deep scattering layer
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2021 ◽  
Vol 8 (12) ◽  
Author(s):  
Fleur Visser ◽  
Onno A. Keller ◽  
Machiel G. Oudejans ◽  
Douglas P. Nowacek ◽  
Annebelle C. M. Kok ◽  
...  

Foraging decisions of deep-diving cetaceans can provide fundamental insight into food web dynamics of the deep pelagic ocean. Cetacean optimal foraging entails a tight balance between oxygen-conserving dive strategies and access to deep-dwelling prey of sufficient energetic reward. Risso's dolphins ( Grampus griseus ) displayed a thus far unknown dive strategy, which we termed the spin dive. Dives started with intense stroking and right-sided lateral rotation. This remarkable behaviour resulted in a rapid descent. By tracking the fine-scale foraging behaviour of seven tagged individuals, matched with prey layer recordings, we tested the hypothesis that spin dives are foraging dives targeting deep-dwelling prey. Hunting depth traced the diel movement of the deep scattering layer, a dense aggregation of prey, that resides deep during the day and near-surface at night. Individuals shifted their foraging strategy from deep spin dives to shallow non-spin dives around dusk. Spin dives were significantly faster, steeper and deeper than non-spin dives, effectively minimizing transit time to bountiful mesopelagic prey, and were focused on periods when the migratory prey might be easier to catch. Hence, whereas Risso's dolphins were mostly shallow, nocturnal foragers, their spin dives enabled extended and rewarding diurnal foraging on deep-dwelling prey.


2021 ◽  
pp. 102669
Author(s):  
Marian Peña ◽  
Itziar Munuera–Fernández ◽  
Enrique Nogueira ◽  
Rafael González-Quirós

2021 ◽  
Vol 194 ◽  
pp. 102560
Author(s):  
Pauline Snoeijs-Leijonmalm ◽  
Harald Gjøsæter ◽  
Randi B. Ingvaldsen ◽  
Tor Knutsen ◽  
Rolf Korneliussen ◽  
...  

2020 ◽  
Vol 96 (2) ◽  
pp. 235-262
Author(s):  
Morag Taite ◽  
Michael Vecchione ◽  
Sheena Fennell ◽  
Louise A Allcock

Many descriptions of paralarval and juvenile cephalopods are poor. By using DNA barcoding, a global bioidentification system for animals, along with morphological investigation, we can confirm species identifications. We have a better chance of eliminating misidentifications and, therefore, documenting the correct abundance and distribution of cephalopods within an area by combining morphological and molecular evidence. The central objectives of this study are to: (1) compare morphological vs molecular identification of cephalopods and (2) determine the occurrence of cephalopods within the deep scattering layer (DSL) within warm core eddies. The specimens reported here were collected between 2014 and 2016 during three transatlantic cruises from Galway, Ireland to St John's, Newfoundland, with a focus on assemblages in warm-core mesoscale eddies on the western part of the transect. Samples were collected from the DSL at multiple stations across mesoscale eddies. In total, 301 cephalopods belonging to 29 species were collected. Not only does our study increase the knowledge of abundance and diversity of pelagic cephalopods in this area, but it also provides sequences for species for which no comparative sequences were previously available. By examining the match/mismatch between morphological and molecular identifications, we highlight a need for revisions in some taxonomic groupings such as the family Cranchiidae.


2019 ◽  
Vol 14 (2) ◽  
pp. 437-449 ◽  
Author(s):  
Caterina R. Giner ◽  
Massimo C. Pernice ◽  
Vanessa Balagué ◽  
Carlos M. Duarte ◽  
Josep M. Gasol ◽  
...  

Abstract Microbial eukaryotes are key components of the ocean plankton. Yet, our understanding of their community composition and activity in different water layers of the ocean is limited, particularly for picoeukaryotes (0.2–3 µm cell size). Here, we examined the picoeukaryotic communities inhabiting different vertical zones of the tropical and subtropical global ocean: surface, deep chlorophyll maximum, mesopelagic (including the deep scattering layer and oxygen minimum zones), and bathypelagic. Communities were analysed by high-tthroughput sequencing of the 18S rRNA gene (V4 region) as represented by DNA (community structure) and RNA (metabolism), followed by delineation of Operational Taxonomic Units (OTUs) at 99% similarity. We found a stratification of the picoeukaryotic communities along the water column, with assemblages corresponding to the sunlit and dark ocean. Specific taxonomic groups either increased (e.g., Chrysophyceae or Bicosoecida) or decreased (e.g., Dinoflagellata or MAST-3) in abundance with depth. We used the rRNA:rDNA ratio of each OTU as a proxy of metabolic activity. The highest relative activity was found in the mesopelagic layer for most taxonomic groups, and the lowest in the bathypelagic. Altogether, we characterize the change in community structure and metabolic activity of picoeukaryotes with depth in the global ocean, suggesting a hotspot of activity in the mesopelagic.


2016 ◽  
Vol 73 (8) ◽  
pp. 2037-2048 ◽  
Author(s):  
Rudy J. Kloser ◽  
Tim E. Ryan ◽  
Gordon Keith ◽  
Lisa Gershwin

Abstract Estimating the biomass of gas-bladdered organisms in the mesopelagic ocean is a simple first step to understanding ecosystem structure. An existing two-frequency (38 and 120 kHz) acoustic and optical probe was lowered to 950 m to estimate the number and size of gas-bladders. In situ target strengths from 38 and 120 kHz and their difference were compared with those of a gas-bladder resonance-scattering model. Predicted mean equivalent spherical radius gas-bladder size varied with depth, ranging from 2.1 mm (shallow) to 0.6 mm (deep). Density of night-time organisms varied throughout the water column and were highest (0.019 m−3) in the 200–300 m depth range. Predictions of 38 kHz volume-backscattering strength (Sv) from the density of gas-bladdered organisms could explain 88% of the vessel's 38 kHz Sv at this location (S 40.9, E 166.7). Catch retained by trawls highlighted the presence of gas-bladdered fish of a similar size range but different densities while optical measurements highlighted the depth distribution and biomass of gas-inclusion siphonophores. Organism behaviour and gear selectivity limits the validation of acoustic estimates. Simultaneous optical verification of multifrequency or broadband acoustic targets at depth are required to verify the species, their size and biomass.


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