Optimal hurricane overwash thickness for maximizing marsh resilience to sea level rise

The interplay between storms and sea level rise, and between ecology and sediment transport governs the behavior of rapidly evolving coastal ecosystems such as marshes and barrier islands. Sediment deposition during hurricanes is thought to increase the resilience of salt marshes to sea level rise by increasing soil elevation and vegetation productivity. We use mesocosms to simulate burial of Spartina alterniflora during hurricane‐induced overwash events of various thickness (0–60 cm), and find that adventitious root growth within the overwash sediment layer increases total biomass by up to 120%. In contrast to most previous work illustrating a simple positive relationship between burial depth and vegetation productivity, our work reveals an optimum burial depth (5–10 cm) beyond which burial leads to plant mortality. The optimum burial depth increases with flooding frequency, indicating that storm deposition ameliorates flooding stress, and that its impact on productivity will become more important under accelerated sea level rise. Our results suggest that frequent, low magnitude storm events associated with naturally migrating islands may increase the resilience of marshes to sea level rise, and in turn, slow island migration rates. Synthesis: We find that burial deeper than the optimum results in reduced growth or mortality of marsh vegetation, which suggests that future increases in overwash thickness associated with more intense storms and artificial heightening of dunes could lead to less resilient marshes.     

mRNA Differential Display in a Microbial Enrichment Culture: Simultaneous Identification of Three Cyclohexanone Monooxygenases from Three Species

mRNA differential display has been used to identify cyclohexanone oxidation genes in a mixed microbial community derived from a wastewater bioreactor. Thirteen DNA fragments randomly amplified from the total RNA of an enrichment subculture exposed to cyclohexanone corresponded to genes predicted to be involved in the degradation of cyclohexanone. Nine of these DNA fragments are part of genes encoding three distinct Baeyer-Villiger cyclohexanone monooxygenases from three different bacterial species present in the enrichment culture. In Arthrobacter sp. strain BP2 and Rhodococcus sp. strain Phi2, the monooxygenase is part of a gene cluster that includes all the genes required for the degradation of cyclohexanone, while in Rhodococcus sp. strain Phi1 the genes surrounding the monooxygenase are not predicted to be involved in this degradation pathway but rather seem to belong to a biosynthetic pathway. Furthermore, in the case of Arthrobacter strain BP2, three other genes flanking the monooxygenase were identified by differential display, demonstrating that the repeated sampling of bacterial operons shown earlier for a pure culture (D. M. Walters, R. Russ, H. Knackmuss, and P. E. Rouvière, Gene 273:305-315, 2001) is also possible for microbial communities. The activity of the three cyclohexanone monooxygenases was confirmed and characterized following their expression in Escherichia coli.