ALBERT

Description: The aims of this project were to improve understanding of the basic life.cycle biology, stock structure, trophic interactions and fisheries exploitation of northeast Atlantic squid, in particular the loliginids Loligo forbesi and Loligo vulgaris. Multivariate analysis of morphometric data and isozyme electrophoresis shows that L. forbesi populations from the coast of mainland Europe are fairly homogeneous, but that those from the Azores are a distinct stock. Loligo forbesi and L. vulgaris are annual species with a peak of breeding in the winter (December-May) throughout the geographical range, and one or more seasonal peaks of recruitment. Loligo are probably batch spawners. Males grow larger than females, mature about 1 month earlier and recruit earlier to the fishery. Sexual maturity occured at two distinct size classes, more obviously in males than females. Fish, including many cimmercially important species, and Crustacea, were the dominant prey of Loligo. The incidence of fish in the diet increases with squid size. Squid of all types are eaten by fish, seals, cetaceans and seabird, although quantitative estimates of consumption by these trophic levels were low. Catches of squid from northeast Atlantic waters increased over the period 1980-1990 but currently supply only a minor component of the European market for squid, the balance being made up by imports. The squid catch in the northern part of the range shows wide fluctuations in abundance by area and by season. The applicability of assessment methods for these stocks is limited by inadequate and inaccurate statistical information, and because nearly all of the catch arises by-catch from finfisheries.

Description: The periodicity of deposition of growth increments in the cuttlebone of juvenile Sepia officinalis was investigated under controlled conditions for a short period after hatching (19 days). The slope of time elapsed and increment counts was significantly different from 1 indicating that lamellae are not deposited on a daily basis. The relationship between increment counts and juvenile length was, however, highly significant. Also significant were the relationships between the number of growth increments and shell length and increment counts and cuttlebone area. These data show that the number of growth increments is related primarily to the growth rate of the juvenile rather than to its chronological age. Taking into account these data, the cuttlebone lamellae cannot be used for age determination in the juvenile cuttlefish just after hatching.

Description: An automated and semi-intelligent voltammetric system is described for trace metal analysis. The system consists of a voltammeter interfaced with a personal computer, a sample changer, 2 peristaltic pumps, a motor burette and a hanging mercury drop electrode. The system carries out fully automatically approximately 5 metal determinations per hour (including at least 3 repetitive scans and calibration by standard addition) at trace levels encountered in clean sea water. The computer program decides what level of standard addition to use and evaluates the data prior to switching to the next sample. Alternatively, the system can be used to carry out complexing ligand titrations with copper whilst recording the labile copper concentration; in this mode up to 8 full titrations are carried out per day. Depth profiles for chromium speciation in the Mediterranean Sea and a profile for copper complexing ligand concentrations in the North Atlantic Ocean measured on board-ship with the system are presented. The chromium speciation was determined using a new method to differentiate between Cr(III) and Cr(VI) utilizing adsorption of Cr(III) on silica particles.

Description: The use of in-line UV-digestion for breakdown of dissolved organic matter (DOM), prior to voltammetric determination of trace metals in natural samples, is discussed in this paper. Destruction of DOM is necessary to free trace metals that are organically complexed and to remove interfering organic surfactants. Complete breakdown of DOM in natural water samples is achieved by in-line UV-digestion using a 100 W medium pressure mercury vapour lamp and a silica coil, at a sample digestion time of 4.5 min. The efficiency of the system is tested with destruction of humic acid, conversion of Cr(III) to Cr(VI), and the release of Ni and Cu from organic complexes in sea water. The in-line application of UV is illustrated by automated voltammetry of nanomolar levels of Cu and Ni in samples from oceanic origin.

Description: Instrumentation and methods are described for collecting surface sea water using pumping with subsequent in-line analysis by stripping voltammetry or chronopotentiometry. The review is illustrated with data for estuarine copper and nickel, and the distribution of nickel in Liverpool Bay.

Description: For over thirty years man has studied “outer space” and installed satellites which watch the surface of the Earth. The great depths of the world ocean are, however, practically unknown and there is an urgent need to put abyssal benthic laboratories into “inner space” in order to study basic phenomena of interest to marine science and climatology as well as man's impact on the oceans. In view of the numerous problems related to global change, as a first step emphasis should first be on the role of the oceans and their inherent processes, which are the focus of such international programmes as the World Ocean Circulation Experiment (WOCE) and the Joint Global Ocean Flux Study (JGOFS). Multi-disciplinary registration of key events at selected key sites investigating the variability in time and space are of the utmost importance. The same methods and techniques must be used for the study of human impacts on the deep oceans caused by mining of metalliferous resources and by waste disposal as well as in basic studies. However, the investigation of the inner space of our planet has certain requirements. As long-term and large-scale investigations become more and more important, development of automized systems, largely independent from research vessels will be required. This will demand high capacities of energy for all technical functions as well as high storage capacities for data and samples. As a consequence the needs for two different—although overlapping—functional approaches are defined for future deep-sea deployments. (A) A system for long-term registration of the natural variability and long-term monitoring of human impacts: (B) A system for short-term observations and short-time experimentations. This report summarizes their technological demands. The envisioned interdisciplinary technology should deliver information on physical, biological and geochemical processes and their variabilities in the deep oceans. The prospected systems need to have the ability for real time video observation, data transfer and experimental manipulation, as well as sensing and sampling facilities with large storage capacities for long-term deployments. Prospective costs of the described multipurpose abyssal benthic laboratory will presumably exceed the funds for deep-sea research of a single country. A joint European effort could solve this problem and help to manifest a leading role for European marine science in international deep-sea and global change research.

Description: The reproductive cycle of the sponge Halichondria panicea was investigated at Boknis Eck in the Western Kiel Bight over 2 yr, and over 1 yr on the island Helgoland in the North Sea and was compared with material collected earlier at Tjärnö at the Swedish west coast. Temperature and salinity were monitored at the different stations in order to determine whether different hydrographic conditions could be linked to differences in seasonal patterns of the reproductive cycle. The results showed H. panicea to be gonochoristic at all stations. The ratio of males to females varied between populations and years, but females predominated consistently. Comparison of the reproductive cycle in the years 1987 and 1989 at the brackish-water station Boknis Eck shows that high ambient winter and spring temperatures in 1989 resulted in a shorter period of oogenesis and earlier larval release, as compared to the year 1987. The reproductive cycle of the sponges at the fully marine station at Helgoland in 1989 and the brackish-water station at Tjärnö in 1978 under temperature and salinity conditions similar to those at Boknis Eck in 1989 showed the same seasonal pattern. We conclude that the lower salinities found at both Boknis Eck and Tjärnö do not cause a delay or slow-down of reproduction at these stations as compared to Helgoland. Under favourable temperature conditions, oogenesis was highly synchronous within the different populations, while it was more spread over time under the low ambient water temperatures at Boknis Eck in 1987.

Description: The winter ice-regime of the 〈80 km wide Alaskan Beaufort Sea shelf is characterized by compression and shearing, resulting in the formation of major grounded pressure ridge systems stabilizing the fast ice on the mid-shelf, and essentially no open-water areas. In contrast, the winter ice-regime of the 500-km wide Laptev Sea shelf is controlled by winds blowing from land to sea, and is therefore dilational. A perennial polynya borders the hundreds of kilometers-wide and very smooth fast ice offshore. In this body of open water, rapidly forming ice is continuously advected offshore by the mean wind field, making the Laptev Sea the single major ice factory for the Arctic Ocean and Transpolar Drift. Conversely, with summer warming this dark polynya turns into an area of high heat gain, which results in the retreat of the ice edge to a much higher latitude and greater distance (〉500 km) from the mainland than in the Beaufort Sea. As a result, the annual freeze-up does not incorporate old, deep-draft ice, and with a lack of compression, such deep-draft ice is not generated in situ, as on the Beaufort Sea shelf. The Laptev Sea has as much as 1000 km of fetch at the end of summer, when freezing storms move in and large (6 m) waves can form. Also, for the first three winter months, the polynya lies inshore at a water depth of only 10 m. Turbulence and freezing are excellent conditions for sediment entrainment by frazil and anchor ice, when compared to conditions in the short-fetched Beaufort Sea. We expect entrainment to occur yearly. Different from the intensely ice-gouged Beaufort Sea shelf, hydraulic bedforms probably dominate in the Laptev Sea. Corresponding with the large volume of ice produced, more dense water is generated in the Laptev Sea, possibly accompanied by downslope sediment transport. Thermohaline convection at the midshelf polynya, together with the reduced rate of bottom disruption by ice keels, may enhance benthic productivity and permit establishment of open-shelf benthic communities which in the Beaufort Sea can thrive only in the protection of barrier islands. Indirect evidence for high benthic productivity is found in the presence of walrus, who also require year-round open water. By contrast, lack of a suitable environment restricts walrus from the Beaufort Sea, although over 700 km farther to the south. We could speculate on other consequences of the different ice regimes in the Beaufort and Laptev Seas, but these few examples serve to point out the dangers of exptrapolating from knowledge gained in the North American Arctic to other shallow Arctic shelf settings.

Description: Despite the Arctic sea ice cover's recognized sensitivity to environmental change, the role of sediment inclusions in lowering ice albedo and affecting ice ablation is poorly understood. Sea ice sediment inclusions were studied in the central Arctic Ocean during the Arctic 91 expedition and in the Laptev Sea (East Siberian Arctic Region Expedition 1992). Results from these investigations are here combined with previous studies performed in major areas of ice ablation and the southern central Arctic Ocean. This study documents the regional distribution and composition of particle-laden ice, investigates and evaluates processes by which sediment is incorporated into the ice cover, and identifies transport paths and probable depositional centers for the released sediment. In April 1992, sea ice in the Laptev Sea was relatively clean. The sediment occasionally observed was distributed diffusely over the entire ice column, forming turbid ice. Observations indicate that frazil and anchor ice formation occurring in a large coastal polynya provide a main mechanism for sediment entrainment. In the central Arctic Ocean sediments are concentrated in layers within or at the surface of ice floes due to melting and refreezing processes. The surface sediment accumulation in central Arctic multi-year sea ice exceeds by far the amounts observed in first-year ice from the Laptev Sea in April 1992. Sea ice sediments are generally fine grained, although coarse sediments and stones up to 5 cm in diameter are observed. Component analysis indicates that quartz and clay minerals are the main terrigenous sediment particles. The biogenous components, namely shells of pelecypods and benthic foraminiferal tests, point to a shallow, benthic, marine source area. Apparently, sediment inclusions were resuspended from shelf areas before and incorporated into the sea ice by suspension freezing. Clay mineralogy of ice-rafted sediments provides information on potential source areas. A smectite maximum in sea ice sediment samples repeatedly occurred between 81°N and 83°N along the Arctic 91 transect, indicating a rather stable and narrow smectite rich ice drift stream of the Transpolar Drift. The smectite concentrations are comparable to those found in both Laptev Sea shelf sediments and anchor ice sediments, pointing to this sea as a potential source area for sea ice sediments. In the central Arctic Ocean sea ice clay mineralogy is significantly different from deep-sea clay mineral distribution patterns. The contribution of sea ice sediments to the deep sea is apparently diluted by sedimentary material provided by other transport mechanisms.

Description: The present paper reviews the literature related to the life cycle of the prymnesiophyte Phaeocystis and its controlling factors and proposes novel hypotheses based on unpublished observations in culture and in the field. We chiefly refer to P. globosa Scherffel as most of the observations concern this species. P. globosa exhibits a complex alternation between several types of free-living cells (non-motile, flagellates, microzoopores and possibly macrozoospores) and colonies for which neither forms nor pathways have been completely identified and described. The different types of Phaeocystis cells were reappraised on the basis of existing microscopic descriptions complemented by unpublished flow cytometric investigations. This analysis revealed the existence of at least three different types of free-living cells identified on the basis of a combination of size, motility and ploidy characteristics: non-motile cells, flagellates and microzoospores. Their respective function within Phaeocystis life cycle, and in particular their involvement in colony formation is not completely understood. Observational evidence shows that Phaeocystis colonies are initiated at the early stage of their bloom each by one free-living cell. The mechanisms controlling this cellular transformation are still uncertain due to the lack of information on the overwintering Phaeocystis fomms and on the cell type responsible for colony induction. The existence of haploid microzoospores released from senescent colonies gives however some support to sexuality involvement at some stages of colony formation. Once colonies are formed, at least two mechanisms were identified as responsible of the spreading of colony form: colony multiplication by colonial division or budding and induction of new colony from colonial cells released in the external medium after colony disruption. The latter mechanism was clearly identified, involving at least two successive cell differentiations in the following sequence: motility development, subsequent flagella loss and settlement to a surface, mucus secretion and colony formation, colonial cell division and colony growth. Aggregate formation, cell motility development and subsequent emigration from the colonies, release of non-motile cells after colony lysis on the other hand, were identified as characteristics for termination of Phaeocystis colony development. These pathways were shown to occur similarly in natural environments. In the early stages of the bloom however, many recently-formed colonies were found on the setae of Chaetoceros spp, suggesting this diatom could play a key-rôle in Phaeocystis bloom inception. Analysis of the possible environmental factors regulating the transition between the different phases of the life cycle, suggested that nutrient status and requirement of a substrate for attachment of free-living cells would be essential for initiation of the colonial form. Physical constraints obviously would be important in determining colony shape and fragmentation although autogenic factors cannot be excluded. Some evidence exists that nutrients regulate colony division, while temperature and nutrient stress would stimulate cell emigration from the colonies.