Abstract
AbstractLow salinity can negatively affect reproduction in estuarine bivalves. The spatial and temporal extents of these effects are important to inform models of population dynamics, environmental risk assessments, restoration efforts, and predictions of climate change effects. A hypothesis of delayed gametogenesis for oysters at low salinity sites was tested relative to their higher salinity counterparts in downstream experimental cages. In 2018, the timing of gametogenesis and spawning was observed June–August for 2-year-old oysters from three distinct ancestries (native, hatchery, aquaculture), outplanted at age 1 month along the salinity gradient (3–30 psu) of a temperate estuary. A second season of data was collected in 2019 from a 3-year-old aquaculture line and mixed-age native adult oysters dredged and transplanted 1 year prior. Dermo was tested in 2019 and prevalence was 1.3% (n = 240). Gametogenesis and spawning were retarded for all ancestries at low salinity relative to higher salinity sites during July and August. The reverse pattern was found in June, with low salinity sites having more advanced gonad index than at a high salinity site. This difference in average gonad index was 2.65 vs 1.46, respectively, for the native line and 2.62 vs 2.08 for aquaculture. Low salinity seemed to not only induce earlier gametogenesis in June, but also extended the reproductive season relative to higher salinity sites. Among oyster ancestries, the aquaculture line stood out as having 30–48% lower gametogenic synchrony within sites, but only in 2018. Because the native oysters used in this study have been restricted to low salinity conditions for many generations, demonstration of their reproductive plasticity across salinities is notable and broadens the range of potential future restoration strategies.
Funder
New York State Water Resources Institute
Hudson River Foundation
College of Agriculture and Life Sciences Charitable Trust, Cornell University
Publisher
Springer Science and Business Media LLC
Subject
Ecology,Aquatic Science,Ecology, Evolution, Behavior and Systematics
Reference83 articles.
1. Able, K. 2005. A re-examination of fish estuarine dependence: Evidence for connectivity between estuarine and ocean habitats. Estuarine, Coastal and Shelf Science 64: 5–17. https://doi.org/10.1016/j.ecss.2005.02.002.
2. AKRF Inc., Hudson River Foundation, Billion Oyster Project, and University of New Hampshire. 2021. 2020 Post-Construction Oyster Monitoring Final Report. PMIS Document Control No. TA_NYSDEC_03527_RPT_ENV. https://www.hudsonriver.org/wp-content/uploads/2021/09/TZB-Final-Report.pdf. Accessed 01/03/23.
3. Andrews, J. D. 1988. Epizootiology of the disease caused by the oyster pathogen Perkinsus marinus and its effects on the oyster industry. American Fisheries Society Species Publication 18: 47–63.
4. Aranda, D.A., M.E. Díaz, F.L. Reynoso, T. Brulé, J. Montero, and E.B. Cárdenas. 2014. Reproductive strategies of the eastern oyster Crassostrea virginica (Gmelin 1791) in tropical lagoons of the Mexican Gulf of Mexico. Journal of Shellfish Research 33: 145–152. https://doi.org/10.2983/035.033.0114.
5. Arnold, T.W. 2010. Uninformative parameters and model selection using Akaike’s information criterion. The Journal of Wildlife Management 74: 1175–1178. https://doi.org/10.1111/j.1937-2817.2010.tb01236.x.
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