ALBERT

Description: The data presented provides new information on the distribution of Antarctic squids and on the summer diet of the emperor penguins. The diet of 58 adult emperor penguins (Aptenodytes forsteri) on the fast ice of the Drescher Inlet, Vestkapp Ice Shelf (72°52′S, 19°25′W) in the eastern Weddell Sea was investigated. Prey consisted principally of squid, fish, krill, amphipods and isopods. Squids were identified by the lower beaks and allometric equations were used to estimate the squid biomass represented. Beaks occurred in 93% of the stomach samples. Each sample contained a mean of 27 beaks (range 1–206). Ninety-two percent of the squids could be identified by the lower beaks and belonged to four families (Onychoteuthidae, Psychroteuthidae, Neoteuthidae and Gonatidae). The most abundant squid was Psychroteuthis glacialis which occurred in 52 samples with lower rostral lengths (LRL) ranging from 1.4–7.2 mm. Forty-five samples contained Alluroteuthis antarcticus (LRL range 1.8–5.8 mm), 17 Kondakovia longimana (LRL range 4–12.1 mm), and four Gonatus antarcticus (LRL range 4.1–6.1 mm). In terms of biomass K. longimana was the most important species taken by the penguins comprising 50% of total estimated squid wet mass (245348 g) in 1990 and 48% in 1992 (154873 g). However, if only fresh beaks were considered for estimations of squid consumption, i.e. beaks that have been accumulated for not longer than 5–6 days in the stomachs, squid diet was of minor importance. Then total squid wet mass accounted for only 4809 g in 1990 and 5445 g in 1992 which implies that one penguin took c.30 g squid d−1 with P. glacialis and A. antarcticus being the most important by mass. The prey composition suggests that emperor penguins take squid at the steep slope regions of the eastern Weddell Sea.

Description: During a study based on catches taken in the northern North Sea by selected Scottish fishing boats during 1985–1992, large numbers of the normally rare short-fin squid, Todaropsis eblanae (Cephalopoda: Ommastrephidae), were recorded in 1987 and 1990. Our findings, supported by data obtained from plankton/young fish surveys in 1988 and 1989, suggest that in northern waters Todaropsis eblanae generally mates and spawns during late summer and early autumn (June-November). Successful hatching events appear to occur during October-March, producing juvenile (stage I) squid in the early part of the year (January-June). Estimations of maximum male reproductive output and female fecundity were up to 130 spermatophores and ~28,000 eggs per individual, respectively.

Description: The cause of decadal climate variability over the North Pacific Ocean and North America is investigated by the analysis of data from a multidecadal integration with a state-of-the-art coupled ocean-atmosphere model and observations. About one-third of the low-frequency climate variability in the region of interest can be attributed to a cycle involving unstable air-sea interactions between the subtropical gyre circulation in the North Pacific and the Aleutian low-pressure system. The existence of this cycle provides a basis for long-range climate forecasting over the western United States at decadal time scales.

Description: The functional morphology of the buccal mass of 23 species of cephalopod (Octopoda, 4 species; Teuthoidea, 17; Sepioidea, 2) was investigated by gross dissection, histology and observations on fresh preparations. Cephalopod beaks lack a joint or articulation point. The jaws slide and rotate around an area rather than a fixed point. During closing the superior mandibular muscle (SMM) provides the force of a bite and the largest movement vector, whilst the inferior mandibular muscle (IMM) acts to retract the upper beak, causing shearing action. Dorsal portions of the lateral mandibular muscles (LMM) flex the upper beak walls outwards, probably to accomodate the backwards sweep of the radula and buccal palps during closing. To open the beaks, the ventral portions to the lateral mandibular muscles pull the rear lateral walls of the two beaks towards each other, moving the lower beak back relative to the upper. The buccal mass weighs more in decapods (0.65-4.34% of body weight) than octopods (0.49-0.77%). The weight difference is mainly accounted for by the size of the superior mandibular muscle. Beak shape and muscle volume are related. Increasing the size of the upper beak hood and lateral wall area results in larger SMM and LMM respectively Increasing hood size in the lower beak increases IMM size, and altering the angle by which the wings meet the lateral wall changes the volume of the SMM and LMM. To accomodate the decapod pointed upper rostrum, the lateral walls of the lower beak have shortened in length, whilst increasing in breadth and surface relief to maintain the area available for muscle insertion. In species with a lateral wall ridge or fold (e.g. Onychoteuthis) this may mark the insertion point of the LMM.

Description: Arm autotomy was induced in a living specimen of Metacrinus rotundus (Echinodermata: Crinoidea). An arm was autotomized at a ligamentary articulation known as a cryptosyzygy, following incision by scissors distal to the break point. Although sessile stalked crinoids cannot entirely escape from a predatory attack by arm autotomy and they do not have an active defense, arm autotomy at cryptosyzygies reduces damage and arm loss by effective distribution, and by minimizing trauma and facilitating subsequent regeneration. The paradigmatic distribution of cryptosyzygies in which arm loss is set at a minimum, compared with the actual distribution, shows that these two patterns are similar and that actual specimens successfully reduce arm loss by the effective distribution of cryptosyzygies. The crinoid branching pattern also affects arm loss, and two different paradigms are discussed: anti-predatory and harvesting. Arm branching patterns of various isocrinids have tended toward the anti-predatory configuration from the Jurassic to the Recent, suggesting that the isocrinids have coped with increased predation. Shallow-water comatulids generally adopt the anti-predatory paradigm in their branching pattern, whereas many deep-water, stalked crinoids adopt a harvesting paradigm, reflecting that shallow-water comatulids receive more predatory attacks than do deep-water crinoids.