180 research outputs found

    Comparative study on lipid quality of distribution and abundance of Mnemiopsis leidyi in the eastern Iranian coasts of Caspian Sea

    Get PDF
    The alien ctenophore Mnemiopsis leidyi which was transported from the Black Sea into the Caspian Sea at the end of 1990s has been negatively affecting ecosystem in this new environment. In this study, spatial and temporal distribution of M.leidyi were studied from a total of stations located along three transects (Amirabad, Babolsar and Nowshar) in the Eeastern Iranian coasts of the Caspian Sea (Mazandaran province) during July 2001 to November 2002. M. leidyi acheived maximum biomass 1024.5 g/m^2 in August-October 2002. Minimum biomass (1.5 g/m^2 of ctenophore were measured in December-Jaunuary 2001. The highest biomass was at the stations with 10m bottom depth (570.7 g/m^2 in autumn and lowest biomass (75.9 g/m^2) was obtained at a station with a 50 m bottom depth in winter. The highest average biomass (641.2 g/m^2) were measured in ~irabad region and the lowest biomass (207.5 g/m^2) observed in Nowshar region. The young specimens (<5 mm) contributed about 90% to the total abundance of the population. The maximum length was 51-55mm which was measured in August. The factors affecting the distribution of M. leidyi in the study area were discussed

    Effect of temperature on clearance rate, daily ration and digestion time of Mnemiopsis leidyi from the southern Caspian Sea

    Get PDF
    The effect of temperature on the main feeding parameters of Mnemiopsis leidyi from the southern Caspian Sea was studied in 2002. The clearance rates and daily rations were estimated from laboratory experiments in a wide range of temperatures from 12 to 27 ºC for M. leidyi of 12–17 mm in length. Clearance rate values changed from 52.5 to 107.3 ml ind-1 h-1. The coefficient Q10 in temperature 12 - 20 ºC was higher than that in 20 - 27 ºC (3.81 and 1.91, respectively). The specific daily ration changed from 1.56±0.19 to 0.24±0.05 mg C mg C-1 day-1 when temperature decreased from 27 ºC to 12 ºC. The direct relationship occurred between daily ration and temperature (R2=0.99). The digestion time decreased with temperature rise and did not display any clear relation to quantity of digested food.

    Zooplankton of the Black Sea and the Eastern Mediterranean: Similarities and dissimilarities

    Get PDF
    A synthesis of data on abundance and biomass of zooplankton in the Eastern Mediterranean (EMED) and the Black Sea shows major differences in the composition and structure of pelagic communities in the two basins. Few Mediterranean planktonic animals have invaded and acclimatised in the Black Sea. The great bulk of Black Sea species is represented by coastal inhabitants that spread throughout the whole basin. This process has been called “neritization” of the Black Sea fauna. Peculiarities in zooplankton assemblages of the Black Sea have been further strengthened over the last few decades due to increasing eutrophication and the massive invasion of the ctenophore Mnemiopsis leidyi. The relative contribution of copepods, cladocerans, chaetognaths, and appendicularians to total zooplankton biomass has notably decreased , whereas gelatinous groups (mainly represented by Mnemiopsis and Aurelia aurita) contributed up to 99% of total wet weight in 1995 in the Black Sea.The basic features of planktonic fauna in the Black Sea are mainly due do the geo-morphological characters of the basin and the limited exchanges with the EMED, that are confined to the surface-subsurface layers in the Dardanelles and Bosphorus Straits. However, the dramatic changes that recently occurred in the structure of zooplankton assemblages seem to have been caused by heavy anthropogenic impact on the pelagic system

    Editorial: Phytoplankton dynamics under climate change

    Get PDF
    Phytoplankton plays an important role in ocean processes, and is well-known to have an enormous positive impact on climate change or more specifically on global warming, by reducing atmospheric CO2 levels through the sinking of produced organic and inorganic matter to the deep ocean (Falkowski, 2012; Beardall and Raven, 2013). However, climate change, with consequences of elevated seawater temperatures and decreased pH levels (Beardall and Raven, 2013), influences phytoplankton dynamics, changing phytoplankton composition, geography and biomass in the oceans (Falkowski and Oliver, 2007; Boyd et al., 2015; Jonkers et al., 2019). Temperature increases could also drive temporal shifts in the onset of the regular annual blooms, their composition, duration and amplitude as well as mismatches in timing between trophic levels (Hinder et al., 2012; Mikaelyan et al., 2015). The overall impact of increased temperature on phytoplankton is not easy to assess due to variable and complex repercussions. For example, increasing temperatures can lead to more stratified waters, especially in summer months, and prevent nutrient replenishment at the ocean surface.info:eu-repo/semantics/publishedVersio

    Increased Chlorophyll Levels in the Southern Caspian Sea Following an Invasion of Jellyfish

    Get PDF
    A significant correlation was observed between satellite derived chlorophyll a (Chl a) concentrations and the biomass of the invasive comb jellyfish Mnemiopsis leidyi in the southern Caspian Sea. By consuming the herbivorous zooplankton, the predatory ctenophore M. leidyi may have caused levels of Chl a to rise to very high values (∼9 mg m−3) in the southern Caspian Sea. There might also be several other factors concurrent with predation effects of M. leidyi influencing Chl a levels in this region, such as eutrophication and climatic changes which play major roles in nutrient, phytoplankton, and zooplankton variations. The decrease in pelagic fishes due to overfishing, natural, and anthropogenic impacts might have provided a suitable environment for M. leidyi to spread throughout this enclosed basin

    Reproduction of the ctenophore, Beroe ovata, in the Caspian Sea water

    Get PDF
    The experiments with Beroe ovata showed that this ctenophore can survive and reproduce in the Caspian Sea water, though at far lower rate than in the Black Sea; larval growth in the Caspian Sea water was also slower and mortality higher. Maximum fecundity of 2210 and 240 eggs recorded in laboratories of Turkey and Iran, respectively. About 34 to 100% of eggs in the Caspian Sea water could not develop and hatch. Larvae were at different stages of development, usually with size between 1.2 to 2mm. The highest number of eggs and larvae were obtained in tanks where Beroe individuals were together with Mnemiopsis leidyi. The poor reproduction of B. ovata in the Caspian Sea water could be due to both the acclimation stress to low salinity and possible damage of individuals during the transportation

    Tuning gastropod locomotion: Modeling the influence of mucus rheology on the cost of crawling

    Get PDF
    Common gastropods such as snails crawl on a solid substrate by propagating muscular waves of shear stress on a viscoelastic mucus. Producing the mucus accounts for the largest component in the gastropod's energy budget, more than twenty times the amount of mechanical work used in crawling. Using a simple mechanical model, we show that the shear-thinning properties of the mucus favor a decrease in the amount of mucus necessary for crawling, thereby decreasing the overall energetic cost of locomotion.Comment: Corrected typo

    From the Allerød to the mid-Holocene: Palynological evidence from the south basin of the Caspian Sea

    Get PDF
    This article has been made available through the Brunel Open Access Publishing Fund. Copyright @ The Authors. This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-No Derivative Works License, which permits non-commercial use, distribution, and reproduction in any medium, provided the original author and source are credited.Pollen and dinoflagellate cysts have been analysed in a core from the south basin of the Caspian Sea, providing a picture of respectively past vegetation and water salinity for the Late Pleistocene to middle Holocene. A relatively sharp lithological change at 0.86 m depth reflects a shift from detrital silts to carbonates-rich fine silts. From this depth upwards, a Holocene chronology is built based on ten radiocarbon dates on ostracod shells and bulk carbonates. From the vegetation point of view, the Late Pleistocene deserts and steppes were partially replaced in the most sheltered areas by an open woodland with Pinus, Juniperus-Hippophae-Elaeagnus and even Alnus-Quercus-Pterocarya and Fraxinus, related to the Allerød palynozone. This was interrupted by the Younger Dryas palynozone when Artemisia reaches a maximum in a first instance followed by a very dry phase with only a slight return of Pinus and Quercus and the rare presence of Ulmus-Zelkova. From 11.5 to 8.4 cal. ka BP, an open landscape dominated by shrubs such as Ephedra and progressively increasing Quercus appeared. The final spread of diverse evergreen and deciduous trees is delayed and occurs after 8.4 cal. ka BP. It is suggested that this delay is caused by an arid climate in the Early Holocene linked to high insolation and perhaps to a lake effect. The dinocyst assemblages fluctuate between slightly brackish (Pyxidinopsis psilata and Spiniferites cruciformis, 7 psu and lower) and more brackish (Impagidinium caspienense, ∼13 psu). In the Lateglacial (Khvalynian highstand), the assemblages remained dominated by relative low salinity taxa. A late and brief increase of salinity occurred prior to 11.2 cal. ka BP associated with the Mangyshlak lowstand. It is suggested that it was caused by a brief drop in meltwater flow from both the north and the southeast (Uzboy) and a likely evaporation increase. This lowstand occurs quasi at the same time as the end of a longer lowstand in the Black Sea. The freshest waters are then inferred as having occurred between 8.4 and ≤4.4 cal. ka BP, linked to a connection with the Amu Darya and the melting glaciers on the Pamir Mountains. The Caspian Sea is a sensitive environment, easily perturbed by global climatic changes, such as the Allerød and Holocene warming, and the Lateglacial and Younger Dryas cooling, as well as by regional changes in its hydrography, such as shifts in the Eurasian meltwater and the Volga and Amu Darya inflows.Centre National de la Recherche Scientifique, Franc
    corecore