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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.

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.

High-resolution 2D seismic reflection data during research cruise MSM63 in April/May 2017 onboard RV Maria S. Merian. The seismic profiles were acquired with a two-105/105-in3-GI-Gun-array shot at 210 bar every 5 seconds and a 150 m-long streamer with 96 channels and 1.5625 m channel spacing. The resulting shot point distance is approximately 8.75-12.5 m at 3.5-5 kn ship speed. The frequency range of the two-GI-Gun-array is 15-500 Hz. The processing included geometry and delay corrections, static corrections, binning to 1.5625 m and bandpass filtering with corner frequencies of 25, 45, 420, and 500 Hz. Furthermore, a normal-move-out-correction (with a constant velocity of 1488 m/s calculated from CTD measurements) was applied and the data were stacked and then migrated using a 2D Stolt algorithm (1500 m/s constant velocity model). Sub-bottom profiler data acquired during cruise MSM63 using Parasound P70 with 4 kHz as the secondary low frequency to obtain seismic images of the upper 100 m below the seafloor with very high vertical resolution (< 15 cm). We applied a frequency filter (low cut 2 kHz, high cut 6 kHz, 2 iterations) and calculated the envelope within the seismic interpretation software IHS Kingdom. Bathymetric data were acquired with the EM712 system mounted to the hull of RV Maria S. Merian. The survey was designed to provide high-resolution bathymetry with 5 x 5 m resolution. We processed the data using MB Systems software (Caress & Chayes, 2017) and included statistical evaluation of soundings that increased the signal-to-noise ratio. The sound velocity profile for multibeam processing was measured at the beginning and at the end of the cruise.

An understanding of the balance of interspecific competition and the physical environment in structuring organismal communities is crucial because those communities structured primarily by their physical environment typically exhibit greater sensitivity to environmental change than those structured predominantly by competitive interactions. Here, using detailed phylogenetic and functional information, we investigate this question in macrofaunal assemblages from Northwest Atlantic Ocean continental slopes, a high seas region projected to experience substantial environmental change through the current century. We demonstrate assemblages to be both phylogenetically and functionally under-dispersed and thus conclude that the physical environment, not competition, may dominate in structuring deep-ocean communities. Further, we find temperature and bottom trawling intensity to be amongst the environmental factors significantly related to assemblage diversity. These results hint that deep-ocean communities are highly sensitive to their physical environment and vulnerable to environmental perturbation, including by direct disturbance through fishing, and indirectly through the changes brought about by climate change.

Seamounts represent ideal systems to study the influence and interdependency of environmental gradients at a single geographic location. These topographic features represent a prominent habitat for various forms of life, including microbiota and macrobiota, spanning benthic as well as pelagic organisms. While it is known that seamounts are globally abundant structures, it still remains unclear how and to which extend the complexity of the seafloor is intertwined with the local oceanographic mosaic, biogeochemistry and microbiology of a seamount ecosystem. Along these lines, the present study aimed to explore whether and to which extend seamounts can have an imprint on the microbial community composition of seawater and of sessile benthic invertebrates, sponges. For our high-resolution sampling approach of microbial diversity (16S rRNA gene Amplicon sequencing) along with measurements of inorganic nutrients and other biogeochemical parameters, we focused on the Schulz Bank seamount ecosystem, a sponge ground ecosystem which is located on the Arctic Mid-Ocean Ridge. Seawater samples were collected at two sampling depths (mid-water: MW, and near-bed water: BW) from a total of 19 sampling sites. With a clustering approach we defined microbial micro-habitats within the pelagic realm at Schulz Bank, which were mapped onto the seamount's topography, and related to various environmental parameters (such as suspended particulate matter (SPM), dissolved inorganic carbon (DIC), silicate (SiO4−), phosphate (PO43−), ammonia (NH4+), nitrate (NO32−), nitrite (NO2), depth, and dissolved oxygen (O2)). The results of our study reveal a seamount effect (sensu stricto) on the microbial mid-water pelagic community up to approximately 200 m above the seafloor. Further, we observed a strong spatial heterogeneity in the pelagic microbial landscape across the seamount, with planktonic microbial communities reflecting oscillatory and circulatory water movements, as well as processes of bentho-pelagic coupling. Depth, NO32−, SiO4−, and O2 concentrations differed significantly between the determined pelagic microbial clusters close to the seafloor (BW), suggesting that these parameters were presumably linked to changes in microbial community structures. Secondly, we assessed the associated microbial community compositions of three sponge species along a depth gradient of the seamount. While sponge-associated microbial communities were found to be mainly species-specific, we also detected significant intra-specific differences between individuals, depending on the pelagic near-bed cluster they originated from. The variable microbial phyla (i.e. phyla which showed significant differences across varying depth, NO32−, SiO4−, O2 concentrations and different from local seawater communities) were distinct for every sponge-species when considering average abundances per species. Variable microbial phyla included representatives of both, those taxa traditionally counted to the variable community fraction, as well as taxa counted traditionally to the core community fraction. Microbial co-occurrence patterns for the three examined sponge species Geodia hentscheli (demosponge, HMA), Lissodendoryx complicata (demosponge, most likely LMA), and Schaudinnia rosea (Hexactinellida, most likely LMA) were distinct from each other. Over all, this study shows that topographic structures such as the Schulz Bank seamount can have an imprint (seamount effect sensu lato) on both, the microbial community composition of seawater and of sessile benthic invertebrates such as sponges by an interplay between the geology, physical oceanography, biogeochemistry and microbiology of seamounts.

The presence-absence data for macrobenthic fauna that has been collected in Mingulay Reef Complex (Scotland, UK) across 79 stations over the years 2003, 2005, 2009, 2010 and 2011. The collection of the benthic samples has been carried out using a Van-Veen grab, mainly from hard habitats (e.g. live and dead coral framework). About 60% of the macrofaunal specimens have been identified at species level using high quality taxonomic keys and advice from taxonomy experts. Most common taxonomic groups analysed here are molluscs, polychaetes, arthropods, bryozoans, anthozoans, tunicates and brachiopods. The collection of the specimens is now deposited at the National Museums of Scotland (see the attached excel file for details). The enviromental data contains information about coordinates and environmental settings at stations where macrobenthic samples mentioned above, were collected. The environmental settings that are included in the file refer to the years 2003, 2005, 2009, 2010, 2011. For more information on the environmental variables have a look in Henry et al. 2010 (doi:10.1007/s00338-009-0577-6) and Henry et al. 2013 (doi:10.5194/bg-10-2737-2013). The environmental variables included in the excel file are: type of macrohabitat (i.e. muddy sand, rubble, rock, live coral, dead framework, live & dead framework), depth (m), slope, ruggedness, broad-scale bathymetric position index, fine-scale bathymetric position index, average current speed (m/s), maximum current speed (m/s), northness, eastness, winter North Atlantic Oscillation Index (same year), winter North Atlantic Oscillation Index (previous year), annual average bottom temperature (same year), annual average bottom salinity (same year). Extraction of bathymetric (depth) and topographic data [slope, aspect, northness, eastness, ruggedness, standardised broad-scale bathymetric position index (BPI; with an inner radius of 1 cell and an outer radius of 5 cells), fine-scale BPI (with an inner radius of 1 cell and an outer radius of 3 cells)] was based on multibeam echosounder data, using the Spatial Analyst and Benthic Terrain Modeler toolboxes in ArcGIS v.10.6.1 Average and maximum current speed values (m/s) were extracted by the ArcGIS v. 10.6.1 Spatial Analyst toolbox using data generated by a high-resolution 3D ocean model created for the MRC by Moreno-Navas et al. (2014). Data for the winter NAOI (DJFM) (Hurrell et al., 2003) were downloaded from the National Center for Atmospheric Research/University Corporation for Atmospheric Research website (climatedataguide.ucar.edu; data accessed on 28/02/2019).

Permafrost thaw and ice wedge degradation lead to drastic landscape changes in the permafrost region. With this data set we investigated the cliff retreat of the Sobo-Sise Cliff (SSC), a high ice-bearing yedoma cliff in the Lena River Delta. The 1,660 m long cliff SSC extends from 72°32'34 N / 128°15'59 E to 72°32'06 N / 128°18'21 E and is located on the Sardakhskaya channel, which is one of the main Lena river branches in the Lena River Delta. Erosion rates for the SSC were determined based on satellite images from different sensors (Corona, Hexagon, Landsat, Planet cube-sat) for the period 1965-2018. Cliff front lines were manually digitized and erosion rates were calculated with the Digital Shoreline Analysis System (DSAS) tool (Himmelstoos et al. 2018). The study Fuchs et al. (2020) (doi:10.3389/feart.2020.00336) shows that the up to 27.7 m high SSC erodes in average 15.7 m yr-1 (2015-2018). During the entire observed time period from 1965-2018, the SSC retreated in average 484 m (ranging from 322 - 680 m). This data set compilation consist of three GIS shapefiles with a corresponding metadata file and a table of the mean annual erosion rates of the yedoma SSC for the time periods 1965-1975, 1975-2000, 2000-2005, 2005-2010, 2010-2015, and 2015-2018, as well as the absolute cliff retreat rates over the entire period 1965-2018, which are derived from remote sensing imagery analyzed with the DSAS tool. In addition, the cliff front lines for each investigated time step are provided as well as the separation between yedoma and alas deposits for each time step. Related trend data for this region, based on Landsat trend analysis are available at: doi:10.1594/PANGAEA.884136 (Nitze, 2018).

International efforts are underway to establish well-connected systems of marine protected areas (MPAs) covering at least 10% of the ocean by 2020. But the nature and dynamics of ocean ecosystem connectivity are poorly understood, with unresolved effects of climate variability. We used 40-year runs of a particle tracking model to examine the sensitivity of an MPA network for habitat-forming cold-water corals in the northeast Atlantic to changes in larval dispersal driven by atmospheric cycles and larval behaviour. Trajectories of Lophelia pertusa larvae were strongly correlated to the North Atlantic Oscillation (NAO), the dominant pattern of interannual atmospheric circulation variability over the northeast Atlantic. Variability in trajectories significantly altered network connectivity and source-sink dynamics, with positive phase NAO conditions producing a well-connected but asymmetrical network connected from west to east. Negative phase NAO produced reduced connectivity, but notably some larvae tracked westward-flowing currents towards coral populations on the mid-Atlantic ridge. Graph theoretical metrics demonstrate critical roles played by seamounts and offshore banks in larval supply and maintaining connectivity across the network. Larval longevity and behaviour mediated dispersal and connectivity, with shorter lived and passive larvae associated with reduced connectivity. We conclude that the existing MPA network is vulnerable to atmospheric-driven changes in ocean circulation.

Comparison of the equatorial upwelling system, the northern coastal upwelling system of the Gulf of Guinea and the tropical Angolan upwelling system.