ALBERT

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: 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.