Methane-consuming archaebacteria in marine sediments.

Large amounts of methane are produced in marine sediments but are then consumed before contacting aerobic waters or the atmosphere. Although no organism that can consume methane anaerobically has ever been isolated, biogeochemical evidence indicates that the overall process involves a transfer of electrons from methane to sulphate and is probably mediated by several organisms, including a methanogen (operating in reverse) and a sulphate-reducer (using an unknown intermediate substrate). Here we describe studies of sediments related to a decomposing methane hydrate. These provide strong evidence that methane is being consumed by archaebacteria that are phylogenetically distinct from known methanogens. Specifically, lipid biomarkers that are commonly characteristic of archaea are so strongly depleted in carbon-13 that methane must be the carbon source, rather than the metabolic product, for the organisms that have produced them. Parallel gene surveys of small-subunit ribosomal RNA (16S rRNA) indicate the predominance of a new archael group which is peripherally related to the methanogenic orders Methanomicrobiales and Methanosarcinales.

Direct observation of the oceanic CO2 increase revisited.

We show, from recent data obtained at specimen North Pacific stations, that the fossil fuel CO2 signal is strongly present in the upper 400 m, and that we may consider areal extrapolations from geochemical surveys to determine the magnitude of ocean fossil fuel CO2 uptake. The debate surrounding this topic is illustrated by contrasting reports which suggest, based upon atmospheric observations and models, that the oceanic CO2 sink is small at these latitudes; or that the oceanic CO2 sink, based upon oceanic data and models, is large. The difference between these two estimates is at least a factor of two. There are contradictions arising from estimates based on surface partial pressures of CO2 alone, where the signal sought is small compared with regional and seasonal variability; and estimates of the accumulated subsurface burden, which correlates well other oceanic tracers. Ocean surface waters today contain about 45 micromol.kg-1 excess CO2 compared with those of the preindustrial era, and the signal is rising rapidly. What limits should we place on such calculations? The answer lies in the scientific questions to be asked. Recovery of the fossil fuel CO2 contamination signal from analysis of ocean water masses is robust enough to permit reasonable budget estimates. However, because we do not have sufficient data from the preindustrial ocean, the estimation of the required Redfield oxidation ratio in the upper several hundred meters is already blurred by the very fossil fuel CO2 signal we seek to resolve.

Surviving the "air evac": medical and logistical issues of evacuating psychiatric patients by air from Korea to the United States.

Active duty soldiers who need a physical evaluation board for incapacitating psychiatric symptoms may be evacuated by air to the United States. The Aeromedical Evacuation (air evac) process involves many overlapping organizations, including the Army, Air Force, command, medical, and flight personnel. There are often communication problems between the different systems. Which soldiers are returned to the United States, how they get there, whether to send a medical attendant, and which medications to use for the flight are discussed. The air evac process is in transition. We hope that this paper will facilitate cooperation between the different systems and improve patient care.

Carbon Dioxide Transport by Ocean Currents at 25{degrees}N Latitude in the Atlantic Ocean.

Measured concentrations of CO(2), O(2), and related chemical species in a section across the Florida Straits and in the open Atlantic Ocean at approximately 25 degrees N, have been combined with estimates of oceanic mass transport to estimate both the gross transport of CO(2) by the ocean at this latitude and the net CO(2) flux from exchange with the atmosphere. The northward flux was 63.9 x 10(6) moles per second(mol/s); the southward flux was 64.6 x 10(6) mol/s. These values yield a net CO(2) flux of 0.7 x 10(6) mol/s (0.26 +/- 0.03 gigaton of C per year) southward. The North Atlantic Ocean has been considered to be a strong sink for atmospheric CO(2), yet these results show that the net flux in 1988 across 25 degrees N was small. For O(2) the equivalent signal is 4.89 x 10(6) mol/s northward and 6.97 x 10(6) mol/s southward, and the net transport is 2.08 x 10(6) mol/s or three times the net CO(2) flux. These data suggest that the North Atlantic Ocean is today a relatively small sink for atmospheric CO(2), in spite of its large heat loss, but a larger sink for O(2) because of the additive effects of chemical and thermal pumping on the CO(2) cycle but their near equal and opposite effects on the CO(2) cycle.

A Climatic Freshening of the Deep Atlantic North of 50{degrees}N over the Past 20 Years.

Observations made in summer 1981 show a significant and widespread decrease in salinity, averaging 0.02 per mil, in deep waters of the subpolar North Atlantic over the past two decades. This implies a relatively rapid response of deep water formation to climatic perturbation.

Biological control of the removal of abiogenic particles from the surface ocean.

Concurrent measurements of particle concentrations in the near-surface water and of particle fluxes in the deep water of the Sargasso Sea show a close coupling between the two for biogenic components. The concentrations of suspended matter appear to follow an annual cycle similar to that of primary production and deepwater particle flux. Although the concentration of particulate aluminum in the surface water appears to vary randomly with respect to that cycle, the removal of aluminum to deep water is intimately linked to the rapid downward transport of organic matter.

Elevated concentrations of actinides in mono lake.

Tetravalent thorium, pentavalent protactinium, hexavalent uranium, and plutonium (oxidation state uncertain) are present in much higher concentrations in Mono Lake, a saline, alkaline lake in eastern central California, than in seawater. Low ratios of actinium to protactinium and of americium to plutonium indicate that the concentrations of trivalent actinides are not similarly enhanced. The elevated concentrations of the ordinarily very insoluble actinides are maintained in solution by natural ligands, which inhibit their chemical removal from the water column, rather than by an unusually large rate of supply.