Se. Calvert et Tf. Pedersen, GEOCHEMISTRY OF RECENT OXIC AND ANOXIC MARINE-SEDIMENTS - IMPLICATIONS FOR THE GEOLOGICAL RECORD, Marine geology, 113(1-2), 1993, pp. 67-88
The distributions of certain minor and trace elements in marine sedime
nts should potentially provide forensic tools for determining the redo
x conditions of the bottom waters at the time of deposition. The abili
ty to identify such conditions in the geological past is important bec
ause (1) current models of the conditions of formation of organic-rich
rocks require re-examination, (2) a method to determine whether the a
real extent of anoxic waters expanded or retracted in response to pala
eoceanographic changes is required, and (3) the effects of such enviro
nmental changes on the geochemical balance of these elements in the oc
ean need to be understood. Recent research has suggested that some min
or and trace elements are precipitated where free dissolved sulphide i
s present (Cu, Cd, Ni, Zn) without undergoing a valency change, wherea
s others undergo a change in valency and are either more efficiently a
dsorbed onto solid surfaces under oxic (1) or anoxic (V) conditions or
are precipitated under anoxic conditions (Cr, Mn, Mo, Re, U, V). Henc
e, the enrichment of these minor and trace elements relative to their
crustal abundances indicates that the host sediments accumulated under
anoxic conditions, although not necessarily under anoxic bottom water
s. Examination of the chemical composition of the sediments of anoxic
basins, continental margin sediments and oxidized deep-sea sediments s
hows that I and Mn enrichments are reliable indicators of bottom water
oxygenation, whereas enrichments of the remaining elements reflect ei
ther bottom water anoxia or element uptake by subsurface anoxic sedime
nts below a relatively thin surficial oxic veneer. Hence, the absence
of metal enrichment in these cases can be taken as firm evidence that
the bottom waters of a basin of sedimentation were not anoxic. These b
ehaviours may be used to propose, for example, that the Holocene sapro
pel in the Black Sea accumulated under oxic bottom waters, whereas the
modern facies reflects its formation under the prevailing intensely a
noxic conditions, and that the Panama Basin bottom waters were not ano
xic during the Last Glacial Maximum when the rate of accumulation of o
rganic carbon increased. Likewise, the enrichment of Mn as a mixed car
bonate phase in some ancient black shales strongly suggests that they
formed under oxic bottom waters rather than anoxic conditions as is co
mmonly assumed.