Ute Schuster

Recent variability of the global ocean carbon sink

We present a new observation-based estimate of the global oceanic carbon dioxide (CO2) sink and its temporal variation on a monthly basis from 1998 through 2011 and at a spatial resolution of 1×1. This sink estimate rests upon a neural network-based mapping of global surface ocean observations of the partial pressure of CO2 (pCO2) from the Surface Ocean CO2 Atlas database. The resulting pCO2 has small biases when evaluated against independent observations in the different ocean basins, but larger randomly distributed differences exist particularly in high latitudes. The seasonal climatology of our neural network-based product agrees overall well with the Takahashi et al. (2009) climatology, although our product produces a stronger seasonal cycle at high latitudes. From our global pCO2 product, we compute a mean net global ocean (excluding the Arctic Ocean and coastal regions) CO2 uptake flux of −1.42 ± 0.53 Pg C yr−1, which is in good agreement with ocean inversion-based estimates. Our data indicate a moderate level of interannual variability in the ocean carbon sink (±0.12 Pg C yr−1, 1𝜎) from 1998 through 2011, mostly originating from the equatorial Pacific Ocean, and associated with the El Nino–Southern Oscillation. Accounting for steady state riverine and Arctic Ocean carbon fluxes our estimate further implies a mean anthropogenic CO2 uptake of −1.99 ± 0.59 Pg C yr−1 over the analysis period. From this estimate plus the most recent estimates for fossil fuel emissions and atmospheric CO2 accumulation, we infer a mean global land sink of −2.82 ± 0.85 Pg C yr−1 over the 1998 through 2011 period with strong interannual variation.

Tracking the variable North Atlantic sink for atmospheric CO2

A Happy Marriage The fluxes of CO2 between the atmosphere and ocean are large and variable, and understanding why the concentration of atmospheric CO2 changes as it does, depends on accurately determining the details of those fluxes. One of the major obstacles in the way of quantifying this exchange is that there are too few measurements available, both temporally and geographically. Watson et al. (p. 1391) report results from a happy marriage of science and commerce—data collected by instruments fitted onto commercial ships plying the waters of the North Atlantic Ocean—that has generated the largest and most comprehensive set of measurements of ocean pCO2 ever collected. These data allow the oceanic CO2 sink to be monitored with unprecedented accuracy and will help researchers precisely map regional interannual air-sea fluxes. Data from instrumented commercial ships reveal substantial interannual variations of carbon dioxide flux between the ocean and the air. The oceans are a major sink for atmospheric carbon dioxide (CO2). Historically, observations have been too sparse to allow accurate tracking of changes in rates of CO2 uptake over ocean basins, so little is known about how these vary. Here, we show observations indicating substantial variability in the CO2 uptake by the North Atlantic on time scales of a few years. Further, we use measurements from a coordinated network of instrumented commercial ships to define the annual flux into the North Atlantic, for the year 2005, to a precision of about 10%. This approach offers the prospect of accurately monitoring the changing ocean CO2 sink for those ocean basins that are well covered by shipping routes.

Gas seep induced interstitial water circulation: observations and environmental implications

Abstract An interstitial water circulation, generated by gas flow through a permeable sediment, was observed at an intertidal site on the Kattegat coast of Denmark. Concentrations of methane dissolved in the interstitial water of the near-surface sediment decreased sharply only centimetres away from gas seeps venting almost pure methane (≈99% methane). Water was driven out of the sediment by the rising bubbles of gas at the seep and was replaced by an equivalent draw-down of overlying, oxygenated water into the surrounding sediment. This process steepened the chemical gradients close to the gas flow channel, with the effects progressively diminishing with increasing distance from the seep. The position of the redox potential discontinuity (RPD) moved by as much as 7 cm deeper into the sediment close to the seep: this effect was less marked, but still detectable, 50 cm away. The degree of displacement from the “normal” sediment profiles depended on the magnitude of the interstitial flow rate. The distribution of pore water pH and sulphate: sodium ratios were also dependent on the flow rate of the circulating water. The concentrations of sulphide, thiosulphate and sulphite in the interstitial water from the top 10 cm of sediment, were high at a seep, decreased to a minimum at 20–30 cm distance, then increased again at 40–50 cm distance. Laboratory experiments confirmed that gas bubbling through a fluid filled permeable matrix generated a flow, out of the sediment at the gas exit and into the sediment over the peripheral surfaces surrounding the outlet. Experimentally determined rates of dispersion, for gas flow rates of 3–20 ml min −1 , for a 40 g l −1 sodium chloride solution, were 62.5 × 10 −9 to 540 × 10 −9 m 2 s −1 , 40–400 times the molecular diffusion coefficient. Linear interstitial fluid velocities of 3–12 mm min −1 , were recorded at 14-3 cm from the seep axis respectively, with a gas flow rate of 5 ml min −1 . Two-dimensional modelling of the experimental system confirmed the flow pattern determined visually with dye. Implications of this process with regard to the recycling rates of elements generally, and of nutrient and waste materials, in particular, are discussed.

PHYSICAL EXCHANGES AT THE AIR-SEA INTERFACE UK-SOLAS Field Measurements

As part of the U.K. contribution to the international Surface Ocean–Lower Atmosphere Study, a series of three related projects—DOGEE, SEASAW, and HiWASE—undertook experimental studies of the processes controlling the physical exchange of gases and sea spray aerosol at the sea surface. The studies share a common goal: to reduce the high degree of uncertainty in current parameterization schemes. The wide variety of measurements made during the studies, which incorporated tracer and surfactant release experiments, included direct eddy correlation fluxes, detailed wave spectra, wind history, photographic retrievals of whitecap fraction, aerosol-size spectra and composition, surfactant concentration, and bubble populations in the ocean mixed layer. Measurements were made during three cruises in the northeast Atlantic on the RRS Discovery during 2006 and 2007; a fourth campaign has been making continuous measurements on the Norwegian weather ship Polarfront since September 2006. This paper provides an overview of the three projects and some of the highlights of the measurement campaigns.

Net community production in the North Atlantic Ocean derived from Volunteer Observing Ship data

The magnitude of marine plankton net community production (NCP) is indicative of both the biologically driven exchange of carbon dioxide between the atmosphere and the surface ocean and the export of organic carbon from the surface ocean to the ocean interior. In this study the seasonal variability in the NCP of five biogeochemical regions in the North Atlantic was determined from measurements of surface water dissolved oxygen and dissolved inorganic carbon (DIC) sampled from a Volunteer Observing Ship (VOS). The magnitude of NCP derived from dissolved oxygen measurements (NCPinline image) was consistent with previous geochemical estimates of NCP in the North Atlantic, with an average annual NCPinline image of 9.5 ± 6.5 mmol O2 m−2 d−1. Annual NCPinline image did not vary significantly over 35° of latitude and was not significantly different from NCP derived from DIC measurements (NCPDIC). The relatively simple method described here is applicable to any VOS route on which surface water dissolved oxygen concentrations can be accurately measured, thus providing estimates of NCP at higher spatial and temporal resolution than currently achieved.

Monitoring and interpreting the ocean uptake of atmospheric CO2

The oceans are an important sink for anthropogenically produced CO2, and on time scales longer than a century they will be the main repository for the CO2 that humans are emitting. Our knowledge of how ocean uptake varies (regionally and temporally) and the processes that control it is currently observation-limited. Traditionally, and based on sparse observations and models at coarse resolution, ocean uptake has been thought to be relatively invariant. However, in the few places where we have enough observations to define the uptake over periods of many years or decades, it has been found to change substantially at basin scales, responding to indices of climate variability. We illustrate this for three well-studied regions: the equatorial Pacific, the Indian Ocean sector of the Southern Ocean, and the North Atlantic. A lesson to take from this is that ocean uptake is sensitive to climate (regionally, but presumably also globally). This reinforces the expectation that, as global climate changes in the future owing to human influences, ocean uptake of CO2 will respond. To evaluate and give early warning of such carbon–climate feedbacks, it is important to track trends in both ocean and land sinks for CO2. Recent coordinated observational programmes have shown that, by organization of an observing network, the atmosphere–ocean flux of CO2 can, in principle, be accurately tracked at seasonal or better resolution, over at least the Northern Hemisphere oceans. This would provide a valuable constraint on both the ocean and (by difference) land vegetation sinks for atmospheric CO2.

Supplement to physical exchanges at the air-sea interface: UK-SOLAS Field Measurements

This document is a supplement to “Physical Exchanges at the Air–Sea Interface: UK–SOLAS Field Measurements,” by Ian M. Brooks, Margaret J. Yelland, Robert C. Upstill-Goddard, Philip D. Nightingale, Steve Archer, Eric d’Asaro, Rachael Beale, Cory Beatty, Byron Blomquist, A. Anthony Bloom, Barbara J. Brooks, John Cluderay, David Coles, John Dacey, Michael DeGrandpre, Jo Dixon, William M. Drennan, Joseph Gabriele, Laura Goldson, Nick Hardman-Mountford, Martin K. Hill, Matt Horn, Ping-Chang Hsueh, Barry Huebert, Gerrit de Leeuw, Timothy G. Leighton, Malcolm Liddicoat, Justin J. N. Lingard, Craig McNeil, James B. McQuaid, Ben I. Moat, Gerald Moore, Craig Neill, Sarah J. Norris, Simon O’Doherty, Robin W. Pascal, John Prytherch, Mike Rebozo, Erik Sahlee, Matt Salter, Ute Schuster, Ingunn Skjelvan, Hans Slagter, Michael H. Smith, Paul D. Smith, Meric Srokosz, John A. Stephens, Peter K. Taylor, Maciej Telszewski, Roisin Walsh, Brian Ward, David K. Woolf, Dickon Young, and Henk Zemmelink (Bull. Amer. Meteor. Soc., 90, 629–644) • ©2009 American Meteorological Society • Corresponding author: Ian M. Brooks, Institute for Climate and Atmospheric Science, School of Earth and Environment, University of Leeds, Leeds LS2 9JT, United Kingdom • E-mail: i.brooks@see.leeds.ac.uk • DOI:10.1175/2008BAMS2578.2

Perspectives and Integration in SOLAS Science

Why a chapter on Perspectives and Integration in SOLAS Science in this book? SOLAS science by its nature deals with interactions that occur: across a wide spectrum of time and space scales, involve gases and particles, between the ocean and the atmosphere, across many disciplines including chemistry, biology, optics, physics, mathematics, computing, socio-economics and consequently interactions between many different scientists and across scientific generations. This chapter provides a guide through the remarkable diversity of cross-cutting approaches and tools in the gigantic puzzle of the SOLAS realm.