ALBERT

Description: Consisting of more than 150 articles written by leading experts, this authoritative reference encompasses the entire field of solid-earth geophysics. It describes in detail the state of current knowledge, including advanced instrumentation and techniques, and focuses on important areas of exploration geophysics. It also offers clear and complete coverage of seismology, geodesy, gravimetry, magnetotellurics and related areas in the adjacent disciplines of physics, geology, oceanography and space science.

Description: A collection of cephalopods from the British Antarctic Survey’s Offshore Biological Programme is described and the cephalopod prey of vertebrate predators at South Georgia is reviewed. Comparison of these data indicates that predators catch larger specimens and a greater diversity of species than nets. There are also differences between samples from different types of net. The RMT 25, the largest research net used to date, has caught most of the species thought to occur in the Scotia Sea but specimens are generally smaller than those taken by predators. Cephalopods which are thought to have potential commercial value are Martialia hyadesi, Kondakovia longimana, Moroteuthis ingens, M. knipovitchi, M. robsoni and Gonatus antarcticus. Other possibilities include species of brachioteuthid, psychroteuthid and neoteuthid. It is likely that Antarctic stocks will be sensitive to exploitation and liable to dramatic fluctuations if overfished. The possible consequences of commercial exploitation of cephalopods for the reproductive success of the vertebrate predators, which prey on cephalopods in the Scotia Sea, are examined.

Description: Antarctic petrels (Thalassoica antarctica) brooding young chicks at Scullin Monolith (67°7′S, 66°42′E), Antarctica, fed fish and crustaceans (87% and 13%, respectively, on a mass basis) to their young. Amounts of solids fed were equivalent to 6.6% of the body mass of adult birds with an empty stomach. The prey comprised species known to occur in the surface layers of the Antarctic ocean in the east wind drift, such as Pleuragramma antarcticum, Notolepis coatsi and Euphausia superba, consistent with the surface feeding habits of Antarctic petrels.

Description: The investigation on the geology of the Sierra Leone Rise contains seismic, petrographic and sedimentological data from the Soviet expedition of R/V »Professor Shtokman«. New results on bottom relief and structure of the Sierra Leone Rise (SLR) are documented in Figs. 1–7. Detailled descriptions of dredge samples of trachyandesites, trachytes, trachyte tuffs, trachybasalts and their tuffs and their chemical composition (Tab. 2) together with the seismic structure of the SLR allow some assumptions on the age and origin of the Rise. The SLR is part of the equatorial Atlantic oceanic crust, that formed in the initial phase of break-up of Gondwana (110–80×106y). During the period 80–90×106 years, when volcanic eruptions were highly intensified in the area, major parts of the SLR have been formed. Some of the volcanic seamounts appeared as islands above sea-level in the Late Cretaceous/Paleocene: the magmatic rocks are more similar to ocean island basalt than to normal oceanic crust. Cenozoic sediments of the SLR reveal continuous sedimentation, which was controlled by surface water productivity, carbonate dissolution and terrigenous matter supply. The Eocene chert sedimentation phase was followed by a period of cyclic carbonate sedimentation. In the Neogene tectonic activity lead to vertical displacements. On several peaked seamounts coral reefs grew. The reef phase was followed by a sinking of the area. At the end of the Neogene the SLR became aseismic. The Late Quaternary sediment cover is studied by means of grab samples and sediment cores from various water depths. The main finding is varying CaCO3 content with depth and with time, controlled mainly by dissolution.

Description: The Quaternary Herchenberg composite tephra cone (East Eifel, FR Germany) with an original bulk volume of 1.17·107 m3 (DRE of 8.2·106 m3) and dimensions of ca. 900·600·90 m (length·width·height) erupted in three main stages: (a) Initial eruptions along a NW-trending, 500-m-long fissure were dominantly Vulcanian in the northwest and Strombolian in the southeast. Removal of the unstable, underlying 20-m-thick Tertiary clays resulted in major collapse and repeated lateral caving of the crater. The northwestern Lower Cone 1 (LC1) was constructed by alternating Vulcanian and Strombolian eruptions. (b) Cone-building, mainly Strombolian eruptions resulted in two major scoria cones beginning initially in the northwest (Cone 1) and terminating in the southeast (Cones 2 and 3) following a period of simultaneous activity of cones 1 and 2. Lapilli deposits are subdivided by thin phreatomagmatic marker beds rich in Tertiary clays in the early stages and Devonian clasts in the later stages. Three dikes intruded radially into the flanks of cone 1. (c) The eruption and deposition of fine-grained uppermost layers (phreatomagmatic tuffs, accretionary lapilli, and Strombolian fallout lapilli) presumably from the northwestern center (cone 1) terminated the activity of Herchenberg volcano. The Herchenberg volcano is distinguished from most Strombolian scoria cones in the Eifel by (1) small volume of agglutinates in central craters, (2) scarcity of scoria bomb breccias, (3) well-bedded tephra deposits even in the proximal facies, (4) moderate fragmentation of tephra (small proportions of both ash and coarse lapilli/bomb-size fraction), (5) abundance of dense ellipsoidal juvenile lapilli, and (6) characteristic depositional cycles in the early eruptive stages beginning with laterally emplaced, fine-grained, xenolith-rich tephra and ending with fallout scoria lapilli. Herchenberg tephra is distinguished from maar deposits by (1) paucity of xenoliths, (2) higher depositional temperatures, (3) coarser grain size and thicker bedding, (4) absence of glassy quenched clasts except in the initial stages and late phreatomagmatic marker beds, and (5) predominance of Strombolian, cone-building activity. The characteristics of Herchenberg deposits are interpreted as due to a high proportion of magmatic volatiles (dominantly CO2) relative to low-viscosity magma during most of the eruptive activity.

Description: The challenges of collecting, transporting, and maintaining healthy wild squids have been nearly as formidable as those of determining the structure and function of ion channels in squid giant axons. The differences are a matter of scale, not complexity. Careful perusal of the literature indicates clearly that failures have been the rule, especially with squids of the genus Loligo. It is an unfortunate fact that the vast majority of biomedical research on Loligo has been done on animals that were moribund when they were prepared for experiments. This was due in most cases to skin damage incurred during capture and transport from the field to the laboratory, and to the secondary infections that invariably followed immediately. Furthermore, the availability of live squids for research is limited seasonally because of the migratory behavior of these fast-swimming invertebrates. Thus any improvements in maintenance, rearing or culture will lead not only to greater availability to meet the demand from researchers, but hopefully to the provision of healthy squids for a wide range of experimentation.

Description: A mechanism exists whereby global greenhouse warning could, by intensifying the alongshore wind stress on the ocean surface, lead to acceleration of coastal upwelling. Evidence from several different regions suggests that the major coastal upwelling systems of the world have been growing in upwelling intensity as greenhouse gases have accumulated in the earth's atmosphere. Thus the cool foggy summer conditions that typify the coastlands of northern California and other similar upwelling regions might, under global warming, become even more pronounced. Effects of enhanced upwelling on the marine ecosystem are uncertain but potentially dramatic.

Description: Because of the implications of shallow gas accumulations to drilling and the integrity of platform foundations, it is important to determine whether gas accumulations can be considered as effectively static, unchanging for the duration of offshore operations, or dynamic. Shallow gas is frequently seen in association with seabed features, such as mud lumps, gas domes and pockmarks. These are considered to have been caused by the escape of gas through the seabed, consequently it can be implied that gas has migrated to, and through, the seabed. This indicates that shallow gas is not static, but it does not suggest a time-scale over which migration occurs. Is shallow gas mobile on a geological or a human time-scale?

Description: Rates of protein synthesis in the whole body and tissues ofOctopus vulgaris collected in September 1985 and 1986 from the Bay of Naples were measured following a flooding dose injection of3H phenylalanine. There were stable phenylalanine free pool-specific radioactivities and linear incorporation of radiolabel into arm-tip protein from 10 to 30 min after the injection. In starved individuals there were no significant differences between the fractional rates of protein synthesis of the following tissues: ventricle, brain, branchial heart, arm tip, gill, stomach, arm, renal appendage and mantle. The mean value (± SE) for all the tissues was 3.02 ± 0.17% d−1. In individuals fed varying amounts of crab, resulting in differing growth rates, there was a linear increase in fractional rates of whole-body protein synthesis with growth rate. A standard 148 g octopus growing at 3.0% d−1 synthesised 0.54 g of protein, with 0.43 g of this protein retained as growth. The proportion of the total protein synthesis which was retained as growth increased with increasing growth rate; at a maximum growth rate of 6% d−1, over 90% of the protein synthesised was retained as growth. The ventricle, arm tip, gill, arm and mantle also showed similar patterns of a linear increase in fractional rates of protein synthesis with increased growth rates. The RNA concentrations in the whole body and tissues increased with increasing growth rates, but the major change was an increase in the efficiency of translation. It is concluded that rapid growth rates inO. vulgaris are brought about by high rates of protein synthesis and high efficiencies of retention of synthesised protein and, therefore, little protein degradation.

Description: Facies patterns within the Pleistocene reef terraces along the Red Sea coast exhibit lateral changes over short distances. These changes reflect either transitions within the depositional environment or they are related to minor or major sea level fluctuations. On the basis of quantitative distributions of biota in the field as well as in thin section it is possible to establish and map these lateral patterns. Important biota are framebuilders and secondary reef encrusters (foraminifers, coralline algae). Frequency distributions of sessile foraminifera and scleractinians are strikingly similar to those of the recent environment within diagenetically unaltered terraces. The marine reef terraces occur in different elevated levels above the present sea level. Morphological steps are caused by onlap during different sea levels, by tectonics, or by erosion during transgression. Although several morphological steps exist which obscure the terrace stratigraphy, only three reef units can be distinguished. Each unit exhibits a lateral facies development, which begins at the shore, covering the whole lagoonal facies and ends at the upper reef slope. Besides this lateral facies pattern vertical patterns occur as well, showing a transgressive sequence in the youngest (lower) and oldest (upper) unit and a regressive one in the middle unit. In top quality outcrops, like wadi sections, it is possible to differentiate within the youngest reef unit between three onlaping reef cycles. Such cycles, however, can not be seen in the middle and oldest formations. The three reef cycles within the youngest unit and the three units as well, exhibit different degrees of diagenetic alterations, which are strongly reflected by a gradual reduction in the number of biota. This reduction may be best described as a process of “sieving”. Where these differences in diagenesis are recorded, they correspond to the age of the reef units. U/Th datations of the investigated terraces reveal an age for the youngest unit between 86,000 and 118,000 years B.P.. During this time three major sea level high stands have occurred, which explain the existence of the three reef cycles. The age of the middle formation is around 205,000 years, while the age for the oldest formation can only be assumed to fit in the time span between 290,000 and 340,000 years B.P.. All these data correspond to other published datations along the Red Sea coast.

Description: This paper presents an analysis of zooplankton net sampling surveys carried out during four expeditions to the Antarctic Peninsula region. Cluster analysis documented two to three site groupings for the epipelagic zone and one mesopelagic site cluster below 200 to 300 m depth. Analysis of species dominance, constancy, diversity and evenness indices did not allow clear designation and separation of communities in terms of these parameters. Computation of a rank correlation matrix for each season allowed the characterization of species groups. There were no perfect indicator species in the very strict sense. The main differences in the composition of the zooplankton between the site clusters were due mainly to changes in abundance rather than to presence or absence of particular species. However, the interpretation of the complex species and site groupings led to the conclusion that we can define three distinct communities: an oceanic, a neritic, and a mesopelagic community beneath 200 to 300 m. A so-called transitional cluster represents a mixing zone created by frequent occurrence of species from both the oceanic and neritic community. The location of the described oceanic and neritic community sites seem to be relatively stable with minor latitudinal changes during the seasons, while occurrence and abundance of most species changes with the time of the year. The usefulness of particular species (e.g. Euphausia superba) as indicator species also change during the year

Description: Polysyncraton lacazei is a colonial tunicate (family didemnidae) living in the NW-mediterranean rocky sublitoral. A thorough scanning of numerous colonies revealed that in spite of an apparently heavy local fouling pressure only one fouling species — a kamptozoan — is encountered with some regularity on Polysyncraton. We try to define the epibiotic situation of sessile marine organisms as composed of four epibiotic parameters: longevity or exposure time (A), epibiont load (E), colonizer pool (CP) and fouling-period (FP). Subsequently, these factors are combined to propose an “Antifouling Potential” index: AFP=(1−E/CP)×A/(FP+A). This index is intended to permit evaluating the relative antifouling defense potency to be expected in a given organism in a given epibiotic situation and to compare different cases of epibiosis and fouling.

Description: Valley-fill ignimbrites of the Middle Laacher See Tephra (MLST) in the proximal depositional fan south of Laacher See volcano are laterally continuous with fine-grained overbank-facies deposits, 0.5–1.5 m thick, covering higher elevations and interfluves between the paleovalleys. The overbank deposits consist of up to 12 ash layers, each 4–10 cm thick, which show internal structures typical of ash-flow transport, such as poor sorting, reverse size-grading of pumice, local normal grading of coarse ash-sized lithics above a fine-grained basal layer, cross-stratification behind obstacles, and erosional unconformities. Thickness, median grain-size, and number of individual layers decrease systematically with distance from the vent. Overbank ash layers thicken at the valley slopes and form discrete valley-fill ignimbrite flow units in the paleochannels with median grain size increasing from ≤63 μm to ≤350 μm. Toward the center of paleochannels, however, the well-defined overbank facies is obscured by mutual erosion of individual flow units. Overlapping data fields in ternary grain-size variation diagrams indicate the overbank facies to have evolved from ash flows chiefly through depletion of lapilli and coarse ash. Overbank-facies ash layers do not represent dust layers resulting from elutriation clouds of ash flows (co-ignimbrite ash) or surge deposits developed on higher ground due to low concentration of solids. They are similar in some parameters to Taupo-type ignimbrite veneer deposits, but are interpreted differently. The thin, fine-grained, Laacher See ash layers are thought to have been deposited from diluted portions of the flow proceeding directly from the eruption column while the main pyroclastic flows were confined to the paleovalleys radiating away from the eruptive center. The wide distribution of the thin ash layers is attributed to the balance of deposition from various flow parts and turbulent entraining and heating of ambient air that sustained sufficient mobility of the diluted flows to spread across hills and level ground.

Description: The sea floor of Fram Strait, the over 2500 m deep passage between the Arctic Ocean and the Norwegian-Greenland Sea, is part of a complex transform zone between the Knipovich mid-oceanic ridge of the Norwegian-Greenland Sea and the Nansen-Gakkel Ridge of the Arctic Ocean. Because linear magnetic anomalies formed by sea-floor spreading have not been found, the precise location of the boundary between the Eurasian and the North American plate is unknown in this region. Systematic surveying of Fram Strait with SEABEAM and high resolution seismic profiling began in 1984 and continued in 1985 and 1987, providing detailed morphology of the Fram Strait sea floor and permitting better definition of its morphotectonics. The 1984 survey presented in this paper provided a complete set of bathymetric data from the southernmost section of the Svalbard Transform, including the Molloy Fracture Zone, connecting the Knipovich Ridge to the Molloy Ridge; and the Molloy Deep, a nodal basin formed at the intersection of the Molloy Transform Fault and the Molloy Ridge. This nodal basin has a revised maximum depth of 5607 m water depth at 79°8.5′N and 2°47′E.

Description: Cephalopod remains were collected, at regular intervals throughout the fledging period, from the stomach contents of chicks of the grey-headed albatrossDiomedea chrysostoma at Bird Island, South Georgia, in 1984 and 1986 and from regurgitations of adults at the nest in 1986. The 1984 sample was taken during a season characterised by abnormal local oceanographic conditions in which the breeding success was very low; in 1986 conditions were normal and breeding success was high. Cephalopod beaks (289 from adults; 5 651 from chicks) were identified, and allometric equations were used to estimate the biomass represented. Five cephalopod species belonging to five families (Gonatidae, Onychoteuthidae, Psychroteuthidae, Ommastrephidae and Cranchiidae) contributed 98% by number and 97% of the biomass fed to chicks. The most important species was the ommastrephid Martialia hyadesi, contributing 68.9 to 77.4% by number and 72.5 to 79.3% of the total biomass fed to chicks. The relative proportions of cephalopod species in the chicks' diet were similar between 1984 and 1986, but the total number and biomass was significantly less in 1984. There is evidence of growth ofM. hyadesi between January and June.