Potential denitrification stimulated by water-soluble organic carbon from plant residues during initial decomposition

Denitrification usually takes place under anoxic conditions and over short periods of time, and depends on readily available nitrate and carbon sources. Variations in CO2 and N2O emissions associated with plant residues have mainly been explained by differences in their decomposability. A factor rarely considered so far is water-extractable organic matter (WEOM) released to the soil during residue decomposition. Here, we examined the potential effect of plant residues on denitrification with special emphasis on WEOM. A range of fresh and leached plant residues was characterized by elemental analyses, 13C-NMR spectroscopy, and extraction with ultrapure water. The obtained solutions were analyzed for the concentrations of organic carbon (OC) and organic nitrogen (ON), and by UV-VIS spectroscopy. To test the potential denitrification induced by plant residues or three different OM solutions, these carbon sources were added to soil suspensions and incubated for 24 h at 20 °C in the dark under anoxic conditions; KNO3 was added to ensure unlimited nitrate supply. Evolving N2O and CO2 were analyzed by gas chromatography, and acetylene inhibition was used to determine denitrification and its product ratio. The production of all gases, as well as the molar (N2O + N2)–N/CO2–C ratio, was directly related to the water-extractable OC (WEOC) content of the plant residues, and the WEOC increased with carboxylic/carbonyl C and decreasing OC/ON ratio of the plant residues. Incubation of OM solutions revealed that the molar (N2O + N2)–N/CO2–C ratio and share of N2O are influenced by the WEOM's chemical composition. In conclusion, our results emphasize the potential of WEOM in largely undecomposed plant residues to support short-term denitrification activity in a typical ˈhot spot–hot momentˈ situation

Novel laser spectroscopic technique for continuous analysis of N2O isotopomers - application and intercomparison with isotope ratio mass spectrometry

RATIONALE Nitrous oxide (N2O), a highly climate-relevant trace gas, is mainly derived from microbial denitrification and nitrification processes in soils. Apportioning N2O to these source processes is a challenging task, but better understanding of the processes is required to improve mitigation strategies. The N2O site-specific 15?N signatures from denitrification and nitrification have been shown to be clearly different, making this signature a potential tool for N2O source identification. We have applied for the first time quantum cascade laser absorption spectroscopy (QCLAS) for the continuous analysis of the intramolecular 15?N distribution of soil-derived N2O and compared this with state-of-the-art isotope ratio mass spectrometry (IRMS). METHODS Soil was amended with nitrate and sucrose and incubated in a laboratory setup. The N2O release was quantified by FTIR spectroscopy, while the N2O intramolecular 15?N distribution was continuously analyzed by online QCLAS at 1?Hz resolution. The QCLAS results on time-integrating flask samples were compared with those from the IRMS analysis. RESULTS The analytical precision (2 sigma) of QCLAS was around 0.3 parts per thousand for the delta 15Nbulk and the 15?N site preference (SP) for 1-min average values. Comparing the two techniques on flask samples, excellent agreement (R2?=?0.99; offset of 1.2 parts per thousand) was observed for the delta 15Nbulk values while for the SP values the correlation was less good (R2?=?0.76; offset of 0.9 parts per thousand), presumably due to the lower precision of the IRMS SP measurements. CONCLUSIONS These findings validate QCLAS as a viable alternative technique with even higher precision than state-of-the-art IRMS. Thus, laser spectroscopy has the potential to contribute significantly to a better understanding of N turnover in soils, which is crucial for advancing strategies to mitigate emissions of this efficient greenhouse gas. Copyright (c) 2012 John Wiley & Sons, Ltd

Dispersive liquid–liquid microextraction using ammonium O,O-diethyl dithiophosphate (DDTP) as chelating agent and graphite furnace atomic absorption spectrometry for the determination of silver in biological samples

A new method for the determination of silver in biological samples is presented in this work. The method involves application of dispersive liquid–liquid microextraction (DLLME) employing ammonium O,O-diethyl dithiophosphate (DDTP) as the chelating agent for extraction and preconcentration of silver prior to quantification using graphite furnace atomic absorption spectrometry (GFAAS). Chloroform and acetone were selected as the extracting and dispersing solvent, respectively, at optimized volumes of 80 mL and 500 mL, respectively. The concentration of DDTP and the extraction time were optimized as 0.01% (m/v) and 10 min, respectively. Pyrolysis (1100 C) and atomization (1800 C) temperatures were optimized using a L'vov platform treated with 400 mg of tungsten as a permanent chemical modifier. The method was proven virtually free from interference from major constituents of biological samples. A detection limit of 2 ng g 1 was obtained with relative standard deviations better than 13% and an enhancement factor of 70 was achieved. The determined concentrations for Ag in certified reference biological samples were in good agreement with the certified values at a 95% statistical confidence limit. The reported method using DLLME and GFAAS presented good analytical performance for Ag determination when compared to other methods available in the literature

Curative resection of a primarily unresectable acinar cell carcinoma of the pancreas after chemotherapy

<p>Abstract</p> <p>Background</p> <p>Acinar cell carcinoma (ACC) represents only 1–2% of pancreatic cancers and is a very rare malignancy. At the time of diagnosis only 50% of the tumors appear to be resectable. Reliable data for an effective adjuvant or neoadjuvant treatment are not available.</p> <p>Case presentation</p> <p>A 65-year old male presented with obstructive jaundice and non-specific upper abdominal pain. MRI-imaging showed a tumor within the head of the pancreas concomitant with Serum-Lipase and CA19-9. During ERCP, a stent was placed. Endosonographic fine needle biopsy confirmed an acinar cell carcinoma. Laparotomy presented an locally advanced tumor with venous infiltration that was consequently deemed unresectable. The patient was treated with five cycles of 5-FU monotherapy with palliative intention. Chemotherapy was well tolerated, and no severe complications were observed. Twelve months later, the patient was in stable condition, and CT-scanning showed an obvious reduction in the size of the tumor. During further operative exploration, a PPPD with resection of the portal vein was performed. Histopathological examination gave evidence of a diffuse necrotic ACC-tumor, all resection margins were found to be negative. Eighteen months later, the patient showed no signs of recurrent disease.</p> <p>Conclusion</p> <p>ACC responded well to 5-FU monochemotherapy. Therefore, neoadjuvant chemotherapy could be an option to reduce a primarily unresectable ACC to a point where curative resection can be achieved.</p

Integrated reduction/oxidation reactions and sorption processes for Cr(VI) removal from aqueous solutions using Laminaria digitata macro-algae

The main goal of this work was the valorization of seaweed Laminaria digitata, after acid pre-treatment, for the remediation of hexavalent chromium solutions. The Cr(VI) removal efficiency by the protonated biomass was studied as a function of different parameters, such as contact time, pH, biomass and Cr(VI) concentration, and temperature. Cr(VI) removal is based on a complex mechanism that includes a reduction of Cr(VI) to Cr(III), through the oxidation of biomass at acidic medium, and further chemical binding of Cr(III) to the negatively charged binding groups, mainly carboxylic groups. The optimum pH for chromium removal, using protonated L. digitata algae, was 2.5. The maximum amount of Cr(VI) reduction by the algae was around 2.1 mmol/g. The uptake capacity of Cr(III) by the oxidized biomass, after Cr(VI) reduction, was higher than by the algae in its original form (protonated algae). Results suggest that the oxidation of the biomass during Cr(VI) reduction, turns other active sites available for Cr(III) binding. Also, the Cr(III) binding from a solution of reduced Cr(VI) was much lower than from a pure Cr(III) solution. The result suggests the presence in solution of Cr(III) complexes with the organic matter released from the algae surface during Cr(VI) reduction. The activation energy obtained for the Cr(VI) reduction by L. digitata was 45 ± 20 kJ mol 1. A kinetic model based on the redox reaction between Cr(VI) species and organic compounds from the biosorbent surface was able to fit well the hexavalent chromium concentration. Trivalent chromium equilibrium biosorption was well described at different chromium concentrations, considering the interaction between carboxylic groups present in the surface of the biomass and Cr(III) in solution

Genetic Evidence for Involvement of Neuronally Expressed S1P1 Receptor in Nociceptor Sensitization and Inflammatory Pain

Sphingosine-1-phosphate (S1P) is a key regulator of immune response. Immune cells, epithelia and blood cells generate high levels of S1P in inflamed tissue. However, it is not known if S1P acts on the endings of nociceptive neurons, thereby contributing to the generation of inflammatory pain. We found that the S1P1 receptor for S1P is expressed in subpopulations of sensory neurons including nociceptors. Both S1P and agonists at the S1P1 receptor induced hypersensitivity to noxious thermal stimulation in vitro and in vivo. S1P-induced hypersensitivity was strongly attenuated in mice lacking TRPV1 channels. S1P and inflammation-induced hypersensitivity was significantly reduced in mice with a conditional nociceptor-specific deletion of the S1P1 receptor. Our data show that neuronally expressed S1P1 receptors play a significant role in regulating nociceptor function and that S1P/S1P1 signaling may be a key player in the onset of thermal hypersensitivity and hyperalgesia associated with inflammation

Inclusive e+^+e−^- production in collisions of pions with protons and nuclei in the second resonance region of baryons

Inclusive e$^+$e$^-$ production has been studied with HADES in $\pi^-$ + p, $\pi^-$ + C and $\pi^- + \mathrm{CH}_2$ reactions, using the GSI pion beam at $\sqrt{s_{\pi p}}$ = 1.49 GeV. Invariant mass and transverse momentum distributions have been measured and reveal contributions from Dalitz decays of $\pi^0$, $\eta$ mesons and baryon resonances. The transverse momentum distributions are very sensitive to the underlying kinematics of the various processes. The baryon contribution exhibits a deviation up to a factor seven from the QED reference expected for the dielectron decay of a hypothetical point-like baryon with the production cross section constrained from the inverse $\gamma$ n$\rightarrow \pi^-$ p reaction. The enhancement is attributed to a strong four-momentum squared dependence of the time-like electromagnetic transition form factors as suggested by Vector Meson Dominance (VMD). Two versions of the VMD, that differ in the photon-baryon coupling, have been applied in simulations and compared to data. VMD1 (or two-component VMD) assumes a coupling via the $\rho$ meson and a direct coupling of the photon, while in VMD2 (or strict VMD) the coupling is only mediated via the $\rho$ meson. The VMD2 model, frequently used in transport calculations for dilepton decays, is found to overestimate the measured dielectron yields, while a good description of the data can be obtained with the VMD1 model assuming no phase difference between the two amplitudes. Similar descriptions have also been obtained using a time-like baryon transition form factor model where the pion cloud plays the major role.Comment: (HADES collaboration