Skip to main content Accessibility help
×
Hostname: page-component-78c5997874-g7gxr Total loading time: 0 Render date: 2024-11-09T19:48:35.288Z Has data issue: false hasContentIssue false

6 - An overview of carbon and sulphur cycling in marine sediments

Published online by Cambridge University Press:  23 September 2009

T. D. Jickells
Affiliation:
University of East Anglia
J. E. Rae
Affiliation:
University of Reading
Get access

Summary

Introduction

In most marine-type sediments (including intertidal ones) organic carbon is the only reducing agent to enter a sediment column. The remainder of the sediment load arrives in its oxidised form, and, with the exception of straightforward compaction, early diagenesis (i.e. the process of change during burial) results directly or indirectly from the flow of electrons. The initial source of the electrons (organic matter) is sequentially oxidised in microbially mediated reactions, using a range of available oxidising agents, and results in some degree of vertical zonation in sediment chemistry (Richards et al., 1965; Froelich et al., 1979). This is because microbial communities outcompete each other for organic carbon (Stumm & Morgan, 1970; Claypool & Kaplan, 1974). However, the resolution of these sediment horizons is likely to be poor because:

  1. (a) although the most important substrate shared by each community is organic carbon, it has been suggested that different communities metabolise different fractions of it, each with a first order rate constant (Berner, 1977). This would produce overlapping or coexistence of zones, unless the competition between communities was for another shared substrate (e.g. nitrate).

  2. (b) the ‘dead cat in the mud’ effect (Coleman, 1985), where the substrates for microbial metabolism do not enter the system as disseminated and reactive particles to give a homogeneous reaction mixture, but rather as poorly sorted, highly concentrated sources of metabolites that may survive beyond zones where they would have been exhausted in a simple layered model. For solid substrates such as organic carbon, iron oxides and manganese oxyhydroxides, this may be an important control on their rate of supply to the reaction.

  3. […]

Type
Chapter
Information
Publisher: Cambridge University Press
Print publication year: 1997

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

Save book to Kindle

To save this book to your Kindle, first ensure [email protected] is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×