scholarly journals Infectious titres of Emiliania huxleyi virus 86 are reduced by exposure to millimolar dimethyl sulfide and acrylic acid

2006 ◽  
Vol 51 (5) ◽  
pp. 2468-2471 ◽  
Author(s):  
Claire Evans ◽  
Gillian Malin ◽  
William H. Wilson ◽  
Peter S. Liss
2010 ◽  
Vol 55 (4) ◽  
pp. 1579-1589 ◽  
Author(s):  
Stephen D. Archer ◽  
Maria Ragni ◽  
Richard Webster ◽  
Ruth L. Airs ◽  
Richard J. Geider

2019 ◽  
Author(s):  
Thomas Klintzsch ◽  
Gerald Langer ◽  
Gernot Nehrke ◽  
Anna Wieland ◽  
Katharina Lenhart ◽  
...  

Abstract. The world’s oceans are considered to be a minor source of methane (CH4) to the atmosphere although the magnitude of total net emissions is highly uncertain. In recent years the origin of the frequently observed in situ CH4 production in the ocean mixed layer has received much attention. Marine algae might contribute to the observed CH4 oversaturation in oxic waters, but so far direct evidence for CH4 production by marine algae has only been provided for the coccolithophore Emiliania huxleyi. In the present study we investigated, next to Emiliania huxleyi, other widespread haptophytes, i.e. Phaeocystis globosa and Chrysochromulina sp. for CH4 formation. Our results of CH4 production and stable carbon isotope measurements provide unambiguous evidence that all three investigated marine algae produce CH4 per se under oxic conditions and at rates ranging from 1.6 ± 0.5 to 2.7 ± 0.7 µg CH4 per g POC (particulate organic carbon) d−1 at a temperature of 20 °C with Chrysochromulina sp. and E. huxleyi showing the lowest and highest rates, respectively. In cultures that were treated with 13C-labelled hydrogen carbonate δ13CH4 values increased with incubation time, clearly resulting from the conversion of 13C-hydrogen carbonate to 13CH4. The addition of 13C labelled dimethyl sulfide, dimethyl sulfoxide and methionine sulfoxide – known algal metabolites that are ubiquitous in marine surface layers - enabled us to clearly monitor the occurrence of 13C-enriched CH4 in cultures of Emiliania huxleyi clearly indicating that methylated sulphur compounds are also precursors of CH4. We propose that CH4 production could be a common process among marine haptophytes likely contributing to CH4 oversaturation in oxic waters.


2020 ◽  
Vol 8 (38) ◽  
pp. 13368-13374
Author(s):  
Muhammad Umair Khan ◽  
Gul Hassan ◽  
Jinho Bae

This paper proposes a novel soft ionic liquid (IL) electrically functional device that displays resistive memory characteristics using poly(acrylic acid) partial sodium salt (PAA-Na+:H2O) solution gel and sodium hydroxide (NaOH) in a thin polydimethylsiloxane (PDMS) cylindrical microchannel.


2020 ◽  
Vol 65 (1) ◽  
pp. 28-41
Author(s):  
Marwa Aly Ahmed ◽  
Júlia Erdőssy ◽  
Viola Horváth

Multifunctional nanoparticles have been shown earlier to bind certain proteins with high affinity and the binding affinity could be enhanced by molecular imprinting of the target protein. In this work different initiator systems were used and compared during the synthesis of poly (N-isopropylacrylamide-co-acrylic acid-co-N-tert-butylacrylamide) nanoparticles with respect to their future applicability in molecular imprinting of lysozyme. The decomposition of ammonium persulfate initiator was initiated either thermally at 60 °C or by using redox activators, namely tetramethylethylenediamine or sodium bisulfite at low temperatures. Morphology differences in the resulting nanoparticles have been revealed using scanning electron microscopy and dynamic light scattering. During polymerization the conversion of each monomer was followed in time. Striking differences were demonstrated in the incorporation rate of acrylic acid between the tetramethylethylenediamine catalyzed initiation and the other systems. This led to a completely different nanoparticle microstructure the consequence of which was the distinctly lower lysozyme binding affinity. On the contrary, the use of sodium bisulfite activation resulted in similar nanoparticle structural homogeneity and protein binding affinity as the thermal initiation.


2015 ◽  
Vol 74 (2) ◽  
pp. 173-185 ◽  
Author(s):  
LJ Darroch ◽  
M Lavoie ◽  
M Levasseur ◽  
I Laurion ◽  
WG Sunda ◽  
...  

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