@article{PerkinsSantosRoseetal.2022,
  author    = {Perkins, Anita K. and Santos, Isaac R. and Rose, Andrew L. and Schulz, Kai G. and Grossart, Hans-Peter and Eyre, Bradley D. and Kelaher, Brendan P. and Oakes, Joanne M.},
  title     = {Production of dissolved carbon and alkalinity during macroalgal wrack degradation on beaches},
  series = {Biogeochemistry},
  volume    = {160},
  journal   = {Biogeochemistry},
  number    = {2},
  publisher = {Springer},
  address   = {Dordrecht},
  issn      = {0168-2563},
  doi       = {10.1007/s10533-022-00946-4},
  pages     = {159 -- 175},
  year      = {2022},
  abstract  = {Marine macroalgae are a key primary producer in coastal ecosystems, but are often overlooked in blue carbon inventories. Large quantities of macroalgal detritus deposit on beaches, but the fate of wrack carbon (C) is little understood. If most of the wrack carbon is respired back to CO2, there would be no net carbon sequestration. However, if most of the wrack carbon is converted to bicarbonate (alkalinity) or refractory DOC, wrack deposition would represent net carbon sequestration if at least part of the metabolic products (e.g., reduced Fe and S) are permanently removed (i.e., long-term burial) and the DOC is not remineralised. To investigate the release of macroalgal C via porewater and its potential to contribute to C sequestration (blue carbon), we monitored the degradation of Ecklonia radiata in flow-through mesocosms simulating tidal flushing on sandy beaches. Over 60 days, 81\% of added E. radiata organic matter (OM) decomposed. Per 1 mol of detritus C, the degradation produced 0.48 +/- 0.34 mol C of dissolved organic carbon (DOC) (59\%) and 0.25 +/- 0.07 mol C of dissolved inorganic carbon (DIC) (31\%) in porewater, and a small amount of CO2 (0.3 +/- 0.0 mol C; ca. 3\%) which was emitted to the atmosphere. A significant amount of carbonate alkalinity was found in porewater, equating to 33\% (0.27 +/- 0.05 mol C) of the total degraded C. The degradation occurred in two phases. In the first phase (days 0-3), 27\% of the OM degraded, releasing highly reactive DOC. In the second phase (days 4-60), the labile DOC was converted to DIC. The mechanisms underlying E. radiata degradation were sulphate reduction and ammonification. It is likely that the carbonate alkalinity was primarily produced through sulphate reduction. The formation of carbonate alkalinity and semi-labile or refractory DOC from beach wrack has the potential to play an overlooked role in coastal carbon cycling and contribute to marine carbon sequestration.},
  language  = {en}
}
@article{DraegerPlessenKieneletal.2019,
  author    = {Dr{\"a}ger, Nadine and Plessen, Birgit and Kienel, Ulrike and Siowinski, Michat and Ramisch, Arne and Tjallingii, Rik and Pinkerneil, Sylvia and Brauer, Achim},
  title     = {Hypolimnetic oxygen conditions influence varve preservation and delta C-13 of sediment organic matter in Lake Tiefer See, NE Germany},
  series = {Journal of paleolimnolog},
  volume    = {62},
  journal   = {Journal of paleolimnolog},
  number    = {2},
  publisher = {Springer},
  address   = {Dordrecht},
  issn      = {0921-2728},
  doi       = {10.1007/s10933-019-00084-2},
  pages     = {181 -- 194},
  year      = {2019},
  abstract  = {Stable carbon isotopes of sediment organic matter (delta C-13(OM)) are widely applied in paleoenvironmental studies. Interpretations of delta C-13(OM), however, remain challenging and factors that influence delta C-13(OM) may not apply across all lakes. Common explanations for stratigraphic shifts in delta C-13(OM) include changes in lake productivity or changes in inputs of allochthonous OM. We investigated the influence of different oxygen conditions (oxic versus anoxic) on the delta C-13(OM) values in the sediments of Lake Tiefer See. We analysed (1) a long sediment core from the deepest part of the lake, (2) two short, sediment-water interface cores from shallower water depths, and (3) OM in the water column, i.e. from sediment traps. Fresh OM throughout the entire water column showed a relatively constant delta C-13(OM) value of approximately -30.5 parts per thousand. Similar values, about -31 parts per thousand, were obtained for well-varved sediments in both the long and short, sediment-water interface cores. In contrast, delta C-13(OM) values from non-varved sediments in all cores were significantly less negative (-29 parts per thousand). The delta C-13(OM) values in the sediment-water interface cores from different water depths differ for sediments of the same age, if oxygen conditions at the time of deposition were different at these sites, as suggested by the state of varve preservation. Sediments deposited from AD 1924 to 1980 at 62m water depth are varved and exhibit delta C-13(OM) values around -31 parts per thousand, whereas sediments of the same age in the core from 35m water depth are not varved and show less negative delta C-13(OM) values of about -29 parts per thousand. The relation between varve occurrence and delta C-13(OM) values suggests that delta C-13(OM) is associated with oxygen conditions because varve preservation depends on hypolimnetic anoxia. A mechanism that likely influences delta C-13(OM) is selective degradation of OM under oxic conditions, such that organic components with more negative delta C-13(OM) are preferably decomposed, leading to less negative delta C-13(OM) values in the remaining, undegraded OM pool. Greater decomposition of OM in non-varved sediments is supported by lower TOC concentrations in these deposits (similar to 5\%) compared to well-varved sediments (similar to 15\%). Even in lakes that display small variations in productivity and terrestrial OM input through time, large spatial and temporal differences in hypolimnetic oxygen concentrations may be an important factor controlling sediment delta C-13(OM).},
  language  = {en}
}