scholarly journals Marine molluscs and fish as biomarkers of pollution stress in littoral regions of the Red Sea, Mediterranean Sea and North Sea

1999 ◽  
Vol 53 (3-4) ◽  
pp. 219-243 ◽  
Author(s):  
Vladimir Bresler ◽  
Avigdor Abelson ◽  
Halim Dizer ◽  
Armin Sturm ◽  
Renate Kratke ◽  
...  
2021 ◽  
Author(s):  
Paolo G. Albano ◽  
Anna Sabbatini ◽  
Jonathan Lattanzio ◽  
Jan Steger ◽  
Sönke Szidat ◽  
...  

<p>The Lessepsian invasion – the largest marine biological invasion – followed the opening of the Suez Canal in 1869 (81 years BP). Shortly afterwards, tropical species also distributed in the Red Sea appeared on Mediterranean shores: it was the dawn of what would become the invasion of several hundred tropical species. The time of the Suez Canal opening coincided with an acceleration in natural history exploration and description, but the eastern sectors of the Mediterranean Sea lagged behind and were thoroughly explored only in the second half of the 20<sup>th</sup> century. Many parts are still insufficiently studied today. Baseline information on pre-Lessepsian ecosystem states is thus scarce. This knowledge gap has rarely been considered by invasion scientists: every new finding of species belonging to tropical clades has been assumed to be a Lessepsian invader.</p><p>We here question this assumption by radiocarbon dating seven individual tests of miliolids – imperforated calcareous foraminifera – belonging to five alleged non-indigenous species. Tests were found in two sediment cores collected at 30 and 40 m depth off Ashqelon, on the Mediterranean Israeli shelf. We dated one <em>Cribromiliolinella milletti </em>(core at 40 m, 20 cm sediment depth), three <em>Nodophthalmidium antillarum </em>(core at 40 m, 35 cm sediment depth), one <em>Miliolinella </em>cf. <em>fichteliana </em>(core at 30 m, 110 cm sediment depth), one <em>Articulina alticostata </em>(core at 40 m, 35 cm sediment depth) and one <em>Spiroloculina antillarum </em>(core at 30 m, 110 cm sediment depth). All foraminiferal tests proved to be of Holocene age, with a median calibrated age spanning between 749 and 8285 years BP. Only one test of <em>N. antillarum</em> showed a 2-sigma error overlapping the time of the opening of the Suez Canal, but with a median age of 1123 years BP. Additionally, a thorough literature search resulted in a further record of <em>S. antillarum</em> in a core interval dated 1820–2064 years BP in Turkey.</p><p>Therefore, these foraminiferal species are not introduced, but native species. They are all circumtropical or Indo-Pacific and in the Mediterranean distributed mostly in the eastern sectors (only <em>S. antillarum</em> occurs also in the Adriatic Sea). Two hypotheses can explain our results: these species are Tethyan relicts that survived the Messinian salinity crisis (5.97–5.33 Ma) and the glacial periods of the Pleistocene in the Eastern Mediterranean, which may have never desiccated completely during the Messinian crisis and which may have worked as a warm-water refugium in the Pleistocene; or they entered the Mediterranean Sea from the Red Sea more recently but before the opening of the Suez Canal, for example during the Last Interglacial (MIS5e) high-stand (125,000 years BP) when the flooded Isthmus of Suez enabled exchanges between the Mediterranean and the Indo-Pacific fauna. The recognition that some alleged Lessepsian invaders are in fact native species influences our understanding of the invasion process, its rates and environmental correlates.</p>


Ocean Science ◽  
2011 ◽  
Vol 7 (5) ◽  
pp. 705-732 ◽  
Author(s):  
F. Gohin

Abstract. Sea surface temperature, chlorophyll, and turbidity are three variables of the coastal environment commonly measured by monitoring networks. The observation networks are often based on coastal stations, which do not provide a sufficient coverage to validate the model outputs or to be used in assimilation over the continental shelf. Conversely, the products derived from satellite reflectance generally show a decreasing quality shoreward, and an assessment of the limitation of these data is required. The annual cycle, mean, and percentile 90 of the chlorophyll concentration derived from MERIS/ESA and MODIS/NASA data processed with a dedicated algorithm have been compared to in-situ observations at twenty-six selected stations from the Mediterranean Sea to the North Sea. Keeping in mind the validation, the forcing, or the assimilation in hydrological, sediment-transport, or ecological models, the non-algal Suspended Particulate Matter (SPM) is also a parameter which is expected from the satellite imagery. However, the monitoring networks measure essentially the turbidity and a consistency between chlorophyll, representative of the phytoplankton biomass, non-algal SPM, and turbidity is required. In this study, we derive the satellite turbidity from chlorophyll and non-algal SPM with a common formula applied to in-situ or satellite observations. The distribution of the satellite-derived turbidity exhibits the same main statistical characteristics as those measured in-situ, which satisfies the first condition to monitor the long-term changes or the large-scale spatial variation over the continental shelf and along the shore. For the first time, climatologies of turbidity, so useful for mapping the environment of the benthic habitats, are proposed from space on areas as different as the southern North Sea or the western Mediterranean Sea, with validation at coastal stations.


2014 ◽  
Vol 17 (4) ◽  
pp. 454-462
Author(s):  
Hamed A. El-Serehy ◽  
Fahad A. Al-Misned ◽  
Nasser S. Abdel-Rahman ◽  
Khaled A. Al-Rasheid

2021 ◽  
Author(s):  
Débora Silva Raposo ◽  
Raphaël Morard ◽  
Christiane Schmidt ◽  
Michal Kucera

<p>In recent decades the “Lessepsian” migration caused a rapid change in the marine community composition due to the invasion of alien species from the Red Sea into the Mediterranean Sea. Among these invaders is the large benthic foraminifera <em>Amphistegina lobifera</em>, a diatom-bearing species that recently reached the invasion front in Sicily. There it copes with colder winters and broader temperature than in its original source, the Red Sea. It is not yet known how (or if) the population from the invasion front has developed adaptation to this new thermal regime. Understanding the modern marine invasive patterns is a crucial tool to predict future invasive successes in marine environments. Therefore, in this study we aim to evaluate the physiological responses to cold temperatures of <em>A. lobifera</em> populations at three different invasive stages: source (Red Sea), early invader (Eastern Mediterranean) and invasion front (Sicily). For this, we conducted a culturing experiment in which we monitored the responses of the foraminifera (growth, motility) to temperatures of 10, 13, 16, 19°C + control (25°C) over four weeks. To address what is the role of their endosymbionts in the adaptation process, we also monitored their photosynthetic activity (Pulse Amplitude Modulation - PAM fluorometer) during the experiment. The growth rate of the foraminifera was reduced for all populations below 19°C as well as the motility, reduced until 16°C and dropping to zero below 13°C. The response of the endosymbionts was however different. There was a reduced photosynthetic activity of the Red Sea and Eastern Mediterranean populations at colder temperatures observed by the lower maximum quantum yield (Fv:Fm) and effective quantum yield (Y(II)), when compared to their initial levels and to the other treatments. In the meantime, the endosymbionts of the Sicily population stood out with the highest photosynthetic activity (Fv:Fm and Y(II)) in the treatments bellow 13 °C (P < 0.05). In conclusion, we observed that while the host responses were similar between the three populations, the endosymbionts from the invasion front population shows the best performance at colder temperatures. This suggests that the photo-symbiosis has an important role in adaptation, most likely being a key factor to the success of past and future migrations.</p>


1982 ◽  
Vol 35 (3) ◽  
pp. 460-465
Author(s):  
Nabil Hilaly

It is recorded that Egypt was the first country to dig a canal to promote world trade; the first canal was dug in the reign of Pharaoh Senusret III (1887–1849 B.C.), to link the Mediterranean Sea with the Red Sea through the Nile delta. This canal, often abandoned due to silting, was reopened for navigation by later Pharaohs and finally by Amro Ibn El Ass in A.D. 640 after which it remained open for 150 years.


2015 ◽  
Vol 42 (12) ◽  
pp. 2363-2373 ◽  
Author(s):  
Michel Bariche ◽  
Martha Torres ◽  
Colin Smith ◽  
Nancy Sayar ◽  
Ernesto Azzurro ◽  
...  

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