Points and dates of tagging and recapture of mature cod in the southern Barents Sea in 1937-1955

Barents cod spawn in the Motovsky Bay during the periods of warming in the Arctic when proportion of mature fish in the population is high enough. Cod spawning is most likely to occur in the Motovsky Bay when large cod forage in southeastern waters, and prespawning fish migrate close by the Murmansk coast. Under such conditions cod spawn in the Motovsky Bay, but low water temperature and slow egg drift toward Murmansk coastal waters delay development of cod eggs. As a result the eggs remain at the first stage for a long time; this causes high egg mortality before hatching. Larvae that survive and become pelagic and then bottom juveniles nevertheless have little chance to survive in winter because they are not biologically ready for overwintering. Thus, delay in egg development at the first stage delays subsequent stages of fish ontogeny, and strongly impairs survival of cod juveniles from the Motovsky Bay.

Verical distribution of Copepoda biomass in the Northwest and tropical Pacific

Quantitative analysis of vertical distribution of copepod families revealed a pattern of variation with depth (from the surface to the greatest ocean depths) in the trophic structure of this taxocenosis in the pelagic Pacific.

Late Oligocene rapid transformations in the South China Sea

Lithobiostratigraphic data indicate that the double reflectors on the seismic profile through Ocean Drilling Program (ODP) Site 1148 represent two unconformities that coincide, respectively, with the lower/upper Oligocene boundary at ~488 mcd, and Oligocene-Miocene boundary at 460 mcd. Two other unconformities, at ~478 and 472 mcd, respectively, were also identified within the upper Oligocene section. Together they erased a sediment record of about 3 Ma from this locality in a period of very active seafloor spreading. The existence of 32.8 Ma marine sediment at the terminated depth (850 mcd) indicates that the initial breakup of the South China Sea (SCS) was probably during 34-33 Ma, close to the Eocene-Oligocene boundary. High sedimentation rates of 60-115 m/my from the much expanded, N350 m lower Oligocene section resulted from rifting and rapid subsidence between 33 and 29 Ma. The mid-Oligocene unconformity at ~28.5 Ma, which also occurred in many parts of the Indo-West Pacific region, was probably related to a significant uplift of the Himalayan-Tibetan Plateau to the west and the initial collision between Indonesia and Australia in the south. A narrowed Indonesian seaway may have accounted for the late Oligocene warming and chalk deposition in the northern South China Sea including the Site 1148 locality. The unconformities and slumps near the Oligocene-Miocene boundary indicate a very unstable tectonic regime, probably corresponding to changes in the rotation of different land blocks and the seafloor spreading ridge from nearly E-W to NE-SW, as recognized earlier at magnetic Anomaly 7. This 25 Ma event also saw the first New Guinea terrane docking at the northern Australian craton. The low sedimentation rate of ~15 m/my in the early to middle Miocene may correspond to another period of rapid seafloor spreading and rapid widespread subsidence that effectively caused sediment source areas to retreat with a rapidly rising sea level. The isostatic nature of these late Oligocene unconformities and slumps with several major collision-uplift events indicate that the rapid changes in the early evolutionary history of the South China Sea were mainly responding to regional tectonic reconfiguration including the uplift-driven southeast extrusion of the Indochina subcontinent.

Vertical distribution of zooplankton biomass in the Sea of Japan

Vertical distribution of total zooplankton biomass and major taxonomic groups are investigated by layers to depths of 2500-3400 m on the basis of three series of net plankton collections. Zooplankton is most abundant above 1500-2000 m. Since true deep-water species do not occur in the Sea of Japan, biomass drops much more sharply at greater depths than it does in the ocean. Since few carnivores inhabit the deep layers, abundant remains of planktonic organisms fall to the bottom, and carnivorous detritovores feeding on these remains are dominant in deep water bottom fauna.

Abundance and biomass of near-surface ichthioplankton in the Western Pacific

During Cruise 50 of R/V Vityaz ichthyoplankton in surface waters was collected by a neuston otter trawl for many days in four study areas of the Western Tropical Pacific. Obtained results describe quantitative distribution of ichthyoplankton and small fishes in surface waters. The near-surface layer of the ocean (about 30-40 cm thick) can be considered as a special biotope, its population forms an independent biocoenosis - hyponeuston. Species composition of this community (particularly, composition of fish components) in the tropical zone has been studied to some degree, but structure of the biocoenosis as well as biomass and quantitative relationships of species have not been investigated at all. In this paper the authors discuss the method of collecting surface samples that is quite suitable for quantitative calculations and also present the first results obtained using this method, which described quantitative distribution of ichthyoplankton and small fishes in surface waters.

Vertical distribution of zooplankton biomass in the Sea of Japan at Station VITYAZ7519

Vertical distribution of common zooplankton species is examined on the base of two series of layer-by-layer net catches down to depth of 3400 m. Differences between the series are significant for most species only near the surface, whereas in deeper layers character of distribution remains the same. Great depths in the Sea of Japan are populated most actively by species performing intensive daily migrations, and less actively by species continuously confined to a definite depth range. Different character of nutrition of the animals apparently determines extent of utilization of deep layers, which are usual for the species.

Ingestion rate and egg production of copepods collected in the upper 20m in the eastern Mediterranean Sea in March and April 2008 during SES_GR1

The ingestion on ciliates and phytoplankton dataset is based on samples taken during April 2008 in Northern Aegean Sea, the area influenced by the Black Sea water outflow. A Lagrangian experiment was established and copepod ingestion was estimated from experiments performed at stations according to the different positions of drifters during the cruise. Copepods for the experiments were obtained with slow non-quantitative tows from the upper 20 m layer of the water column using 200 µm mesh size nets fitted with a large non-filtering cod end. For the grazing experiments we used the following copepod species: Centropages typicus and Calanus helgolandicus according to the relevant reference (Bamstedt et al. 2000). Copepod clearance rates on ciliates were calculated according to Frost equations (Frost 1972). Ingestion rates were calculated by multiplying clearance rates by the initial standing stocks (Bamstedt et al. 2000). The egg production dataset is based on samples taken during April 2008 in Northern Aegean Sea, the area influenced by the Black Sea water outflow. A Lagrangian experiment was established and copepod egg production was estimated from experiments performed at stations according to the different positions of drifters during the cruise. Egg production rates of the dominant calanoid copepods were determined by incubation of fertilised females (eggs female/day) collected in the 0-20m layer. Copepod egg production was measured for the copepods Centropages typicus, Calanus helgolandicus. On board experiments for the estimation of copepod egg production were taken place. For the estimation of copepod production (mgC/ m**2 /day), lengths (copepods and eggs) were converted to body carbon (Hopcroft et al., 1998) and production was estimated from biomass and weight-specific egg production rates, by assuming that those rates are representative for juvenile specific growth rates (Berggreen et al., 1988).

Ingestion rate on ciliates and phytoplankton collected in the upper 100m in the eastern Mediterranean Sea based on samples from August-September 2008 during SES_GR2

The SES_GR2_Copepod Ingestion on ciliates and phytoplankton dataset is based on samples taken during August-September 2008 in Ionian Sea, Libyan Sea, Southern Aegean Sea and Northern Aegean Sea. Ingestion rates were estimated from experiments performed at all the third priority stations during the cruise according to DoW of Sesame project. Copepods for the experiments were obtained with slow non-quantitative tows from the upper 100 m layer of the water column using 200 µm mesh size nets fitted with a large non-filtering cod end. For the grazing experiments we used the following copepod species: Clausocalanus furcatus, Oithona spp. Temora stylifera and Acartia spp according to the relevant reference (Bamstedt et al. 2000). Copepod clearance rates on ciliates were calculated according to Frost equations (Frost 1972). Ingestion rates were calculated by multiplying clearance rates by the initial standing stocks (Bamstedt et al. 2000).