The influence of surface state and saturation state on the dissolution kinetics of biogenic aragonite in seawater
Clicks: 5
ID: 308722
1989
Article Quality & Performance Metrics
Overall Quality
Not rated
Combines reader engagement with the AI quality analysis. This
article has not been analysed, so there is no overall score —
reader engagement is measured and shown alongside.
Reader Engagement
Steady Performance
1.2
/100
5 views
1 readers
AI Quality Assessment
Not analyzed
Readership in this journal
SteadyRanked #100 of 8,486 articles by views in american journal of science
Most read
Least read
Bar heights use a square-root scale. Only the 120 most-read articles are drawn; the journal has 8,486 in total.
Mint this article as an NFT
Not yet mintedCreate a permanent, verifiable on-chain record of this article on the Scimatic Network. The NFT is held in your Journament account, and you can withdraw it to your own wallet at any time.
5
SUSD
one-off · no wallet required
Abstract
Laboratory observations of aragonite dissolution in seawater, under temperature and pressure conditions that approximate the natural oceanic environment, indicate that R = k{prime}((CO{sup 2{minus}}{sub 3}){sub s} - (CO{sup 2{minus}}{sub 3})){sup n} is an appropriate expression describing the dependence of dissolution rate on seawater saturation, state, where R is aragonite dissolution rate in percent per day, (CO{sup 2{minus}}{sub 3}){sub s} is the carbonate ion concentration at saturation, and (CO{sup 2{minus}}{sub 3}) is the in-situ carbonate ion concentration. Under conditions in which the influence of surface alteration is minimized, plots of dissolution rate, R, versus ((CO{sup 2{minus}}{sub 3}){sub s} - (CO{sup 2{minus}}{sub 3})) approach linearity. Consequently, in the absence of surface alteration effects, our results suggest that the reaction order, n, in the above expression should be equal to one. Use of single pteropod shells in extended experimental sequences indicates that progressive roughening of the shell surface by dissolution can substantially enhance shell dissolution rates. Surface alteration leads to variable values of the rate constant, k{prime}, in the expression above. For rate measurements obtained at increasing degrees of both undersaturation and shell roughness, the multiplicative factors k{prime} and ((CO{sup 2{minus}}{sub 3}){sub s} - (CO{sup 2{minus}}{sub 3})) give rise to curvature in plotsmore » of rate versus ((CO{sup 2{minus}}{sub 3}){sub s} - (CO{sup 2{minus}}{sub 3})). For models in which variations in k{prime} are not explicitly acknowledged, dissolution rates are generally described successfully with reaction orders (n) greater than one. Our experiments, performed at variable pressure, were modeled using several realistic partial molar volume changes ({delta} V) for aragonite dissolution in seawater.« less
| Reference Key |
openalex_W1966671539
Use this key to autocite in the manuscript while using
SciMatic Manuscript Manager or Thesis Manager
|
|---|---|
| Authors | James G. Acker, Robert H. Byrne |
| Journal | american journal of science |
| Year | 1989 |
| DOI |
10.2475/ajs.289.9.1098
|
| URL | |
| Keywords | Keywords not found |
Citations
No citations found. To add a citation, contact the admin at info@scimatic.org
Comments
No comments yet. Be the first to comment on this article.