TY - JOUR A1 - Radosavljevic, Boris A1 - Lantuit, Hugues A1 - Knoblauch, Christian A1 - Couture, Nicole A1 - Herzschuh, Ulrike A1 - Fritz, Michael T1 - Arctic nearshore sediment dynamics - an example from Herschel Island - Qikiqtaruk, Canada JF - Journal of marine science and engineering N2 - Increasing arctic coastal erosion rates imply a greater release of sediments and organic matter into the coastal zone. With 213 sediment samples taken around Herschel Island-Qikiqtaruk, Canadian Beaufort Sea, we aimed to gain new insights on sediment dynamics and geochemical properties of a shallow arctic nearshore zone. Spatial characteristics of nearshore sediment texture (moderately to poorly sorted silt) are dictated by hydrodynamic processes, but ice-related processes also play a role. We determined organic matter (OM) distribution and inferred the origin and quality of organic carbon by C/N ratios and stable carbon isotopes delta C-13. The carbon content was higher offshore and in sheltered areas (mean: 1.0 wt.%., S.D.: 0.9) and the C/N ratios also showed a similar spatial pattern (mean: 11.1, S.D.: 3.1), while the delta C-13 (mean: -26.4 parts per thousand VPDB, S.D.: 0.4) distribution was more complex. We compared the geochemical parameters of our study with terrestrial and marine samples from other studies using a bootstrap approach. Sediments of the current study contained 6.5 times and 1.8 times less total organic carbon than undisturbed and disturbed terrestrial sediments, respectively. Therefore, degradation of OM and separation of carbon pools take place on land and continue in the nearshore zone, where OM is leached, mineralized, or transported beyond the study area. KW - permafrost KW - Arctic Ocean KW - stable carbon isotopes KW - nitrogen KW - sediment KW - chemistry KW - sediment dynamics KW - Beaufort Sea KW - grain size Y1 - 2022 U6 - https://doi.org/10.3390/jmse10111589 SN - 2077-1312 VL - 10 IS - 11 PB - MDPI CY - Basel ER - TY - JOUR A1 - Mai-Linde, Yasemin A1 - Linker, Torsten T1 - Radical clock probes to determine carbohydrate radical stabilities JF - Organic letters N2 - Carbohydrate radical stabilities in the 1- and 2-position have been determined by a radical clock approach, starting from cyclopropanated sugars with xanthates as precursors. Various hexoses and pentoses afforded 1-deoxy sugars as main products, indicating that anomeric radicals are more stable than radicals in the 2-position. An additional influence of the configurations on radical stabilities has been observed. Our results should be interesting for the understanding of 1,2-radical rearrangements in carbohydrate chemistry and offer an easy access to deoxy-vinyl sugars. KW - stereoselective-synthesis KW - convenient synthesis KW - chemistry KW - cyclopropanation KW - mechanism KW - glycals KW - beta-(acyloxy)alkylrear KW - rangement KW - sugars Y1 - 2020 U6 - https://doi.org/10.1021/acs.orglett.0c00111 SN - 1523-7060 SN - 1523-7052 VL - 22 IS - 4 SP - 1525 EP - 1529 PB - American Chemical Society CY - Washington ER - TY - JOUR A1 - Grewe, Volker A1 - Brinkop, Sabine A1 - Joeckel, Patrick A1 - Shin, Seoleun A1 - Reich, Sebastian A1 - Yserentant, Harry T1 - On the theory of mass conserving transformations for Lagrangian methods in 3D atmosphere-chemistry models JF - Meteorologische Zeitschrift KW - Lagrangian modelling KW - chemistry KW - transformations Y1 - 2014 U6 - https://doi.org/10.1127/0941-2948/2014/0552 SN - 0941-2948 SN - 1610-1227 VL - 23 IS - 4 SP - 441 EP - 447 PB - Schweizerbart CY - Stuttgart ER -