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Data refer to export fluxes of carbonate produced by calcifying phytoplankton (coccolithophores), and coccolith-CaCO₃ percent contribution to total carbonate flux across the tropical North Atlantic, from upwelling affected NW Africa, via three ocean sites along 12°N to the Caribbean. Sampling was undertaken by means of a spatial array of four time-series sediment traps (i.e., CB at 21°N 20°W; M1U at 12°N 23°W; M2U at 14°N 37°W; M4U at 12°N 49°W; Guerreiro et al., 2021) collecting particle fluxes in two-week intervals, from October 2012 to February 2014, allowing to track temporal changes along the southern margin of the North Atlantic central gyre. Auxiliary PIC (Particulate Inorganic Carbon) data from NASA's Ocean Biology Processing Group (https://oceancolor.gsfc.nasa.gov) are also provided for the sediment sampling period at all four trap sites. Particle flux data (mg/m²/d) of CaCO₃, organic matter, particulate organic carbon (POC), biogenic silica (bSiO₂) and unspecified residual fraction are provided for sediment trap site CB.

We report the results of an aquaria-based experiment testing the effects of suspended particles generated during potential mining activities, on a common habitat-building coral species in the Azores, Dentomuricea aff. meteor. Corals were collected from the summit of Condor Seamount (Azores, NE Atlantic) at depths between 185-210 m in August 2014. Coral fragments were maintained in 10-L aquaria and exposed to three experimental treatments for a period of four weeks at the DeepSeaLab aquaria facilities (Okeanos-University of the Azores): (1) control conditions (no added sediments); (2) suspended polymetallic sulphide (PMS) particles; (3) suspended quartz particles. PMS particles were obtained by grinding PMS inactive chimney rocks collected at the hydrothermal vent field Lucky Strike. Both particle types were delivered at a concentration of 25 mg L-1. The putative effects of PMS particles were evaluated through measurements of the coral physiological responses at the levels of the organism (oxygen consumption, ammonium excretion), tissue (bioaccumulation of metals) and cell (enzyme activity and gene expression).

Since 2001, current velocities have been measured continuously as part of a multilateral collaboration, the Prediction and Research Moored Array in the Tropical Atlantic (PIRATA), that regularly services a moored observatory located at 0°N, 23°W. Here, we present 20 years of full-depth current velocity observations at 0°N, 23°W. With the presented current velocity data product, we aim to provide an important and accessible reference data set against which models and reanalysis output could be validated. The velocity time series will also be helpful for studies focusing on long-term climate variability to search for connections with changes in the equatorial circulation over the last 20 years. Earlier versions of this data product have already been used in a variety of studies and provided a significant contribution to an overall improved understanding of equatorial ocean dynamics. The moored observatory at 0°N, 23°W is an ongoing example of a successful multinational collaboration extending over more than two decades.

TALDICE (TALos Dome Ice CorE) is a 1620 m deep ice core drilled at Talos Dome, an ice dome located at the edge of the East Antarctic Plateau in the Ross Sea Sector. Here are presented new measurements on TALDICE ice core used to define the TALDICE-deep1 chronology between 1438 m and 1548 m depth. The new age scale extends the climate record for the Ross Sea Sector of the East Antarctic Ice Sheet back to MIS 10.1. Here we present new measurements on the deeper part of the TALDICE ice core.

Data refer to export fluxes of calcifying phytoplankton (coccolithophores) across the tropical North Atlantic, from upwelling affected NW Africa, via three ocean sites along 12°N to the Caribbean. Sampling was undertaken by means of a spatial array of four time-series sediment traps (i.e., CB at 21°N 20°W; M1U at 12°N 23°W; M2U at 14°N 37°W; M4U at 12°N 49°W; Guerreiro et al., 2017) collecting particle fluxes in two-week intervals, from October 2012 to February 2014, allowing to track temporal changes along the southern margin of the North Atlantic central gyre. Auxiliary environmental data regarding the mixed layer depth (MLD) are provided for the sampling period at all four trap sites, while Sea Surface Temperature (SST), wind velocity, daily precipitation and sea surface Chl-a concentrations are only provided for sites M1 and CB. All data in supplement to Guerreiro et al. (2019), with links to Guerreiro et al. (2017) and Korte et al. (2017, 2020) (see https://doi.pangaea.de/10.1594/PANGAEA.881457).

The data submitted is used in a comparative analysis of the diet of one of the globally most numerous myctophids, the Glacier lantern fish Benthosema glaciale, across four deep basins of the North-Atlantic. B. glaciale is a small fish species that contribute to carbon flux to the deep basins of the open ocean, and is thus considered an important element of the biological carbon pump (BCP). Data submitted is length and weight of fish analyzed for stomach content. In addition there are available taxonomic information, weight and number of prey items of each fish that has stomach content, as long as it has been possible to assign prey to a species or other taxonomic category. Unidentified prey usually had a high degree of digestion and individual items could not be counted, but could be weighed. Sampling were undertaken onboard the RV G.O. Sars during a six week long transatlantic scientific survey from Bergen (Norway) to Nuuk (Greenland) and back to Bergen in May and June 2013. Samples of B. glaciale for stomach content analysis were collected from three Harstad trawl hauls and 16 Macroplankton trawl hauls. The Harstad trawl is a graded (variable mesh size), small mid-water trawl with 20 m vertical opening and 15 m wing spread (Godø et al., 1993). The Macroplankton trawl on the other hand is a light pelagic trawl that has a nominal 6x6 m trawl opening and mesh size of 3 mm square light opening (8 mm stretched, knot to knot) from the trawl mouth along the entire trawl length to the cod-end (Hassel et al., 2017; Klevjer et al., 2020).

A global compilation of in situ data is vital to evaluate the quality of ocean-colour satellite data records. Here, we describe data compiled for the validation of ocean-colour products from the ESA Ocean Colour Climate Change Initiative (OC-CCI). The data were acquired from several sources (including, inter alia, MOBY, BOUSSOLE, AERONET-OC, SeaBASS, NOMAD, MERMAID, AMT, ICES, HOT, GeP&CO) and span the period from 1997 to 2021. Observations of the following variables were compiled: spectral remote-sensing reflectance, concentration of chlorophyll-a, spectral inherent optical properties, spectral diffuse attenuation coefficient and total suspended matter. The data were obtained from multi-project archives acquired via open internet services, or from individual projects, acquired directly from data providers. Methodologies were implemented for homogenisation, quality control and merging of all data. No changes were made to the original data, other than averaging of observations that were close in time and space, elimination of some points after quality control and conversion to a standard format. The result is a merged table available in text format. Metadata of each in situ measurement (original source, cruise or experiment, principal investigator) were propagated throughout the work and made available in the final table. By making the metadata available, provenance is better documented, and it is also possible to analyse each set of data separately. This paper also describes the changes that were made to the compilation in relation to the previous version.

Coccolithophores are globally important marine calcifying phytoplankton that utilize a haplo-diplontic life cycle. The haplo-diplontic life cycle allows coccolithophores to divide in both life cycle phases and potentially expands coccolithophore niche volume. Research has, however, to date largely overlooked the life cycle of coccolithophores and has instead focused on the diploid life cycle phase of coccolithophores. Through the synthesis and analysis of global scanning electron microscopy (SEM) coccolithophore abundance data (n=2534), we find that calcified haploid coccolithophores generally constitute a minor component of the total coccolithophore abundance (≈ 2 %–15 % depending on season). However, using case studies in the Atlantic Ocean and Mediterranean Sea, we show that, depending on environmental conditions, calcifying haploid coccolithophores can be significant contributors to the coccolithophore standing stock (up to ≈30 %). Furthermore, using hypervolumes to quantify the niche of coccolithophores, we illustrate that the haploid and diploid life cycle phases inhabit contrasting niches and that on average this allows coccolithophores to expand their niche by ≈18.8 %, with a range of 3 %–76 % for individual species. Our results highlight that future coccolithophore research should consider both life cycle stages, as omission of the haploid life cycle phase in current research limits our understanding of coccolithophore ecology. Our results furthermore suggest a different response to nutrient limitation and stratification, which may be of relevance for further climate scenarios. Our compilation highlights the spatial and temporal sparsity of SEM measurements and the need for new molecular techniques to identify uncalcified haploid coccolithophores. Our work also emphasizes the need for further work on the carbonate chemistry niche of the coccolithophore life cycle.

In July 2017, we collected apparent resistivity data (ohm-m) in a sub-aquatic permafrost environment on the southern coastline of the Bykovsky Peninsula in northeast Siberia. The project goal was to determine the depth to the top of frozen sediment for multiple submerged landscapes. The submerged landscapes included ice-rich Yedoma permafrost, permafrost that had undergone prior thermokarst (Alases), and a former lagoon (i.e. offshore at the lagoon's coastline positions in earlier years). The data was collected with an IRIS Syscal Pro Deep Marine resistivity system that was equipped with a GPS and an echo-sounder to record water depths. The geoelectric cable had an electrode separation of 10 m and the electrodes were arranged in a reciprocal Wenner Schlumberger array. The offset between the first electrode and the boat was approximately 10 m.

CTDO measurements were acquired on the major research cruises performed as part of the SFB 754 or other projects . Seabird 911plus systems equipped with dual temperature-conductivity-oxygen sensors were employed. All systems had a 24-bottle water sampling rosette with 10 l Niskin bottles. On some cruises only 22 bottles were mounted to accommodate a lowered Acoustic Doppler Current Profiler for deep ocean current observations. Water sampling, processing, and calibration followed GO-SHIP recommendations (Swift, 2010; McTaggart et al., 2010; Uchida et al., 2010) and included the recommended steps Data Conversion, Sensor Time-Alignment, Creation of Bottle Files, Outlier Removal, Pressure Sensor Filtering, Conductivity Cell Thermal Mass Correction, Ship Roll Correction and Deck Offset Correction by Loop Editing, as well as Derivation of Calculated Properties. After these steps, conductivity and oxygen readings were calibrated against values determined with salinometry and Winkler titration , respectively. Finally, the downcast data was averaged over 1 dbar wide intervals. An independent upcast calibration was used to obtain calibrated CTDO values coincident with the discrete water samples.