Spatial and temporal dynamics of European hake (Merluccius merluccius) in the North Sea

2018 ◽  
Vol 75 (6) ◽  
pp. 2033-2044 ◽  
Author(s):  
Arved Staby ◽  
Jon Egil Skjæraasen ◽  
Audrey J Geffen ◽  
Daniel Howell

Abstract Catches of European hake (Merluccius merluccius) in the North Sea have increased substantially during the last decade, even though there is no directed commercial fishery of hake in this area. We analysed the spatial distributions of hake in the northern the parts of its range, (where it is less well-studied), using ICES international bottom trawl survey data from 1997 to 2015. We examine length-frequency distributions for (i) distinct modes enabling the assignment of fish into categories which likely corresponded to the ages 1, 2, and 3+ and (ii) patterns of seasonal spatial distribution for the different groups. Age categories 1 and 2 fish were most abundant in the northern North Sea, and appear to remain in the North Sea until 2 years of age, when they move into deeper waters. Their distribution has expanded into the western-central North Sea in the last decade. Age category 3+ fish were most abundant in the northern and central North Sea during summer, indicating a seasonal influx of large individuals into this area likely associated with spawning activity. The distribution of these older fish has gradually expanded westward in both seasons.

2014 ◽  
Vol 71 (6) ◽  
pp. 1342-1355 ◽  
Author(s):  
Xochitl Cormon ◽  
Christophe Loots ◽  
Sandrine Vaz ◽  
Youen Vermard ◽  
Paul Marchal

Spatial interactions between saithe (Pollachius virens) and hake (Merluccius merluccius) were investigated in the North Sea. Saithe is a well-established species in the North Sea, while occurrence of the less common hake has recently increased in the area. Spatial dynamics of these two species and their potential spatial interactions were explored using binomial generalized linear models (GLM) applied to the International Bottom Trawl Survey (IBTS) data from 1991 to 2012. Models included different types of variables: (i) abiotic variables including sediment types, temperature, and bathymetry; (ii) biotic variables including potential competitors and potential preys presence; and (iii) spatial variables. The models were reduced and used to predict and map probable habitats of saithe, hake but also, for the first time in the North Sea, the distribution of the spatial overlap between these two species. Changes in distribution patterns of these two species and of their overlap were also investigated by comparing species’ presence and overlap probabilities predicted over an early (1991–1996) and a late period (2007–2012). The results show an increase in the probability over time of the overlap between saithe and hake along with an expansion towards the southwest and Scottish waters. These shifts follow trends observed in temperature data and might be indirectly induced by climate changes. Saithe, hake, and their overlap are positively influenced by potential preys and/or competitors, which confirms spatial co-occurrence of the species concerned and leads to the questions of predator–prey relationships and competition. Finally, the present study provides robust predictions concerning the spatial distribution of saithe, hake, and of their overlap in the North Sea, which may be of interest for fishery managers.


2015 ◽  
Vol 73 (4) ◽  
pp. 1115-1126 ◽  
Author(s):  
Jeroen van der Kooij ◽  
Sascha M.M. Fässler ◽  
David Stephens ◽  
Lisa Readdy ◽  
Beth E. Scott ◽  
...  

Abstract Fisheries independent monitoring of widely distributed pelagic fish species which conduct large seasonal migrations is logistically complex and expensive. One of the commercially most important examples of such a species in the Northeast Atlantic Ocean is mackerel for which up to recently only an international triennial egg survey contributed to the stock assessment. In this study, we explore whether fisheries acoustic data, recorded opportunistically during the English component of the North Sea International Bottom Trawl Survey, can contribute to an improved understanding of mackerel distribution and provide supplementary data to existing dedicated monitoring surveys. Using a previously published multifrequency acoustic mackerel detection algorithm, we extracted the distribution and abundance of schooling mackerel for the whole of the North Sea during August and September between 2007 and 2013. The spatio-temporal coverage of this unique dataset is of particular interest because it includes part of the unsurveyed summer mackerel feeding grounds in the northern North Sea. Recent increases in landings in Icelandic waters during this season suggested that changes have occurred in the mackerel feeding distribution. Thus far it is poorly understood whether these changes are due to a shift, i.e. mackerel moving away from their traditional feeding grounds in the northern North Sea and southern Norwegian Sea, or whether the species' distribution has expanded. We therefore explored whether acoustically derived biomass of schooling mackerel declined in the northern North Sea during the study period, which would suggest a shift in mackerel distribution rather than an expansion. The results of this study show that in the North Sea, schooling mackerel abundance has increased and that its distribution in this area has not changed over this period. Both of these findings provide, to our knowledge, the first evidence in support of the hypothesis that mackerel have expanded their distribution rather than moved away.


Author(s):  
Simon Jennings ◽  
John Lancaster ◽  
Andrew Woolmer ◽  
John Cotter

The assemblages of attached and freeliving epibenthic species in the North Sea are described, based on analysis of samples collected with a small beam trawl. Clustering of survey sites based on the presence or absence of attached species indicated that three regions had characteristic assemblages: the northern North Sea, the central North Sea from 55 to 57°N and the southern North Sea. Clustering of sites based on counts of free-living epibenthic species also revealed that the sites formed three major groups but these corresponded to regions in the north-east North Sea, the northern and western central North Sea and the southern and eastern central North Sea. Species which contributed most to the similarity within and dissimilarity between groups were identified. The environmental factors which best accounted for the grouping of sites were depth, winter temperature and the temperature difference between winter and summer for attached species and depth and the temperature difference between winter and summer for free-living species. The species richness of attached and free-living epibenthic species was higher in the central and northern North Sea than in the south. The number of abundant (Hill's N1) and very abundant (Hill's N2) free-living species also increased from south to north.


Minerals ◽  
2018 ◽  
Vol 8 (12) ◽  
pp. 564 ◽  
Author(s):  
Andrew Morton ◽  
Paula McGill

Correlation of hydrocarbon reservoir sandstones is one of the most important economic applications for heavy mineral analysis. In this paper, we review the fundamental principles required for establishing correlation frameworks using heavy mineral data, and illustrate the applications of a wide variety of heavy mineral techniques using a number of case studies from hydrocarbon reservoirs in the North Sea and adjacent areas. The examples cover Triassic red-bed successions in the central North Sea and west of Shetland, which have been subdivided and correlated using provenance-sensitive ratio data and mineral morphologies; Middle Jurassic paralic sandstones in the northern North Sea, correlated using garnet geochemistry; Upper Jurassic deep water sandstones in the northern North Sea, discriminated using rutile geochemistry and detrital zircon age data; and the “real-time” application of the technique at well site in Devonian-Carboniferous fluvio-lacustrine sandstones of the Clair Field, west of Shetland.


2016 ◽  
Vol 13 (8) ◽  
pp. 2511-2535 ◽  
Author(s):  
Fabian Große ◽  
Naomi Greenwood ◽  
Markus Kreus ◽  
Hermann-Josef Lenhart ◽  
Detlev Machoczek ◽  
...  

Abstract. Low oxygen conditions, often referred to as oxygen deficiency, occur regularly in the North Sea, a temperate European shelf sea. Stratification represents a major process regulating the seasonal dynamics of bottom oxygen, yet, lowest oxygen conditions in the North Sea do not occur in the regions of strongest stratification. This suggests that stratification is an important prerequisite for oxygen deficiency, but that the complex interaction between hydrodynamics and the biological processes drives its evolution. In this study we use the ecosystem model HAMSOM-ECOHAM to provide a general characterisation of the different zones of the North Sea with respect to oxygen, and to quantify the impact of the different physical and biological factors driving the oxygen dynamics inside the entire sub-thermocline volume and directly above the bottom. With respect to oxygen dynamics, the North Sea can be subdivided into three different zones: (1) a highly productive, non-stratified coastal zone, (2) a productive, seasonally stratified zone with a small sub-thermocline volume, and (3) a productive, seasonally stratified zone with a large sub-thermocline volume. Type 2 reveals the highest susceptibility to oxygen deficiency due to sufficiently long stratification periods (>  60 days) accompanied by high surface productivity resulting in high biological consumption, and a small sub-thermocline volume implying both a small initial oxygen inventory and a strong influence of the biological consumption on the oxygen concentration. Year-to-year variations in the oxygen conditions are caused by variations in primary production, while spatial differences can be attributed to differences in stratification and water depth. The large sub-thermocline volume dominates the oxygen dynamics in the northern central and northern North Sea and makes this region insusceptible to oxygen deficiency. In the southern North Sea the strong tidal mixing inhibits the development of seasonal stratification which protects this area from the evolution of low oxygen conditions. In contrast, the southern central North Sea is highly susceptible to low oxygen conditions (type 2). We furthermore show that benthic diagenetic processes represent the main oxygen consumers in the bottom layer, consistently accounting for more than 50 % of the overall consumption. Thus, primary production followed by remineralisation of organic matter under stratified conditions constitutes the main driver for the evolution of oxygen deficiency in the southern central North Sea. By providing these valuable insights, we show that ecosystem models can be a useful tool for the interpretation of observations and the estimation of the impact of anthropogenic drivers on the North Sea oxygen conditions.


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.


Author(s):  
C.P. Lynam ◽  
M.J. Attrill ◽  
M.D. Skogen

Oceanographically based mechanisms are shown to explain the spatial variation in the climatic relationship between the abundance of medusae (Aurelia aurita and Cyanea spp. of the class Scyphozoa), in the North Sea between 1971 and 1986 during June–August, and the winter (December–March) North Atlantic Oscillation Index (NAOI). A scyphomedusa population to the west of Denmark shows a strong inverse relationship between medusa abundance and fluctuations in the NAOI; the NAOI correlates strongly (P < 0.001) with both annual sea surface temperature (SST) at 6.5°E 56.5°N (1950–2008) and with winter precipitation on the Danish coast at Nordby (1900–2008) suggesting a direct link between the influence of climate and medusae abundance. In contrast, scyphomedusa abundance and distribution in the northern North Sea appears to be influenced by oceanic and mixed water inflow, which may overwhelm or mask any direct climatic influence on jellyfish abundance. Similarly, advection can also explain much of the interannual variability (1959–2000) in the abundance of other gelatinous zooplankton taxa (Cnidaria, Ctenophora and Siphonophora) in the northern North Sea as identified by the capture of gelatinous tissue and nematocysts (stinging cells) in Continuous Plankton Recorder samples. Jellyfish (Scyphozoa) in the southern North Sea may benefit from low temperature anomalies and the long-term effects of global warming might suppress Aurelia aurita and Cyanea spp. populations there. However, the biological response to temperature is complex and future research is required in this area.


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.


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