Analysis of correlations between time series with the use of the phase spectrum

In connection with the problem of revealing cause-effect relations among different climatic characteristics, methods for determining the dependence between time series on the basis of selected auto-and cross-covariance functions and periodograms expressed in terms of the Fourier coefficients of the initial series are discussed. Real time series do not always satisfy the conditions of statistical stationarity, so that their analysis requires a combination of statistical and deterministic approaches. The possibility of using the above numerical characteristics in relation to such series is considered. Characteristic features of describing finite segments of time series with the use of their Fourier coefficients is studied in detail. The main emphasis is on the determination of the time shifts (delays) at which the covariance between the series is maximal. The problems that appear during a practical implementation of the periodogram method for shift estimation are discussed. A previously unknown formula that is necessary for further studies and relates the Fourier transform of a selected correlation function to the periodogram of the series is derived.     

Methods of fitting the Fisher-Tippett type 1 extreme value distribution

Methods are described for estimating the parameters of the Fisher-Tippet Type 1 extreme value distribution and associated return values from measured extremes, such as maximum wave height. A comparison of these methods, with simulated data, shows that those using Gumbel's plotting position are least satifactory. Maximum likelihood methods give the smallest mean square errors, but the very much simpler method of moments is nearly as good.     

Acoustic reflectors in the surface layers of deep sea sediments

Using ultrasonic scanning it is possible to display the position of an acoustic discontinuity within a sediment core and the amplitude of the reflected signal which results from it. From these results it has been possible to examine the effect of variations in the geotechnical properties on the reflection of compressional waves at normal incidence within the core at a frequency of 100 kHz. The occurrence of acoustic reflectors in the surface layers of North Atlantic sediments has also been examined.Two ultrasonic scanning systems for the non-destructive testing of marine sediment cores have been developed. The performance of the two systems has been evaluated using the results from measurements made on a suite of marine sediment cores from the North Atlantic in conjunction with X-ray scanning and geological analysis of the same cores.     

Trace metals and hydrocarbons in sediments from the Southampton water region,with particular reference to the influence of oil refinery effluent

The concentrations of a number of trace metals (Co, Ni, Cu, Zn, Ag, Cd and Hg) have been determined in sediments from cores collected in the Southampton Water region. Measurements of total hydrocarbons were also made on several of the cores. Markedly elevated concentrations of copper, up to 362 μg/g dry wt, were found in sediments which were collected close to the discharge points of oil refinery outfalls and which also showed concentrations of total hydrocarbons considerably greater than the background levels for the estuary. The results of selective chemical extractions showed that much of the copper was present in the non-lattice fraction of the sediment. Although the concentrations of Co, Ni, Zn and Cd were significantly correlated with those of copper in the core showing the highest concentrations of this element, these metals were not enhanced in comparison with the levels found in several other parts of the estuary. Variations in concentrations of metals in sediments throughout the estuary were not correlated with differences in organic carbon content.     

Chlorinated hydrocarbons in seawater: Analytical method and levels in the northeastern Pacific

A method is described for analyzing nanogram quantities of chlorinated hydrocarbons from 1-1 samples of seawater. Seawater samples are pumped through a copper column containing a mixture by weight of 5% activated carbon powder, 10% MgO and 85% refined diatomaceous earth. The chlorinated hydrocarbons in the seawater are adsorbed or trapped on the column and subsequently eluted with 30% benzene in acetone (v/v) for analysis by gas-liquid chromatography.This procedure was used to analyze chlorinated hydrocarbon levels in samples collected off the southern California coast. We suggest that anthropogenic chlorinated hydrocarbons can be used for the investigation of large-scale ocean currents and mixing processes.