REMINERALIZATION RATES, RECYCLING, AND STORAGE OF CARBON IN AMAZON SHELF SEDIMENTS

Citation
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
Citations number
97
Categorie Soggetti
Oceanografhy
Journal title
ISSN journal
02784343
Volume
16
Issue
5-6
Year of publication
1996
Pages
753 - 786
Database
ISI
SICI code
0278-4343(1996)16:5-6<753:RRRASO>2.0.ZU;2-6
Abstract
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.