De. Hammond et al., EARLY DIAGENESIS OF ORGANIC MATERIAL IN EQUATORIAL PACIFIC SEDIMENTS - STOICHIOMETRY AND KINETICS, Deep-sea research. Part 2. Topical studies in oceanography, 43(4-6), 1996, pp. 1365-1412
Benthic incubation chambers and sediment pore water profiles were used
to study early diagenesis of organic matter in equatorial Pacific sed
iments. Replicate measurements with a flux chamber covering 720 cml in
dicated that the spatial variability of oxygen, TCO2, alkalinity, nitr
ate and silica fluxes at a single station did not exceed 10-35%. In co
ntrast, diffusive fluxes of oxygen from replicate cores covering 70 cm
(2) at a single station often showed greater variation. In January 199
2, benthic oxygen consumption was fairly constant along the equator fr
om 103 degrees W to 140 degrees W at 0.6-0.8 mmol m(-2) day(-1). In No
vember 1992, consumption was roughly symmetrical across the equator al
ong 140 degrees W, with rates of 0.6-0.8 mmol m(-2) day(-1) between 2
degrees S and 2 degrees N, declining to rates of 0.1-0.2 mmol m(-2) da
y(-1) at 12 degrees S and 9 degrees N. Pore water oxygen profiles were
fit with a reaction-diffusion model equation to evaluate reaction kin
etics. Most profiles were adequately fit with a model that assumed rea
ction rates declined exponentially with depth, but at low latitudes be
tter fits often were obtained with a model that assumed decomposing or
ganic matter has two labile components and that each decays with first
-order kinetics and decreases exponentially with depth. Results of bot
h fits indicate that at least 70% of the organic matter degradation oc
curs within the upper 1-2 cm of sediment. At the low-latitude stations
fit with the two-component model, 70-90% of the flux is attributable
to the more labile component which has an average 1/e penetration dept
h of 0.4+/-0.1 cm. The more refractory component at these stations has
a penetration depth of 4.4+/-0.4 cm. From estimates of sediment mixin
g rates, the mean life of all degrading organic matter at the higher l
atitude stations is 4-55 years, while at the stations fit with the two
-component model, the lifetime of the more labile fraction is weeks to
months, and the lifetime of the less labile component is 40-300 years
. A third carbon fraction exists at all stations that is far more refr
actory. The O-2:CO2 stoichiometry of remineralization is -1.45+/-0.17,
and the C:N ratio is 8+/-1. Both ratios are in good agreement with th
ose observed from sediment trap and hydrographic studies in the water
column, and suggest that degrading organic matter has about 70% of its
carbon in -CH2O- groups and 30% in -CH2- groups. The C:P atom ratios
for benthic remineralization differ by a factor of 3 for the two cruis
es, showing substantial temporal variability and de-coupling from carb
on, although the mean for the two cruises (170+/-85) is not significan
tly different than remineralization ratios observed in the water colum
n. The aerally-integrated benthic respiration rate for the equatorial
Pacific upwelling region is at least 25% of the integrated respiration
rate for the continental margin (slope + rise) areas of the Pacific,
emphasizing the importance of the equatorial Pacific sediments as a ma
jor site of benthic carbon recycling. Benthic carbon remineralization
rates determined during the past decade near the equator and 140 degre
es W have varied by a factor of 2, which is not surprising given the s
hort lifetime of the majority of the carbon degrading. The temporal pa
tterns of carbon remineralization rates resemble those of sea-surface
temperature, suggesting that benthic carbon oxidation at this site may
reflect water column productivity over relatively short timescales. C
opyright (C) 1996 Elsevier Science Ltd.