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2022 ◽  
Vol 248 ◽  
pp. 106192
Author(s):  
Rafael Schroeder ◽  
Paulo R. Schwingel ◽  
Edgar Pinto ◽  
Agostinho Almeida ◽  
Alberto T. Correia

2022 ◽  
Vol 248 ◽  
pp. 106224
Author(s):  
Guelson Batista Silva ◽  
Lisa Elma Ailloud ◽  
Justin Monin Amandé ◽  
Rafael Ferreira Muniz ◽  
Fabio Hissa Vieira Hazin ◽  
...  

2022 ◽  
Vol 248 ◽  
pp. 106211
Author(s):  
D. Gaertner ◽  
L. Guéry ◽  
N. Goñi ◽  
J. Amande ◽  
P. Pascual Alayon ◽  
...  

2022 ◽  
Author(s):  
Alexander L. Peace ◽  
Jordan J.J. Phethean

ABSTRACT It is well established that plate-tectonic processes operate on a global scale and that spatially separate but temporally coincident events may be linked. However, identifying such links in the geological record and understanding the mechanisms involved remain speculative. This is particularly acute during major geodynamic events, such as the dispersal of supercontinents, where multiple axes of breakup may be present as well as coincidental collisional events. To explore this aspect of plate tectonics, we present a detailed analysis of the temporal variation in the mean half rate of seafloor spreading in the Indian and Atlantic Oceans, as well as plate-kinematic attributes extracted from global plate-tectonic models during the dispersal of Gondwana since ca. 200 Ma. Our analysis shows that during the ~20 m.y. prior to collision between India and Asia at ca. 55 Ma, there was an increase in the mean rate of seafloor spreading in the Indian Ocean. This manifests as India rapidly accelerating toward Asia. This event was then followed by a prompt deceleration in the mean rate of Indian Ocean seafloor spreading after India collided with Asia at ca. 55 Ma. Since inception, the mean rate of seafloor spreading in the Indian Ocean has been generally greater than that in the Atlantic Ocean, and the period of fastest mean half spreading rate in the Indian Ocean was coincident with a slowdown in mean half seafloor spreading rate in the competing Atlantic Ocean. We hypothesize that faster and hotter seafloor spreading in the Indian Ocean resulted in larger ridge-push forces, which were transmitted through the African plate, leading to a slowdown in Atlantic Ocean spreading. Following collision between India and Asia, and a slowdown of Indian Ocean spreading, Atlantic spreading rates consequently increased again. We conclude that the processes in the Indian and Atlantic Oceans have likely remained coupled throughout their existence, that their individual evolution has influenced each other, and that, more generally, spreading in one basin inevitably influences proximal regions. While we do not believe that ridge push is the main cause of plate motions, we consider it to have played a role in the coupling of the kinematic evolution of these oceans. The implication of this observation is that interaction and competition between nascent ocean basins and ridges during supercontinent dispersal exert a significant control on resultant continental configuration.


Author(s):  
Gillian R. Foulger ◽  
Laurent Gernigon ◽  
Laurent Geoffroy

ABSTRACT We propose a new, sunken continent beneath the North Atlantic Ocean that we name Icelandia. It may comprise blocks of full-thickness continental lithosphere or extended, magma-inflated continental layers that form hybrid continental-oceanic lithosphere. It underlies the Greenland-Iceland-Faroe Ridge and the Jan Mayen microplate complex, covering an area of ~600,000 km2. It is contiguous with the Faroe Plateau and known parts of the submarine continental rifted margin offshore Britain. If these are included in a “Greater Icelandia,” the entire area is ~1,000,000 km2 in size. The existence of Icelandia needs to be tested. Candidate approaches include magnetotelluric surveying in Iceland; ultralong, full-crust-penetrating reflection profiling along the length of the Greenland-Iceland-Faroe Ridge; dating zircons collected in Iceland; deep drilling; and reappraisal of the geology of Iceland. Some of these methods could be applied to other candidate sunken continents that are common in the oceans.


2022 ◽  
Vol 48 (1) ◽  
pp. 3-8
Author(s):  
Keith D. Mullin ◽  
Lisa Steiner ◽  
Charlotte Dunn ◽  
Diane Claridge ◽  
Laura González García ◽  
...  

Zootaxa ◽  
2022 ◽  
Vol 5091 (2) ◽  
pp. 393-400
Author(s):  
CÉDRIC D’UDEKEM D’ACOZ ◽  
FLORENCE GULLY ◽  
MARC COCHU ◽  
ARTHUR ANKER

The rare symbiotic alpheid shrimp Salmoneus erasimorum Dworschak, Abed-Navandi & Anker, 2000 was previously known from a single specimen collected with a suction pump on the Croatian coast in the Adriatic Sea, together with its host, the ghost shrimp, Gilvossius tyrrhenus (Petagna, 1792). A second record of S. erasimorum is presented here, with a diagnosis and the first colour photographs, based on a single specimen collected in northern Brittany, France, also with a suction pump, but without its host. This is also the first record of the species on the European coast of the Atlantic Ocean. An annotated list and a key to the species of Salmoneus currently known from the eastern Atlantic and the Mediterranean Sea are provided.  


Eos ◽  
2022 ◽  
Vol 103 ◽  
Author(s):  
Jack Lee

Simulations reveal the influence of reduced and enhanced wind stress on the Atlantic Meridional Overturning Circulation.


2022 ◽  
Vol 8 ◽  
Author(s):  
Vanda Brotas ◽  
Glen A. Tarran ◽  
Vera Veloso ◽  
Robert J. W. Brewin ◽  
E. Malcolm S. Woodward ◽  
...  

Phytoplankton biomass, through its proxy, Chlorophyll a, has been assessed at synoptic temporal and spatial scales with satellite remote sensing (RS) for over two decades. Also, RS algorithms to monitor relative size classes abundance are widely used; however, differentiating functional types from RS, as well as the assessment of phytoplankton structure, in terms of carbon remains a challenge. Hence, the main motivation of this work it to discuss the links between size classes and phytoplankton groups, in order to foster the capability of assessing phytoplankton community structure and phytoplankton size fractionated carbon budgets. To accomplish our goal, we used data (on nutrients, photosynthetic pigments concentration and cell numbers per taxa) collected in surface samples along a transect on the Atlantic Ocean, during the 25th Atlantic Meridional Transect cruise (AMT25) between 50° N and 50° S, from nutrient-rich high latitudes to the oligotrophic gyres. We compared phytoplankton size classes from two methodological approaches: (i) using the concentration of diagnostic photosynthetic pigments, and assessing the abundance of the three size classes, micro-, nano-, and picoplankton, and (ii) identifying and enumerating phytoplankton taxa by microscopy or by flow cytometry, converting into carbon, and dividing the community into five size classes, according to their cell carbon content. The distribution of phytoplankton community in the different oceanographic regions is presented in terms of size classes, taxonomic groups and functional types, and discussed in relation to the environmental oceanographic conditions. The distribution of seven functional types along the transect showed the dominance of picoautotrophs in the Atlantic gyres and high biomass of diatoms and autotrophic dinoflagellates (ADinos) in higher northern and southern latitudes, where larger cells constituted the major component of the biomass. Total carbon ranged from 65 to 4 mg carbon m–3, at latitudes 45° S and 27° N, respectively. The pigment and cell carbon approaches gave good consistency for picoplankton and microplankton size classes, but nanoplankton size class was overestimated by the pigment-based approach. The limitation of enumerating methods to accurately resolve cells between 5 and 10 μm might be cause of this mismatch, and is highlighted as a knowledge gap. Finally, the three-component model of Brewin et al. was fitted to the Chlorophyll a (Chla) data and, for the first time, to the carbon data, to extract the biomass of three size classes of phytoplankton. The general pattern of the model fitted to the carbon data was in accordance with the fits to Chla data. The ratio of the parameter representing the asymptotic maximum biomass gave reasonable values for Carbon:Chla ratios, with an overall median of 112, but with higher values for picoplankton (170) than for combined pico-nanoplankton (36). The approach may be useful for inferring size-fractionated carbon from Earth Observation.


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