Description: Seamounts are amongst the most common physiographic structures of the deep-ocean landscape, but remoteness and geographic complexity have limited the systematic collection of integrated and multidisciplinary data in the past. Consequently, important aspects of seamount ecology and dynamics remain poorly studied. We present a data collection of ocean currents and raw acoustic backscatter from shipboard Acoustic Doppler Current Profiler (ADCP) measurements during six cruises between 2004 and 2015 in the tropical and subtropical Northeast Atlantic to narrow this gap. Measurements were conducted at seamount locations between the island of Madeira and the Portuguese mainland (Ampère, Seine Seamount), as well as east of the Cape Verde archipelago (Senghor Seamount). The dataset includes two-minute ensemble averaged continuous velocity and backscatter profiles, supplemented by spatially gridded maps for each velocity component, error velocity and local bathymetry.

Description: The deep sea is among the largest, most biologically diverse, yet least-explored ecosystems on Earth. Baseline information on deep-sea biodiversity is crucial for understanding ecosystem functioning and for detecting community changes. Here, we established a baseline of cephalopod community composition and distribution off Cabo Verde, an archipelago in the eastern tropical Atlantic. This baseline served to test the hypothesis that Cabo Verde is biogeographically separated from other Macaronesian archipelagos and allowed the identification of cephalopod species which may play a role in the Macaronesian carbon cycle and oceanic food web. To investigate cephalopod community composition, this study used 746 individual cephalopods obtained by nets (0–1000 m) and 52 cephalopod encounters during video surveys with either towed camera (0–2500 m) or manned submersible (0–375 m). Additionally, environmental DNA (eDNA) metabarcoding on 105 seawater samples (50–2500 m), using an 18S rRNA universal cephalopod primer pair, and a species-specific primer pair for Taningia danae resulted in the detection of 32 cephalopod taxa. When combined, the three methods detected a total of 87 taxa, including 47 distinct species. Each method contributed between 7 and 54% of taxa that were not detected by the other methods, indicating that multiple methodological approaches are needed for optimal deep-sea cephalopod biodiversity assessments. This study documents the occurrences of six species and three genera for the first time in waters surrounding Cabo Verde. Video surveys and eDNA analysis detected Taningia danae recurrently (100–2500 m). eDNA metabarcoding proved to be a powerful tool for cephalopod biodiversity monitoring and complementary to traditional sampling methods. When also including literature records, Cabo Verde hosts at least 102 cephalopod taxa including 30 families and 64 benthic and pelagic species. The total number and species composition of Cabo Verde cephalopods is similar to the Canary Islands and Azores, two known cephalopod biodiversity hotspots, but the Cabo Verde octopus fauna seems to differ. Due to a range of life history characteristics, we hypothesize that the squids Taningia danae (Octopoteuthidae) and Sthenoteuthis pteropus (Ommastrephidae) are important in the carbon cycle of Macaronesia. As a cephalopod biodiversity hotspot Cabo Verde could function as a model region to investigate cephalopod biology and ecology in a rapidly changing Atlantic Ocean.

Description: Gelatinous zooplankton can be present in high biomass and taxonomic diversity in planktonic oceanic food webs, yet the trophic structuring and importance of this “jelly web” remain incompletely understood. To address this knowledge gap, we provide a holistic trophic characterization of a jelly web in the eastern tropical Atlantic, based on δ13C and δ15N stable isotope analysis of a unique gelatinous zooplankton sample set. The jelly web covered most of the isotopic niche space of the entire planktonic oceanic food web, spanning 〉 3 trophic levels, ranging from herbivores (e.g., pyrosomes) to higher predators (e.g., ctenophores), highlighting the diverse functional roles and broad possible food web relevance of gelatinous zooplankton. Among gelatinous zooplankton taxa, comparisons of isotopic niches pointed to the presence of differentiation and resource partitioning, but also highlighted the potential for competition, e.g., between hydromedusae and siphonophores. Significant differences in spatial (seamount vs. open ocean) and depth‐resolved patterns (0–400 m vs. 400–1000 m) pointed to additional complexity, and raise questions about the extent of connectivity between locations and differential patterns in vertical coupling between gelatinous zooplankton groups. Added complexity also resulted from inconsistent patterns in trophic ontogenetic shifts among groups. We conclude that the broad trophic niche covered by the jelly web, patterns in niche differentiation within this web, and substantial complexity at the spatial, depth, and taxon level call for a more careful consideration of gelatinous zooplankton in oceanic food web models. In light of climate change and fishing pressure, the data presented here also provide a valuable baseline against which to measure future trophic observations of gelatinous zooplankton communities in the eastern tropical Atlantic.

Description: Data represent isotopic values of plankton community of the eastern tropical Atlantic. Main focus was given to the trophic position of gelatinous zooplankton within the oceanic food web. Sampling was conducted during November and December 2015 on board R/V “MARIA S. MERIAN” (cruise MSM49) at 8 stations in Cape Verdean waters in the ETA, including a shallow seamount (Senghor Seamount, 100-3300 m) and its northwestern and southeastern slopes, a cyclonic eddy, and four oceanic stations. Net sampling was conducted using two types of multiple opening/closing nets and environmental sampling systems (MOCNESS), one with 1 m2 ( three nets, mesh size: 2 mm; and six nets, mesh size: 335 µm) and one with 10 m2 opening (five nets, mesh size: 1.5 mm), towed at a speed of 2 kn. Sampling depth intervals were targeted at 0-50, 50-100, 100-200, 200-400, 400-600, and 600-1000 m. Samples from replicate tows at the same depth and station were pooled for analyses.

Description: Net catches of cephalopods were obtained during the cruises POS320/2 (March 2005), MSM49 (November/December 2015) and WH383 (March/April 2015) off Cabo Verde at a total of 18 stations at depths between 0 and 1000 m. Cephalopods were caught during POS320/2 with either a Isaacs-Kidd midwater trawl (IKMT) with a 6 m2 net opening, 4 mm mesh size equipped with a flowmeter, a Hydro-Bios Multinet Maxi with a 0.5 m2 net opening and 500 µm mesh size between the surface and 250 m water depth, or an 80 feet bottom trawl. Net sampling during MSM49 was conducted with two types of multiple opening/closing nets (MOCNESS) and an IKMT. The smaller MOCNESS had a net opening of 1 m2 opening (three nets with a mesh size of 2 mm and six nets with a mesh size of 335 μm) and the larger MOCNESS a net opening of 10 m2 opening (five nets, mesh size: 1.5 mm) and were deployed between the surface to 1000 m. The IKMT had a net opening of 7 m2 and ended in a cod end of 500 µm mesh size. It was deployed to a maximum depth of 500 m. During WH383 a pelagic trawl ('Aalnetz', Engel Netze, Bremerhaven, Germany) with a mouth opening of 16 x 30 m, length of 150 m including multiple opening-closing device, 260 meshes by 180 cm stretched mesh size at the front, a cod end 20 mm stretched mesh-opening and a 1.8 mm inlet sewn into last 1 m of cod end was used with a multisampler (Construction Services AS, Bergen, Norway) allowing depth-stratified sampling. During WH383 three strata (mean vertical extension of ca. 40 m) were trawled mostly during night and one time during daytime at depths between 30 and 700 m in horizontal tows for 30 minutes per stratum with a mean speed of three knots (2.8-3.3 kn). During this cruise, night trawls took place at 22:00 local time, and the day-time trawl at 12:00 local time. Onboard, cephalopods were identified morphologically to the lowest taxonomic level possible (species, genus or family), and whole specimens were preserved in formalin as voucher. In addition, tissue samples of some specimen were collected and preserved in ethanol for barcoding and the genetic reference database used for eDNA metabarcoding. Pelagic video transects with the Pelagic In-Situ Observation System (PELAGIOS, (Hoving et al., 2019a)) were conducted during the cruises MSM49 (Christiansen et al., 2016) (transects between 30 and 1000 m, total towing duration 〉 80h), MSM61 (Fiedler et al., 2020) (transects between 80 and 1200 m, total hours of observations 〉 32h), POS520 (Hoving et al., 2018, p. 520) (transects between 30 and 2500 m, total hours of observations 27h), POS532 (Hoving et al., 2019b) (transects between 30 and 990 m, total hours of observations 19h) and M119 (Brandt, 2016) (transects between 50 and 700 m, total hours of observations 〉 20h) between 2015 and 2019 (Figure 1). PELAGIOS is a battery powered, high-definition camera system that is towed horizontally via a single-wired conductive sea-cable at 0.5 m s -1. Around 0.45 m2 of the water column in front of the camera is illuminated with an LED array. The attached depth sensor and/or a sensor for conductivity, temperature and depth (CTD) with oxygen sensor allows for hydrographic measurements and depth monitoring during transects. Pelagic video transects were conducted between 11-33 minutes per depth, towing the camera horizontally at specified depths. A deep-sea telemetry system allows for transmission of a low-resolution preview of the recorded video. During the cruises POS520 and POS532 the manned submersible JAGO (GEOMAR, Helmholtz Centre for Ocean Research) was used for 30 deployments of about four hours each between the surface and 350 m water depth. During the dives, video was recorded by a high-resolution camera. The videos taken during the PELAGIOS and JAGO dives were annotated manually using the Video Annotation and Reference System (VARS) developed at the Monterey Bay Aquarium Research Institute, which allows annotation and congruent collection of video frames. We also provide raw data on environmental DNA samples taken during POS532 in February 2019 at five stations. The stations off the islands Santo Antão and Fogo were close to the coast (maximum sampled depth 2500 m), CVOO was a reference station in the open ocean (maximum sampled depth 3000 m) and the stations Cyclone and Anticyclone were located eddies that had formed in the wake of Fogo and had propagated southwards (maximum sampled depths 2200 and 600 m, respectively). Per sampled depth, three biological replicates of two liters of seawater each were collected from three different 10 liter Niskin bottles mounted on a CTD rosette. For filtration, 0.22 µm pore size Sterivex-GP filter (Merck Millipore) were directly connected to the Niskin bottle with sterile tubing. The weight of the water in the Niskin bottles was sufficient to filter two liters of seawater per filter. The filters were closed with sterile plastic caps and stored at -80°C until further processing in the laboratory.

Description: Onboard, cephalopods were identified morphologically to the lowest taxonomic level possible (species, genus or family), and whole specimens were preserved in formalin as voucher. In addition, tissue samples of some specimen were collected and preserved in ethanol for barcoding and the genetic reference database used for eDNA metabarcoding.

Description: Pelagic video transects with the Pelagic In-Situ Observation System (PELAGIOS, (Hoving et al., 2019a)) were conducted during the cruises MSM49 (Christiansen et al., 2016) (transects between 30 and 1000 m, total towing duration 〉 80h), MSM61 (Fiedler et al., 2020) (transects between 80 and 1200 m, total hours of observations 〉 32h), POS520 (Hoving et al., 2018, p. 520) (transects between 30 and 2500 m, total hours of observations 27h), POS532 (Hoving et al., 2019b) (transects between 30 and 990 m, total hours of observations 19h) and M119 (Brandt, 2016) (transects between 50 and 700 m, total hours of observations 〉 20h) between 2015 and 2019 (Figure 1). PELAGIOS is a battery powered, high-definition camera system that is towed horizontally via a single-wired conductive sea-cable at 0.5 m s -1. Around 0.45 m2 of the water column in front of the camera is illuminated with an LED array. The attached depth sensor and/or a sensor for conductivity, temperature and depth (CTD) with oxygen sensor allows for hydrographic measurements and depth monitoring during transects. Pelagic video transects were conducted between 11-33 minutes per depth, towing the camera horizontally at specified depths. A deep-sea telemetry system allows for transmission of a low-resolution preview of the recorded video. During the cruises POS520 and POS532 the manned submersible JAGO (GEOMAR, Helmholtz Centre for Ocean Research) was used for 30 deployments of about four hours each between the surface and 350 m water depth. During the dives, video was recorded by a high-resolution camera. The videos taken during the PELAGIOS and JAGO dives were annotated manually using the Video Annotation and Reference System (VARS) developed at the Monterey Bay Aquarium Research Institute, which allows annotation and congruent collection of video frames. We also provide raw data on environmental DNA samples taken during POS532 in February 2019 at five stations. The stations off the islands Santo Antão and Fogo were close to the coast (maximum sampled depth 2500 m), CVOO was a reference station in the open ocean (maximum sampled depth 3000 m) and the stations Cyclone and Anticyclone were located eddies that had formed in the wake of Fogo and had propagated southwards (maximum sampled depths 2200 and 600 m, respectively). Per sampled depth, three biological replicates of two liters of seawater each were collected from three different 10 liter Niskin bottles mounted on a CTD rosette. For filtration, 0.22 µm pore size Sterivex-GP filter (Merck Millipore) were directly connected to the Niskin bottle with sterile tubing. The weight of the water in the Niskin bottles was sufficient to filter two liters of seawater per filter. The filters were closed with sterile plastic caps and stored at -80°C until further processing in the laboratory.

Description: Net catches of cephalopods were obtained during the cruises POS320/2 (March 2005), MSM49 (November/December 2015) and WH383 (March/April 2015) off Cabo Verde at a total of 18 stations at depths between 0 and 1000 m. Cephalopods were caught during POS320/2 with either a Isaacs-Kidd midwater trawl (IKMT) with a 6 m2 net opening, 4 mm mesh size equipped with a flowmeter, a Hydro-Bios Multinet Maxi with a 0.5 m2 net opening and 500 µm mesh size between the surface and 250 m water depth, or an 80 feet bottom trawl. Net sampling during MSM49 was conducted with two types of multiple opening/closing nets (MOCNESS) and an IKMT. The smaller MOCNESS had a net opening of 1 m2 opening (three nets with a mesh size of 2 mm and six nets with a mesh size of 335 μm) and the larger MOCNESS a net opening of 10 m2 opening (five nets, mesh size: 1.5 mm) and were deployed between the surface to 1000 m. The IKMT had a net opening of 7 m2 and ended in a cod end of 500 µm mesh size. It was deployed to a maximum depth of 500 m. During WH383 a pelagic trawl ('Aalnetz', Engel Netze, Bremerhaven, Germany) with a mouth opening of 16 x 30 m, length of 150 m including multiple opening-closing device, 260 meshes by 180 cm stretched mesh size at the front, a cod end 20 mm stretched mesh-opening and a 1.8 mm inlet sewn into last 1 m of cod end was used with a multisampler (Construction Services AS, Bergen, Norway) allowing depth-stratified sampling. During WH383 three strata (mean vertical extension of ca. 40 m) were trawled mostly during night and one time during daytime at depths between 30 and 700 m in horizontal tows for 30 minutes per stratum with a mean speed of three knots (2.8-3.3 kn). During this cruise, night trawls took place at 22:00 local time, and the day-time trawl at 12:00 local time. Onboard, cephalopods were identified morphologically to the lowest taxonomic level possible (species, genus or family), and whole specimens were preserved in formalin as voucher.

Description: Gelatinous zooplankton can be present in high biomass and taxonomic diversity in planktonic oceanic food webs, yet the trophic structuring and importance of this “jelly web” remain incompletely understood. To address this knowledge gap, we provide a holistic trophic characterization of a jelly web in the eastern tropical Atlantic, based on δ13C and δ15N stable isotope analysis of a unique gelatinous zooplankton sample set. The jelly web covered most of the isotopic niche space of the entire planktonic oceanic food web, spanning 〉 3 trophic levels, ranging from herbivores (e.g., pyrosomes) to higher predators (e.g., ctenophores), highlighting the diverse functional roles and broad possible food web relevance of gelatinous zooplankton. Among gelatinous zooplankton taxa, comparisons of isotopic niches pointed to the presence of differentiation and resource partitioning, but also highlighted the potential for competition, e.g., between hydromedusae and siphonophores. Significant differences in spatial (seamount vs. open ocean) and depth-resolved patterns (0–400 m vs. 400–1000 m) pointed to additional complexity, and raise questions about the extent of connectivity between locations and differential patterns in vertical coupling between gelatinous zooplankton groups. Added complexity also resulted from inconsistent patterns in trophic ontogenetic shifts among groups. We conclude that the broad trophic niche covered by the jelly web, patterns in niche differentiation within this web, and substantial complexity at the spatial, depth, and taxon level call for a more careful consideration of gelatinous zooplankton in oceanic food web models. In light of climate change and fishing pressure, the data presented here also provide a valuable baseline against which to measure future trophic observations of gelatinous zooplankton communities in the eastern tropical Atlantic.