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 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.

Description: First culture results are presented from four major experiments (lasting up to 478 days) on the commercially important squid species, Loligo forbesi Steenstrup, Details are provided on eggs, hatching, feeding, growth, survival, behaviour and sexual maturation. Best survival during the critical first 75 days was 15%. The hatchlings (up to 4.9mm mantle length, ML) are the largest among the genus Loligo, and the largest squid grown was a male 155mm ML and 124g. First schooling was observed only 40–50 days post-hatching. Spawning was not achieved although males reached maturity, females had maturing ova and mating was observed. The largest giant axon measured was 425μm in diameter (from a female 130mm ML), a size suitable for most biomedical applications. Laboratory data suggest a 2-year life cycle compared to fishery data which suggest a 1-year cycle.

Description: Loligo forbesi Steenstrup is a commercially and biomedically important species raneing from Scotland to North Africa and from the Azores Islands in the central Atlantic east through the Mediterranean Sea and Red Sea. Eggs were collected from Plymouth. England and from the Azores and the hatchlings were reared to adult size in recirculating seawater systems. Growth data were obtained primarily from mortalities during the course of three culture experiments which lasted 360, 240 and 480 days. Loligo forbesi hatched at a size of 5–9mg (3.0–4.6mm mantle length, ML) and grew to a maximum size of 124g (155 mm ML) in 413 days. In all experiments, growth was exponential in form for at least the first 3 months at rales of 5.8, 5.1 and 3.6% body weight per day (BW/d) at mean temperatures of 14.1, 14.0 and 13.1°C respectively. In one short-term experiment, month-old squids grew at 8.0% BW/d at 17.4°C. Growth beyond 3 months was slower and either logarithmic (as described by the power function) or exponential in form. Growth rates gradually declined to 1–2% BW/d, Analyses of mantle length growth confirmed the wet weight results. There was no evidence of sexual dimorphism in the laboratory populations, which were of small size, and the length-weight (L-W) relationships were found to be similar to those of field populations. Growth rates during the exponential growth phase appeared very sensitive to temperature, with a 1°C difference changing growth rate by 2% BW/d and producing a three-fold difference in weight at 90 days post-hatching. These dramatic effects of temperature on adult size and lifespan in nature are discussed. It is hypothesized that the small size of mature laboratory-reared squids was due to low culture temperatures during the first 3 months.