Cabana G, Rasmussen JB (1994) Modelling food chain structure and contaminant bioaccumulation using stable nitrogen isotopes. Nature 372:255–257

    Article  CAS  Google Scholar 

  • Carter MW, Shoup DE, Dettmers JM, Wahl DH (2010) Effects of turbidity and cover on prey selectivity of adult smallmouth bass. Trans Am Fish Soc 139:353–361

    Article  Google Scholar 

  • Chen M, Daroub SH, Lang TA, Diaz OA (2006) Specific conductance and ionic characteristics of farm canals in the Everglades Agricultural Area. J of Environ Qual 35:141–150

    Article  Google Scholar 

  • Chick JH, McIvor CC (1994) Patterns in the abundance and composition of fishes among beds of different macrophytes: Viewing a littoral zone as a landscape. Can J Fish Aquat Sci 51:2873–2882

    Article  Google Scholar 

  • Chick JH, Ruetz CR III, Trexler JC (2004) Spatial scale and abundance patterns of large fish communities in freshwater marshes of the Florida Everglades. Wetlands 24:652–664

    Article  Google Scholar 

  • Corrales J, Naja GM, Dziuba C, Rivero RG, Orem W (2011) Sulfate threshold target to control methylmercury levels in wetland ecosystems. Sci Tot Environ 409:2156–2162

    Article  CAS  Google Scholar 

  • Crump KL, Trudeau VL (2009) Critical review: mercury-induced reproductive impairment in fish. Environ Tox Chem 28:895–907

    Article  CAS  Google Scholar 

  • Dibble ED, Harrel SL (1997) Largemouth bass diets in two aquatic plant communities. J Aquat Plant Manag 35:74–78

    Google Scholar 

  • Dierberg FE, DeBusk TA, Jerauld M, Gu B (2014) Appendix 3B-1: evaluation of factors influencing methylmercury accumulation in South Florida marshes. In: 2014 South Florida environmental report—volume I. South Florida Water Management District, West Palm Beach

  • Fink L (2003) Appendix 2B-1: The effect of dryout and burn on the Everglades mercury cycle. In: 2003 Everglades consolidated report. South Florida Water Management District, West Palm Beach

  • Florida Administrative Code (2008) Chapter 62-160 Quality Assurance. Tallahassee, FL

  • Gabriel MC, Howard N, Osborne TZ (2014) Fish mercury and surface water sulfate relationships in the Everglades Protection Area. Environ Manag 53:583–593. doi:10.1007/s00267-013-0224-4

    Article  Google Scholar 

  • Gilmour CC, Henry EA (1991) Mercury methylation in aquatic systems affected by acid deposition. Environ Pollut 71:131–169

    Article  CAS  Google Scholar 

  • Gilmour CC, Henry EA, Mitchell R (1992) Sulfate stimulation of mercury methylation in freshwater sediments. Environ Sci Technol 26:2281–2287

    Article  CAS  Google Scholar 

  • Gilmour CC, Riedel GS, Ederington MC, Bell JT, Benoit JM, Gill GA, Stordal MC (1998) Methylmercury concentrations and production rates across a trophic gradient in the northern Everglades. Biogeochem 40(2/3):327–345

    Article  CAS  Google Scholar 

  • Gilmour CC, Podar M, Bullock AL, Graham AM, Brown SD, Somenahally AC, Johs A, Hurt RA Jr, Baily KL, Elias DA (2013) Mercury methylation by novel microorganisms from new environments. Environ Sci Technol 47:11810–11820

    Article  CAS  Google Scholar 

  • Gu B, Howard N (2014) Attachment C: annual permit compliance monitoring report for mercury in the stas. In: Germain G (ed) 2014. Appendix 3-1: annual permit report for the Everglades stormwater treatment areas. 2014 South Florida Environmental Report—volume III, South Florida Water Management District, West Palm Beach

  • Guentzel JL, Landing WM, Gill GA, Pollman CD (1995) Atmospheric depositon of mercury in the Florida FAMS project (1992–1994). Water Air Soil Pollut 80:393–402

    Article  CAS  Google Scholar 

  • Guentzel JL, Landing WM, Gill GA, Pollman CD (2001) Process influencing rainfall deposition of mercury in the Florida. Environ Sci Technol 35:863–873

    Article  CAS  Google Scholar 

  • Gutknecht J (1981) Inorganic mercury (Hg2+) transport through lipid bilayer membranes. J Mem Biol 61:61–66

    Article  CAS  Google Scholar 

  • Gutreuter S, Childress WM (1990) Evaluation of condition indices for estimation of growth of largemouth bass and white crappie. N Amer J Fish Manag 10(4):434–441

    Article  Google Scholar 

  • Håkanson L (1980) The quantitative impact of pH, bioproduction and Hg-contamination on the Hg-content of fish (pike). Environ Pollut 1:285–304

    Article  Google Scholar 

  • Harwell MC, Surratt DD, Barone DM, Aumen NG (2008) Conductivity as a tracer of agricultural and urban runoff to delineate water quality impacts in the northern Everglades. Environ Monit Assess 147:445–462

    Article  CAS  Google Scholar 

  • Heck KL Jr, Crowder LB (1991) Habitat structure and predator-prey interactions in vegetated aquatic systems. In: Bell SS, McCoy SS, Mushinsky HR (eds) Habitat structure: the physical arrangement of objects in space. Chapman and Hall, New York, pp 281–299

    Chapter  Google Scholar 

  • Henson JC (1991) Quantitative description and development of a species-specific standard growth form for Largemouth Bass with the application to the relative weight index. Master’s thesis, Texas A&M University College Station, TX

  • Huckabee JW, Elwood JW, Hildebrand SG (1979) Accumulation of mercury in freshwater biota. In: Nriagu JO (ed) Biogeochemistry of mercury in the environment. Elsevier/North Holland Biomedial, New York, pp 227–302

    Google Scholar 

  • Hutchings JA (1993) Adaptive life histories affected by age-specific survival and growth rate. Ecology 74:673–684

    Article  Google Scholar 

  • Ireland PA (2010) Changes in native aquatic vegetation, associated fish assemblages, and food habits of largemouth bass (Micropterus salmoides) following the addition of triploid grass carp to manage hydrilla (Hydrilla verticillata) in lake Conroe, TX. Masters Thesis, Texas A & M. College Station, TX

  • Julian P (2013) Mercury hotspot identification in Water Conservation Area 3, Florida USA. Annu GIS 19:79–88

    Article  Google Scholar 

  • Julian II P, et al. (2015) Chapter 3B: mercury and sulfur environmental assessment for the Everglades. In: 2015 South Florida environmental report—volume I, South Florida Water Management District, West Palm Beach

  • Julian II P, Payne G, Xue SK (2013) Chapter 3A: Water quality in the everglades protection area. In: 2013 South Florida environmental report—volume I, South Florida Water Management District, West Palm Beach

  • Julian II P, Gu B, Frydenborg R, Lange T, Wright AL, McCray JM (2014) Chapter 3B: mercury and sulfur environmental assessment for the Everglades. In: 2014 South Florida environmental report—volume I, South Florida Water Management District, West Palm Beach

  • Kidd KA, Schindler DW, Muir DCG, Lockhart WL, Heslein RH (1995) High concentrations of toxaphene in fishes from a subartic lake. Science 269:240–242

    Article  CAS  Google Scholar 

  • Kvangarsnes K, Frantzen S, Julshamn K, Saethre LJ, Nedreaas K, Maage A (2012) Distribution of mercury in a gadoid fish species, tusk (Brosme brosme), and its implication for food safety. J Food Sci Eng 2:603–615

    CAS  Google Scholar 

  • Lange TR, Royals HE, Connor LL (1993) Influence of water chemistry on mercury concentration in largemouth bass from Florida lakes. Trans Am Fish Soci 122:74–84

    Article  CAS  Google Scholar 

  • Le Cren ED (1951) The length-weight relationship and seasonal cycle in gonad weight and condition in the perch (Perca fluviatillis). J Ani Ecol 20:201–219

    Article  Google Scholar 

  • Light SS, Dineen JW (1994) Water control in the everglades: a historical perspective. In: Davis S, Ogden J (eds) Everglades: the ecosystem and its restoration. St. Lucie Press, Delray Beach, pp 47–84

    Google Scholar 

  • Liu G, Cai Y, O’Driscoll N (2012) Environmental chemistry and toxicology of mercury. Wiley, Hoboken

    Google Scholar 

  • Loftus WF (2000) Accumulation and fate of mercury in an Everglades aquatic food web. Dissertation, Florida International University, Miami, FL

  • Lorenzoni M, Dorr AJM, Erra R, Giovionazzo G, Mearelli M, Selvi S (2002) Growth and reproduction of largemouth bass (Micropterus salmoides Lacepede, 1802) in Lake Trasimeno (Umbria, Italy). Fish Res 56:89–95

    Article  Google Scholar 

  • McCormick PV, Harvey JW, Crawford ES (2011) Influence of changing water sources and mineral chemistry on Everglades ecosystem. Crit Rev Environ Sci Technol 41(S1):28–63

    Article  CAS  Google Scholar 

  • McMichael Jr, RH (2000) Fisheries independent monitoring program operating procedure manual. Report No. IHR2000-05. Florida Fish and Wildlife Research Institute, Saint Petersburg, FL

  • Michelutti N, Blais JM, Mallory ML, Brash J, Thienpont J, Kimpe LE, Douglas MSV, Smol JP (2010) Trophic position influences the efficacy of seabirds as metal biovectors. Proc Natl Acad Sci 107:10543–10548

    Article  CAS  Google Scholar 

  • Miranda LE, Pugh LL (1997) Relationship between vegetation coverage and abundance, size, and diet of juvenile largemouth bass during winter. N Am J Fish Manag 17:601–610

    Article  Google Scholar 

  • Myers RL, Ewel JJ (1990) Ecosystems of Florida. University of Central Florida Press, Orlando

    Google Scholar 

  • Neumann RM, Murphy BR (1992) Seasonal relationships of relative weight to body composition in white crappie, Pomoxis annularis Rafineque. Aquac Fish Manag 23:243–251

    Google Scholar 

  • Ogden JC, Robertson WB Jr, Davis GE, Schmidt TW (1973) Pesticides, polychlorinated biphenols and heavy metals in upper food chain levels, Everglades national park and vicinity. National Park Service Everglades National Park, Homestead

    Google Scholar 

  • Olson MH (1996) Ontogenetic niche shift in largemouth bass: variability and consequences for first-year growth. Ecology 77:179–190

    Article  Google Scholar 

  • Orem W, Gilmour C, Axelrad D, Krabbenhoft D, Schedit D, Kalla P, McCormick P, Gabriel M, Aiken G (2011) Sulfur in the South Florida ecosystem: distribution, sources, biogeochemistry, impacts, and management for restoration. Crit Rev Environ Sci Technol 41(S1):249–288

    Article  CAS  Google Scholar 

  • Pickhardt OC, Stepnova M, Fisher NS (2006) Contrasting uptake routes and tissue distributions of inorganic and methylmercury in mosquitofish (Gambusia affinis) and redear sunfish (Lepomis microlophus). Environ Toxicol Chem 25(8):2132–2142

    Article  CAS  Google Scholar 

  • Rader RB, Richardson CJ (1992) The effects of nutrient enrichment on algae and macroinvertebrates in the Everglades: a Review. Wetlands 12:121–135

    Article  Google Scholar 

  • Ravichandran M (2004) Interactions between mercury and dissolved organic matter—a review. Chemosphere 55:319–331

    Article  CAS  Google Scholar 

  • Rawlik Jr PS, Kendall C, Bemis BE, Wankel SD (2002) A conceptual model for seasonal changes in foodwebs in the Everglades: implications for mercury bioaccumulation. Technical report, South Florida Water Management District, West Palm Beach

  • Rodgers DW, Beamish FWH (1983) Water quality modifies uptake of water borne methylmercury by rainbow trout, Salmo gairdneri. Can J Fish Aquat Sci 40:824–828

    Article  CAS  Google Scholar 

  • Rumbold DG, Niemczyk SL, Fink LE, Chandrasekhar T, Harkanson B, Laine A (2001) Mercury in eggs and feathers of great egrets (Ardea albus) from the Florida Everglades. Arch Environ Contam Toxicol 41:501–507

    Article  CAS  Google Scholar 

  • Sammons SM, Maceina MJ (2006) Changes in diet and food consumption of largemouth bass following large-scale hydrilla reduction in Lake Seminole, Georgia. Hydrobiologia 560(1):109–120

    Article  Google Scholar 

  • Shoup DE, Callahan SP, Wahl DH, Pierce CL (2007) Size-specific growth of bluegill, largemouth bass and channel catfish in relation to prey availability and limnological variables. J Fish Biol 70:21–34

    Article  Google Scholar 

  • Sklar F, Dreschel T (2013) Chapter 6: Everglades research and evaluation. In: 2013 South Florida environmental report—volume I, South Florida Water Management District, West Palm Beach

  • Skyllberg U (2008) Competition among thiols and inorganic sulfides and polysulfides for Hg and MeHg in wetlands soils and sediments under suboxic conditions: Illumination of controversies and implications for MeHg production. J Geophys Res 113:G00C03. doi:10.1029/2008JG000745

    Google Scholar 

  • Spry DJ, Wiener JD (1991) Metal bioavailability and toxicity to fish in low-alkalinity lakes: a Critical Review. Environ Pollut 71:243–304

    Article  CAS  Google Scholar 

  • Stumm W, Morgan JJ (1996) Aquatic chemistry: chemical equilibria and rates in natural waters, 3rd edn. Wiley, Hoboken

    Google Scholar 

  • Swanson HK, Johnston TA, Leggett WC, Bodaly RA, Doucett RR, Cunjak RA (2003) Trophic positions and mercury bioaccumulation in rainbow smelt (Osmerus mordax) and native forage fishes in northwestern Ontario lakes. Ecosyst 6:289–299

    Article  CAS  Google Scholar 

  • United States Environmental Protection Agency (1991) Methods for the determination of metals in environmental samples. EPA-600/4-191-010, Atlanta, GA, USA

  • Wege GJ, Andersen RO (1978) Relative weight (Wr): a new index of condition for largemouth bass. pp 79–91, In: Novinger GD, Dillard JG (eds) New approaches to the management of small impoundments. North Central Division, American Fisheries Society, Special Publication 5, Bethesda

  • Wiener JG (1987) Metal contamination of fish in low-pH lakes and potential implications for piscivorous wildlife. Transact N Am Wildlife Nat Res Conf 52:645–657

    Google Scholar 

  • Zheng S, Gu B, Zhou Q, Li Y (2013) Variation of mercury in the inflow and outflow of a constructed treatment wetland in south Florida, USA. Ecol Eng 61:419–425

    Article  Google Scholar 

Download references

Acknowledgments

We would like to thank Garth Redfield, Thomas Dreschel, Peter Rawlik, Brad Robbins, Meifang Zhou, and two anonymous reviewers for their review and input that ultimately improved the quality of this manuscript. Additionally we would like to acknowledge all of the current and past South Florida Water Management District and Florida Fish and Wildlife Conservation Commission staff involved in the collection and laboratory analysis of the data used in this manuscript. Without their hard work, dedication and ample supply of blood (to feed the mosquitoes) this work would not be possible.

Conflict of interest

The authors declare that they have no conflict of interest.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Paul Julian II.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Julian, P., Gu, B. Mercury accumulation in largemouth bass (Micropterus salmoides Lacépède) within marsh ecosystems of the Florida Everglades, USA. Ecotoxicology 24, 202–214 (2015). https://doi.org/10.1007/s10646-014-1373-9

Download citation

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10646-014-1373-9

Keywords

Navigation