The influence of air-sea fluxes on atmospheric oxygen can be separated from terrestrial influences using the tracer Atmospheric Potential Oxygen (APO).  Data collected by the Scripps atmospheric oxygen flask sampling network exhibits interannual variability in APO coherent over the northern hemisphere.  The timing of these changes correlates with climatic changes in the North Pacific.

The remote sensing of CO₂ from satellites is an exciting new and rapidly developing field in carbon cycle research. Satellite sensors have the potential to provide a wealth of information on atmospheric CO₂, covering many regions that are scarsely monitored the ground based observational networks. Satellite measurements could significantly strengthen the power of inverse modelling computations in tracing sources and sinks of CO₂. The main challenge, however, is to reach the measurement accuracy needed to resolve the important CO₂ concentration gradients. The current generation of satellite instruments from which CO₂ can be retrieved is expected to meet the requirements only partly, as the instruments were not originally designed to measure CO₂. Nevertheless interesting results come out as we will show for the Sciamachy instrument. A particularly difficult aspect is the determination of the airmass factor, which is needed to translate the observed optical thickness into a column averaged dry air mixing ratio. The airmass factor is influenced by e.g. clouds, aerosols, air pressure, and orography. So far the uncertainty assessments have mainly relied on theoretical investigations and ground-based measurements. The measurements from Sciamachy allow us to verify these studies, and some of the methods that have been proposed to reduce or eliminate the errors. We will demonstrate this with the main focus on aerosols. Error assessments using in-flight data will be indispensable for improving future instruments.

GOSAT is a satellite to measure the column densities of CO₂ and CH₄ from space globally, and it is scheduled to be launched in 2008. It has a short wavelength infrared (SWIR) Fourier transform spectrometer (FTS) which measures both the ground surface scattered solar light over land and the right reflected light (sun-glint) over ocean. Column densities of CO₂ and CH₄ will be retrieved from the SWIR (i.e. 1.6 µm and 2.0 µm bands) data and the optical path length from oxygen A-band (0.76 µm). A cloud and aerosol sensor composed of three spectral image sensors (0.380, 0.678 and 1.62 µm) is equipped, viewing the wider area than FTS. This is a joint project among Ministry of Environment of Japan (MOE), National Insitutite for Environmental Studies (NIES) and Japan Aerospace Exploration Agency (JAXA).

Measurements of the partial pressure of CO₂ in surface seawater (pCO₂^w) have been made frequently and extensively in the western North Pacific (3-35°N, 132-142°E) since 1990. Based on the time series analysis of pCO₂^w data, we obtained a “climatological view” of seasonal variation in pCO₂^w in the western North Pacific. We have examined the relationship between pCO₂^w and sea surface temperature (SST). The pCO₂^w–SST relationship varies spatially and temporally. The pCO₂^w showed an average growth rate of 1.6 µatm yr^-1 (nearly equal to that of the air, pCO₂^a) with large variability (±8.9µatm yr^-1). In 1998, larger growth rates of pCO₂^w occurred in the subtropical gyre and the western equatorial Pacific, which was probably associated with the 1997/98 El Niño phenomena. To know processes affecting long-term variations in pCO₂^w, we have examined seasonal variation in growth rate of pCO₂^w. The linear growth rate of pCO₂^w during the winter season ranged from 1.3±0.2 to 2.1±0.2µatm yr^-1 with an average of 1.7±0.2µatm yr^-1. During spring/summer seasons, the average growth rate of pCO₂^w was larger than 2µatm yr^-1 north of 27°N, and within the range from 0 to 1µatm yr^-1 in the North Equatorial Current. These increases were mostly caused by the oceanic uptake of anthropogenic CO₂, and to some extent, other processes controlling the pCO₂^w change: thermodynamic effect, lateral transport and vertical mixing, and biological activity.

To examine vertical distributions of the O₂/N₂ ratio in the stratosphere, air samples were collected using a cryogenic sampler over Sanriku, Japan and Syowa, Antarctica. It was clearly seen that d(O₂/N₂), as well as simultaneously measured d¹⁵N of N₂ and d¹⁸O of O₂, decreased gradually with increasing height in the stratosphere. The observed profiles of stratospheric ï€ d¹⁵N and d¹⁸O were in good agreement with those calculated using a steady state 1-dimensional eddy-diffusion/molecular-diffusion model suggesting that the upward decrease of stratospheric d(O₂/N₂) is caused by O₂ and N₂ molecules fractionated differently by gravity. The stratospheric d(O₂/N₂) corrected for the gravitational separation indicated that the average value at heights above 20-25 km over Sanriku was always higher than the upper tropospheric d(O₂/N₂) value over Japan at the corresponding time, and that it has decreased secularly, as was found in the troposphere.

High-quality data of total inorganic carbon (TCO₂) and other oceanographic parameters have been acquired repeatedly between 1994 and 2003 along 137ºE (WOCE P9) in the western North Pacific. They indicate the significant increase in TCO₂, apparent oxygen utilization (AOU) and preformed TCO₂ in the water columns between 20ºN and 30ºN, in particular, in the North Pacific Subtropical Mode Water (NPSTMW). The increase in the preformed TCO₂ suggests the 0.9 to 1.1 mol m^-2 yr^-1 accumulation of the anthropogenic CO₂ in this region. However, the change in the preformed TCO₂ associated with the change in the formation region and/or advection of NPSTMW is also suggested.

We have constructed an estimate of annual-mean surface fluxes of carbon dioxide for the period 1992-6 using observational constraints from the atmosphere and from the ocean interior. The method interprets in situ observations of carbon dioxide concentration in the ocean and atmosphere using transport estimates from global circulation models.

In recent years our knowledge of gas exchange across the air-sea interface at the process level has improved as a consequence of new instrumentation and novel use of injected and natural tracers.  However, there remains significant uncertainty in the extrapolation of these results to larger scales, especially for studies focusing on global-scale processes such as the earth's carbon cycle.

We examine the growth-rate of atmospheric CO₂ in 2002 and 2003. Observations show consecutive increases of greater than 2 ppmv per year for the first time on the Mauna Loa record. We use a statistical regression to show that increasing anthropogenic emissions and ENSO activity are unable to account for the CO₂ growth-rates of 1992 and 1993 following the Pinatubo volcanic eruption, or the anomalously high growth-rate of 2003. Increased forest fires in the northern hemisphere, consistent with remote-sensing and carbon monoxide measurements, seem likely to have contributed significantly to the 2003 anomaly. We hypothesise that the hot and dry Eurasian summer of 2003 led to an increase in forest fire emissions from Siberia, and may also have directly suppressed land-carbon uptake. Model results lead us to expect a steady increase in airborne fraction as climate change weakens the natural carbon sink and accelerates CO₂ rise.