A high-resolution three-dimensional numerical study of intermediate water formation in the Levantine Sea

1998 ◽  
Vol 103 (C9) ◽  
pp. 18497-18511 ◽  
Author(s):  
A. Lascaratos ◽  
K. Nittis
Water ◽  
2019 ◽  
Vol 11 (9) ◽  
pp. 1781 ◽  
Author(s):  
Elisabeth Kubin ◽  
Pierre-Marie Poulain ◽  
Elena Mauri ◽  
Milena Menna ◽  
Giulio Notarstefano

Levantine intermediate water (LIW) is formed in the Levantine Sea (Eastern Mediterranean) and spreads throughout the Mediterranean at intermediate depths, following the general circulation. The LIW, characterized by high salinity and relatively high temperatures, is one of the main contributors of the Mediterranean Overturning Circulation and influences the mechanisms of deep water formation in the Western and Eastern Mediterranean sub-basins. In this study, the LIW and Levantine deep water (LDW) formation processes are investigated using Argo float data from 2001 to 2017 in the Northwestern Levantine Sea (NWLS), the larger area around Rhodes Gyre (RG). To find pronounced events of LIW and LDW formation, more than 800 Argo profiles were analyzed visually. Events of LIW and LDW formation captured by the Argo float data are compared to buoyancy, heat and freshwater fluxes, sea surface height (SSH), and sea surface temperature (SST). All pronounced events (with a mixed layer depth (MLD) deeper than 250 m) of dense water formation were characterized by low surface temperatures and strongly negative SSH. The formation of intermediate water with typical LIW characteristics (potential temperature > 15 °C, salinity > 39 psu) occurred mainly along the Northern coastline, while LDW formation (13.7 °C < potential temperature < 14.5 °C, 38.8 psu < salinity < 38.9 psu) occurred during strong convection events within temporary and strongly depressed mesoscale eddies in the center of RG. This study reveals and confirms the important contribution of boundary currents in ventilating the interior ocean and therefore underlines the need to rethink the drivers and contributors of the thermohaline circulation of the Mediterranean Sea.


Author(s):  
H.A. Cohen ◽  
T.W. Jeng ◽  
W. Chiu

This tutorial will discuss the methodology of low dose electron diffraction and imaging of crystalline biological objects, the problems of data interpretation for two-dimensional projected density maps of glucose embedded protein crystals, the factors to be considered in combining tilt data from three-dimensional crystals, and finally, the prospects of achieving a high resolution three-dimensional density map of a biological crystal. This methodology will be illustrated using two proteins under investigation in our laboratory, the T4 DNA helix destabilizing protein gp32*I and the crotoxin complex crystal.


Author(s):  
Kenneth H. Downing ◽  
Hu Meisheng ◽  
Hans-Rudolf Went ◽  
Michael A. O'Keefe

With current advances in electron microscope design, high resolution electron microscopy has become routine, and point resolutions of better than 2Å have been obtained in images of many inorganic crystals. Although this resolution is sufficient to resolve interatomic spacings, interpretation generally requires comparison of experimental images with calculations. Since the images are two-dimensional representations of projections of the full three-dimensional structure, information is invariably lost in the overlapping images of atoms at various heights. The technique of electron crystallography, in which information from several views of a crystal is combined, has been developed to obtain three-dimensional information on proteins. The resolution in images of proteins is severely limited by effects of radiation damage. In principle, atomic-resolution, 3D reconstructions should be obtainable from specimens that are resistant to damage. The most serious problem would appear to be in obtaining high-resolution images from areas that are thin enough that dynamical scattering effects can be ignored.


Author(s):  
Hirano T. ◽  
M. Yamaguchi ◽  
M. Hayashi ◽  
Y. Sekiguchi ◽  
A. Tanaka

A plasma polymerization film replica method is a new high resolution replica technique devised by Tanaka et al. in 1978. It has been developed for investigation of the three dimensional ultrastructure in biological or nonbiological specimens with the transmission electron microscope. This method is based on direct observation of the single-stage replica film, which was obtained by directly coating on the specimen surface. A plasma polymerization film was deposited by gaseous hydrocarbon monomer in a glow discharge.The present study further developed the freeze fracture method by means of a plasma polymerization film produces a three dimensional replica of chemically untreated cells and provides a clear evidence of fine structure of the yeast plasma membrane, especially the dynamic aspect of the structure of invagination (Figure 1).


Author(s):  
C. Abegg ◽  
Graham de Vahl Davis ◽  
W.J. Hiller ◽  
St. Koch ◽  
Tomasz A. Kowalewski ◽  
...  

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