assessing ecosystem functional equivalence between
TRANSCRIPT
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Assessing Ecosystem Functional Equivalence between Constructed and Natural Oyster
Reefs
Kevin S. Dillon and Mark S. Peterson
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Increase marsh habitat & complexity Stabilize marsh edge Trophic mediators Metrics of restoration have been measured
relative to cultch, design, & depth Most studies focus on larger, subtidal
reefs Little attention to small, intertidal reefs
particularly in the Northern Gulf Coast
Why small, intertidal oyster reefs?
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Research Objectives Assess the ecological equivalency
of natural vs. constructed reefs Measure the trajectory of colonization and
ecological functions on natural vs. constructed oyster reefs over 2 years
Assess changes in faunal assemblages Quantify food-web dynamics using stable
isotope analysis – Restore the isotopes, restore the function
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Study Site Grand Bay National Estuarine Research Reserve
Retrograding delta Freshwater inputs small Microtidal
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Methods Natural reefs were
assessed pre-deployment Determine and quantify
faunal assemblage Quantify oyster density
Construct oyster reefs & designate natural reefs Deployed randomly assigned
sampling units, interspersed in constructed reefs
Construct reefs with 30-35% coverage
Establish upland and lowland stakes
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Methods
Artificial reef cultch deployed in August 2006
Natural and constructed reefs sampled every 6 months for 2 years
3 sample trays from each reef harvested
Samples washed through 500 µm sieve
ID & quantify oyster spat, seed, adults and other fauna
Samples were freeze dried, acid washed, rinsed, dried and ground to a fine powder for SI analysis.
Samples analyzed for δ13C and δ15N values with a Thermo Delta V Advantage stable isotope ratio mass spectrometer coupled to a Costech elemental analyzer
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RESULTS
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15008
Summary of Total Macrofauna Collected Over Two Years
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Stable Isotopes in Ecology Stable C and N isotopes can be traced through food webs with predictable fractionation and mixing at various trophic levels
13C show very little enrichment (~1 ‰) in tissues with trophic transfer and is useful in tracing C sources through the food web
15N shows an enrichment of 2-4‰ with each trophic transfer and can be used to determine an organisms trophic level Isotope ratios are expressed as parts per thousand differences from a standard material:
δX = [(Rsample / Rstandard) – 1] x 1000 where X is the stable isotope (13C, 15N), R is the corresponding ratio of heavy to light isotopes (13C/12C or 15N/14N)
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Primary Producers and Plankton 13C vs. 15N
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November 2006
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May 2007
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0
5
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15
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25
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35Sa
linity
Date
Salinity - Bayou Cumbest Grand Bay SWMP data
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December 2007
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May 2008
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BC CR NR Balanus sp. x Crassostrea virginica spat x x x Crassostrea virginica seedling x x Ischidium recurvum x Melita sp. x x Panopeus herbstii x Xanthid crabs x x Capitellidae x Eunicidae x
List of unbiqitous taxa used in the cluster analysis and SIMPROF tests by bayou pooled by reef type and Spring 2007 and 2008 periods.
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BC-Nat 2007 BC-Con 2007 BC-Nat 2008 BC-Nat 2008
CR-Nat 2007 CR-Con 2008 CR-Nat 2008 CR-Con 2007
NR-Nat 2007 NR-Con 2007 NR-Nat 2008 NR-Con 2008
SIMPROF test, p < 0.05
SIMPROF test, p < 0.05
SIMPROF test, p < 0.05
Cluster analysis similarity profiles 13C
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CONCLUSIONS Density of oyster spat and seed are greater in constructed reefs. Taxa richness is greater in all constructed reefs Increases over time Assemblages vary between subsystems Artificial constructed reefs at long term site were had similar community structure and stable isotope values after 15 months Reef trophic structure: Amphipods < Crabs/Mussels < Oysters/Polycheates < Shrimps < Barnacles < Large Polycheates and Fish (Gobies/Toadfish) Spatial and temporal variability in 13C (and 34S) values with salinity
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