Meridional zonation of the Barents Sea ecosystem inferred from satellite remote sensing and in situ bio-optical observations

The Barents Sea is a productive, shallow, high-latitude marine ecosystem with complex hydrographic conditions. Zonal hydrographic bands defined by a coastal current. North Atlantic Water, the Polar Front, and the seasonally variable marginal ice edge zone create a meridional zonation of the ecosystem during the spring-summer transition. The features reveal themselves in satellite imagery and by high-resolution (vertical and horizontal) physical-optical-biological sampling.
Surprisingly, the long-term (7-year) mean of Coastal Zone Color Scanner (CZCS) imagery reveals the Barents Sea as an anomalous "blue-water" regime at high latitudes that are otherwise dominated by satellite-observed surface blooms. A combination of satellite imagery and in situ bio-optical analyses indicate that this pattern is caused by strong stratification in summer with surface nutrient depletion. The onset of stratification of the entire region is linked to the extent of the winter ice edge: cold years with extensive sea ice apparently stratify early due to ice melt; warm years stratify later, perhaps due to weaker thermal stratification of the Atlantic waters (e.g. Skjoldal et al. 1987). The apparent "low chlorophyll" indicated by the CZCS 7-year mean is partly due to sampling error whereby the mean is dominated by images taken later in the summer. In fact, massive blooms of subsurface phytoplankton embedded in the pycnocline persist throughout the summer and maintain substantial rates of primary production. Further, these subsurface blooms that are not observed by satellite are responsible for dramatic gradients in the beam (c₁) and spectral diffuse (k) attenuation coefficients. The Barents Sea exemplifies the need to couple satellite observations with spatially and temporally resolved biogeographic ecosystem models in order to estimate the integrated water column primary production, mass flux or spectral light attenuation coefficients.     

On the excitation of resonant double Kelvin waves in the Barents Sea Opening

In the northern Barents Sea Opening (BSO) the K₁ tidal energy is predominant in the diurnal tidal frequency band, suggesting the generation of a topographic wave with the K₁ tidal frequency. Tidal energy of the K₁ component becomes strong where bottom topography undulates in the BSO and the scale of the undulation is close to the wavelength of the K₁ wave. An analytical model is developed to investigate the energy enhancement mechanism of the tidally induced topographic wave due to a resonance between tidal current, a topographic wave and periodic topography. The wave excited by the resonance is identified as a resonant double Kelvin wave (DKW) and the significant K₁ energy in the BSO could be due to the excitation of the resonant DKW.     

Distribution and life history of krill from the Barents Sea

Krill from the Barents Sea were studied on six cruises from 1985 to 1989. Thysanoessa inermis and T. longicaudata were the dominant species, while T. raschii and Meganyctiphanes norvegica were rarer in the studied areas. The two dominant species T. inermis and T. longicaudata are mainly found in the Atlantic. Water and they do not to a large extent penetrate into Arctic water masses in the northern Barents Sea. M. norvegica is a more strict boreal species that does not occur as extensively in the Barents Sea as do the Thysanoessa species. The mean population abundance ranged from 1 to 61 individuals m⁻² for T. inermis and from 2 to 52 ind. M⁻² for T. longicaudata . The mean dry weight biomass of these two species ranged from 14 to 616 and from 19 to 105 mg⁻². Length frequency distributions indicate a life span of just over two years for T. inermis and T. longicaudata . Growth took place from about April to autumn with no apparent growth during winter. Maturation and spawning seem to occur after two years for T. inermis and one year for T. longicaudata . Main spawning occurred from May to June coinciding with the spring phytoplankton bloom. Captive spawners of T. inermis (total length 17-22 mm) shed 30-110 eggs per female in a single batch.     

Palynodebris analysis of a shallow core from the Barents Sea

A quantitative study of palynomorphs and palynodebris in a shallow core from the central part of Bjørnøyrenna, western Barents Sea, is presented. The core could be subdivided into a lower part characterized by a complete dominance of reworked plant debris of Mesozoic age and an upper part with considerable input of first cycle algal debris and dinoflagellate cysts. Two hypotheses are suggested to explain this radical change in palynodebris composition. Either it represents a transition from a situation with permanent ice to normal marine conditions, or the absence of first cycle plant debris in the lower part of the core is caused by a masking of this component due to extremely high input of glacially eroded material from the bordering shallow parts of the Barents Sea. The present study shows that palynodebris analysis may contribute important information to the study of composition and depositional environment of Quaternary marine sediments in the area.     

Phytoplankton dynamics in the Barents Sea estimated from chlorophyll budget models

Pigment budgets use chlorophyll a and phaeopigment standing stock in combination with their photo-oxidation and sedimentation rates in the euphotic zone to estimate phytoplankton growth and grazing by micro- and macrozooplankton. Using this approach, average phytoplankton growth in the euphotic zone of the Barents Sea was estimated at 0.17 and 0.14 d⁻¹ during spring of 1987 and 0.018 and 0.036 d⁻¹ during late- and postbloom conditions in summer of 1988. Spring growth was 65% lower than the estimates from radiocarbon incorporation, supporting a 33% pigment loss during grazing. Macrozooplankton grazing and cell sinking were the main loss terms for phytoplankton during spring while microzooplankton grazing was dominant in summer.
In contrast to tropical and temperate waters, Arctic waters are characterized by a high phaeopigment: chlorophyll a ratio in the seston. Photooxidation rates of phaeopigments at in situ temperatures (0 ± 1°C) are lower than in temperate waters and vary by a factor of 2 for individual forms (0.009 to 0.018 m⁻²mol⁻¹). The phaeopigment fraction in both the suspended and sedimenting material was composed of seven main compounds that were isolated using high-performance liquid chromatography and characterized by spectral analysis. The most abundant phaeopigment in the sediment traps, a phaeo-phorbide-like molecule of intermediate polarity (phaeophorbide a₃), peaked in abundance in the water column below the 1% isolume for PAR (60-80 m) and showed the highest rate of photooxidation. This phaeopigment was least abundant in the seston when phytoplankton was dominated by prymnesiophytcs but increased its abundance in plankton dominated by diatoms. This distribution suggests that larger grazers feeding on diatoms are the main producers of this phaeopigment.     

Surface temperatures of the Barents Sea

Temperature conditions in the Barents Sea are determined by the quality and quantity of the inflowing Atlantic water from the west and by processes taking part in the Barents Sea itself, in particular as a consequence of winter cooling and ice formation. The field of inflow to the Barents Sea during the period 1977-1987 has been studied. The surface winter temperatures within the Barents Sea vary in parallel with variations in the deeper layers of the inflowing water masses, whereas the surface temperatures in summer have a different variation pattern which is most likely dependent on the summer heating process.     

Global observation of off-great-circle propagation of Long-Period surface waves

In the current generation of global dispersion maps of surface waves, the long-wavelength structure seems to be very well determined. There is general agreement in the patterns of global phase velocity anomalies up to harmonic degree 16. However, the shorter-wavelength structure varies significantly between published maps, and it appears that this part of the models depends strongly on the inversion technique and on the data set of surface-wave dispersion (usually phase measurements). Polarization data depend on the lateral gradient of phase velocity and hence are more sensitive to shorter-wavelength structure than phase data; thus, including these data should enhance resolution. In this paper, I demonstrate that polarization data of long-period surface waves (80 s), as a function of frequency, can be reliably measured using a multitaper technique. the resulting off-great-circle arrival angles of the surface-wave packets are relatively easy to interpret within a ray-theoretical framework. Our data base of three-component recordings is now large enough to provide useful constraints on global dispersion maps, particularly on the shorter-wavelength parts. Apart from the phase velocity model itself, a possible misorientation of the horizontal components at each station is included in a non-linear inversion as an additional independent model parameter. This gives a significant improvement in the fit to the data. Misorientations of more than 3° are probable for at least four of the 37 stations investigated.     

Primary production of the northern Barents Sea

The majority of the arctic waters are only seasonally ice covered; the northern Barents Sea, where freezing starts at 80 to 81°N in September, is one such area. In March, the ice cover reaches its greatest extension (74-75°N). Melting is particularly rapid in June and July, and by August the Barents Sea may be ice free. The pelagic productive season is rather short, 3 to 3.5 months in the northern part of the Barents Sea (north of the Polar Front, 75°N), and is able to sustain an open water production during only half of this time when a substantial part of the area is free of ice. Ice algal production starts in March and terminates during the rapid melting season in June and July, thus equalling the pelagic production season in duration.
This paper presents the first in situ measurements of both pelagic and ice-related production in the northern Barents Sea: pelagic production in summer after melting has started and more open water has become accessible, and ice production in spring before the ice cover melts. Judged by the developmental stage of the plankton populations, the northern Barents Sea consists of several sub-areas with different phytoplankton situations. Estimates of both daily and annual carbon production have been based on in situ measurements. Although there are few sampling stations (6 phytoplankton stations and 8 ice-algae stations), the measurements represent both pelagic bloom and non-bloom conditions and ice algal day and night production. The annual production in ice was estimated to 5.3 g Cm^-2, compared to the pelagic production of 25 to 30 g Cm^-2 south of Kvitøya and 12 to 15 g Cm^-2 further north. According to these estimates ice production thus constitutes 16% to 22% of the total primary production of the northern Barents Sea, depending on the extent of ice-free areas.     

A study of the climatic system in the Barents Sea

The climatic conditions in the Barents Sea are mainly determined by the influx of Atlantic Water. A homogeneous wind-driven numerical current model was used to calculate the fluctuations in the volume flux of Atlantic Water to the Barents Sea which are caused by local wind forcing. The study period is from 1970 to 86. When compared with observed variations in temperature, ice coverage, and air pressure, the results show remarkably good agreement between all three parameters. The climate system of the Barents Sea is discussed with emphasis on the interrelations and feedback mechanisms between air, sea, and ice.     

Aerial strip surveys of polar bears in the Barents Sea

Aerial strip surveys of polar bears in the Barents Sea were performed by helicopter in winter 1987. The number of bears within 100 m on each side of the helicopter was counted. A total of 263.6 km² was surveyed and 21 bears were counted. Most of the bears were found in the southern part of the area, which indicates that the southwestern ice edge area in the Barents Sea is a very important winter habitat for polar bears.     

Photosynthesis-irradiance relationships in natural phytoplankton populations of the Barents Sea

An analysis is made of the photosynthesis-irradiance relationships in natural phytoplankton populations in the Barents Sea. The data set comprises 232 experiments carried out during a 10-year period, both in open and ice-covered waters. The variability on the P-I parameters is discussed and examined in relation to the variation in a variety of environmental conditions. The results suggest that in the Barents Sea, as in other Arctic areas, phytoplankton photosynthesis is mainly controlled by physical variables. However, control of the phytoplankton stock, i.e. by zooplankton grazing, seems also to have a considerable indirect influence on P-I parameters, especially after the spring bloom and the depletion of winter nutrients.     

Micromonas pusilla (Prasinophyceae) as part of pico-and nanoplankton communities of the Barents Sea

Micromonas pusilla (Butcher) Manton & Parke appears to be a prominent member of the Barents Sea picoplankton community as revealed by the serial dilution culture method. Cell numbers frequently exceeded 10⁷ cells 1⁻¹, though they usually varied between 10³and 10⁶ cells l⁻¹. A number of other identified and unidentified taxa were recorded and quantified. Distribution relative to the marginal ice zone is reported.     

Calanus in North Norwegian fjords and in the Barents Sea

The Physical environment of a North Norwegian fjord and of the Atlantic and Arctic domains of the Barents Sea are described. The seasonal variation of primary production and biomass of the most important copepod species are described in order to contrast regional differences in the timing of the plankton cycles. Analysis of the seasonal variation in the biomass of six different copepod species in Balsfjorden clearly demonstrate the importance of Calanus finmarchkus as a spring and early summer form, whereas Pseudoculanus acuspes , the most important smaller form, reaches the highest biomass later during the productive season. In the Atlantic part of the Barents Sea, C. finmarchkus is the dominant herbivorous form. The next most important species, Pseudocalanus sp. and M. longa , play a less important role here than in Balsfjorden. In the Arctic domain, the smaller copepod forms appear to have been replaced in trophodynamic terms by the youngest year-group (C-CIII) of C. glacialis , which prevails during the Arctic summer and autumn periods. The coupling between primary producers and Calanus on a seasonal basis is addressed through the grazing and the vertical organisation of the plant-herbivore community. The productivity of these two Calanus species is considered in relation to the seasonal and inter-annual variation in climate; although different mechanisms are utilised, cold periods tend to lower Calanus productivity both in the Arctic and the Atlantic domains of the Barents Sea. Interannual variations in Calanus biomass and productivity are discussed in the perspective of endemic and advective processes.     

Dynamics of plankton growth in the Barents Sea: model studies

1-D and 3-D models of plankton production in the Barents Sea are described and a few simulations presented. The 1-D model has two compartments for phytoplankton (diatoms and P. pouchelii) , three for limiting nutrients (nitrate, ammonia and silicic acid), and one compartment called "sinking phytoplankton". This model is coupled to a submodel of the important herbivores in the area and calculates the vertical distribution in a water column. Simulations with the 3-D model indicate a total annual primary production of 90-120g C m⁻² yr⁻¹ in Atlantic Water and 20-50g C m⁻² yr⁻¹ in Arctic Water, depending on the persistence of the ice cover during the summer.
The 3-D model takes current velocities, vertical mixing, ice cover, and temperature from a 3-D hydrodynamical model. Input data are atmospheric wind, solar radiation, and sensible as well as latent heat flux for the year 1983. The model produces a dynamic picture of the spatial distribution of phytoplankton throughout the spring and summer. Integrated primary production from March to July indicates that the most productive area is Spitsbcrgenbanken and the western entrance to the Barents Sea. i.e. on the northern slope of Tromsøflaket.