The distribution and concentration of particulate biogenic silica in surface waters of Prydz Bay, Antarctica, during the austral summer of 2011

2013 ◽  
Vol 23 (4) ◽  
pp. 211-216
Author(s):  
Chuanyu HU ◽  
Chen SHEN ◽  
Haisheng ZHANG
2005 ◽  
Vol 2 (1) ◽  
pp. 56 ◽  
Author(s):  
Sylvia Sander ◽  
Jonathan P. Kim ◽  
Barry Anderson ◽  
Keith A. Hunter

Environmental Context. The bioavailability of dissolved metals in natural waters is directly affected by metal-sequestering agents. These agents include soil-derived matter and compounds released by microorganisms, since copper can support or inhibit aquatic microorganisms depending on concentration. During summer the levels of copper increase in surface waters, an effect intuitively attributable to increased ultraviolet light degrading the sequestering agents more effectively, leading to a concurrent release of the metal. This paper shows that the amount of degradation attributable to light is too low to explain the metal release and that a biological influence may instead be responsible. Abstract. The influence of UVB irradiation on the Cu2+ binding by natural organic ligands in six alpine lakes on the South Island, New Zealand, has been investigated using competitive ligand equilibration with salicylaldoxime and detection by cathodic stripping voltammetry (CLE-CSV). During austral summer 2002–2003 the total dissolved Cu ([Cu]T), the concentration of strong Cu2+-binding ligands ([L]T), and their conditional stability constant K´´ were determined in surface samples of all six lakes. All lakes exhibited appreciable concentrations of a strong Cu2+ binding ligand with similar K´´ values and concentrations always exceeding [CuT], thus dominating Cu2+ speciation. Four lakes (Hayes, Manapouri, Wanaka, Te Anau) showed no appreciable trend in [LT] throughout the summer, whereas in Lakes Wakatipu and Hawea [LT] increased steadily throughout this period. Laboratory UVB irradiation of lake water samples using a 400 W mercury lamp with a Pyrex glass filter (λ > 280 nm) showed that Cu2+-binding ligands are destroyed by UVB radiation, causing [L]T to decrease with a rate of –0.588 nmol L–1 h–1 (r2 0.88). From this we calculate that the in situ ligand destruction rate by UVB in summer for surface waters of these lakes is too small to significantly affect [LT], and conclude that variations in ligand concentrations must result from seasonally variable biological factors.


2015 ◽  
Vol 120 (8) ◽  
pp. 5836-5849 ◽  
Author(s):  
Liyang Zhan ◽  
Liqi Chen ◽  
Jiexia Zhang ◽  
Jinpei Yan ◽  
Yuhong Li ◽  
...  

PLoS ONE ◽  
2014 ◽  
Vol 9 (6) ◽  
pp. e98849 ◽  
Author(s):  
Martha Valiadi ◽  
Stuart C. Painter ◽  
John T. Allen ◽  
William M. Balch ◽  
M. Debora Iglesias-Rodriguez

Polar Biology ◽  
1991 ◽  
Vol 11 (5) ◽  
pp. 293-304 ◽  
Author(s):  
Eva-Maria Nöthig ◽  
Bodo von Bodungen ◽  
Qingbo Sui

2018 ◽  
Author(s):  
Christos Panagiotopoulos ◽  
Mireille Pujo Pay ◽  
Mar Benavides ◽  
France Van Wambeke ◽  
Richard Sempéré

Abstract. The distribution and dynamics of dissolved organic carbon (DOC) and dissolved combined neutral sugars (DCNS) were studied across an increasing oligotrophic gradient (−18 to −22° N latitude) spanning from the Melanesian Archipelago (MA) area to the western part of the south Pacific gyre (WGY), in austral summer, as a part of the OUTPACE project. Our results showed DOC and DCNS concentrations exhibited little differences among the MA and WGY areas (0–200 m: 55–78 µMC for DOC and 1.5–2 µMC for DCNS), however, a deeper penetration of DOC was noticeable at 150 m depth at the WGY area. This finding was also reflected to the DOC and semi-labile DOC (DOCSL) stocks values (integration 0–200 m) for which we found higher values in the WGY than the MA area. The high excess DOCSL measured in WGY was characterized by a high residence time (130 ± 31 days (n = 3)) about three times higher than the MA region (Tr = 40 ± 7 days (n = 8)) suggesting an accumulation of the semi-labile DOM in the surface waters of WGY. DCNS yields (DCNS-C x DOC−1 %) also followed this pattern with higher values recorded in the WGY (3.2 ± 1.3 %) than MA (2.8 ± 0.8 %) highlighting the presence of semi-labile dissolved organic material (DOM) in the form of polysaccharides. These polysaccharides also exhibited a higher residence time in WGY (Tr = 8 ± 4 days, n = 3) than in MA (Tr = 3 ± 1days, n = 8) suggesting that this DCNS pool persists longer in the surface waters of the WGY. The accumulation of DOCSL in the surface waters of WGY is probably due to the very slow bacterial degradation due to nutrient limitation indicating that biologically produced DOC can be stored in the euphotic layer for a very long period.


2011 ◽  
Vol 8 (6) ◽  
pp. 11041-11088 ◽  
Author(s):  
S. F. Henley ◽  
A. L. Annett ◽  
R. S. Ganeshram ◽  
D. S. Carson ◽  
K. Weston ◽  
...  

Abstract. A high resolution time-series analysis of stable carbon isotopic signatures in particulate organic carbon (δ13CPOC) and associated biogeochemical parameters in sea ice and surface waters provides an insight into the factors affecting δ13CPOC in the coastal western Antarctic Peninsula (WAP) sea ice environment. The study covers two austral summer seasons in Ryder Bay, northern Marguerite Bay between 2004 and 2006. A shift in diatom species composition during the 2005/2006 summer bloom to near-complete biomass dominance of Proboscia inermis is strongly correlated with a large ~10‰ negative isotopic shift in δ13CPOC that cannot be explained by a concurrent change in concentration or isotopic signature of CO2. We hypothesise that the δ13CPOC shift may be driven by the contrasting biochemical mechanisms and utilisation of carbon-concentrating mechanisms in different diatom species. These short-lived yet pronounced negative δ13CPOC excursions drive a 4‰ decrease in the seasonal average δ13CPOC signal, which is transferred to sediment traps and core-top sediments and consequently has the potential for preservation in the sedimentary record. This 4‰ difference between seasons of contrasting sea ice conditions and upper water column stratification matches the full amplitude of glacial-interglacial Southern Ocean δ13CPOC variability and, as such, we invoke phytoplankton species changes as a potentially important factor influencing sedimentary δ13CPOC. We also find significantly higher δ13CPOC in sea ice than surface waters, consistent with autotrophic carbon fixation in a semi-closed environment and possible contributions from post-production degradation, biological utilisation of HCO3- and production of exopolymeric substances (EPS). This study demonstrates the importance of surface water diatom speciation effects and isotopically heavy sea ice-derived material for δ13CPOC in Antarctic coastal environments and underlying sediments, with consequences for the utility of diatom-based δ13CPOC in the sedimentary record.


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