TY - JOUR
T1 - Burrowing fauna mediate alternative stable states in the redox cycling of salt marsh sediments
AU - van de Velde, Sebastiaan J.
AU - Hidalgo-Martinez, Silvia
AU - Callebaut, Ine
AU - Antler, Gilad
AU - James, Rebecca K.
AU - Leermakers, Martine
AU - Meysman, Filip J.R.
N1 - Funding Information:
The research leading to these results was financially supported by the Belgian American Educational Foundation (postdoctoral fellowship to SVDV) and the Research Foundation Flanders (PhD fellowship to SVDV). FJRM was financially supported by the European Research Council under the European Union's Seventh Framework Program (FP/2007-2013) through ERC Grant 306933, by the Research Foundation Flanders via FWO grant G031416N, and the Netherlands Organization for Scientific Research (VICI grant 016.VICI.170.072). GA acknowledges financial support by the Israel Science Foundation (grant No. 2361/19). The HR-ICP-MS instrument was financed by the HERCULES Foundation (Code: UABR/11/010). The authors would like to thank Jurian Brasser, Peter Van Breugel, Jan Sinke, Jan Peene, Yvonne van der Maas, Pieter Van Rijswijk of NIOZ Yerseke and David Verstraeten of the Vrije Universiteit Brussel for the analysis of the pore-water and sediment samples. Additionally, we would like to thank Kirsten Imhoff and Timothy F. Ferdelman from the Max Planck Institute for Marine Microbiology for the analysis of the elemental sulphur samples.
Funding Information:
The research leading to these results was financially supported by the Belgian American Educational Foundation (postdoctoral fellowship to SVDV) and the Research Foundation Flanders (PhD fellowship to SVDV). FJRM was financially supported by the European Research Council under the European Union’s Seventh Framework Program ( FP/2007-2013 ) through ERC Grant 306933 , by the Research Foundation Flanders via FWO grant G031416N , and the Netherlands Organization for Scientific Research (VICI grant 016.VICI.170.072 ). GA acknowledges financial support by the Israel Science Foundation (grant No. 2361/19). The HR-ICP-MS instrument was financed by the HERCULES Foundation (Code: UABR/11/010 ). The authors would like to thank Jurian Brasser, Peter Van Breugel, Jan Sinke, Jan Peene, Yvonne van der Maas, Pieter Van Rijswijk of NIOZ Yerseke and David Verstraeten of the Vrije Universiteit Brussel for the analysis of the pore-water and sediment samples. Additionally, we would like to thank Kirsten Imhoff and Timothy F. Ferdelman from the Max Planck Institute for Marine Microbiology for the analysis of the elemental sulphur samples.
Publisher Copyright:
© 2020 Elsevier Ltd
PY - 2020/5/1
Y1 - 2020/5/1
N2 - The East Anglian salt marsh system (UK) has recently generated intriguing data with respect to sediment biogeochemistry. Neighbouring ponds in these salt marshes show two distinct regimes of redox cycling: the sediments are either iron-rich and bioturbated, or they are sulphide-rich and unbioturbated. No conclusive explanation has yet been given for this remarkable spatial co-occurrence. Here, we quantify the geochemical cycling in both pond types, using pore-water analyses and solid-phase speciation. Our results demonstrate that differences in solid-phase carbon and iron inputs are likely small between pond types, and so these cannot act as the direct driver of the observed redox dichotomy. Instead, our results suggest that the presence of bioturbation plays a key role in the transition from sulphur-dominated to iron-dominated sediments. The presence of burrowing fauna in marine sediments stimulates the mineralisation of organic matter, increases the iron cycling and limits the build-up of free sulphide. Overall, we propose that the observed dichotomy in pond geochemistry is due to alternative stable states, which result from non-linear interactions in the sedimentary iron and sulphur cycles that are amplified by bioturbation. This way, small differences in solid phase input can result in very different regimes of redox cycling due to positive feedbacks. This non-linearity in the iron and sulphur cycling could be an inherent feature of marine sediments, and hence, alternative stable states could be present in other systems.
AB - The East Anglian salt marsh system (UK) has recently generated intriguing data with respect to sediment biogeochemistry. Neighbouring ponds in these salt marshes show two distinct regimes of redox cycling: the sediments are either iron-rich and bioturbated, or they are sulphide-rich and unbioturbated. No conclusive explanation has yet been given for this remarkable spatial co-occurrence. Here, we quantify the geochemical cycling in both pond types, using pore-water analyses and solid-phase speciation. Our results demonstrate that differences in solid-phase carbon and iron inputs are likely small between pond types, and so these cannot act as the direct driver of the observed redox dichotomy. Instead, our results suggest that the presence of bioturbation plays a key role in the transition from sulphur-dominated to iron-dominated sediments. The presence of burrowing fauna in marine sediments stimulates the mineralisation of organic matter, increases the iron cycling and limits the build-up of free sulphide. Overall, we propose that the observed dichotomy in pond geochemistry is due to alternative stable states, which result from non-linear interactions in the sedimentary iron and sulphur cycles that are amplified by bioturbation. This way, small differences in solid phase input can result in very different regimes of redox cycling due to positive feedbacks. This non-linearity in the iron and sulphur cycling could be an inherent feature of marine sediments, and hence, alternative stable states could be present in other systems.
KW - Alternative stable states
KW - Bioturbation
KW - Marine sediments
KW - Redox cycling
KW - Salt marshes
UR - http://www.scopus.com/inward/record.url?scp=85081244516&partnerID=8YFLogxK
U2 - 10.1016/j.gca.2020.02.021
DO - 10.1016/j.gca.2020.02.021
M3 - Article
AN - SCOPUS:85081244516
SN - 0016-7037
VL - 276
SP - 31
EP - 49
JO - Geochimica et Cosmochimica Acta
JF - Geochimica et Cosmochimica Acta
ER -