scholarly journals Why do jellyfish bloom in Norwegian waters and what can be done to recover the ecosystems in the North Sea and on the Norwegian coast?

Author(s):  
Johannes Hamre

The ecosystems with their relationships between fish species and stocks, have been established by evolution for millions of years, but during the last 50 years, the ecosystems in the North Sea and along the Norwegian coast have been changed fundamentally by fisheries. The North Sea mackerel stock has been depleted and its feeding grounds have been invaded by the Western mackerel which spawns west of Ireland. This stock is now very rich in numbers and occupies the North Sea, the Norwegian Sea and the western Barents Sea. If the trend continues, mackerel may outcompete many of the other fish stocks in the area. Traditionally and until the beginning of the 1970s, there was a large stock of sandeel spawning in the North Sea and on the Norwegian coast. Sandeel juveniles was an important food source for a wide range of species, including sea mammals and birds. The fact that this stock has also been overfished, may explain many changes observed in the ecosystem on the west coast of Norway, for example a large reduction in the populations of sea birds. There are several instances where ecosystems shift to sustain jellyfish blooms in response to depletion of forage fish stocks. This was registered in Namibia in the 1990’s, where the pilchard stock was decimated and the biomass of jellyfish soon became overwhelming. On the west-coast of Norway, there are now frequent blooms of jellyfish, yet another indication that a controlling factor is missing in the system, in this case sandeel, which is a key species in the transfer of nutrients from zooplankton to higher trophic levels in the area. In this paper, I give a description of the situation and some suggested measures that should be taken in fisheries management.

2017 ◽  
Author(s):  
Johannes Hamre

The ecosystems with their relationships between fish species and stocks, have been established by evolution for millions of years, but during the last 50 years, the ecosystems in the North Sea and along the Norwegian coast have been changed fundamentally by fisheries. The North Sea mackerel stock has been depleted and its feeding grounds have been invaded by the Western mackerel which spawns west of Ireland. This stock is now very rich in numbers and occupies the North Sea, the Norwegian Sea and the western Barents Sea. If the trend continues, mackerel may outcompete many of the other fish stocks in the area. Traditionally and until the beginning of the 1970s, there was a large stock of sandeel spawning in the North Sea and on the Norwegian coast. Sandeel juveniles was an important food source for a wide range of species, including sea mammals and birds. The fact that this stock has also been overfished, may explain many changes observed in the ecosystem on the west coast of Norway, for example a large reduction in the populations of sea birds. There are several instances where ecosystems shift to sustain jellyfish blooms in response to depletion of forage fish stocks. This was registered in Namibia in the 1990’s, where the pilchard stock was decimated and the biomass of jellyfish soon became overwhelming. On the west-coast of Norway, there are now frequent blooms of jellyfish, yet another indication that a controlling factor is missing in the system, in this case sandeel, which is a key species in the transfer of nutrients from zooplankton to higher trophic levels in the area. In this paper, I give a description of the situation and some suggested measures that should be taken in fisheries management.


Zootaxa ◽  
2006 ◽  
Vol 1203 (1) ◽  
pp. 39
Author(s):  
ALISON M. MCCARTHY ◽  
SARAH GERKEN ◽  
DAVID MCGRATH ◽  
GRACE P. MCCORMACK

The validity of Pseudocuma gilsoni B|cescu 1950 has been questioned in the past. The recent discovery of material in Irish waters, and in the North Sea, confirms the presence of the species in the North East Atlantic and provides the opportunity to present a full redescription. A new genus, Monopseudocuma, is erected to accommodate the species. A neotype is designated from the West coast of Ireland.


2020 ◽  
Author(s):  
Jan Niklas Macher ◽  
Berry B. van der Hoorn ◽  
Katja T. C. A. Peijnenburg ◽  
Lodewijk van Walraven ◽  
Willem Renema

AbstractZooplankton are key players in marine ecosystems, linking primary production to higher trophic levels. The high abundance and high taxonomic diversity renders zooplankton ideal for biodiversity monitoring. However, taxonomic identification of the zooplankton assemblage is challenging due to its high diversity, subtle morphological differences and the presence of many meroplanktonic species, especially in coastal seas. Molecular techniques such as metabarcoding can help with rapid processing and identification of taxa in complex samples, and are therefore promising tools for identifying zooplankton communities. In this study, we applied metabarcoding of the mitochondrial cytochrome c oxidase I gene to zooplankton samples collected along a latitudinal transect in the North Sea, a shelf sea of the Atlantic Ocean. Northern regions of the North Sea are influenced by inflow of oceanic Atlantic waters, whereas the southern parts are characterised by more coastal waters. Our metabarcoding results indicated strong differences in zooplankton community composition between northern and southern areas of the North Sea, particularly in the classes Copepoda, Actinopterygii (ray-finned fishes) and Polychaeta. We compared these results to the known distributions of species reported in previous studies, and by comparing the abundance of copepods to data obtained from the Continuous Plankton Recorder (CPR). We found that our metabarcoding results are mostly congruent with the reported distribution and abundance patterns of zooplankton species in the North Sea. Our results highlight the power of metabarcoding to rapidly assess complex zooplankton samples, and we suggest that the technique could be used in future monitoring campaigns and biodiversity assessments.HighlightsZooplankton communities are different in northern and southern areas of the North SeaMetabarcoding results are consistent with known species distributions and abundanceMetabarcoding allows for fast identification of meroplanktonic species


2020 ◽  
Author(s):  
Oceana ◽  
Helena Álvarez ◽  
Allison L. Perry ◽  
Jorge Blanco ◽  
Silvia Garcia ◽  
...  

To help fill gaps in knowledge about marine biodiversity in the North Sea, Oceana carried out two eight week research expeditions, in 2016 and 2017. Oceana’s surveys documented a wide range of habitats and species that are considered priorities for conservation, under national, EU, and international frameworks that recognise them as threatened and/or establish legal requirements for their protection.Oceana’s research has underscored the fact that much remains to be discovered about marine life on the seabed of the North Sea. Continued research is critical for informing efforts to recover biodiversity, an urgent priority in the face of the multiple, intense pressures facing the North Sea’s marine habitats and species.


Ocean Science ◽  
2017 ◽  
Vol 13 (2) ◽  
pp. 315-335 ◽  
Author(s):  
Robert Marsh ◽  
Ivan D. Haigh ◽  
Stuart A. Cunningham ◽  
Mark E. Inall ◽  
Marie Porter ◽  
...  

Abstract. The European Slope Current provides a shelf-edge conduit for Atlantic Water, a substantial fraction of which is destined for the northern North Sea, with implications for regional hydrography and ecosystems. Drifters drogued at 50 m in the European Slope Current at the Hebridean shelf break follow a wide range of pathways, indicating highly variable Atlantic inflow to the North Sea. Slope Current pathways, timescales and transports over 1988–2007 are further quantified in an eddy-resolving ocean model hindcast. Particle trajectories calculated with model currents indicate that Slope Current water is largely recruited from the eastern subpolar North Atlantic. Observations of absolute dynamic topography and climatological density support theoretical expectations that Slope Current transport is to first order associated with meridional density gradients in the eastern subpolar gyre, which support a geostrophic inflow towards the slope. In the model hindcast, Slope Current transport variability is dominated by abrupt 25–50 % reductions of these density gradients over 1996–1998. Concurrent changes in wind forcing, expressed in terms of density gradients, act in the same sense to reduce Slope Current transport. This indicates that coordinated regional changes of buoyancy and wind forcing acted together to reduce Slope Current transport during the 1990s. Particle trajectories further show that 10–40 % of Slope Current water is destined for the northern North Sea within 6 months of passing to the west of Scotland, with a general decline in this percentage over 1988–2007. Salinities in the Slope Current correspondingly decreased, evidenced in ocean analysis data. Further to the north, in the Atlantic Water conveyed by the Slope Current through the Faroe–Shetland Channel (FSC), salinity is observed to increase over this period while declining in the hindcast. The observed trend may have broadly compensated for a decline in the Atlantic inflow, limiting salinity changes in the northern North Sea during this period. Proxies for both Slope Current transport and Atlantic inflow to the North Sea are sought in sea level height differences across the FSC and between Shetland and the Scottish mainland (Wick). Variability of Slope Current transport on a wide range of timescales, from seasonal to multi-decadal, is implicit in sea level differences between Lerwick (Shetland) and Tórshavn (Faroes), in both tide gauge records from 1957 and a longer model hindcast spanning 1958–2012. Wick–Lerwick sea level differences in tide gauge records from 1965 indicate considerable decadal variability in the Fair Isle Current transport that dominates Atlantic inflow to the northwest North Sea, while sea level differences in the hindcast are dominated by strong seasonal variability. Uncertainties in the Wick tide gauge record limit confidence in this proxy.


Clay Minerals ◽  
2006 ◽  
Vol 41 (1) ◽  
pp. 151-186 ◽  
Author(s):  
M. Wilkinson ◽  
R. S. Haszeldine ◽  
A. E. Fallick

AbstractThe principal clays of the northern and central North Sea are illite (sometimes with interlayered smectite) and kaolin. Chlorite is only locally important. Although it has been proposed that kaolin within North Sea sandstones is detrital in origin, the majority of workers have concluded that it is authigenic, largely the product of feldspar alteration. Kaolin is found within a wide range of sedimentary settings (and within shales) apparently defying the notion that kaolin is an indicator of meteoric water deposition. Within sandstones, the earliest authigenic kaolin has a vermiform morphology, the distribution of which is controlled by the availability of detrital mica to act as a nucleus, and the composition of the post-depositional porewaters. This vermiform kaolin formed in meteoric water, the presence of which is easily accounted for below sub-aerial exposure surfaces in non-marine formations, and below unconformities over marine units. In fully marine sands, and even marine shale units, kaolin still occurs. It has therefore been suggested that even these locations have been flushed with meteoric water.Early vermiform kaolin recrystallizes to a more blocky morphology as burial proceeds, at least in the Brent Group. Blocky kaolin has been reported as growing before, synchronously with, and after the formation of quartz overgrowths, though oxygen isotope studies support low-temperature growth, pre-quartz. Blocky kaolin may form during meteoric flushing associated with lower Cretaceous uplift and erosion, though it is found in fault blocks that are thought to have remained below sea level. Here, the kaolin may form in stagnant meteoric water, relics of the post-depositional porewater. It has also been proposed that the blocky kaolin grew in ascending basinal waters charged with carboxylic acids and CO2, though this hypothesis is not supported by stable oxygen isotope data. Some of the blocky kaolin is dickite, the stable polymorph above ∼100°C.Fibrous illite occurs almost ubiquitously within the clastic sediments of the North Sea. An early pore-lining phase has been interpreted as both infiltrated clastic clay, and as an early diagenetic phase. Early clays may have been quite smectite-rich illites, or even discrete smectites. Later, fibrous illite is undoubtedly neoformed, and can degrade reservoir quality significantly. Both within sandstones and shales, there is an apparent increase in the K content deeper than 4 km of burial, which could be due to dilution of the early smectite-rich phase by new growth illite, or to the progressive illitization of existing I-S. Much of the ‘illite’ that has been dated by the K-Ar method may therefore actually be I-S.The factors that control the formation of fibrous illite are only poorly known, though temperature must play a role. Illite growth has been proposed for almost the entire range of diagenetic temperatures (e.g. 15–20°C, Brent Group; 35–40°C, Oxfordian Sand, Inner Moray Firth; 50–90°C, Brae formation; 100–110°C, Brent Group; 130–140°C, Haltenbanken). It seems unlikely that there is a threshold temperature below which illite growth is impossible (or too slow to be significant), though this is a recurring hypothesis in the literature. Instead, illite growth seems to be an event, commonly triggered by oil emplacement or another change in the physiochemical conditions within the sandstone, such as an episode of overpressure release. Hence fibrous illite can grow at any temperature encountered during diagenesis.Although there is an extensive dataset of K-Ar ages of authigenic illites from the Jurassic of the North Sea, there is no consensus as to whether the data are meaningful, or whether the purified illite samples prepared for analysis are so contaminated with detrital phases as to render the age data meaningless. At present it is unclear about how to resolve this problem, though there is some indication that chemical micro-analysis could help. It is a common belief that illite ages record the timing of oil charge, and so can be used to calibrate basin models.Grain-coating Fe-rich chlorite cements can preserve exceptional porosity during burial. They are found in marginal marine sandstones, formed during diagenesis from precursor Fe-rich clays such as berthierine or verdine.


2005 ◽  
Vol 62 (7) ◽  
pp. 1205-1215 ◽  
Author(s):  
J. Alheit ◽  
C. Möllmann ◽  
J. Dutz ◽  
G. Kornilovs ◽  
P. Loewe ◽  
...  

Abstract The index of the North Atlantic Oscillation, the dominant mode of climatic variability in the North Atlantic region, changed in the late 1980s (1987–1989) from a negative to a positive phase. This led to regime shifts in the ecology of the North Sea (NS) and the central Baltic Sea (CBS), which involved all trophic levels in the pelagial of these two neighbouring continental shelf seas. Increasing air and sea surface temperatures, which affected critical physical and biological processes, were the main direct and indirect driving forces. After 1987, phytoplankton biomass in both systems increased and the growing season was extended. The composition of phyto- and zooplankton communities in both seas changed conspicuously, e.g. dinoflagellate abundance increased and diatom abundance decreased in the CBS. Key copepod species that are essential in fish diets experienced pronounced changes in biomass. Abundance of Calanus finmarchicus (NS) and Pseudocalanus sp. (CBS) fell to low levels, whereas C. helgolandicus (NS) and Temora longicornis and Acartia spp. (CBS) were persistently abundant. These changes in biomass of different copepod species had dramatic consequences on biomass, fisheries, and landings of key fish species: North Sea cod declined, cod in the CBS remained at low levels, and CBS sprat reached unprecedented high biomass levels resulting in high yields. The synchronous regime shifts in NS and CBS resulted in profound changes in both marine ecosystems. However, the reaction of fish populations to the bottom-up mechanisms caused by the same climatic shift was very different for the three fish stocks.


1960 ◽  
Vol 67 (4) ◽  
pp. 351-362 ◽  
Author(s):  
A. D. McIntyre

SynopsisFrom a faunistic survey in Scottish waters, concentrated mainly in the sea lochs of the north-west coast and in the deep water in the North Sea off the east coast, thirty-two species of polychætes are listed which have not previously been recorded from these areas. Seven of the species are new records for British coastal waters or for the North Sea.


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