128 research outputs found
Carbon isotopic evidence for microbial control of carbon supply to Orca Basin at the seawaterâbrine interface
© The Author(s), 2013. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Biogeosciences 10 (2013): 3175-3183, doi:10.5194/bg-10-3175-2013.Orca Basin, an intraslope basin on the Texas-Louisiana continental slope, hosts a hypersaline, anoxic brine in its lowermost 200 m in which limited microbial activity has been reported. This brine contains a large reservoir of reduced and aged carbon, and appears to be stable at decadal time scales: concentrations and isotopic composition of dissolved inorganic (DIC) and organic carbon (DOC) are similar to measurements made in the 1970s. Both DIC and DOC are more "aged" within the brine pool than in overlying water, and the isotopic contrast between brine carbon and seawater carbon is much greater for DIC than DOC. While the stable carbon isotopic composition of brine DIC points towards a combination of methane and organic carbon remineralization as its source, radiocarbon and box model results point to the brine interface as the major source region for DIC, allowing for only limited oxidation of methane diffusing upwards from sediments. This conclusion is consistent with previous studies that identify the seawaterâbrine interface as the focus of microbial activity associated with Orca Basin brine. Isotopic similarities between DIC and DOC suggest a different relationship between these two carbon reservoirs than is typically observed in deep ocean basins. Radiocarbon values implicate the seawaterâbrine interface region as the likely source region for DOC to the brine as well as DIC.This work
was funded by the WHOI Postdoctoral Scholar program, NSF
Cooperative Agreement for the Operation of a National Ocean
Sciences Accelerator Mass Spectrometry Facility (OCE-0753487),
and the US National Science Foundationâs Emerging Frontiers
program (award 0801741 to SBJ)
Triacylglycerol profiling of microalgae strains for biofuel feedstock by liquid chromatographyâhigh-resolution mass spectrometry
Biofuels from photosynthetic microalgae are quickly gaining interest as a viable carbon-neutral energy source. Typically, characterization of algal feedstock involves breaking down triacylglycerols (TAG) and other intact lipids, followed by derivatization of the fatty acids to fatty acid methyl esters prior to analysis by gas chromatography (GC). However, knowledge of the intact lipid profile could offer significant advantages for discovery stage biofuel research such as the selection of an algal strain or the optimization of growth and extraction conditions. Herein, lipid extracts from microalgae were directly analyzed by ultra-high pressure liquid chromatographyâmass spectrometry (UHPLC-MS) using a benchtop Orbitrap mass spectrometer. Phospholipids, glycolipids, and TAGs were analyzed in the same chromatographic run, using a combination of accurate mass and diagnostic fragment ions for identification. Using this approach, greater than 100 unique TAGs were identified over the six algal strains studied and TAG profiles were obtained to assess their potential for biofuel applications. Under the growth conditions employed, Botryococcus braunii and Scenedesmus obliquus yielded the most comprehensive TAG profile with a high abundance of TAGs containing oleic acid
Targeted metabolomics reveals proline as a major osmolyte in the chemolithoautotroph Sulfurimonas denitrificans
© The Author(s), 2018. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in MicrobiologyOpen 7 (2018): e00586, doi:10.1002/mbo3.586.Chemoautotrophic bacteria belonging to the genus Sulfurimonas in the class
Campylobacteria are widespread in many marine environments characterized by redox
interfaces, yet little is known about their physiological adaptations to different environmental
conditions. Here, we used liquid chromatography coupled with tandem
mass spectrometry (LC-MS/
MS) in a targeted metabolomics approach to study the
adaptations of Sulfurimonas denitrificans to varying salt concentrations that are found
in its natural habitat of tidal mudflats. Proline was identified as one of the most abundant
internal metabolites and its concentration showed a strong positive correlation
with ionic strength, suggesting that it acts as an important osmolyte in S. denitrificans.
2,3-dihydroxypropane-
1-
sulfonate
was also positively correlated with ionic strength,
indicating it might play a previously unrecognized role in osmoregulation. Furthermore,
the detection of metabolites from the reductive tricarboxylic acid cycle at high internal
concentrations reinforces the importance of this pathway for carbon fixation in
Campylobacteria and as a hub for biosynthesis. As the first report of metabolomic data
for an campylobacterial chemolithoautotroph, this study provides data that will be
useful to understand the adaptations of Campylobacteria to their natural habitat at
redox interfaces.NSF, Grant/Award Number: OCE-
1136727 and OCE-1154320; Woods Hole
Oceanographic Institution; U.S. Geological
Surve
Advances in Sample Preparation at the National Ocean Sciences Accelerator Mass Spectrometry Facility (NOSAMS): Investigation of Carbonate Secondary Standards
The development of robust sample preparation techniques for ocean science research has been a hallmark of
NOSAMS since its inception. Improvements to our standard methods include reducing the minimum size of the
samples we can analyze, building modular graphite reactors of different sizes that we can swap in and out
depending on our sample stream, and modifying our carbonate acidification methods to improve handling of the
smaller samples we now receive. A relatively new instrument, the Ramped PyrOx, which allows the separation
of organic matter into thermal fractions, has attracted much interest as a research and development tool. We will
also discuss our progress on incorporating a Picarro isotope analyzer into our sample preparation options
14C and 13C characteristics of higher plant biomarkers in Washington margin surface sediments
Author Posting. © The Author(s), 2012. This is the author's version of the work. It is posted here by permission of Elsevier for personal use, not for redistribution. The definitive version was published in Geochimica et Cosmochimica Acta 105 (2013): 14-30, doi:10.1016/j.gca.2012.11.034.Plant wax lipids and lignin phenols are the two most common classes of molecular markers that are used to trace vascular plant-derived OM in the marine environment. However, their 13C and 14C compositions have not been directly compared, which can be used to constrain the flux and attenuation of terrestrial carbon in marine environment. In this study, we describe a revised method of isolating individual lignin phenols from complex sedimentary matrices for 14C analysis using high pressure liquid chromatography (HPLC) and compare this approach to a method utilizing preparative capillary gas chromatography (PCGC). We then examine in detail the 13C and 14C compositions of plant wax lipids and lignin phenols in sediments from the inner and mid shelf of the Washington margin that are influenced by discharge of the Columbia River. Plant wax lipids (including n-alkanes, n-alkanoic (fatty) acids, n-alkanols, and n-aldehydes) displayed significant variability in both ÎŽ13C (-28.3 to -37.5 â°) and â14C values (-204 to +2 â°), suggesting varied inputs and/or continental storage and transport histories. In contrast, lignin phenols exhibited similar ÎŽ13C values (between -30 to -34 â°) and a relatively narrow range of â14C values (-45 to -150 â°; HPLC-based mesurement) that were similar to, or younger than, bulk OM (-195 to -137 â°). Moreover, lignin phenol 14C age correlated with the degradation characteristics of this terrestrial biopolymer in that vanillyl phenols were on average ~500 years older than syringyl and cinnamyl phenols that degrade faster in soils and sediments. The isotopic characteristics, abundance, and distribution of lignin phenols in sediments suggest that they serve as promising tracers of recently biosynthesized terrestrial OM during supply to, and dispersal within the marine environment. Lignin phenol 14C measurements may also provide useful constraints on the vascular plant end member in isotopic mixing models for carbon source apportionment, and for interpretation of sedimentary records of past vegetation dynamics.
Key words: 14C and 13C composition, radiocarbon age, plant wax lipids, lignin phenols, Washington margin, marine carbon cycling, terrestrial organic matterGrants OCE-9907129, OCE-0137005, and OCE-0526268 (to TIE) from the National Science Foundation (NSF) supported this research
How Far Can a Short Leadership and Management Programme Address the Challenges for First Line Social Work Managers? An Evaluation of One of the Skills for Care Leadership and Management Demonstration Sites
Ibrutinib for Relapsed / Refractory CLL: A UK and Ireland Analysis of Outcomes in 315 patients
In 2014, ibrutinib was made available for relapsed/refractory chronic lymphocytic leukaemia (CLL) patients. The UK CLL Forum collected data from UK/Ireland patients with a minimum of 1 year follow-up with pre-planned primary endpoints; the number of patients still on therapy at 1 year (Discontinuation Free Survival; DFS) and 1 year overall survival (OS). With a median 16 months follow-up, data on 315 patients demonstrated 1 year DFS of 73.7% and 1 year OS of 83.8%. Patients with better pre-treatment performance status (PS 0/1 vs 2+) had superior DFS (77.5% vs 61.3%;p14 days and had OS of 89.7%, while 26% of patients had dose reductions and 13% had temporary treatment breaks >14 days. We could not demonstrate a detrimental effect of dose reductions alone (1 year OS: 91.7%), but patients who had first year treatment breaks > 14 days, particularly permanent cessation of ibrutinib had both reduced 1 year OS (68.5%) and also a statistically significant excess mortality rate beyond one year. Although outcomes appear inferior to the RESONATE trial (1 year OS;90%: PFS;84%), this may partly reflect the inclusion of PS 2+ patients and that 17.5% of patients permanently discontinued ibrutinib due to an event other than disease progression
Quality of Graphite Target for Biological/Biomedical/Environmental Applications of 14C-Accelerator Mass Spectrometry
Catalytic graphitization for 14C-accelerator mass spectrometry (14C-AMS) produced various forms of elemental carbon. Our high-throughput Zn reduction method (C/Fe = 1:5, 500 °C, 3 h) produced the AMS target of graphite-coated iron powder (GCIP), a mix of nongraphitic carbon and Fe3C. Crystallinity of the AMS targets of GCIP (nongraphitic carbon) was increased to turbostratic carbon by raising the C/Fe ratio from 1:5 to 1:1 and the graphitization temperature from 500 to 585 °C. The AMS target of GCIP containing turbostratic carbon had a large isotopic fractionation and a low AMS ion current. The AMS target of GCIP containing turbostratic carbon also yielded less accurate/precise 14C-AMS measurements because of the lower graphitization yield and lower thermal conductivity that were caused by the higher C/Fe ratio of 1:1. On the other hand, the AMS target of GCIP containing nongraphitic carbon had higher graphitization yield and better thermal conductivity over the AMS target of GCIP containing turbostratic carbon due to optimal surface area provided by the iron powder. Finally, graphitization yield and thermal conductivity were stronger determinants (over graphite crystallinity) for accurate/precise/high-throughput biological, biomedical, and environmental14C-AMS applications such as absorption, distribution, metabolism, elimination (ADME), and physiologically based pharmacokinetics (PBPK) of nutrients, drugs, phytochemicals, and environmental chemicals
Neurotic illness in the families of children with asthma and wheezy bronchitis: a general practice population study
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