Elsevier

Organic Geochemistry

Volume 27, Issues 5–6, 15 November 1997, Pages 195-212
Organic Geochemistry

What happens to terrestrial organic matter in the ocean?

https://doi.org/10.1016/S0146-6380(97)00066-1Get rights and content

Abstract

Each year rivers transport approximately 0.25×1015 g of dissolved (<0.5 μm) organic carbon (DOC) and 0.15×1015 g of particulate (>0.5 μm) organic carbon (POC) from continents to the ocean. Global discharge of riverine DOC is sufficient alone to sustain turnover of the entire pool of organic carbon dissolved in seawater. Similarly, the input of terrestrial POC by rivers is adequate to supply all the organic carbon buried in marine sediments. Because riverine organic matter consists of highly degraded, nitrogen-poor remains of terrestrial organisms, it might be expected to suffer minimal respiration in the ocean. One of the biggest mysteries in the global carbon cycle, therefore, is that only a small fraction of the organic matter dissolved in seawater and preserved in marine sediments appears to be land-derived. Either our global budgets and distribution estimates are greatly in error, or both dissolved and particulate organic matter of terrestrial origin suffer rapid and remarkably extensive remineralization at sea. Although many uncertainties remain, recent studies provide growing evidence for destruction of both dissolved and particulate terrestrial organic matter in the ocean. The mechanisms by which these huge masses of organic materials might be so rapidly oxidized following discharge are largely unknown. This report focuses on the transport and transformations of land-derived organic matter in the ocean, highlighting recent research on the patterns and processes involved.

Introduction

The question of the fate of terrestrial organic matter (TOM) in the ocean has intrigued scientists for decades (Waksman, 1933; Bader, 1956; Handa, 1977; Deuser, 1988) and is key to understanding the global carbon cycle (Berner, 1989) and its anthropogenic perturbations (Siegenthaler and Sarmiento, 1993). TOM represents a huge source of reduced carbon (approximately 0.4×1015 g C yr−1) to the marine environment (Schlesinger and Melack, 1981), integrates drainage basin processes, and incorporates bioactive elements whose cycling modulates the biosphere over geologic time (Meybeck, 1982; Thurman, 1985). Organic remains of terrestrial organisms preserved in marine sediments provide one of the most extensive records of life on the continents, whose continuously eroding surfaces are ephemeral over millennia and seldom preserved (Judson, 1968). Organic substances unique to land plants label continental debris from specific regions, imprinting marine deposits with information concerning proximity to continents, wind strength and other climatically-related variables (Summons, 1993). Successful environmental reconstructions and searches for fossil fuels often hinge on an understanding of processes controlling the distributions and destinies of TOM in fluvial/marine systems.

Many circumstances appear to favor efficient dispersion and sensitive detection of TOM in marine environments. Rivers alone discharge sufficient DOC to support the turnover of DOC throughout the ocean (Williams and Druffel, 1987) and enough POC to account for all the organic carbon now being buried in marine sediments (Berner, 1989; Hedges and Keil, 1995). Aeolian inputs of TOM are challenging to determine, but at open ocean sites appear to be comparable to the delivery rate of marine-derived organic matter to the seafloor (Zafiriou et al., 1985), and hence are geochemically significant (Peltzer and Gagosian, 1989). The major ultimate source of TOM is vascular plants, which are confined essentially to land and characteristically contain high concentrations of recalcitrant, nitrogen-free biomacromolecules such as lignin, tannin, suberin and cutin (de Leeuw and Largeau, 1993). These “higher” plants have distinctive stable carbon isotope compositions (Fry and Sherr, 1984) and produce a host of unique lipids (Simoneit, 1977; Peltzer and Gagosian, 1989) which can be used as sensitive biomarkers of terrestrial origin (Hedges, 1990; Prahl et al., 1994). Despite its large input, relative resistance to microbial degradation and multiple biomarkers, there is surprisingly little evidence that TOM persists as a major component of organic mixtures in sea-water and marine sediments (Hedges and Keil, 1995). Either our global budgets and tracer methods are terribly flawed, or the ocean has remarkable means of ridding itself of TOM while preserving organic matter of planktonic origin. This geochemical conundrum will be reviewed in the following discussion, along with possible methods for its resolution.

Section snippets

Reservoirs and fluxes of terrestrial organic matter

It is helpful to evaluate the question of the marine fate of TOM within the context of the global carbon cycle (Siegenthaler and Sarmiento, 1993; Hedges and Oades, in press). Most organic matter is stored on land within terrestrial biota (570 gigatons C; 1 Gt=1×1015 g), plant litter (70 Gt C; Post, 1993) and surface (0–100 cm) soils (1600 Gt C; Eswaran et al., 1993). Assuming that litter and biomass are compositionally similar (Huc, 1980; Goñi and Hedges, 1990a), the total inventory of above-ground

Compositional and molecular tracers of TOM

A key requirement for defining the marine fate of TOM is to distinguish and quantify this often-small component in complex water and sedimentary mixtures. Discriminating TOM in marine settings usually boils down to identifying isotopic signatures and biochemicals characteristic of vascular plants (Hedges, 1990; Prahl et al., 1994). These almost exclusively terrestrial flora have evolved a variety of physiological adaptations and structural biomacromolecules (e.g. lignin and hemicelluloses) to

Determining TOM concentrations and fates in the ocean

Rather than attempting a comprehensive review of the literature on TOM in the ocean, we will address two questions: (a) “What is our present understanding of the types, quantities and dynamics of terrestrial organic matter in the World Ocean?” and (b) “How might new methods be applied to improve this knowledge?” This discussion will highlight recent research on dissolved TOM in the ocean and on particulate TOM off the well-studied Washington and northern Brazil coasts. We will begin with

Future research directions

Although recent studies involving a variety of measurements and strategies provide consistent evidence that dissolved and particulate TOM are rapidly and extensively remineralized in the ocean, it has been extremely difficult to identify the processes involved and the settings in which they operate. Where do we go from here to better define the fate of TOM in the ocean? This question will be discussed along the themes of improved: (a) measurements of bulk properties, (b) applications of

Acknowledgements

The authors thank Anthony Aufdenkampe, Peter Hernes, Matt McCarthy, Michael Peterson, Fred Prahl, Crystal Thimsen, Elizabeth Tsamakis and George Wolff for constructive comments on drafts of this manuscript. This is manuscript 2178 from the School of Oceanography, University of Washington, 88 from the CAMREX group, and 1013 from the University of Texas Marine Science Institute. This research was funded in part by US NSF grants OCE-9401903 and DEB-9408676 to JH, OCE-9402081 to RK and OCE-9413843

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