Identification of storm surge events over the German Bight from atmospheric reanalysis and climate model data

A new procedure for the identification of storm surge situations for the German Bight is developed and applied to reanalysis and global climate model data. This method is based on the empirical approach for estimating storm surge heights using information about wind speed and wind direction. Here, we hypothesize that storm surge events are caused by high wind speeds from north- westerly direction in combination with a large-scale wind storm event affecting the North Sea region. The method is calibrated for ERA-40 data, using the data from the storm surge atlas for Cuxhaven. It is shown that using information of both wind speed and direction as well as large-scale wind storm events improves the identification of storm surge events. To estimate possible future changes of potential storm surge events, we apply the new identification approach to an ensemble of three transient climate change simulations performed with the ECHAM5/MPIOM model under A1B greenhouse gas scenario forcing. We find an increase in the total number of potential storm surge events of about 12 % [(2001–2100)–(1901–2000)], mainly based on changes of moderate events. Yearly numbers of storm surge relevant events show high interannual and decadal variability and only one of three simulations shows a statistical significant increase in the yearly number of potential storm surge events between 1900 and 2100. However, no changes in the maximum intensity and duration of all potential events is determined. Extreme value statistic analysis confirms no frequency change of the most severe events

A Thermophilic Ionic Liquid-Tolerant Cellulase Cocktail for the Production of Cellulosic Biofuels

Generation of biofuels from sugars in lignocellulosic biomass is a promising alternative to liquid fossil fuels, but efficient and inexpensive bioprocessing configurations must be developed to make this technology commercially viable. One of the major barriers to commercialization is the recalcitrance of plant cell wall polysaccharides to enzymatic hydrolysis. Biomass pretreatment with ionic liquids (ILs) enables efficient saccharification of biomass, but residual ILs inhibit both saccharification and microbial fuel production, requiring extensive washing after IL pretreatment. Pretreatment itself can also produce biomass-derived inhibitory compounds that reduce microbial fuel production. Therefore, there are multiple points in the process from biomass to biofuel production that must be interrogated and optimized to maximize fuel production. Here, we report the development of an IL-tolerant cellulase cocktail by combining thermophilic bacterial glycoside hydrolases produced by a mixed consortia with recombinant glycoside hydrolases. This enzymatic cocktail saccharifies IL-pretreated biomass at higher temperatures and in the presence of much higher IL concentrations than commercial fungal cocktails. Sugars obtained from saccharification of IL-pretreated switchgrass using this cocktail can be converted into biodiesel (fatty acid ethyl-esters or FAEEs) by a metabolically engineered strain of E. coli. During these studies, we found that this biodiesel-producing E. coli strain was sensitive to ILs and inhibitors released by saccharification. This cocktail will enable the development of novel biomass to biofuel bioprocessing configurations that may overcome some of the barriers to production of inexpensive cellulosic biofuels

Some Mercuration Reactions of Substituted Pyrroles

Mercuration of N-unsubstituted pyrroles with mercury(II) acetate results in immediate precipitation of the N-mercurated derivative, which is insoluble in virtually all organic solvents. If the pyrrole N atom is protected (e.g. with Me, CH2OCH2Ph, or CO2t-Bu) then mercuration takes place efficiently at unsubstituted pyrrole carbons. Subsequent palladium/olefin (Heck-type) reactions afford the corresponding pyrrole acrylate when, for example, the olefin is methyl acrylate; deprotection (when the N-substituent is CH2OCH2Ph or CO2t-Bu) then affords the required carbon-substituted pyrrole. Attempts to deprotect the N-methylpyrroles were unsuccessful. © 1989, American Chemical Society. All rights reserved