Seagrasses have received considerable attention over the past 2 decades because of the multiple ecological roles they play in estuarine and coastal ecosystems and concerns over worldwide losses of seagrass habitat due to direct and indirect human impacts. Restoration and conservation efforts are underway in some areas of the world, but progress may be limited by the paucity of information on the role of seeds in bed dynamics. Although flowering occurs in most of the 58 seagrass species, seed germination data exist for only 19 of the 42 species that have some period of dormancy, with only 93 published references to field and/or laboratory studies. This review addresses critical issues in conservation and restoration of seagrasses involving seed dormancy (e.g. environmental vs physiological), existence and type of seed bank (transient or persistent), and factors influencing seed germination (e.g. salinity, temperature, light). Results of many earlier published studies relating seed germination to various environmental factors may need re-examination given more recent published data which show a confounding influence of oxygen level on the germination process. We highlight the importance of conducting ecologically meaningful germination studies, including germination experiments conducted in sediments. We also identify questions for future research that may figure prominently in landscape level questions regarding protected marine or estuarine reserves, habitat fragmentation, and restoration.
We examined responses of water-column conditions, sediment-water fluxes, ecosystem metabolism, and nutrient export in the Back River estuary during the past three decades following multiple phases of nutrient load reductions from a large wastewater treatment plant. Total nitrogen (TN) loads from the treatment plant declined from 7000 kg N d À1 in the mid-1980s to 1500 kg N d À1 following the implementation of enhanced nutrient removal in late 2017. Total phosphorus (TP) loads declined by ~90% from peaks in the mid-1980s-1990s and have been stable ever since. In response, TN and TP concentrations measured since 1985 show declines that generally mirror that of loads from the treatment plant, and box model computations suggest significant reductions in nutrient export to adjacent Chesapeake Bay. As a consequence, water-column chlorophyll a (Chl a) concentrations have declined modestly over the record, despite inter-annual variability. This reduction in Chl a coincided with a reduced frequency of nitrogen and phosphorus concentrations that would saturate phytoplankton growth, as well as reductions in ecosystem gross primary production and respiration derived from high-frequency oxygen time-series. Sediment-water fluxes of dissolved nitrogen, phosphorus, and oxygen, as well as associated sediment concentrations of nitrogen, phosphorus, and carbon also declined over the record. These temporal patterns were reproduced in a 35-yr model simulation that suggests a relatively rapid response to reduced organic matter deposition changes. Finally, the recycling of ammonium for a given TN load declined substantially, consistent with high observed rates of denitrification, indicating that well-mixed estuaries can recover relatively rapidly in response to nutrient remediation.
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