Calcite dissolution driven by benthic mineralization in the deep-sea: in situ measurements of Ca 2+ , pH, pCO 2 and O 2

Wenzhöfer, Frank; Adler, M.; Kohls, Oliver; Hensen, Christian; Strotmann, B.; Boehme, Susan E.; Schulz, Horst D

doi:10.1016/s0016-7037(01)00620-2

Cited by 92 publications

(44 citation statements)

References 47 publications

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“…The software has been described in great detail elsewhere (e.g. Adler et al, 2000Adler et al, , 2001Wenzhöfer et al, 2001;Pfeifer et al, 2002). Notably, CoTReM has already been successfully applied to model transport processes and geochemical reactions at two mud volcanoes of the Eastern Mediterranean (Haese et al, 2003(Haese et al, , 2006.…”

Section: Geochemical Modeling With "Cotrem"mentioning

confidence: 99%

Interaction between hydrocarbon seepage, chemosynthetic communities, and bottom water redox at cold seeps of the Makran accretionary prism: insights from habitat-specific pore water sampling and modeling

et al. 2012

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Abstract. The interaction between fluid seepage, bottom water redox, and chemosynthetic communities was studied at cold seeps across one of the world's largest oxygen minimum zones (OMZ) located at the Makran convergent continental margin. Push cores were obtained from seeps within and below the core-OMZ with a remotely operated vehicle. Extracted sediment pore water was analyzed for sulfide and sulfate concentrations. Depending on oxygen availability in the bottom water, seeps were either colonized by microbial mats or by mats and macrofauna. The latter, including ampharetid polychaetes and vesicomyid clams, occurred in distinct benthic habitats, which were arranged in a concentric fashion around gas orifices. At most sites colonized by microbial mats, hydrogen sulfide was exported into the bottom water. Where macrofauna was widely abundant, hydrogen sulfide was retained within the sediment.Numerical modeling of pore water profiles was performed in order to assess rates of fluid advection and bioirrigation. While the magnitude of upward fluid flow decreased from 11 cm yr −1 to <1 cm yr −1 and the sulfate/methane transition (SMT) deepened with increasing distance from the central gas orifice, the fluxes of sulfate into the SMT did not significantly differ (6.6-9.3 mol m −2 yr −1 ). Depth-integrated rates of bioirrigation increased from 120 cm yr −1 in the central habitat, characterized by microbial mats and sparse macrofauna, to 297 cm yr −1 in the habitat of large and few small vesicomyid clams. These results reveal that chemosynthetic macrofauna inhabiting the outer seep habitats below the core-OMZ efficiently bioirrigate and thus transport sulfate down into the upper 10 to 15 cm of the sediment. In this way the animals deal with the lower upward flux of methane in outer habitats by stimulating rates of anaerobic oxidation of methane (AOM) with sulfate high enough to provide hydrogen sulfide for chemosynthesis. Through bioirrigation, macrofauna engineer their geochemical environment and fuel upward sulfide flux via AOM. Furthermore, due to the introduction of oxygenated bottom water into the sediment via bioirrigation, the depth of the sulfide sink gradually deepens towards outer habitats. We therefore suggest thatin addition to the oxygen levels in the water column, which determine whether macrofaunal communities can develop or not -it is the depth of the SMT and thus of sulfide production that determines which chemosynthetic communities are able to exploit the sulfide at depth. We hypothesize that large vesicomyid clams, by efficiently expanding the sulfate zone down into the sediment, could cut off smaller or less mobile organisms, as e.g. small clams and sulfur bacteria, from the sulfide source.

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Section: Geochemical Modeling With "Cotrem"mentioning

confidence: 99%

Interaction between hydrocarbon seepage, chemosynthetic communities, and bottom water redox at cold seeps of the Makran accretionary prism: insights from habitat-specific pore water sampling and modeling

et al. 2012

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“…A box volume is assigned to each node according to simple geometrical calculations, and the flux itself is approximated by finite differences. The model has been thoroughly tested and verified in a number of studies Wenzhöfer et al, 2001;Pfeifer et al, 2002;Hensen et al, 2003). The conceptual model consists of the oxidation of OM in welloxigenated milieus according to Froelich et al (1979) OM+138O 2 → 106CO 2 +16HNO 3 +122H 2 O+H 3 PO 4 (2) with OM having a Redfield composition of 106:16:1 (C:N:P) and silica dissolution…”

Section: Model Description and Setupmentioning

confidence: 99%

Microbial mediation of benthic biogenic silica dissolution

Holstein

Hensen

2009

Geo-Mar Lett

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Pore water profiles from 24 stations in the South Atlantic (located in the Guinea, Angola, Cape, Guyana, and Argentine basins) show good correlations of oxygen and silicon, suggesting microbially mediated dissolution of biogenic silica. We used simple analytical transport and reaction models to show the tight coupling of the reconstructed process kinetics of aerobic respiration and silicon regeneration. A generic transport and reaction model successfully reproduced the majority of Si pore water profiles from aerobic respiration rates, confirming that the dissolution of biogenic silica (BSi) occurs proportionally to O 2 consumption. Possibly limited to well-oxygenated sediments poor in BSi, benthic Si fluxes can be inferred from O 2 uptake with satisfactory accuracy. Compared to aerobic respiration kinetics, the solubility of BSi emerged as a less influential parameter for silicon regeneration. Understanding the role of bacteria for silicon regeneration requires further investigations, some of which are outlined. The proposed aerobic respiration control of benthic silicon cycling is suitable for benthic-pelagic models. The empirical relation of BSi dissolution to aerobic respiration can be used for regionalization assessments and estimates of the silicon budget to increase the understanding of global primary and export production patterns.

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“…For example, nutrients produced during the re-mineralization of organic matter at the deep seafloor are ultimately used by phytoplankton to produce organic matter that fuels secondary production. At the same time, organic-matter degradation and re-mineralisation contribute to carbon biogeochemical cycling in the ocean, and help to buffer the ocean against pH changes and the effects of ocean acidification Wenzhöfer et al, 2001;Cerrano et al, 2013). The health and sustainable functioning of the planet are therefore highly dependent on the deep sea (defined here as > 200 m), which accounts for more than 95% of the volume of the Earth's oceans.…”

Section: Introductionmentioning

confidence: 99%

Major impacts of climate change on deep-sea benthic ecosystems

Sweetman

Thurber

Smith

et al. 2017

Elementa: Science of the Anthropocene

282

297

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The deep sea encompasses the largest ecosystems on Earth. Although poorly known, deep seafloor ecosystems provide services that are vitally important to the entire ocean and biosphere. Rising atmospheric greenhouse gases are bringing about significant changes in the environmental properties of the ocean realm in terms of water column oxygenation, temperature, pH and food supply, with concomitant impacts on deep-sea ecosystems. Projections suggest that abyssal (3000-6000 m) ocean temperatures could increase by 1°C over the next 84 years, while abyssal seafloor habitats under areas of deep-water formation may experience reductions in water column oxygen concentrations by as much as 0.03 mL L -1 by 2100. Bathyal depths (200-3000 m) worldwide will undergo the most significant reductions in pH in all oceans by the year 2100 (0.29 to 0.37 pH units). O 2 concentrations will also decline in the bathyal NE Pacific and Southern Oceans, with losses up to 3.7% or more, especially at intermediate depths. Another important environmental parameter, the flux of particulate organic matter to the seafloor, is likely to decline significantly in most oceans, most notably in the abyssal and bathyal Indian Ocean where it is predicted to decrease by 40-55% by the end of the century. Unfortunately, how these major changes will affect deep-seafloor ecosystems is, in some cases, very poorly understood. In this paper, we provide a detailed overview of the impacts of these changing environmental parameters on deep-seafloor ecosystems that will most likely be seen by 2100 in continental margin, abyssal and polar settings. We also consider how these changes may combine with other anthropogenic stressors (e.g., fishing, mineral mining, oil and gas extraction) to further impact deep-seafloor ecosystems and discuss the possible societal implications.

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Calcite dissolution driven by benthic mineralization in the deep-sea: in situ measurements of Ca 2+ , pH, pCO 2 and O 2

Cited by 92 publications

References 47 publications

Interaction between hydrocarbon seepage, chemosynthetic communities, and bottom water redox at cold seeps of the Makran accretionary prism: insights from habitat-specific pore water sampling and modeling

Interaction between hydrocarbon seepage, chemosynthetic communities, and bottom water redox at cold seeps of the Makran accretionary prism: insights from habitat-specific pore water sampling and modeling

Microbial mediation of benthic biogenic silica dissolution

Major impacts of climate change on deep-sea benthic ecosystems

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