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The effects of boat propeller scarring intensity on nekton abundance in subtropical seagrass meadows

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Abstract

Seagrasses play a critical role in the function and structure of coastal ecosystems, and they are an important habitat for a variety of marine organisms. Damage to seagrass beds caused by boat propeller scarring is significant in many areas. This study was designed to assess the impact of varying scarring intensities on nekton density. We selected ten replicate (10 m×25 m quadrats) sites representing four distinct scarring intensities: reference (0%), low (5% or less), moderate (5–15%), and severe (>15%). Sites were sampled in 2003–2004 for nekton during four seasons (summer, fall, winter, and spring) using epibenthic sleds. There were eight taxa numerically dominant in all seasons and an additional four seasonally dominant species. We were unable to detect a significant effect of propeller scarring on nekton density at any scarring level. Additionally, regression analysis indicated no relationship between scarring intensity and nekton density. These results suggest that propeller scarring intensities of up to ca. 27% may not impact nekton densities. However, seagrass loss, higher scarring intensity, and scale may play a critical role in determining the impact of propeller scarring on nekton.

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References

  • Attrill MJ, Strong JA, Rowden AA (2000) Are macroinvertebrate communities influenced by seagrass structural complexity? Ecography 23:114–121

    Article  Google Scholar 

  • Beck MW, Heck KL, Able KW, Childers DL, Eggleston DB, Gillanders BM, Halpern B, Hays CG, Hoshino K, Minello TJ, Orth RJ, Sheridan PF, Weinstein MP (2001) The identification, conservation, and management of estuarine and marine nurseries for fish and invertebrates. BioScience 5:633–641

    Article  Google Scholar 

  • Bell SS, Hall MO, Soffian S, Madley K (2002) Assessing the impact of boat propeller scars on fish and shrimp utilizing seagrass beds. Ecol Appl 12:206–217

    Article  Google Scholar 

  • Britton JC, Morton B (1997) Shore ecology of the Gulf of Mexico, 3rd edn. University of Texas Press, Austin

    Google Scholar 

  • Castellanos DL, Rozas LP (2001) Nekton use of submerged aquatic vegetation, marsh, and shallow unvegetated bottom in the Atchafalaya River Delta, a Louisiana tidal freshwater ecosystem. Estuaries 24:184–197

    Article  Google Scholar 

  • Dawes CJ, Andorfer J, Rose C, Uranowski C, Ehringer N (1997) Regrowth of the seagrass Thalassia testudinum into propeller scars. Aquat Bot 59:139–155

    Article  Google Scholar 

  • Doak DF, Marino PC, Kareiva PM (1992) Spatial scale mediates the influence of habitat fragmentation on dispersal success: implications for conservation. Theor Popul Biol 41:315–336

    Article  Google Scholar 

  • Dunton KH, Schonberg SS (2002) Assessment of propeller scarring in seagrass beds of the south Texas coast. J Coast Res 37:100–110

    Google Scholar 

  • Eggleston DB, Elis WE, Etherington LL, Dahlgren CP, Posey MH (1999) Organism responses to habitat fragmentation and diversity: habitat colonization by estuarine macrofauna. J Exp Mar Biol Ecol 236:107–132

    Article  Google Scholar 

  • Eleuterius LN (1987) Seagrass ecology along the coasts of Alabama, Louisiana, and Mississippi. In: Durako MJ, Phillips RC, Lewis RR (eds) Proceedings of the symposium on subtropical–tropical seagrasses of the Southeastern United States. Florida Marine Research Publication No. 42. Florida Department of Natural Resources, St. Petersburg

  • Fahrig L, Merriam G (1994) Conservation of fragmented populations. Conserv Biol 8:50–59

    Article  Google Scholar 

  • Fonseca MS, Bell SS (1998) Influence of physical setting on seagrass landscapes near Beaufort, North Carolina, USA. Mar Ecol Prog Ser 171:109–121

    Article  Google Scholar 

  • Haila Y (2002) A conceptual genealogy of fragmentation research: from island biogeography to landscape ecology. Ecol Appl 12:321–334

    Google Scholar 

  • Heck KL, Thoman TA (1981) Experiments on predator–prey interactions in vegetated aquatic habitats. J Exp Mar Biol Ecol 53:125–134

    Article  Google Scholar 

  • Heck KL, Thoman TA (1984) The nursery role of seagrass meadows in the upper and lower reaches of the Chesapeake Bay. Estuaries 7:70–92

    Article  Google Scholar 

  • Heck KL, Coen LD, Morgan SG (2001) Pre- and post-settlement factors as determinants of juvenile blue crab Callinectes sapidus abundance: results from the north-central Gulf of Mexico. Mar Ecol Prog Ser 222:163–176

    Article  Google Scholar 

  • Heck KL, Hays G, Orth RJ (2003) Critical evaluation of the nursery role hypothesis for seagrass meadows. Mar Ecol Prog Ser 253:123–136

    Article  Google Scholar 

  • Hemminga MA, Duarte CM (2000) Seagrass ecology. Cambridge University Press, Cambridge

    Book  Google Scholar 

  • Holt SA, Kitting CL, Arnold CR (1983) Distribution of young red drums among different sea-grass meadows. Trans Am Fish Soc 112:267–271

    Article  Google Scholar 

  • Hovel KA, Lipcius RN (2002) Effects of seagrass habitat fragmentation on juvenile blue crab survival and abundance. J Exp Mar Biol Ecol 271:75–98

    Article  Google Scholar 

  • Levin P, Petrik R, Malone J (1997) Interactive effects of habitat selection, food supply and predation on recruitment of an estuarine fish. Oecologia 112(1):55–63

    Article  CAS  Google Scholar 

  • Lipton DW, Wellman KF, Shiefer IC, Weiher RF (1995) Economic valuation of natural resources—a handbook for coastal resource policymakers. NOAA Coastal Ocean Program Decision Analysis Series No. 5. NOAA Coastal Ocean Office, Silver Spring

  • McGarigal K, Cushman SA (2002) Comparative evaluation of experimental approaches to the study of habitat fragmentation effects. Ecol Appl 12(2):335–345

    Article  Google Scholar 

  • Minello TJ (1999) Nekton densities in shallow estuarine habitats of Texas and Louisiana and the identification of essential fish habitat. In: Benaka LR (eds) Fish habitat: essential fish habitat, and rehabilitation. American Fisheries Society, Bethesda

    Google Scholar 

  • Minello TJ, Webb JW (1997) Use of natural and created Spartina alterniflora salt marshes by fishery species and other aquatic fauna in Galveston Bay, Texas, USA. Mar Ecol Prog Ser 151(1–3):165–179

    Article  Google Scholar 

  • Onuf CP (1994) Seagrasses, dredging and light in Laguna Madre, Texas, U.S.A. Est Coast Shelf Sci 39:75–91

    Article  Google Scholar 

  • Orth RJ, Heck KL, Van Montfrans JV (1984) Faunal communities in seagrass beds: a review of the influence of plant structure and prey characteristics on predator–prey relationships. Estuaries 7:339–350

    Article  Google Scholar 

  • Quammen ML, Onuf CP (1993) Laguna Madre—seagrass changes continue decades after salinity reduction. Estuaries 16:302–310

    Article  Google Scholar 

  • Robbins BD, Bell SS (1994) Seagrass landscapes: a terrestrial approach to the marine subtidal environment. Trends Ecol Evol 9:301–304

    Article  CAS  Google Scholar 

  • Rooker JR, Holt GJ, Holt SA (1998) Vulnerability of newly settled red drum (Sciaenops ocellatus) to predatory fish: is early-life survival enhanced by seagrass meadows. Mar Biol 131:145–151

    Article  Google Scholar 

  • Rozas LP, Minello TJ (1998) Nekton use of salt marsh, seagrass, and nonvegetated habitats in a south Texas (USA) estuary. Bull Mar Sci 63:481–501

    Google Scholar 

  • Rozas LP, Odum WE (1988) Occupation of submerged aquatic vegetation by fishes: testing the roles of food and refuge. Oecologia 77:101–106

    Article  Google Scholar 

  • Sargent FJ, Leary TJ, Crewz D, Jruer CR (1995) Scarring of Florida’s seagrasses: assessment and management options. Technical Report TR-1. Florida Marine Research Institute, St. Petersburg

  • Saunders DA, Hobbs RJ, Margules CR (1991) Biological consequences of ecosystem fragmentation: a review. Conserv Biol 5:18–32

    Article  Google Scholar 

  • SCPT (Seagrass Conservation Plan for Texas) (1999) Texas Parks and Wildlife, Austin

  • Short FT, Burdick DM, Kaldy JE (1995) Mesocosm experiments quantify the effects of eutrophication on eelgrass, Zostera marina. Limnol Oceanogr 40:740–749

    Article  Google Scholar 

  • Short FT, Wyllie-Echeverria S (1996) Natural and human induced disturbance of seagrasses. Environ Conserv 23:12

    Article  Google Scholar 

  • Stunz GW, Minello TJ (2001) Habitat-related predation on juvenile wild-caught and hatchery-reared red drum Sciaenops ocellatus (Linnaeus). J Exp Mar Biol Ecol 260:13–25

    Article  Google Scholar 

  • Stunz GW, Minello TJ, Levin PS (2002a) A comparison of early juvenile red drum densities among various habitat types in Galveston Bay, Texas. Estuaries 25:76–85

    Article  Google Scholar 

  • Stunz GW, Minello TJ, Levin PS (2002b) Growth of newly settled red drum Sciaenops ocellatus in different estuarine habitat types. Mar Ecol Prog Ser 238:227–236

    Article  Google Scholar 

  • Summerson HC, Peterson CH (1984) Role of predation in organizing benthic communities of a temperate-reef zone seagrass bed. Mar Ecol Prog Ser 15:63–77

    Article  Google Scholar 

  • Tomasko DA, Lapointe BE (1991) Productivity and biomass of Thalassia testudinum as related to water column availability and epiphyte levels: field observations and experimental studies. Mar Ecol Prog Ser 75:9–17

    Article  Google Scholar 

  • Uhrin AV, Holmquist JG (2003) Effects of propeller scarring on macrofaunal use of the seagrass Thalassia testudinum. Mar Ecol Prog Ser 250:61–70

    Article  Google Scholar 

  • Zieman JC (1976) The ecological effects of physical damage from motor boats on turtle grass beds in southern Florida. Aquat Bot 2:127–139

    Article  Google Scholar 

  • Zimmerman RJ, Minello TJ (1984) Densities of Penaeus aztecus, Penaeus setiferus, and other natant macrofauna in a Texas salt marsh. Estuaries 7:421–433

    Article  Google Scholar 

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Acknowledgements

We would like to thank the Members of the Fisheries Ecology Lab at Texas A&M University-Corpus Christi for their help on this project. Special thanks to Brooke Stanford, Ryan Fikes, Megan Reese, Amanda Bushon, and Annette Cardona for their hours of assistance in the field and laboratory, and to Steve Moore for producing Fig. 1. We gratefully acknowledge the comments and input by Chris Onuf. We would like to thank Ken Dunton of UTMSI and Richard Watson for flights over the study area. We would also like to thank anonymous reviewers for comments that greatly improved the earlier drafts of the manuscript.

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Correspondence to Gregory W. Stunz.

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Communicated by P.W. Sammarco, Chauvin

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Burfeind, D.D., Stunz, G.W. The effects of boat propeller scarring intensity on nekton abundance in subtropical seagrass meadows. Marine Biology 148, 953–962 (2006). https://doi.org/10.1007/s00227-005-0136-9

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  • DOI: https://doi.org/10.1007/s00227-005-0136-9

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