Description: Recently the influence of an electric light on the capture of the main groups of deep sea animals by a midwater trawl was described and discussed (Clarke & Pascoe, 1985). With regard to fish it was shown that at depths close to 800 m the total number, the total volume, the volume of the ten largest and the volume of the single largest fish all increased significantly when an electric light was used on the headline of the trawl when compared with controls with the light off. These experiments were carried out both in the Bay of Biscay and off Madeira.

Description: The effect of two 70 W underwater electric lamps on the catch rate of a commercial bottom otter trawl was determined by comparative trials both at night and in daylight. It was found that, although the overall numbers and weights of fish caught did not differ, most of the species which were caught in large enough numbers for a judgement to be made showed a reaction to light. Three species, Trachurus trachurus, Merlangius merlangus and Trisopterus minutus were attracted and four species, Eutriglagurnardus, Micromesistius poutassou, Merluccius merluccius and Limanda limanda were scared off by light. The possible use of lights to further the development of selective commercial bottom trawling by attracting or scaring particular species is discussed.

Description: Growth laminations were first noted in squid statoliths by Clarke (1966), who suggested they might be useful for age determination. Spratt (1978) presented a detailed age analysis of Loligo opalescens Berry, 1911, arguing that some rings in the cephalopod statolith were deposited daily, as are fish otoliths (Panella, 1971). Growth rings in Illex illecebrosus (Lesueur, 1921) statoliths were illustrated by Lipinski (1978) with similar interpretation to that of Spratt (op. cit.). Several further attempts have been made to validate and/or to discuss age determination from statoliths (Hurley, Drew & Radtke, 1979; Hurley et al. 1983; Wiborg, 1979; Hurley & Beck, 1980; Kristensen, 1980; Lipinski, 1980, 1981; Rosenberg, Wiborg & Bech, 1981; Martins, 1982; Radtke, 1983; Dawe et al. 1984), and several other attempts are in preparation (R. J. Hanlon, G. V. Hurley, M. R. Clarke & R. L. Radtke, personal communications).

Description: The importance of feeding pattern is well documented in fish (Jenkins & Green, 1977; Simenstad & Cailliet, 1986) but there are not many reported studies in cephalopods. Feeding patterns, as defined by Jenkins & Green (1977) have been studied, to our knowledge, only in Todarodes pacificus (Okiyama, 1965), Loligo pealei (Vovk, 1972), Loligo opalescens (Karpov & Cailliet, 1978), Illex illecebrosus (Amaratunga et ah, 1979; Amaratunga, 1980) and Nototodarus gouldi (O'Sullivan & Cullen, 1983). Boyle (1983) dealt with aspects of feeding in several cephalopod species but not specifically with feeding pattern. Aspects of feeding in Sepia officinalis have been reviewed by Nixon (1987). The present work describes the daily feeding pattern in Sepia officinalis from data collected in the field.

Description: Santorini volcanic field has had 12 major (1–10 km3 or more of magma), and numerous minor, explosive eruptions over the last ~ 200 ka. Deposits from these eruptions (Thera Pyroclastic Formation) are well exposed in caldera-wall successions up to 200 m thick. Each of the major eruptions began with a pumice-fall phase, and most culminated with emplacement of pyroclastic flows. Pyroclastic flows of at least six eruptions deposited proximal lag deposits exposed widely in the caldera wall. The lag deposits include coarse-grained lithic breccias (andesitic to rhyodacitic eruptions) and spatter agglomerates (andesitic eruptions only). Facies associations between lithic breccia, spatter agglomerate, and ignimbrite from the same eruption can be very complex. For some eruptions, lag deposits provide the only evidence for pyroclastic flows, because most of the ignimbrite is buried on the lower flanks of Santorini or under the sea. At least eight eruptions tapped compositionally heterogeneous magma chambers, producing deposits with a range of zoning patterns and compositional gaps. Three eruptions display a silicic–silicic + mafic–silicic zoning not previously reported. Four eruptions vented large volumes of dacitic or rhyodacitic pumice, and may account for 90% or more of all silicic magma discharged from Santorini. The Thera Pyroclastic Formation and coeval lavas record two major mafic-to-silicic cycles of Santorini volcanism. Each cycle commenced with explosive eruptions of andesite or dacite, accompanied by construction of composite shields and stratocones, and culminated in a pair of major dacitic or rhyodacitic eruptions. Sequences of scoria and ash deposits occur between most of the twelve major members and record repeated stratocone or shield construction following a large explosive eruption. Volcanism at Santorini has focussed on a deep NE–SW basement fracture, which has acted as a pathway for magma ascent. At least four major explosive eruptions began at a vent complex on this fracture. Composite volcanoes constructed north of the fracture were dissected by at least three caldera-collapse events associated with the pyroclastic eruptions. Southern Santorini consists of pryoclastic ejecta draped over a pre-volcanic island and a ridge of early- to mid-Pleistocene volcanics. The southern half of the present-day caldera basin is a long-lived, essentially non-volcanic, depression, defined by topographic highs to the south and east, but deepened by subsidence associated with the main northern caldera complex, and is probably not a separate caldera.

Description: Orbulina universa d'Orbigny is a spinose planktonic foraminifer which occurs throughout surface waters of the tropical, subtropical and transition zones of the world ocean (Bé & Tolderlund, 1971). This species is unique among planktonic Foraminifera in that its life cycle is composed of two growth stages. The juvenile stage is a trochospiral form which is enclosed within a terminal spherical chamber in the adult stage. O. universa is relatively omnivorous, and consumes a variety of prey that range in size and quality from phytoplankton to copepods (Bé et al. 1977; Anderson et al. 1979; Spindler et al. 1984). In addition, each individual harbors several thousand zooxanthellae which presumably are an additional source of nutrition for the foraminifer (Be et al. 1977; Hemleben & Spindler, 1983; Spero & Parker, 1985).

Description: Cephalopods may be divided into five types according to their buoyancy. Members of several families such as the Octopodidae, Loliginidae and Ommastrephidae are negatively buoyant and must swim to stay in midwater and are therefore highly muscular animals. Others have mechanisms to make them neutrally buoyant so they can remain suspended in midwater without effort. Nautilus, Spirula and cuttlefishes have low pressure gas-filled chambers and their flesh is muscular and non-buoyant (Denton & Gilpin-Brown, 1973). Squids of one family, the Gonatidae, have a low density oil in their livers to give buoyancy but most of their body is muscular. Some oceanic octopods have very watery tissues in which lighter chloride ions replace sulphate ions (Denton & Shaw, 1961). In 12 of the 26 teuthoid families the buoyancy is provided by low-density ammonia-rich solution in their body and head tissues or in an expanded coelomic cavity (Clarke, Denton & Gilpin-Brown, 1979). These ammoniacal squids are extremely abundant in the oceans of the world and form a large part of the diet of birds, cetaceans, seals and fish (Clarke, 1977). When their biomass is estimated from their utilization by predators it is important to know their properties as food and, in particular, their calorific values. As pointed out by Croxall & Prince in a review of the calorific values of cephalopods (1982), all the known values are of muscular, negatively buoyant species because they are of value as food for humans but no measurements have been made on the ammoniacal or oily species which are probably as important, or even more important, in the economy of the ocean (Clarke, 1983).

Description: Cephalopod beaks recovered from stomach samples taken from l 4 sea bird species in the southern Benguela region off Southern Africa and from one species at Sub-Antarctic Marion Island, were identified as far as possible, counted and the lower rostral lengths (LRLs) measured. Dorsal mantle lengths (DMLs) and body masses of the cephalopods eaten were estimated. The results of analyses by percentage frequency of occurrence and numerical abundance are discussed with reference to present knowledge of the distribution of cephalopods eaten by sea birds in the areas studied. Division of the cephalopod component of seabird diets into species which float, and species which sink, after death indicates that the birds forage on dead or moribund cephalopods on the surface, rather than catching live bioluminescent cephalopods at night.

Description: Surveys of the interdial macrofauna and sediment characters of Nigg Bay, Moray Firth, were carried out between 1981 and 1985. Permanent stations were located at the intersections of a half-kilometre grid covering the entire interdial area and sampled for infauna using replicate cores. Estimates were also made of mussel and lugworm densities from quadrats and cast counts respectively. The biomass of selected species that constitute important resources for higher tropic levels were also estimated. The sediment for each station was analysed for median particle diameter and slit content. The infaunal data were analysed by Detrended Correspondence Analysis. This indicated that tida height was the most important factor governing the distribution and abundance of the interdial communities. Sediment characters were only poorly related to distribution patterns. The bay has a rich fauna and is biologically similar to other outer bays of the Moray Firth, which, like Nigg, are important areas for wildfowl and waders. Comparison of survey data from different years indicate that there are natural cycles in some sediment and biological characters of Nigg Bay.