TY - JOUR
T1 - Early diagenetic remineralization of sedimentary organic C in the Gulf of Papua deltaic complex (Papua New Guinea)
T2 - Net loss of terrestrial C and diagenetic fractionation of C isotopes
AU - Aller, Robert C.
AU - Blair, Neal E.
N1 - Funding Information:
We are indebted to Gregg Brunskill and the Australian Institute of Marine Science for organizing, heading, and supporting the TROPICS program within which this research was carried out. Indispensable aid was provided by Josephine Aller, Angelos Hannides, Vanessa Madrid, J. P. Walsh, Irena Zagorskis, John Pfistner, Gregg Brunskill, Chuck Nittrouer, and many additional indentured scientific party and crew. Laboratory assistance was supplied primarily by Zhongbin Zhu, Kelly Peeler, and Christina Heilbrun. The Masters and crews of the R/V Harry Messel and R/V Franklin provided the expertise, hard work, and good nature to make it all happen. We thank two anonymous reviewers for helpful, critical comments. Supported by USA NSF grant OCE 9818574 and OCE0219919.
PY - 2004/4/15
Y1 - 2004/4/15
N2 - Oceania supplies ∼40% of the global riverine flux of organic carbon, approximately half of which is injected onto broad continental shelves and processed in shallow deltaic systems. The Gulf of Papua, on the south coast of the large island of New Guinea, is one such deltaic clinoform complex. It receives ∼4 Mt yr-1 particulate terrestrial organic carbon with initial particle Corg loading ∼0.7 mg m-2. Corg loading is reduced to ∼0.3 mg m-2 in the topset-upper foreset zones of the delta despite additional inputs of mangrove and planktonic detritus, and high net sediment accumulation rates of 1-4 cm yr-1. Carbon isotopic analyses (δ13C, Δ14C) of ΣCO2 and Corg demonstrate rapid (<100 yr) remineralization of both terrestrial (δ13C <-28.6) and marine Corg (δ13C ∼-20.5) ranging in average age from modern (bomb) (Δ14C ∼60) to ∼1000 yr (Δ14C ∼-140). Efficient and rapid remineralization in the topset-upper foreset zone is promoted by frequent physical reworking, bioturbation, exposure, and reoxidation of deposits. The seafloor in these regions, particularly <20 m, apparently functions as a periodically mixed, suboxic batch reactor dominated by microbial biomass. Although terrestrial sources can be the primary metabolic substrates at inshore sites, relatively young marine Corg often preferentially dominates pore water ΣCO2 relative to bulk Corg in the upper foreset. Thus a small quantity of young, rapidly recycled marine organic material is often superimposed on a generally older, less reactive terrestrial background. Whereas the pore water ΣCO2 reflects both rapidly cycled marine and terrestrial sources, terrestrial material dominates the slower overall net loss of Corg from particles in the topset-upper foreset zone (i.e. recycled marine Corg leaves little residue). Preferential utilization of Corg subpools and diagenetic fractionation of C isotopes supports the reactive continuum model as a conceptual basis for net decomposition kinetics. Early diagenetic fractionation of C isotopes relative to the bulk sedimentary Corg composition can produce changes in 14C activity independent of radioactive decay. In the Gulf of Papua topset-upper foreset, Δ14C of pore water ΣCO2 averaged ∼ 300‰ greater than Corg sediment between ∼1-3 m depth in deposits. Diagenetic fractionation and decomposition aging of sedimentary Corg compromises simple application of 14C for determination of sediment accumulation rates in diagenetically reactive deposits.
AB - Oceania supplies ∼40% of the global riverine flux of organic carbon, approximately half of which is injected onto broad continental shelves and processed in shallow deltaic systems. The Gulf of Papua, on the south coast of the large island of New Guinea, is one such deltaic clinoform complex. It receives ∼4 Mt yr-1 particulate terrestrial organic carbon with initial particle Corg loading ∼0.7 mg m-2. Corg loading is reduced to ∼0.3 mg m-2 in the topset-upper foreset zones of the delta despite additional inputs of mangrove and planktonic detritus, and high net sediment accumulation rates of 1-4 cm yr-1. Carbon isotopic analyses (δ13C, Δ14C) of ΣCO2 and Corg demonstrate rapid (<100 yr) remineralization of both terrestrial (δ13C <-28.6) and marine Corg (δ13C ∼-20.5) ranging in average age from modern (bomb) (Δ14C ∼60) to ∼1000 yr (Δ14C ∼-140). Efficient and rapid remineralization in the topset-upper foreset zone is promoted by frequent physical reworking, bioturbation, exposure, and reoxidation of deposits. The seafloor in these regions, particularly <20 m, apparently functions as a periodically mixed, suboxic batch reactor dominated by microbial biomass. Although terrestrial sources can be the primary metabolic substrates at inshore sites, relatively young marine Corg often preferentially dominates pore water ΣCO2 relative to bulk Corg in the upper foreset. Thus a small quantity of young, rapidly recycled marine organic material is often superimposed on a generally older, less reactive terrestrial background. Whereas the pore water ΣCO2 reflects both rapidly cycled marine and terrestrial sources, terrestrial material dominates the slower overall net loss of Corg from particles in the topset-upper foreset zone (i.e. recycled marine Corg leaves little residue). Preferential utilization of Corg subpools and diagenetic fractionation of C isotopes supports the reactive continuum model as a conceptual basis for net decomposition kinetics. Early diagenetic fractionation of C isotopes relative to the bulk sedimentary Corg composition can produce changes in 14C activity independent of radioactive decay. In the Gulf of Papua topset-upper foreset, Δ14C of pore water ΣCO2 averaged ∼ 300‰ greater than Corg sediment between ∼1-3 m depth in deposits. Diagenetic fractionation and decomposition aging of sedimentary Corg compromises simple application of 14C for determination of sediment accumulation rates in diagenetically reactive deposits.
UR - http://www.scopus.com/inward/record.url?scp=1842788887&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=1842788887&partnerID=8YFLogxK
U2 - 10.1016/j.gca.2003.10.028
DO - 10.1016/j.gca.2003.10.028
M3 - Article
AN - SCOPUS:1842788887
SN - 0016-7037
VL - 68
SP - 1815
EP - 1825
JO - Geochmica et Cosmochimica Acta
JF - Geochmica et Cosmochimica Acta
IS - 8
ER -