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1.
Pelagic-Benthic Coupling in the Nordic Seas: The Role of Episodic Events   总被引:3,自引:0,他引:3  
Abstract. The consequences of the following episodic phenomena for the pelagic-benthic coupling in the Nordic Seas are illustrated: (1) Advection of water masses between fjords and shelf environments, (2) freshwater run-off and vertical stability, (3) dynamics of the marginal ice zone in the central and northern Barents Sea and the Polar Ocean, (4) drift patterns of sinking particles along the North Norwegian coast, (5) advection of zooplankton into subarctic fjords and the southern Barents Sea, zooplankton overwintering and composition, and (6) transport of organic particulate matter from the Barents Sea shelf. It is shown that physical processes in the north-eastern North Atlantic and Polar Ocean can be strongly variable on time scales of days to decades. They have a significant influence on the dynamics of pelagic-benthic coupling. The physical oceanography influences the vertical and horizontal particle flux not only directly (mixing, advection, up- and down-welling), but also indirectly through its impact on the biota (for example radiation, wind, ice cover, freshwater run-off and overwintering, advection and retention of zooplankton). Understanding pelagic-benthic coupling at high latitudes depends even more on a best possible understanding of the physical oceanography and the time scales involved than elsewhere.  相似文献   
2.
Geological history from the late Palaeoproterozoic to early Neoproterozoic is dominated by the formation of the supercontinent Columbia, and its break-up and re-amalgamation into the next supercontinent, Rodinia. On a global scale, major orogenic events have been tied to the formation of either of these supercontinents, and records of extension are commonly linked to break-up events. Presented here is a synopsis of the geological evolution of southwest Fennoscandia during the ca. 1.9–0.9 Ga period. This region records a protracted history of continental growth and reworking in a long-lived accretionary orogen. Three major periods of continental growth are defined by the Transscandinavian Igneous Belt (1.86–1.66 Ga), Gothian (1.66–1.52 Ga), and Telemarkian (1.52–1.48 Ga) domains. The 1.47–1.38 Ga Hallandian–Danopolonian period featured reorganization of the subduction zone and over-riding plates, with limited evidence for continental collision. During the subsequent 1.38–1.15 Ga interval, the region is interpreted as being located inboard of a convergent margin that is not preserved today and hosted magmatism and sedimentation related to inboard extensional events. The 1.15–0.9 Ga period is host to Sveconorwegian orogenesis that marks the end of this long-lived accretionary orogen and features significant crustal deformation, metamorphism, and magmatism. Collision of an indenter, typically Amazonia, is commonly inferred for the cause of widespread Sveconorwegian orogenesis, but this remains inconclusive. An alternative is that orogenesis merely represents subduction, terrane accretion, crustal thickening, and burial and exhumation of continental crust, along an accretionary margin. During the Mesoproterozoic, southwest Fennoscandia was part of a much larger accretionary orogen that grew on the edge of the Columbia supercontinent and included Laurentia and Amazonia amongst other cratons. The chain of convergent margins along the western Pacific is the best analogue for this setting of Proterozoic crustal growth and tectonism.  相似文献   
3.
The U–Pb ages, REE content, and oxygen isotopic composition of zircon rims developed within a major shear zone in the Kalak Nappe Complex (KNC), Arctic Norway have been determined along with the age of monazite crystals. Different generations of granitic veins have been distinguished based on both field criteria and monazite ages of 446 ± 3 and 424 ± 3 Ma. Within each of these veins, inherited zircon cores are mantled by homogeneous low CL-response zircon rims which yield a range of concordant U–Pb dates of ca. 470–360 Ma. Significant numbers of zircon rims coincide with the timing of monazite crystallization. The zircon rims have moderate light REE enrichment compared to cores, distinctive (Sm/La) n values of less than 12, and La between 0.3 and 10 ppm. This indicates free elemental exchange between newly formed zircon rims and the surrounding matrix. The rims have calculated accumulated alpha-radiation dosages corresponding with a crystalline structure and δ18O values of 1‰. This implies rim crystallization directly from a zirconium-saturated hydrothermal fluid which was modified by some silicate melt. Growth of the zircon rims was prolonged and locally variable due to preferential fluid flow. A third type of zircon can be recognized, forming both rims and cores, with high alpha-radiation doses, and significant enrichment in La, Pr, and Eu. These are interpreted as low-temperature hydrothermally altered metamict zircons. The high volatile input and partial melting in the shear zone favoured prolonged zircon rim growth due to its ability to easily nucleate on inherited seeds. On the other hand, monazite, susceptible to dissolution and re-growth, crystallized in brief episodes, as has been predicted from theoretical phase diagrams. From a regional perspective, these results elucidate cryptic Ar–Ar cooling ages, providing the first record of a Late Ordovician heating and cooling phase within the KNC prior to the climactic Scandian collision.  相似文献   
4.
The Hardangervidda-Rogaland Block within southwest Norway is host to ~1.52 to 1.48 Ga continental building and variable reworking during the ~1.1 to 0.9 Ga Sveconorwegian orogeny. Due to the lack of geochronological and geochemical data, the timing and tectonic setting of early Mesoproterozoic magmatism has long been ambiguous. This paper presents zircon U–Pb–Hf–O isotope data combined with whole-rock geochemistry to address the age and petrogenesis of basement units within the Suldal region, located in the centre of the Hardangervidda-Rogaland Block. The basement comprises variably deformed grey gneisses and granitoids that petrologically and geochemically resemble mature volcanic arc lithologies. U–Pb ages confirm that magmatism occurred from ~1,521 to 1,485 Ma, and conspicuously lack any xenocrystic inheritance of distinctly older crust. Hafnium isotope data range from εHf(initial) +1 to +11, suggesting a rather juvenile magmatic source, but with possible involvement of late Palaeoproterozoic crust. Oxygen isotope data range from mantle-like (δ18O ~5 ‰) to elevated (~10 ‰) suggesting involvement of low-temperature altered material (e.g., supracrustal rocks) in the magma source. The Hf–O isotope array is compatible with mixing between mantle-derived material with young low-temperature altered material (oceanic crust/sediments) and older low-temperature altered material (continent-derived sediments). This, combined with a lack of xenoliths and xenocrysts, exposed older crust, AFC trends and S-type geochemistry, all point to mixing within a deep-crustal magma-generation zone. A proposed model comprises accretion of altered oceanic crust and the overlying sediments to a pre-existing continental margin, underthrusting to the magma-generation zone and remobilisation during arc magmatism. The geodynamic setting for this arc magmatism is comparable with that seen in the Phanerozoic (e.g., the Sierra Nevada and Coast Range batholiths), with compositions in the Suldal Sector reaching those of average upper continental crust. As within these younger examples, factors that drive magmatism towards the composition of the average continental crust include the addition of sedimentary material to magma source regions, and delamination of cumulate material. Underthrusting of sedimentary materials and their subsequent involvement in arc magmatism is perhaps a more widespread mechanism involved in continental growth than is currently recognised. Finally, the Suldal Arc magmatism represents a significant juvenile crustal addition to SW Fennoscandia.  相似文献   
5.
Food webs and carbon flux in the Barents Sea   总被引:6,自引:3,他引:6  
Within the framework of the physical forcing, we describe and quantify the key ecosystem components and basic food web structure of the Barents Sea. Emphasis is given to the energy flow through the ecosystem from an end-to-end perspective, i.e. from bacteria, through phytoplankton and zooplankton to fish, mammals and birds. Primary production in the Barents is on average 93 g C m−2 y−1, but interannually highly variable (±19%), responding to climate variability and change (e.g. variations in Atlantic Water inflow, the position of the ice edge and low-pressure pathways). The traditional focus upon large phytoplankton cells in polar regions seems less adequate in the Barents, as the cell carbon in the pelagic is most often dominated by small cells that are entangled in an efficient microbial loop that appears to be well coupled to the grazing food web. Primary production in the ice-covered waters of the Barents is clearly dominated by planktonic algae and the supply of ice biota by local production or advection is small. The pelagic–benthic coupling is strong, in particular in the marginal ice zone. In total 80% of the harvestable production is channelled through the deep-water communities and benthos. 19% of the harvestable production is grazed by the dominating copepods Calanus finmarchicus and C. glacialis in Atlantic or Arctic Water, respectively. These two species, in addition to capelin (Mallotus villosus) and herring (Clupea harengus), are the keystone organisms in the Barents that create the basis for the rich assemblage of higher trophic level organisms, facilitating one of the worlds largest fisheries (capelin, cod, shrimps, seals and whales). Less than 1% of the harvestable production is channelled through the most dominating higher trophic levels such as cod, harp seals, minke whales and sea birds. Atlantic cod, seals, whales, birds and man compete for harvestable energy with similar shares. Climate variability and change, differences in recruitment, variable resource availability, harvesting restrictions and management schemes will influence the resource exploitation between these competitors, that basically depend upon the efficient energy transfer from primary production to highly successful, lipid-rich zooplankton and pelagic fishes.  相似文献   
6.
This paper reports estimates of trophic flows of carbon off the Galician coast from a 1D ecological model, which are compared with field data from a two week Lagrangian drift experiment. The model consists of 9 biological components: nitrate, ammonium, >5μm phytoplankton, <5μm phytoplankton, heterotrophic nanoflagellates/dinoflagellates (5–20 μm), heterotrophic dinoflagellates (>20 μm), ciliates, fast sinking detritus and slow sinking detritus. Calculations were made for the fluxes of carbon between biological components within the upper 45m of the water column. The temporal development of primary production during the simulation period of two weeks was in good agreement with field estimates, which varied between 248 and 436mgC.m−2.d−1. Heterotrophic nanoflagellates had the greatest impact on carbon flux, with a grazing rate of 168mgC.m−2.d−1. Herbivorous grazing by microzooplankton amounted to 215mgC.m−2.d−1, whereas grazing by copepods on phytoplankton was 35mgC.m−2 d−1. Copepods grazing on microzooplankton was minor (0.47mgC.m−2.d−1) and the export flux from the upper 45m was 302mgC.m−2.d−1. Sensitivity analyses, in which the grazing parameters (i.e the functional relationship between ingestion and food concentration) were changed, were carried out on the heterotrophic dinoflagellate, ciliate and heterotrophic nanoflagellates/dinoflagellate components of the model. These changes did not alter the temporal development of heterotrophic nanoflagellates/dinoflagellates biomass significantly, but ciliates and heterotrophic dinoflagellates were more sensitive to variations in the grazing parameters. The overall conclusion from this modelling study is that the coupling between small phytoplankton and heterotrophic nanoflagellates was the quantitatively most important process controlling carbon flow in this region.  相似文献   
7.
8.
Abstract

The Barents Sea is divided into a northern and a southern part by the Polar Front (at about 75–76° N) where Atlantic waters descend under Arctic waters. Near to and north of the Polar Front, the spring bloom of phytoplankton is triggered by the stability induced in the upper 20 m by the melting of ice. The pycnocline is too strong to be eroded by wind. Primary productivity after the bloom is therefore small and largely regenerative. Underneath the pycnocline there is a 3–5 m thick layer characterized by dense, slow‐growing algal populations. New productivity north of the Polar Front is no more than 40 g C m?2 a?1.

In permanently open waters south of the Polar Front, the spring bloom starts in early May. Rhythmic wind‐induced mixing related to the atmospheric low‐pressure belt reaches an average 40–60 m depth in the growth season, and secondary phytoplankton maxima may arise. As a result, new annual productivity is more than doubled, i.e. 90 g C m?2 a?1, relative to the same system without wind. Although productivity is highest south of the Polar Front, it is more concentrated north of it, in the sense that high new production is mainly related to a 20–50 km wide belt that sweeps the area following the ice edge northwards while the ice melts through the summer.  相似文献   
9.
The physical and biological environment of the Barents Sea is characterised by large variability on a wide range of scales. Results from a numerical ocean model, SINMOD, are presented showing that the physical variability is partly forced by changes in annual net ice import. The mean contribution from ice import in the simulation period (1979–2007) is about 40% of the total amount of ice melted each year. The annual ice import into the Barents Sea varies between 143 and 1,236 km3, and this causes a substantial variability in the amount of annual ice melt in the Barents Sea. This in turn impacts the freshwater content. The simulated freshwater contribution from ice is 0.02 Sv on average and 0.04 Sv at maximum. When mixed into a mean net Atlantic Water (AW) inflow of 1.1 Sv with a salinity of 35.1, this freshwater addition decreases the salinity of the modified AW to 34.4 and 33.9 for the mean and maximum freshwater fluxes, respectively. Ice import may thus be important for the Barents Sea production of Arctic Ocean halocline water which has salinity of about 34.5. The changes in the ice melt the following summer due to ice import also affect the formation of dense water in the Barents Sea by changing stratification, altering the vertical mixing rates and affecting heat loss from the warm AW. The model results thus indicate that ice import from the Arctic has a great impact on water mass modification in the Barents Sea which in turn impacts the ventilation of the Arctic Ocean.  相似文献   
10.
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