• European Marine Science
• 2013-2022close
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Long chain alkyl diols form a group of lipids occurring widely in marine environments. Recent studies have suggested several palaeoclimatological applications for proxies based on their distributions, but also revealed uncertainties about their applicability. Here we evaluate the use of long chain 1,14-alkyl diol indices for reconstruction of temperature and upwelling conditions by comparing index values, obtained from a comprehensive set of marine surface sediments, with environmental factors like sea surface temperature (SST), salinity and nutrient concentrations. Previous cultivation efforts indicated a strong effect of temperature on the degree of saturation and the chain length distribution of long chain 1,14-alkyl diols in Proboscia spp., quantified in the diol saturation index (DSI) and diol chain length index (DCI), respectively. However, values of these indices in surface sediments show no relationship with annual mean SST of the overlying water. It remains unknown what determines the DSI, although our data suggests that it may be affected by diagenesis, while the relationship between temperature and DCI may be different for different Proboscia species. In addition, contributions of algae other than Proboscia diatoms may affect both indices, although our data provide no direct evidence for additional long chain 1,14-alkyl diol sources. Two other indices using the abundance of 1,14-diols vs. 1,13-diols and C30 1,15-diols have previously been applied as indicators for upwelling intensity at different locations. The geographical distribution of their values supports the use of 1,14 diols vs. 1,13 diols [C28 + C30 1,14-diols]/[(C28 + C30 1,13-diols) + (C28 + C30 1,14-diols)] as a general indicator for high nutrient or upwelling conditions.

Atmospheric _p_CO~2~ is a critical component of the global carbon system and is considered to be the major control of Earth's past, present and future climate. Accurate and precise reconstructions of its concentration through geological time are, therefore, crucial to our understanding of the Earth system. Ice core records document _p_CO~2~ for the past 800 kyrs, but at no point during this interval were CO~2~ levels higher than today. Interpretation of older _p_CO~2~ has been hampered by discrepancies during some time intervals between two of the main ocean-based proxy methods used to reconstruct _p_CO~2~: the carbon isotope fractionation that occurs during photosynthesis as recorded by haptophyte biomarkers (alkenones) and the boron isotope composition (δ^11^B) of foraminifer shells. Here we present alkenone and δ^11^B-based _p_CO~2~ reconstructions generated from the same samples from the Plio-Pleistocene at ODP Site 999 across a glacial-interglacial cycle. We find a muted response to _p_CO~2~ in the alkenone record compared to contemporaneous ice core and δ^11^B records, suggesting caution in the interpretation of alkenone-based records at low _p_CO~2~ levels. This is possibly caused by the physiology of CO~2~ uptake in the haptophytes. Our new understanding resolves some of the inconsistencies between the proxies and highlights that caution may be required when interpreting alkenone-based reconstructions of _p_CO~2~.

The data relate to a paper submitted to Quaternary Science Reviews. All the data support a study of the last 94 ka recorded in core MD03-2611 and an adjacent multicore MD03-MUC 3 taken on the fringe of one of the Murray Canyons offshore Kangaroo Island. Additional data pertain to core SS0206-GC15 taken offshore Victoria south of Warrnambool, but its record only spans the last 25ka. The records are at high resolution and cover a multitude of parameters. Radiocarbon dates for these cores are presented in the supplementary section of this paper.

The reconstruction of the stable carbon isotope evolution in atmospheric CO2 (d13Catm ), as archived in Antarctic ice cores, bears the potential to disentangle the contributions of the different carbon cycle fluxes causing past CO2 variations. Here we present a new record of d13Catm before, during and after the Marine Isotope Stage 5.5 (155 000 to 105 000 years BP). The record was derived with a well established sublimation method using ice from the EPICA Dome C (EDC) and the Talos Dome ice cores in East Antarctica. We find a 0.4 permil shift to heavier values between the mean d13Catm level in the Penultimate (~ 140 000 years BP) and Last Glacial Maximum (~ 22 000 years BP), which can be explained by either (i) changes in the isotopic composition or (ii) intensity of the carbon input fluxes to the combined ocean/atmosphere carbon reservoir or (iii) by long-term peat buildup. Our isotopic data suggest that the carbon cycle evolution along Termination II and the subsequent interglacial was controlled by essentially the same processes as during the last 24 000 years, but with different phasing and magnitudes. Furthermore, a 5000 years lag in the CO2 decline relative to EDC temperatures is confirmed during the glacial inception at the end of MIS 5.5 (120 000 years BP). Based on our isotopic data this lag can be explained by terrestrial carbon release and carbonate compensation.

Much of our understanding of Earth's past climate states comes from the measurement of oxygen and carbon isotope variations in deep-sea benthic foraminifera. Yet, major intervals in those records that lack the temporal resolution and/or age control required to identify climate forcing and feedback mechanisms. Here we document 66 million years of global climate by a new high-fidelity Cenozoic global reference benthic carbon and oxygen isotope dataset (CENOGRID). Using recurrence analysis, we find that on timescales of millions of years Earth's climate can be grouped into Hothouse, Warmhouse, Coolhouse and Icehouse states separated by transitions related to changing greenhouse gas levels and the growth of polar ice sheets. Each Cenozoic climate state is paced by orbital cycles, but the response to radiative forcing is state dependent.

Acoustic estimates of herring and blue whiting abundance were obtained during the surveys using the Simrad ER60 scientific echosounder. The allocation of NASC-values to herring, blue whiting and other acoustic targets were based on the composition of the trawl catches and the appearance of echo recordings. To estimate the abundance, the allocated NASC -values were averaged for ICES-squares (0.5° latitude by 1° longitude). For each statistical square, the unit area density of fish (rA) in number per square nautical mile (N*nm-2) was calculated using standard equations (Foote et al., 1987; Toresen et al., 1998). To estimate the total abundance of fish, the unit area abundance for each statistical square was multiplied by the number of square nautical miles in each statistical square and then summed for all the statistical squares within defined subareas and over the total area. Biomass estimation was calculated by multiplying abundance in numbers by the average weight of the fish in each statistical square then summing all squares within defined subareas and over the total area. The Norwegian BEAM soft-ware (Totland and Godø 2001) was used to make estimates of total biomass.

We used a multibeam echosounder (Reson7125) front-mounted onto the ROV Isis (Dive D333, DY081 expedition) to map the terrain of a vertical feature marking the edge of a deep-sea glacial trough (Labrador Sea, [63°51.9'N, 53°16.9'W, depth: 650 to 800 m]). After correction of the ROV navigation (i.e. merging of USBL and DVL), bathymetry [m] and backscatter [nominal unit] were extracted at a resolution of 0.3 m and different terrain descriptors were computed: Slope, Bathymetric Position Index (BPI), Terrain Ruggedness Index, Roughness, Mean and Gaussian curvatures and orientations (Northness and Eastness), at scales of 0.9, 3 and 9 m. Using a Principal Component Analysis (PCA), the terrain descriptors enabled to retrieve 4 terrain clusters and their associated confusion index, to investigate the spatial heterogeneity of the terrain. This approach also underlined the presence of geomorphic features in the wall terrain. The extraction of the backscatter intensity for the first time considering vertical terrains, opens space for further acquisition and processing development. Using photographs collected by the ROV Isis (Dive D334, DY081 expedition), epibenthic fauna was annotated. Each image was linked to a terrain cluster in the 3D space and pooled into 20-m² bins of images. A Bray-Curtis dissimilarity matrix was constructed from morphospecies abundances. This enabled to test for differences of assemblage composition among clusters. Few species appeared more abundant in particular clusters such as L. pertusa in high-roughness cluster. However, nMDS suggested differences in assemblage composition but these dissimilarities were not strongly delineated. Whereas the design of this study may have limited distinctive differences among assemblages, this shows the potential of this cost-effective method of top-down habitat mapping to be applied in undersampled benthic habitat in order to provide a priori knwoledge for defining appropriate sampling design.

These datasets were used to describe the diversity, ecology and role of non-scleractinian corals on scleractinian cold-water coral carbonate mounds in the Logachev Mound Province, Rockall Bank, NE Atlantic. Cold-water coral carbonate mounds, created by framework-building scleractinian corals, are also important habitats for non-scleractinian corals, whose ecology and role are understudied in deep-sea environments. In total ten non-scleractinian species were identified, which were mapped out along eight ROV video transects. Eight species were identified as black corals (three belonging to the family Schizopathidae, one each to the Leiopathidae, Cladopathidae, and Antipathidae and two to an unknown family) and two as gorgonians (Isididae and Plexauridae). The most abundant species were Leiopathes sp. and Parantipathes sp. 2. Areas with a high diversity of non-scleractinian corals are interpreted to offer sufficient food, weak inter-species competition and the presence of heterogeneous and hard settlement substrates. A difference in the density and occurrence of small vs. large colonies of Leiopathes sp. was also observed, which is likely related to a difference in the stability of the substrate they choose for settlement. Non-scleractinian corals, especially black corals, are an important habitat for crabs, crinoids, and shrimps in the Logachev Mound Province.

Radar-detected internal layering contains information on past accumulation rates and patterns. In this study, we assume that the radar layers are isochrones, and use the layer stratigraphy in combination with ice-core measurements and numerical methods to retrieve accumulation information for the northern part of central Greenland. Measurements of the dielectric properties of an ice core from the NEEM (North Greenland Eemian Ice Drilling) site, allow for correlation of the radar layers with volcanic horizons to obtain an accurate age of the layers. We obtain 100 a averaged accumulation patterns for the period 1311-2011 for a 300 by 350 km area encompassing the two ice-core sites: NEEM and NGRIP (North Greenland Ice Core Project). Our results show a clear trend of high accumulation rates west of the ice divide and low accumulation rates east of the ice divide. At the NEEM site, this accumulation pattern persists throughout our study period with only minor temporal variations in the accumulation rate. In contrast, the accumulation rate shows more pronounced temporal variations (based on our centennial averages) from 170 km south of the NEEM site to the NGRIP site. We attribute this variation to shifts in the location of the high?low accumulation boundary away from the ice divide.

Jellyfishes have functionally replaced several overexploited commercial stocks of planktivorous fishes. This is paradoxical, because they use a primitive prey capture mechanism requiring direct contact with the prey, whereas fishes use more efficient visual detection. We have compiled published data to show that, in spite of their primitive life-style, jellyfishes exhibit similar instantaneous prey clearance and respiration rates as their fish competitors and similar potential for growth and reproduction. To achieve this production, they have evolved large, water-laden bodies that increase prey contact rates. Although larger bodies are less efficient for swimming, optimization analysis reveals that large collectors are advantageous if they move through the water sufficiently slowly.