Accumulation in Svalbard glaciers deduced from ice cores with nuclear tests and Chernobyl reference layers

Mean net annual balance and the related spatio-temporal variations have been determined on the basis of well-dated artificial layers in shallow ice cores (Chernobyl, 1986, and atmospheric thermonuclear tests, mainly in 1961-62 in Novaya Zemlya). Seventy ice cores from 13 Svalbard glaciers have been analysed. On each glacier, in its accumulation area and at the highest elevation, one ice core was recovered down to about 40 m and sampled for radioactivity measurements to determine the 1986 and 1962-63 layer (1954 was the initial date of the nuclear tests). For each glacier, at least five complementary ice cores from the accumulation area were analysed to determine the Chernobyl reference layer. Six ice cores exhibit both the Chernobyl and nuclear tests layers and are of special interest in this study.
This work provides new data on the deposition rates of natural and artificial radioisotopes. Using ice cores samples from the Arctic glaciers, even with superimposed ice accumulation, it is possible to distinguish between the Chernobyl and the nuclear tests fallouts. This work also shows that the mean annual net balance did not significantly change for at least five ice core locations in the Svalbard glaciers for the two periods extending from 1963 to 1986 to the recent date of drilling.     

Ocean bottom seismograph

The ocean bottom seismograph described in this paper has been developed primarily for recording earthquakes on the mid-oceanic ridges. The instrument is suitable for dropping onto the most rugged areas of the ocean floor. Acoustic tracking with the ship's precision echo sounder enables it to be located there relative to both the topography of the sea bed and the ship. The outputs of a 3-component seismometer and a hydrophone are recorded in FM form on a low-power magnetic tape recorder designed specifically for the instrument.     

Laboratory study of wave and turbulence velocities in a broad-banded irregular wave surf zone

The characteristics of wave and turbulence velocities created by a broad-banded irregular wave train breaking on a 1:35 slope were studied in a laboratory wave flume. Water particle velocities were measured simultaneously with wave elevations at three cross-shore locations inside the surf zone. The measured data were separated into low-frequency and high-frequency time series using a Fourier filter. The measured velocities were further separated into organized wave-induced velocities and turbulent velocity fluctuations by ensemble averaging. The broad-banded irregular waves created a wide surf zone that was dominated by spilling type breakers. A wave-by-wave analysis was carried out to obtain the probability distributions of individual wave heights, wave periods, peak wave velocities, and wave-averaged turbulent kinetic energies and Reynolds stresses. The results showed that there was a consistent increase in the kurtosis of the vertical velocity distribution from the surface to the bottom. The abnormally large downward velocities were produced by plunging breakers that occurred from time to time. It was found that the mean of the highest one-third wave-averaged turbulent kinetic energy values in the irregular waves was about the same as the time-averaged turbulent kinetic energy in a regular wave with similar deep-water wave height to wavelength ratio. It was also found that the correlation coefficient of the Reynolds stress varied strongly with turbulence intensity. Good correlation between u′ and w′ was obtained when the turbulence intensity was high; the correlation coefficient was about 0.3–0.5. The Reynolds stress correlation coefficient decreased over a wave cycle, and with distance from the water surface. Under the irregular breaking waves, turbulent kinetic energy was transported downward and landward by turbulent velocity fluctuations and wave velocities, and upward and seaward by the undertow. The undertow in the irregular waves was similar in vertical structure but lower in magnitude than in regular waves, and the horizontal velocity profiles under the low-frequency waves were approximately uniform.     

Modeling environmental effects on the size-structured energy flow through marine ecosystems. Part 2: Simulations

Numerical simulations using a physiologically-based model of marine ecosystem size spectrum are conducted to study the influence of primary production and temperature on energy flux through marine ecosystems. In stable environmental conditions, the model converges toward a stationary linear log–log size-spectrum. In very productive ecosystems, the model predicts that small size classes are depleted by predation, leading to a curved size-spectrum.It is shown that the absolute level of primary production does not affect the slope of the stationary size-spectrum but has a nonlinear effect on its intercept and hence on the total biomass of consumer organisms (the carrying capacity). Three domains are distinguished: at low primary production, total biomass is independent from production changes because loss processes dominate dissipative processes (biological work); at high production, ecosystem biomass is proportional to primary production because dissipation dominates losses; an intermediate transition domain characterizes mid-production ecosystems. Our results enlighten the paradox of the very high ecosystem biomass/primary production ratios which are observed in poor oceanic regions. Thus, maximal dissipation (least action and low ecosystem biomass/primary production ratios) is reached at high primary production levels when the ecosystem is efficient in transferring energy from small sizes to large sizes. Conversely, least dissipation (most action and high ecosystem biomass/primary production ratios) characterizes the simulated ecosystem at low primary production levels when it is not efficient in dissipating energy.Increasing temperature causes enhanced predation mortality and decreases the intercept of the stationary size spectrum, i.e., the total ecosystem biomass. Total biomass varies as the inverse of the Arrhenius coefficient in the loss domain. This approximation is no longer true in the dissipation domain where nonlinear dissipation processes dominate over linear loss processes. Our results suggest that in a global warming context, at constant primary production, a 2–4 °C warming would lead to a 20–43% decrease of ecosystem biomass in oligotrophic regions and to a 15–32% decrease of biomass in eutrophic regions.Oscillations of primary production or temperature induce waves which propagate along the size-spectrum and which amplify until a “resonant range” which depends on the period of the environmental oscillations. Small organisms oscillate in phase with producers and are bottom-up controlled by primary production oscillations. In the “resonant range”, prey and predators oscillate out of phase with alternating periods of top-down and bottom-up controls. Large organisms are not influenced by bottom-up effects of high frequency phytoplankton variability or by oscillations of temperature.     

Stable abundance,but changing size structure in grenadier fishes (Macrouridae) over a decade (1998–2008) in which deepwater fisheries became regulated

A ten-year time series (1998–2008) from a trawl survey of the continental slope of the NE Atlantic was analyzed to assess temporal variation in the abundance and length frequency of seven species of deepwater grenadier fish. This period coincided (in 2003) with the regulation of deepwater fisheries in this area. None of the species declined in numbers or biomass over the period, and 2 species significantly increased. This suggests that the declines in abundance of these deepwater species following the onset of fishing in the 1970s may now have stabilized, albeit at much lower levels than the virgin biomass. Although two metrics of body size (mean length and maximum length) did not show any evidence for consistent decrease over time, there were significant changes in the overall length–frequency distributions. The species found in shallower depths (500 m) had a greater number of larger individuals in 2008 whereas those found deeper (1500 m) tended to have a greater number of smaller individuals. This suggests the presence of a lagged indirect effect of fishing on species that live beyond the actual depths that fishing takes place.