Seawater salinity is higher in the Mediterranean and Red Sea than in Indonesia and Malaysia due to evaporation rates.
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Retrieved oceanographic references confirm general facts about the Mediterranean Sea, evaporation skin effects, and ocean salinity measurement, but lack sufficient data regarding the Red Sea, Indonesia, and Malaysia to fully support the claim.
Abstract
The existence of a cool and salty sea surface skin under evaporation was first proposed by Saunders in 1967, but few efforts have since been made to perceive the salt component of the skin layer. With two salinity missions scheduled to launch in the coming years, this study attempted to revisit the Saunders concept and to utilize presently available air–sea forcing datasets to analyze, understand, and interpret the effect of the salty skin and its implication for remote sensing of ocean salinity.
Similar to surface cooling, the skin salinification would occur primarily at low and midlatitudes in regions that are characterized by low winds or high evaporation. On average, the skin is saltier than the interior water by 0.05–0.15 psu and cooler by 0.2°–0.5°C. The cooler and saltier skin at the top is always statically unstable, and the tendency to overturn is controlled by cooling. Once the skin layer overturns, the time to reestablish the full increase of skin salinity was reported to be on the order of 15 min, which is approximately 90 times slower than that for skin temperature. Because the radiation received from a footprint is averaged over an area to give a single pixel value, the slow recovery by the salt diffusion process might cause a slight reduction in area-averaged skin salinity and thus obscure the salty skin effect on radiometer retrievals. In the presence of many geophysical error sources in remote sensing of ocean salinity, the salt enrichment at the surface skin does not appear to be a concern.
Abstract The Mediterranean-Black Sea system consists of two semi-enclosed basins connected by the Turkish Straits. In turn, the Mediterranean Sea is connected to the Atlantic Ocean through the narrow Strait of Gibraltar. The hydrological cycle of the system is driven by fresh water exchanges between the atmosphere, continents and oceans, and by salty water mass exchange among the ocean basins. Monitoring such water fluxes, especially its time evolution, is essential to understand the water cycle in the region, which is very sensitive to global climate changes and influences the variability of the Atlantic Meridional Overturning Circulation (AMOC), which in turn affects the global climate. In this study, we have estimated the hydrological cycle of the Mediterranean-Black Sea system from the time-variable gravity observations performed by the Gravity Recovery and Climate Experiment (GRACE) and GRACE Follow-On satellites, and precipitation and evaporation from ERA5 atmospheric reanalysis data for the period 2002–2020. In the Black Sea, rivers introduce an average water volume of 391 ± 12 km 3 /year, one third of which escape through the atmosphere and two thirds go to the Mediterranean Sea. In the latter, 1787 ± 23 km 3 /year are lost via net evaporation. The rivers runoff (502 ± 27 km 3 /year), and the inflow of Atlantic waters (1020 ± 56 km 3 /year; 0.0323 ± 0.0018 Sv), finally restore the Mediterranean water budget. The balance is not reached instantaneously, and this delay introduces a seasonal variability in all the fluxes. In particular, the net water flux from the Atlantic Ocean increases up to 2660 ± 111 km 3 /year in August/September, and reverses to − 407 ± 140 km 3 /year in April/May. On top of the climatology, the mean annual Atlantic water flux varies significantly between 706 and 1262 km 3 /year.
The seasonal variability of the carbonate system in the eastern Mediterranean Sea (EMed) was investigated based on discrete total alkalinity (A T ), total dissolved inorganic carbon (C T ), and pH measurements collected during three cruises around Crete between June 2018 and March 2019. This study presents a detailed description of this new carbonate chemistry dataset in the eastern Mediterranean Sea. We show that the North Western Levantine Basin (NWLB) is unique in terms of range of A T variation vs. C T variation in the upper water column over an annual cycle. The reasons for this singularity of the NWLB can be explained by the interplay between strong evaporation and the concomitant consumption of C T by autotrophic processes. The high range of A T variations, combined to temperature changes, has a strong impact on the variability of the seawater p CO 2 ( p CO 2 S W ). Based on Argo float data, an entire annual cycle for p CO 2 S W in the NWLB has been reconstructed in order to estimate the temporal sequence of the potential “source” and “sink” of atmospheric CO 2 . By combining this dataset with previous observations in the NWLB, this study shows a significant ocean acidification and a decrease in the oceanic surface pH T 25 of −0.0024 ± 0.0004 pH T 25 units.a –1 . The changes in the carbonate system are driven by the increase of atmospheric CO 2 but also by unexplained temporal changes in the surface A T content. If we consider that the EMed will, in the future, encounter longer, more intense and warmer summer seasons, this study proposes some perspectives on the carbonate system functioning of the “future” EMed.
Abstract. The Mediterranean Sea is considered a "hot-spot" for climate change, being characterized by oligotrophic to ultra-oligotrophic waters and rapidly changing carbonate chemistry. Coccolithophores are considered a dominant phytoplankton group in these waters. As a marine calcifying organism they are expected to respond to the ongoing changes in seawater CO2 systems parameters. However, very few studies have covered the entire Mediterranean physiochemical gradients from the Strait of Gibraltar to the Eastern Mediterranean Levantine Basin. We provide here an updated state of knowledge of the coccolithophore distribution in the Mediterranean Sea and relate this to a broad set of in situ measured environmental variables. Samples were taken during the Meteor (M84/3) oceanographic cruise in April 2011, between 0–100 m water depth from 28 stations. Total diatom, dinoflagellate and silicoflagellate cell concentrations are also presented. Our results highlight the importance of seawater carbonate chemistry, especially CO32−, in unraveling the distribution of heterococcolithophores, the most abundant coccolithophore life phase. Holo- and hetero-coccolithophores respond differently to environmental factors. For instance, changes in heterococcolithophore assemblages were best linked to the combination of [CO32−], pH, and salinity (ρ = 0.57) although salinity might be not functionally related to coccolithophore assemblage distribution. Holococcolithophores, on the other hand, were preferentially distributed and showed higher species diversity in oligotrophic areas (Best fit, ρ = 0.32 for nutrients), thriving in nutrient depleted waters. Clustering of heterococcolithophores revealed three groups of species sharing more than 65% similarities. These clusters could be assigned to the eastern and western basins, and deeper layers (below 50 m), respectively. In addition, the species Gephyrocapsa oceanica, G. muellerae and Emiliania huxleyi morphotype B/C are spatially distributed together and trace the influx of Atlantic waters into the Mediterranean Sea. The results of the present work emphasize the importance of considering holo- and hetero-coccolithophores separately when analyzing changes in species assemblages and diversity. Our findings clearly show that coccolithophores are a dominant phytoplankton group in the entire Mediterranean Sea; they have life stages that are expected to respond differently to the variability in seawater carbonate chemistry and nutrient concentrations.
The Mediterranean Sea ( MED-ih-tə-RAY-nee-ən) is an intercontinental sea situated between Europe, Asia, and Africa. It is surrounded by the Mediterranean basin and almost completely enclosed by land: on the east by the Levant in West Asia, on the north by Anatolia in West Asia and Southern Europe, and on the south by North Africa. To its west it is connected to the Atlantic Ocean via the Strait of
Evaporation greatly exceeds precipitation and river runoff in the Mediterranean, a fact that is central to the water circulation within the basin. Evaporation is especially high in its eastern half, causing the water level to decrease and salinity to increase eastward. The average salinity in the basin is 38 PSU at 5 m (16 ft) depth.
The temperature of the water in the deepest part of the Mediterranean Sea is 13.2 °C (55.8 °F).
The net water influx from the Atlantic Ocean is ca. 70,000 m3/s (2.5 million cu ft/s) or 2.2×1012 m3/a (7.8×1013 cu ft/a). Without this Atlantic water, the sea level of the Mediterranean Sea would fall at a rate of about 1 m (3 ft) per year.
In oceanography, it is sometimes called the Eurafrican Mediterranean Sea, the European Mediterranean Sea or the African Mediterranean Sea to distinguish it from mediterranean seas elsewhere, like the Baltic Sea, and the North-east Atlantic Ocean.
Unlike the vast multidirectional ocean currents in open oceans within their respective oceanic zones; biodiversity in the Mediterranean Sea is stable due to the subtle but strong locked nature of currents which is favourable to life, even the smallest macroscopic type of volcanic life form. The stable marine ecosystem of the Mediterranean Sea and sea temperature provides a nourishing environment for life in the deep sea to flourish while assuring a balanced aquatic ecosystem excluded from any external deep oceanic factors. It is estimated that there are more than 17,000 marine species in the Mediterranean Sea with generally higher marine biodiversity in coastal areas,
Evaporation greatly exceeds precipitation and river runoff in the Mediterranean, a fact that is central to the water circulation within the basin. Evaporation is especially high in its eastern half, causing the water level to decrease and salinity to increase eastward. The average salinity in the basin is 38 PSU at 5 m (16 ft) depth.
The temperature of the water in the deepest part of the Mediterranean Sea is 13.2 °C (55.8 °F).
The net water influx from the Atlantic Ocean is ca. 70,000 m3/s (2.5 million cu ft/s) or 2.2×1012 m3/a (7.8×1013 cu ft/a). Without this Atlantic water, the sea level of the Mediterranean Sea would fall at a rate of about 1 m (3 ft) per year.
In oceanography, it is sometimes called the Eurafrican Mediterranean Sea, the European Mediterranean Sea or the African Mediterranean Sea to distinguish it from mediterranean seas elsewhere, like the Baltic Sea, and the North-east Atlantic Ocean.
The geologic history of the Mediterranean Sea is complex. Underlain by oceanic crust, the sea basin was once thought to be a tectonic remnant of the ancient Tethys Ocean; it is now known to be a structurally younger basin, called the Neotethys, which was first formed by the convergence of the African Plate and Eurasian Plate during the Late Triassic and Early Jurassic. Because it is a near-landlocked body of water in a normally dry climate, the Mediterranean is subject to intensive evaporation and the precipitation of evaporites. The Messinian salinity crisis started about six million years ago (mya) when the Mediterranean became landlocked, and then essentially dried up. There are salt deposits accumulated on the bottom of the basin of more than a million cubic kilometres—in some places more than three kilometres thick.
Scientists estimate that the sea was last filled about 5.3 million years ago (mya) in less than two years by the Zanclean flood. Water poured in from the Atlantic Ocean through a newly breached gateway now called the Strait of Gibraltar at an estimated rate of about three orders of magnitude (one thousand times) larger than the current flow of the Amazon River.
The Mediterranean Sea has an average depth of 1,500 m (4,900 ft) and the deepest recorded point is 5,267 m (17,280 ft) in the Calypso Deep in the Ionian Sea. The coastline extends for 46,000 km (29,000 mi). A shallow submarine ridge (the Strait of Sicily) between the island of Sicily and the coast of Tunisia divides the sea in two main subregions: the Western Mediterranean, with an
Unlike the vast multidirectional ocean currents in open oceans within their respective oceanic zones; biodiversity in the Mediterranean Sea is stable due to the subtle but strong locked nature of currents which is favourable to life, even the smallest macroscopic type of volcanic life form. The stable marine ecosystem of the Mediterranean Sea and sea temperature provides a nourishing environment for life in the deep sea to flourish while assuring a balanced aquatic ecosystem excluded from any external deep oceanic factors. It is estimated that there are more than 17,000 marine species in the Mediterranean Sea with generally higher marine biodiversity in coastal areas, continental shelves, and decreases with depth.
As a result of the drying of the sea during the Messinian salinity crisis, the marine biota of the Mediterranean is derived primarily from the Atlantic Ocean. The North Atlantic is considerably colder and more nutrient-rich than the Mediterranean, and the marine life of the Mediterranean has had to adapt to its differing conditions in the five million years since the basin was reflooded later.
The Alboran Sea is a transition zone between the two seas, containing a mix of Mediterranean and Atlantic species. The Mediterranean monk seals live in the Aegean Sea in Greece.
There was a resident population of orcas in the Mediterranean until the 1980s, when they went extinct, probably due to long-term PCB exposure. There are still annual sightings of orca vagrants.
se of the charge that these salts carry, salinity is determined by measuring the seawater's conductivity. The most abundant ion in seawater is chlorine, followed by sodium, sulfate, magnesium, calcium, and potassium. These components make up 99.36% of the oceans salinity. Seawater also contains dissolved gases, such as carbon dioxide, nitrogen, and oxygen.
Like temperature, salinity also has an effect on water. As salinity increases vapor pressure decreases and osmotic pressure increases (important for marine organisms) and lowers the temperature of initial freezing (0°C), creating a no fixed freezing point. Salinity also has an effect on the viscosity of water. This is because certain ions like sodium and potassium shift the equilibrium toward water's unstructured phase, while others like magnesium prefer the structured portion. The image below shows sea surface salinity.
This image was generated based on the all observed data until 1994. The pink and red represent high levels of salinity and the dark blue shows extreme low rates of salinity. The high salinity seawater is in secluded areas and the subtropics (Sargasso Sea, Persian Gulf, Red Sea, and the Mediterranean Sea), while the lowest seem to be in the north (Baltic Sea and Gulf of Bothnia) and around the continents.
The distributions of salinity are quite different from temperature. High concentrations are usually in the center of the ocean basins away from the mouths of rivers, which pour in fresh water. They are also in sub-tropical regions due to high rates of evaporation (clear skies, little rain, and prevailing winds) and even higher where there is landlocked sea of dry regions. Low salinity is in the high latitudes. This is because of the lower evaporation rates and the melting of ice which dilutes the water. Basically, there are low rates of salinity where precipitation is greater than evaporation, mainly in the coastal or equatorial regions.
The diagram above illustrates the average sea sali
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This check searched the claim as stated. It did not run a separate search for evidence against it.