Microbial community structure and function in the Levantine Basin of the eastern Mediterranean

被引:57
|
作者
Tanaka, Tsuneo
Zohary, Tamar
Krom, Michael D.
Law, Cliff S.
Pitta, Paraskevi
Psarra, Stella
Rassoulzadegan, Fereidoun
Thingstad, T. Frede
Tselepides, Anastasios
Woodward, E. Malcolm S.
Flaten, Gro Anita Fonnes
Skjoldal, Evy Foss
Zodiatis, George
机构
[1] Univ Paris 06, Stn Zool, LOV, CNRS, F-06234 Villefranche Sur Mer, France
[2] Univ Bergen, Dept Biol, Marine Microbiol Res Grp, Bergen, Norway
[3] Univ Leeds, Sch Earth & Environm Sci, Earth & Biosphere Inst, Leeds, W Yorkshire, England
[4] Natl Inst Water & Atmospher Res, Wellington, New Zealand
[5] Plymouth Marine Lab, Plymouth, Devon, England
[6] Oceanog Inst, Hellen Ctr Marine Res3, Iraklion, Crete, Greece
[7] Univ Cyprus, Oceanog Ctr, Nicosia, Cyprus
关键词
microbial food web; oligotrophic system; Cyprus warm-core eddy; mesopelagic layer; bathypelagic layer; eastern; Mediterranean; WARM-CORE EDDY; LAGRANGIAN PHOSPHATE-ADDITION; SUB-ARCTIC PACIFIC; TOP-DOWN CONTROL; BACTERIAL PRODUCTION; BACTERIOPLANKTON DISTRIBUTION; BIOGEOCHEMICAL FLUXES; PHOSPHORUS LIMITATION; PHYTOPLANKTON BIOMASS; PRIMARY PRODUCTIVITY;
D O I
10.1016/j.dsr.2007.06.008
中图分类号
P7 [海洋学];
学科分类号
0707 ;
摘要
During May 2001 and May 2002, the structure and function of the microbial community within and outside the Cyprus quasi-stationary warm-core eddy in the Levantine Basin of the eastern Mediterranean was studied down to the depth of the bathypelagic layer. We present here the detailed description of the microbial food web in one of the most oligotrophic and P-starved marine systems on earth. The isothermal layer was at the depth between 20 and 260/300m at the core of the eddy, and between 20 and 100/110m outside. Nitrate and phosphate were found at higher concentration between 100 and 500/800 m outside the eddy compared within the core of the eddy, but the vertical diffusive flux of nitrate and phosphate across the pycnocline was higher within the core of the eddy. There were only minor differences in microbial abundance in the euphotic, layers of the two sites. It is suggested that the differences in the areal supply of nutrients to the isothermal layer, between the two sites, resulted in essentially a similar volumetric supply of nutrients to the euphotic layer. This suggests that the results of this study can be applied to describe the microbial food web within the euphotic layer over the larger area of the Levantine Basin, which exhibits ultra-oligotrophic and P-starved conditions. Primary production and abundances of the microbial community were somewhat higher in May 2001 than in May 2002, possibly because of higher nutrient fluxes in the euphotic layer, which are probably the result of deeper winter mixing in 2001, although a later onset of winter mixing or increased dust supply could not be discounted. In the euphotic layer, heterotrophs (bacteria, heterotrophic nanoflagellates (HNF), and ciliates) dominated (60-70%) the microbial carbon biomass. Heterotrophic ciliates were found to be much more abundant in the upper 50 m of the water column, while no consistent pattern wasfound for bacteria and HNF throughout the euphotic layer. Autotrophs showed a maximum distribution at the deep chlorophyll maximum found between 100 and 130m. In the euphotic layer, the relationships between biomass and production for phytoplankton and bacteria suggested a higher top-down control on the phytoplankton in the upper similar to 50 in and a consistently tight top-down control on the bacterial biomass throughout the euphotic layer. The phosphate addition experiment in the Cyprus Eddy suggests that the close predator-prey relationships within the microbial heterotrophic community were required for the rapid transfer of a limiting element to higher trophic levels without biomass oscillations in the P-fertilized surface mixed layers (0-20m). The results from the unmodified system in this study suggested that the rapid P transfer mechanisms would function only in the upper similar to 50m, while the element transfer would be based on a predator-prey relationship with more conceivable biomass oscillations in the deeper waters (similar to 100-160m) of the euphotic layer. In the Mediterranean Sea, nutrient concentrations, POC export, and integrated chlorophyll and primary production all tend to decrease toward the east. Our results together with a literature survey showed that abundances of the microbial components in the euphotic layer were not consistently lower in the study area than in the northwestern Mediterranean and that abundances of bacteria and HNF found in the mesopelagic and bathypelagic layers of the study area were within the reported ranges and quite similar to those found in the northwestern Mediterranean. This suggests that the oligotrophic status and the lw export production are not reflected in the abundance of the microbial components down to the bathypelagic layer of the eastern Mediterranean. (C) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1721 / 1743
页数:23
相关论文
共 50 条
  • [31] Seasonal patterns of coccolithophores in the ultra-oligotrophic South-East Levantine Basin, Eastern Mediterranean Sea
    Keuter, Sabine
    Silverman, Jacob
    Krom, Michael D.
    Sisma-Ventura, Guy
    Yu, Juntau
    Tsemel, Anat
    Ben-Ezra, Tal
    Sher, Daniel
    Reich, Tom
    Koplovitz, Gil
    Frada, Miguel J.
    MARINE MICROPALEONTOLOGY, 2022, 175
  • [32] Seasonal patterns of coccolithophores in the ultra-oligotrophic South-East Levantine Basin, Eastern Mediterranean Sea
    Keuter, Sabine
    Silverman, Jacob
    Krom, Michael D.
    Sisma-Ventura, Guy
    Yu, Juntau
    Tsemel, Anat
    Ben -Ezra, Tal
    Sher, Daniel
    Reich, Tom
    Koplovitz, Gil
    Frada, Miguel J.
    MARINE MICROPALEONTOLOGY, 2022, 175
  • [33] Is dinitrogen fixation significant in the Levantine Basin, East Mediterranean Sea?
    Yogev, Tali
    Rahav, Eyal
    Bar-Zeev, Edo
    Man-Aharonovich, Dikla
    Stambler, Noga
    Kress, Nurit
    Beja, Oded
    Mulholland, Margaret R.
    Herut, Barak
    Berman-Frank, Ilana
    ENVIRONMENTAL MICROBIOLOGY, 2011, 13 (04) : 854 - 871
  • [34] CURRENTS, WATER MASSES, EDDIES AND JETS IN THE MEDITERRANEAN LEVANTINE BASIN
    HECHT, A
    PINARDI, N
    ROBINSON, AR
    JOURNAL OF PHYSICAL OCEANOGRAPHY, 1988, 18 (10) : 1320 - 1353
  • [35] Synechococcus dynamics in the Levantine basin shelf waters (northeastern Mediterranean)
    Uysal, Z.
    Koksalan, I.
    MEDITERRANEAN MARINE SCIENCE, 2010, 11 (02): : 277 - 294
  • [36] Water column distribution of stable isotopes and carbonate properties in the South-eastern Levantine basin (Eastern Mediterranean): Vertical and temporal change
    Sisma-Ventura, G.
    Yam, R.
    Kress, N.
    Shemesh, A.
    JOURNAL OF MARINE SYSTEMS, 2016, 158 : 13 - 25
  • [37] Planktonic dinoflagellates of the northern Levantine Basin, northeastern Mediterranean Sea
    Polat, Sevim
    Koray, Tufan
    EUROPEAN JOURNAL OF PROTISTOLOGY, 2007, 43 (03) : 193 - 204
  • [38] Community structure and population genetics of Eastern Mediterranean polychaetes
    Chatzigeorgiou, Giorgos
    Sarropoulou, Elena
    Vasileiadou, Katerina
    Brown, Christina
    Faulwetter, Sarah
    Kotoulas, Giorgos
    Arvanitidis, Christos D.
    FRONTIERS IN MARINE SCIENCE, 2014, 1
  • [39] Thaliacean distribution and abundance in the northern part of the Levantine Sea (Crete and Cyprus) during the eastern Mediterranean climatic transient, and a comparison with the western Mediterranean basin
    Weikert, Horst
    Godeaux, Jean E. A.
    HELGOLAND MARINE RESEARCH, 2008, 62 (04) : 377 - 387
  • [40] Atmospheric deposition of inorganic phosphorus in the Levantine Basin, eastern Mediterranean: Spatial and temporal variability and its role in seawater productivity
    Markaki, Z
    Oikonomou, K
    Kocak, M
    Kouvarakis, G
    Chaniotaki, A
    Kubilay, N
    Mihalopoulos, N
    LIMNOLOGY AND OCEANOGRAPHY, 2003, 48 (04) : 1557 - 1568