Sequence structure emission in The Red Rectangle Bands

We report high resolution (R~37,000) integral field spectroscopy of the central region (r<14arcsec) of the Red Rectangle nebula surrounding HD44179. The observations focus on the 5800A emission feature, the bluest of the yellow/red emission bands in the Red Rectangle. We propose that the emission feature, widely believed to be a molecular emission band, is not a molecular rotation contour, but a vibrational contour caused by overlapping sequence bands from a molecule with an extended chromophore. We model the feature as arising in a Polycyclic Aromatic Hydrocarbon (PAH) with 45-100 carbon atoms.Comment: 13 pages, 9 figures, accepted for publication in ApJ. A version of the paper with full resolution figures is available at: http://www.aao.gov.au/local/www/rgs/Sequence-Structure

The new onset of dysphagia four years after anterior cervical discectomy and fusion: Case report and literature review.

Background: Dysphagia is a common complication immediately following anterior cervical spine surgery. However, its onset more than 1-year postoperatively is rare. Case Description: A 45-year-old male initially underwent a C3-4 and C5-6 anterior cervical discectomy and fusion (ACDF). At age 49, 4 years later, he presented with worsening dysphagia accompanied by neck and right upper extremity pain. Radiographs demonstrated an extruded left C3 screw, which had migrated into the prevertebral soft tissues at the C4-C5 level; there was also loosening of the right C3 screw. The subsequent barium swallow study revealed that the screw was embedded in the pharyngeal wall. The patient required a two-stage operation; first, to remove the anterior instrumentation, and second, to perform a posterior instrumented C2-T2 fusion. Conclusion: A barium swallow study and other dynamic imaging are a valuable component of the diagnostic workup and therapeutic intervention to evaluate the delayed onset dysphagia following an ACDF

Current assessment of the Red Rectangle band problem

In this paper we discuss our insights into several key problems in the identification of the Red Rectangle Bands (RRBs). We have combined three independent sets of observations in order to try to define the constraints guiding the bands. We provide a summary of the general behavior of the bands and review the evidence for a molecular origin of the bands. The extent, composition, and possible absorption effects of the bands are discussed. Comparison spectra of the strongest band obtained at three different spectral resolutions suggests that an intrinsic line width of individual rotational lines can be deduced. Spectroscopic models of several relatively simple molecules were examined in order to investigate where the current data are weak. Suggestions are made for future studies to enhance our understanding of these enigmatic bands

Effect of Gas Atmosphere on Catalytic Behaviour of Zirconia, Ceria and Ceria Zirconia Catalysts in Valeric Acid Ketonization

[EN] Ketonization of valeric acid, which can be obtained by lignocellulosic biomass conversion, was carried out in a fixed bed flow reactor over ZrO2, 5-20 % CeO2/ZrO2 and CeO2 both under hydrogen and nitrogen stream at 628 K and atmospheric pressure. Regardless gas-carrier 10 wt% CeO2/ZrO2 was found to show higher catalytic activity compared to zirconia per se as well as other ceria modified zirconia while ceria per se exhibited very low catalytic activity. All catalysts provided higher acid conversion in H-2 than in N-2 whereas selectivity to 5-nonanone was insensitive to gas atmosphere. XRD, FTIR, UV-Vis DRS, XPS, HRTEM methods were applied to characterize catalysts in reduced and unreduced states simulating corresponding reaction conditions during acid ketonization. XRD did not reveal any changes in zirconia and ceria/zirconia lattice parameters as well as crystalline phase depending on gas atmosphere while insertion of ceria in zirconia caused notable increase in lattice parameter indicating some distortion of crystalline structure. According to XPS, FTIR and UV-Vis methods, the carrier gas was found to affect catalyst surface composition leading to alteration in Lewis acid sites ratio. Appearance of Zr3+ cations was observed on the ZrO2 surface after hydrogen pretreatment whereas only Zr4+ cations were determined using nitrogen as a gas-carrier. These changes of catalyst's surface cation composition affected corresponding activity in ketonization probably being crucial for reaction mechanism involving metal cations catalytic centers for acid adsorption and COO- stabilization at the initial step.Financial support from the Russian Foundation of Basic Research (RFBR Grant No 11-03-94001-CSIC) is gratefully acknowledged. This work was supported by the Federal Program "Scientific and Educational Cadres of Russia'' (Grant No 2012-1.5-12-000-1013-002). The authors also wish to thank Dr. Evgeniy Gerasimov, Dr. Igor Prosvirin, Dr. Demid Demidov from the Department of Physicochemical Methods at the Boreskov Institute of Catalysis for TEM and XPS measurements.Zaytseva, YA.; Panchenko, VN.; Simonov, MN.; Shutilov, AA.; Zenkovets, GA.; Renz, M.; Simakova, IL.... (2013). Effect of Gas Atmosphere on Catalytic Behaviour of Zirconia, Ceria and Ceria Zirconia Catalysts in Valeric Acid Ketonization. Topics in Catalysis. 56(9-10):846-855. https://doi.org/10.1007/s11244-013-0045-yS846855569-10Alonso DM, Bond JQ, Dumesic JA (2010) Green Chem 12:1493–1513Serrano-Ruiz JC, Wang D, Dumesic JA (2010) Green Chem 12:574–577Malhotra SL, Wong RW, Breton MP (2002) Patent US 6461417Westfechtel A, Breucker C, Gutsche B, Jeromin L, Eierdanz H, Baumann H, Schmid KH, Nonnenkamp W (1993) Patent DE 4121117Seipel W, Hensen H, Boyxen N (2001) Patent DE 19958521Tomlinson AD (2001) Patent WO 2001094522Glinski M, Kijenski J, Jakubowski A (1995) Appl Catal A Gen 128:209–217Glinski M, Kijenski J (2000) React Kinet Catal Lett 69:123–128Parida K, Mishra HK (1999) J Mol Catal A Chem 139:73–80Serrano-Ruiz JC, Dumesic JA (2009) Green Chem 11:1101–1104Serrano-Ruiz JC, Dumesic JA (2009) ChemSusChem 2:581–586Leung A, Boocock DGB, Konar SK (1995) Energy Fuels 9:913–920Gaertner CA, Serrano-Ruiz JC, Braden DJ, Dumesic JA (2010) Ind Eng Chem Res 49:6027–6033Saito N (1996) Patent JP 08198796Yakerson VI, Rubinshtein AM, Gorskaya LA (1970) Patent GB 1208802Graille J, Pioch D (1991) Patent EP 457665Pioch D, Lescure R, Graille J (1995) Ol Corps Gras Lipides 2:386–389Mueller-Erlwein E, Rosenberger B (1990) Chem Ing Tech 62:512–513Corma A, Renz M, Schaverien C (2008) ChemSusChem 1:739–741Bayer (1911) Patent DE 256622Vavon G, Apchie A (1928) Bull Soc Chim 43:667–677Thorpe JF, Kon GAR (1941) Org Synth 1:192–194Nagashima O, Sato S, Takahashi R, Sodesawa T (2005) J Mol Catal A Chem 227:231–239Klein-Homann W (1988) Patent DE 3709765Stubenrauch J, Brisha E, Vohs JM (1996) Catal Today 28:431–441Pulido A, Oliver-Tomas B, Renz M, Boronat M, and Corma A (2013) ChemSusChem 6:141–151Hendren TS, Dooley KM (2003) Catal Today 85:333–351Novothy R, Paulsen S (1963) Patent DE 1158050Kim KS, Barteau MA (1990) J Catal 125:353–375Pestman R, Van Duijne A, Pieterse JAZ, Ponec V (1995) J Mol Catal A 103:175–180Martinez R, Huff MC, Barteau MA (2004) J Catal 222:404–409Matsuoka K, Tagawa K (1985) Patent JP 61207354Shutilov AA, Simonov MN, Zaytseva YuA, Zenkovets GA, and Simakova IL (2013) Kinet Catal 54:184–192Kuriacose JC, Swaminathan R (1969) J Catal 14:348–354Swaminathan R, Kuriacose JC (1970) J Catal 16:357–362Cressely J, Farkhani D, Deluzarche A, Kiennemann A (1984) Mater Chem Phys 11:413–431Kuriacose JC, Jewur SS (1977) J Catal 50:330–341Renz M, Corma A (2004) Eur J Org Chem 2004:2036–2039Taimoor AA, Favre-Reguillon A, Vanoye L, Pitault I (2012) Catal Sci Technol 2:359–363Kustov LM (1997) Top Catal 4:131–144Emmanuel NM (1978) Usp Khim 8:1329–1396Kaspar J, Fornasiero P (2002) In: Trovarelli A (ed) Catalysis by ceria and related materials. Imperial College Press, LondonReddy DD, Chowdhury B, Smirniotis PG (2001) Appl Catal A Gen 211:19–30Rango R, Kaspar G, Meriani S, di Monte R, Graziani M (1994) Catal Lett 24:107–112Rao G, Sahu H (2001) Proc Indian Acad Sci (Chem Sci) 113:651–658Navío JA, Hidalgo MC, Colón G, Botta SG, Litter MI (2001) Langmuir 17:202–210Timofeeva MN, Jhung SH, Hwang YK, Kim DK, Panchenko VN, Melgunov MS, Chesalov YA, Chang JS (2007) Appl Catal A Gen 317:1–10Kaneko H, Taku S, Tamaura Y (2011) Sol Energy 85:2321–2330Maia TA, Assaf JM, Assaf EM (2012) Mater Chem Phys 132:1029–1034Zhou HP, Si R, Song WG, Yan CH (2009) J Solid State Chem 182:2475–2485Si R, Zhang YW, Li SJ, Lin BX, Yan CH (2004) J Phys Chem B 108:12481–12488Hadjivanov KI, Vayssilov GN (2002) Adv Catal 47:307–511Vivier L, Duprez D (2010) ChemSusChem 3:654–678Vidruk R, Landau MV, Herskowitz M, Ezersky V, Goldbourt A (2011) J Catal 282:215–227Binet C, Daturi M, Lavalley JC (1999) Catal Today 50:207–225Conesa J (1995) Surf Sci 339:337–35

Russia’s Legal Transitions: Marxist Theory, Neoclassical Economics and the Rule of Law

We review the role of economic theory in shaping the process of legal change in Russia during the two transitions it experienced during the course of the twentieth century: the transition to a socialist economy organised along the lines of state ownership of the means of production in the 1920s, and the transition to a market economy which occurred after the fall of the Soviet Union in the 1990s. Despite differences in methodology and in policy implications, Marxist theory, dominant in the 1920s, and neoclassical economics, dominant in the 1990s, offered a similarly reductive account of law as subservient to wider economic forces. In both cases, the subordinate place accorded to law undermined the transition process. Although path dependence and history are frequently invoked to explain the limited development of the rule of law in Russia during the 1990s, policy choices driven by a deterministic conception of law and economics also played a role.This is the author accepted manuscript. The final version is available from Springer via http://dx.doi.org/10.1007/s40803-015-0012-

Insights into the ceria-catalyzed ketonization reaction for biofuels applications

The ketonization of small organic acids is a valuable reaction for biorenewable applications. Ceria has long been used as a catalyst for this reaction; however, under both liquid and vapor phase conditions, it was found that given the right temperature regime of about 150-300 °C, cerium oxide, which was previously believed to be a stable catalyst for ketonization, can undergo bulk transformations. This result, along with other literature reports, suggest that the long held belief of two separate reaction pathways for either bulk or surface ketonization reactions are not required to explain the interaction of cerium oxide with organic acids. X-ray photon spectroscopy, scanning electron microscopy, and temperature programmed decomposition results supported the formation of metal acetates and explained the occurrence of cerium reduction as well as the formation of cerium oxide/acetate whiskers. After thermogravimetry/mass spectrometry and FT-IR experiments, a single reaction sequence is proposed that can be applied to either surface or bulk reactions with ceria

The Chlorophyll Catabolite, Pheophorbide a, Confers Predation Resistance in a Larval Tortoise Beetle Shield Defense

Larval insect herbivores feeding externally on leaves are vulnerable to numerous and varied enemies. Larvae of the Neotropical herbivore, Chelymorpha alternans (Chrysomelidae:Cassidinae), possess shields made of cast skins and feces, which can be aimed and waved at attacking enemies. Prior work with C. alternans feeding on Merremia umbellata (Convolvulaceae) showed that shields offered protection from generalist predators, and polar compounds were implicated. This study used a ubiquitous ant predator, Azteca lacrymosa, in field bioassays to determine the chemical constitution of the defense. We confirmed that intact shields do protect larvae and that methanol-water leaching significantly reduced shield effectiveness. Liquid chromatography-mass spectrometry (LC-MS) of the methanolic shield extract revealed two peaks at 20.18 min and 21.97 min, both with a molecular ion at m/z 593.4, and a strong UV absorption around 409 nm, suggesting a porphyrin-type compound. LC-MS analysis of a commercial standard confirmed pheophorbide a (Pha) identity. C. alternans shields contained more than 100 μg Pha per shield. Shields leached with methanol-water did not deter ants. Methanol-water-leached shields enhanced with 3 μg of Pha were more deterrent than larvae with solvent-leached shields, while those with 5 μg additional Pha provided slightly less deterrence than larvae with intact shields. Solvent-leached shields with 10 μg added Pha were comparable to intact shields, even though the Pha concentration was less than 10% of its natural concentration. Our findings are the first to assign an ecological role for a chlorophyll catabolite as a deterrent in an insect defense

Sorting Signals, N-Terminal Modifications and Abundance of the Chloroplast Proteome

Characterization of the chloroplast proteome is needed to understand the essential contribution of the chloroplast to plant growth and development. Here we present a large scale analysis by nanoLC-Q-TOF and nanoLC-LTQ-Orbitrap mass spectrometry (MS) of ten independent chloroplast preparations from Arabidopsis thaliana which unambiguously identified 1325 proteins. Novel proteins include various kinases and putative nucleotide binding proteins. Based on repeated and independent MS based protein identifications requiring multiple matched peptide sequences, as well as literature, 916 nuclear-encoded proteins were assigned with high confidence to the plastid, of which 86% had a predicted chloroplast transit peptide (cTP). The protein abundance of soluble stromal proteins was calculated from normalized spectral counts from LTQ-Obitrap analysis and was found to cover four orders of magnitude. Comparison to gel-based quantification demonstrates that ‘spectral counting’ can provide large scale protein quantification for Arabidopsis. This quantitative information was used to determine possible biases for protein targeting prediction by TargetP and also to understand the significance of protein contaminants. The abundance data for 550 stromal proteins was used to understand abundance of metabolic pathways and chloroplast processes. We highlight the abundance of 48 stromal proteins involved in post-translational proteome homeostasis (including aminopeptidases, proteases, deformylases, chaperones, protein sorting components) and discuss the biological implications. N-terminal modifications were identified for a subset of nuclear- and chloroplast-encoded proteins and a novel N-terminal acetylation motif was discovered. Analysis of cTPs and their cleavage sites of Arabidopsis chloroplast proteins, as well as their predicted rice homologues, identified new species-dependent features, which will facilitate improved subcellular localization prediction. No evidence was found for suggested targeting via the secretory system. This study provides the most comprehensive chloroplast proteome analysis to date and an expanded Plant Proteome Database (PPDB) in which all MS data are projected on identified gene models