ALBERT

Description: The fur seal, Arctocephalus gazella, population at Mossman Peninsula (Laurie Island) was studied from 1985 to 1987. Weekly counts were carried out at a 4 km bachelor haul-out beach from December through June. Maxima of 2 240, 2 787 and 5 196 juvenile and adult males were counted during March of the respective years. Census data indicate an increase in the non-breeding population of 13.5% between 1985–1986 and 46.5% between 1986–1987.

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: In the Antarctic there are large unexploited stocks of cephalopods with high potential commercial value and there are two important fisheries for squid in the cool temperate waters of the Southern Ocean, adjacent to the Antarctic, in the Atlantic and Pacific sectors. Squid fisheries can develop very rapidly, and if this were to happen in the Antarctic before adequate management plans could be established, there would be serious consequences for the squid stocks, and also for the vertebrate predator populations which depend on them. It is especially important to increase our knowledge of the Antarctic cephalopod species, their distribution and role in the food chain, and to understand their life cycles

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: At ODP Site 661 from the continental margin of Northwest Africa, authigenic clinoptilolites were investigated in detail. Based on chemical data, crystal size and shape and their intergrowth with associated mineral phases, two types of clinoptilolite (type A and B) occur representing different diagenetic conditions under which the formation of zeolites took place. Clinoptilolite type A was found in a sediment section comprises numerous hiatuses and stratigraphically condensed sediments and could have been formed during early diagenesis. In contrast, clinoptilolite type B was precipitated in Campanian sediments during later diagenesis, after the transformation from opal-A to opal-CT had taken place. At Site 661, the silica source for the authigenesis of both clinoptilolite types is biogenic opal. Volcanic ash material occurs, but in low amounts and thus is not a prerequisite for the formation of clinoptilolite at Site 661.

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: Respiration and nitrogen excretion rates of mature adult Loligo forbesi were investigated at the Roscoff Laboratory (North Brittany, France) during individual short-term incubation experiments in January 1986. The squids were in post-digestive condition and not actively swimming. Both oxygen uptake and nitrogen excretion are continuous processes. The metabolic rates of this active nektonic species (145 ml kg-1 h-1 oxygen uptake, 18.56 μg g-1 h-1 ammonia excretion) are distinctly higher than those of benthic cephalopods. Proteins constitute the main metabolic substrate for energetic needs. Besides ammonia, urea is also continuously released, in amounts ranging from 5 to 16% of ammonia-excretion values.

Description: The diets of five breeding seabird species were investigated on Adélie Land in January–February 1982. Stomach contents of Adélie penguins, Pygoscelis adeliae, were sampled by a water off-loading method and of Procellariiformes by spontaneous regurgitation. Diet compositions by mass were: Adélie penguin (79% euphausiid, 18% fish, 3% squid); Cape pigeon, Daption capense, (64% euphausiid, 29% fish, 7% carrion); Antarctic fulmar, Fulmarus glacialoides, (64% euphausiid, 20% carrion, 16% fish); snow petrel, Pagodroma nivea, (95% fish, 2% euphausiid, 1% carrion) and Wilson's stormpetrel, Oceanites oceanicus, (39% fish, 37% euphausiid, 13% carrion, 12% various crustaceans). The present Adélie penguin diet is consistent with those reported in other studies, given our knowledge of geographical variation in food availability. Differences in the diets of fulmarine petrels appear to relate to differences in foraging areas. The snow petrel is a fish-eating bird associated with pack-ice. Cape pigeon and Antarctic fulmar are mainly krill-eaters and we infer segregation along a neritic/oceanic gradient because of the importance of the neritic Euphausia crystallorophias in the former and the oceanic E. superba in the latter.

Description: The foraging behaviour of fur seals and two species of surface feeding seabirds was observed over swarms of vertically migrating krill along the Antarctic Peninsula in July 1987. Fur Seal haul out patterns were correlated with krill in the upper 30 m of the water column. Krill moved to the surface at night; seals subsequently foraged from 1400-0700 hours before returning to floes. Foraging was continuous through the night. Dive duration decreased as krill moved up to the surface; shorter dives may have been more successful than longer ones. It is possible that very deep dives, which occur early in a foraging bout, represent more of an attempt to assess krill depth and distribution rather than being a genuine foraging effort. Seabirds responded to the presence of a surface krill swarm by circling over it and foraging; krill at depths greater than 30 m elicited directional flight and low frequencies of prey capture attempts. Both Snow Petrels and Antarctic Terns preyed on krill, but each species approached the swarms from different habitats. Snow Petrels primarily overflew areas covered by ice; terns preferred open water. This suggested that prey encounters are essentially opportunistic, although the search for prey is limited to rather specific marine habitats. This feature may be important to our understanding of the factors that determine the pelagic distribution of seabirds.

Description: The diet of the emperor penguin Aptenodytes forsteri in the eastern Weddell Sea, Antarctica was studied during October and November 1986 by stomach content analysis. Emperor penguins fed mainly on Antarctic krill Euphausia superba, Antarctic silverfish Pleuragramma antarcticum and squid Psychroteuthis glacialis. Benthic prey was not found. The prey composition suggests two different feeding strategies, shallow dives exploring the rugged underside of sea ice where krill is taken, and deep dives when mesopelagic fish and squid are consumed. Chicks were fed on average every 1.44 days.