Rc. Aller et al., REMINERALIZATION RATES, RECYCLING, AND STORAGE OF CARBON IN AMAZON SHELF SEDIMENTS, Continental shelf research, 16(5-6), 1996, pp. 753-786
Diagenetic reactions and redox properties of Amazon shelf sediments ar
e characterized by extensive vertical and lateral regions of Fe and Mn
cycling. This is in contrast to many temperate estuarine and shelf de
posits where S can dominate early diagenesis, but may be typical of we
t-tropical regions draining highly weathered terrain with energetic co
astlines. Although the major pathways of C-org remineralization in sur
fical sediments apparently differ from previously studied areas, the a
bsolute magnitude and relative importance of benthic decomposition on
the Amazon shelf are comparable to many shallow water regions of equiv
alent depth range (10-40 m). Net Sigma CO2 production over the upper s
imilar to 1-2 m of deposits is >50 mmol m(-2) d(-1) and has a predomin
antly planktonic isotopic composition (delta(13)C similar to-21 to -22
parts per thousand), indicating that marine organic matter largely dr
ives diagenetic reactions and that greater than or similar to 20% of a
verage water-column primary production is metabolized on the seafloor.
The Sigma CO2 production rates in the upper 0-5 cm of sediment tend t
o increase slightly alongshelf away from the turbid river mouth, but a
re relatively uniform within cross-shelf transects at any given season
and independent of net sedimentation rate. Near uniformity in surface
decomposition rates, despite substantial offshore increases in water-
column productivity and net accumulation at the delta front, implies r
apid cross-shelf particle exchange by estuarine circulation and tidal
currents. Build-up patterns of pore-water Sigma CO2 indicate in some c
ases that the upper similar to 20 cm was deposited only a few days pri
or to core collection. Benthic Sigma CO2 production is highest during
periods of low or falling river flow, but no dramatic seasonality occu
rs. O-2 penetrates similar to 2-4 mm into sediments and diffusive O-2
uptake averages similar to 13 mmol m(-2) d(-1) annually. Anaerobic met
abolism accounts for >75% of sedimentary remineralization, but C/S bur
ial ratios are usually >6 (average world shelf similar to 2.8). Season
al patterns in sedimentary Fe oxidation states indicate that sediments
can be partially reoxidized to depths similar to 0.6- 1 m during eros
ion/redeposition and that subsequent Fe reduction can account for much
of the anaerobic decomposition. Diffusive Sigma CO2 fluxes and pore-w
ater inventories imply substantial loss of remineralized C to authigen
ic sedimentary-carbonate formation or flux imbalances due to nonsteady
-state ingrowth of disturbed pore-water profiles. Reoxidation of metab
olites and nutrient release to the water column occur during massive p
hysical remobilization of sediments. The total benthic N remineralizat
ion flux (recycled) is comparable to external riverine and shelf-upwel
ling fluxes. During stable seabed periods, however, little or no co-re
mineralized N (NH4+, NO3-, NO2-) or P escapes diffusively into overlyi
ng water, indicating the potential for loss of up to similar to 100% o
f the benthic remineralized N (by denitrification) and P (during authi
genic mineral precipitation and adsorption). Overall, the shelf appare
ntly acts as an efficient, fluidized-bed denitrification processor (si
milar to 50% recycled N) but an inefficient burial sink for riverine a
nd upwelled N. In contrast to the atmospheric sink for N, rapidly rege
nerated P is eventually lost to the open ocean during sediment resuspe
nsion and desorption into the overlying water. Approximately 90% of th
e remineralized Sigma CO2 production flux escapes the sediment and sim
ilar to 10% is permanently hurled as authigenic carbonate. Despite reo
xidation and carbonate dissolution during reworking, net burial of C i
s similar to 5 x 10(12) g C-total per year, of which similar to 25-30%
is carbonate from remineralized organics (similar to 70% of this frac
tion is marine) similar to 20% is residual marine C-org, and the remai
ning similar to 50% is residual terrestrial C-org. ''Refractory'' terr
estrial POC is apparently subject to repetitive co-oxidation and redox
cycling, resulting in remineralization of similar to 65-70% of input
and leaving less than similar to 30-35% of the riverine POC flux store
d on the shelf.