ALBERT

Description: High-resolution seismic reflection and Sea Beam bathymetric data provide insights into the processes of sediment offscraping and accretion in the Middle America Trench off southern Mexico. Thick terrigenous sediments that are transported down Ometepec Canyon and accumulate along the trench floor are scraped off the oceanic plate and accreted in thrust packets to the lower trench slope. The packets offscraped represent most of the trench strata. Underlying hemipelagic deposits that accumulate on the seafloor seaward of the trench are subducted landward of the toe of the slope. Horizontal displacement on the thrust is less than 1 km. Leading edge folds are the surface expressions of the thrusts and strike subparallel to the base of the trench slope. The folds are continuous for as much as 10 km and have amplitudes as high as 200 m and wavelengths of 0.5 to 2 km. Folds are best developed along sections of the trench with interbedded silty turbidite and mud deposits. Fold are absent where thick coarse-grained fan deposits occur. Thickening of the thrust packets occurs by large-scale thrust duplication, by layer-parallel shortening, and by deposition of material that slumps off the leading edge of older upslope thrust blocks.

Description: We have determined the centroid depths and source mechanisms of 12 large earthquakes on transform faults of the northern Mid-Atlantic Ridge from an inversion of long-period body waveforms. The earthquakes occurred on the Gibbs, Oceanographer, Hayes, Kane, 15°20′, and Vema transforms. We have also estimated the depth extent of faulting during each earthquake from the centroid depth and the fault width. For five of the transforms, earthquake centroid depths lie in the range 7–10 km beneath the seafloor, and the maximum depth of seismic faulting is 14–20 km. On the basis of a comparison with a simple thermal model for transform faults, this maximum depth of seismic behavior corresponds to a nominal temperature of 900° ± 100°C. In contrast, the nominal temperature limiting the maximum depth of faulting during oceanic intraplate earthquakes with strike-slip mechanisms is 700° ± 100°C. The difference in these limiting temperatures may be attributed to the different strain rates characterizing intraplate and transform fault environments. Three large earthquakes on the 15°20′ transform have shallower centroid depths of 4–5 km and a maximum depth of seismic faulting of 10 km, corresponding to a limiting temperature of 600°C. The shallower extent of seismic behavior along the 15°20′ transform may be related to a recent episode of extension across the transform associated with the northward migration of the triple junction among North American, South American, and African plates to its present position near the transform. The source mechanisms for all events in this study display the strike-slip motion expected for transform fault earthquakes; slip vector azimuths agree to within 2°–3° of the local strike of the zone of active faulting. The only anomalies in mechanism were for two earthquakes near the western end of the Vema transform which occurred on significantly nonvertical fault planes. Secondary faulting, occurring either precursory to or near the end of the main episode of strike-slip rupture, was observed for five of the 12 earthquakes. For three events the secondary faulting was characterized by reverse motion on fault planes striking oblique to the trend of the transform. In all three cases the site of secondary reverse faulting is near a compressional jog in the current trace of the active transform fault zone. We find no evidence to support the conclusions of Engeln, Wiens, and Stein that oceanic transform faults in general are either hotter than expected from simple thermal models or weaker than normal oceanic lithosphere.

Description: Maturing females of the octopod Japetella diaphana (Hoyle) develop a luminous oral ring. Studies of specimens of different size show that this structure develops from a muscular ring which undergoes great cellular proliferation, associated with gradual degeneration of the original muscle. The light‐producing cells (photocytes) have a relatively uniform cytoplasm whose most characteristic components are small mitochondria, granular aggregates and microtubular or microfibrillar bundles. It is concluded that the original muscle tissue is not transformed directly into luminous tissue. Possible uses of the luminescence are discussed, based on the postures adopted by live specimens in shipboard aquaria.

Description: The cuttlefish ingests much skeleton from the crustaceans and fish it preys upon. The skeletal pieces are relatively large and their dimensions bear a close relationship to the length of the buccal mass and diameter of the oesophagus. The structures of the buccal mass are instrumental in the breakdown of prey and orientation of long pieces of skeleton to ensure their entry into the oesophagus. Many pieces of skeletal material present in the stomach contents still have attached muscles, showing that there is little, or no, external digestion. Skeletal material may be important for long-term maintenance of young Sepia in captivity.

Description: The diet of the king penguin Aptenodytes patagonicus at Marion Island was examined throughout the year by analysis of stomach samples. Fish accounted for 87% by wet mass, 75% by numbers and 69% by reconstituted mass. Their proportional importance by wet mass increased from 68% during winter to almost 100% in summer and probably reflects a real increase in their local availability. Squid comprised most of the remainder with crustaceans forming less than 1% of the diet by numbers. Prey items were generally small, the most abundant being three species of myctophid fish, Krefftichthys anderssoni, Protomyctophum tenisonì and Electrona carlsbergi, and a squid Kondakovia longimana. King penguins took both juvenile and adult Krefftichthys anderssoni and P. tenisoni, but only adult E. carlshergi. The juvenile and adult modal size classes of K. anderssoni and P. tenisoni increased from March through to February and the proportion of juvenile to adult fish increased in winter. The increase in the modal size class of the K. anderssoni/P. tenisoni complex during the year probably reflects growth of the fish, rather than movement of different populations in and out of the area exploited by king penguins. All squid consumed were probably juveniles. The modal size class of Kondakovia longimana increased from March to August, but in September to October smaller squid again formed a large proportion of the squid component of the diet. Numbers of measurable squid beaks recovered from November to February were low. This is the first time that mesopelagic myctophid fish have been shown to comprise a major component of the diet of a vertebrate predator in the Southern Ocean.

Description: In the animal kingdom evolutionary size changes involved increasing, decreasing and stationary patterns. Planktic and benthic Foraminifera chiefly increased their size during evolution. This increase, however, did not always occur gradually, but could be interrupted by periods when the animals maintained or even decreased in size. The rate of the size increase is different for the various species examined, some benthic forms grew only 10% during the Oligocene-Pleistocene interval, while for others this figure was up to 96%. Some benthic species increased in size in certain areas, but not in others. It is not improbable that some phylogenetic trends of planktic Foraminifera representing, according to stratigraphers, the evolution of one species into another, represent in reality, from the biological point of view, specimens of the same species which changed their size and in addition some minor morphological traits which are encompassed by the normal span of intraspecific variability. A comprehensive understanding and explanation of the size change of Foraminifera needs much additional research.

Description: The diets of adult Macaroni penguins Eudyptes chrysolophus chrysolophus and Southern rockhopper penguins E. chrysocome chrysocome were analysed quantitatively at Marion Island, southern Indian Ocean, throughout two successive chick-rearing seasons. The diets were broadly similar. Crustaceans were the predominant prey type comprising, overall, 90% by mass and 98% by numbers in Macaroni penguins and 96% by mass and 99% by numbers in rockhopper penguins. Nauticaris marionis was the predominant crustacean eaten by both penguin species in 1983–84, but Euphausia vallentini and Thysanoessa vicina predominated in 1984–85. Themisto gaudichaudii was present in appreciable numbers only in Macaroni penguins. Fish was not found in measurable quantities in either species in 1983–84, but contributed 5% and 4% of the mass of the diet in Macaroni and rockhopper penguins, respectively, when calculated in terms of the original biomass of food ingested. In 1984–85, however, fish comprised 10% and 6% of observed mass and c. 25% and 14% of original biomass ingested in Macaroni and rockhopper penguins, respectively. Pelagic myctophids, predominantly Krefftichthys anderssoni, Protomyctophum tenisoni and P. normani between 0·01 and 8·3 g, were the most commonly identified fish prey, but Macaroni penguins took an appreciable number of Electrona carlsbergi in 1983–84. Cephalopods made up between 1 % and 3% of the diet by mass in both penguin species and between 5% and 13% of original biomass ingested. Predominant cephalopods eaten were Kondakovia longimana and an unidentified octopus species. The relative proportions of each prey type change throughout chick-rearing, with pelagic fish and cephalopods comprising a larger proportion later in the season when the penguins were assumed to be foraging farther from their breeding sites. Dietary segregation of the two species appears to be related to the difference in the timing of the breeding season, which begins three to four weeks earlier in Macaroni penguins.