Formation of (nitrooxy)organosulfates from organic peroxides and S(IV) via daytime and nighttime chemistry

Author(s):  
Martin Brüggemann ◽  
Matthieu Riva ◽  
Clement Dubois ◽  
Anke Mutzel ◽  
Christian George ◽  
...  

<p>Sulfur and nitrogen containing organic compounds, such as organosulfates (OSs) and nitrooxy organosulfates (NOSs), are recognized to be ubiquitously present in secondary organic aerosol (SOA). However, little is known about the chemical mechanisms or the required conditions for the formation of these compounds in the ambient atmosphere. Earlier studies have commonly suggested that OSs are predominantly formed through the reaction of organic gaseous epoxides with acidic sulfate particles. However, this epoxide pathway often fails to explain the formation of (N)OSs from monoterpenes. Moreover, recent studies highlight the potential role of gas-phase SO<sub>2</sub> and organic peroxides for the formation of OSs, which might serve as predominant precursors for OSs and NOSs from atmospheric monoterpene oxidation.</p><p>Here, we conducted a series of chamber experiments to elucidate the formation mechanisms of (N)OSs from α-pinene oxidation during daytime and nighttime conditions. In particular, we focused on the role of organic peroxides and S(IV) (i.e., gas-phase SO<sub>2</sub> and particulate SO<sub>3</sub><sup>2–</sup>) in contrast to organic epoxides and isotope-labelled particulate sulfate (i.e., S(VI)). SOA particles were analyzed online by extractive electrospray ionization coupled with high-resolution Orbitrap mass spectrometry (EESI-Orbitrap MS) allowing an unambiguous identification of OS and NOS species with a high time resolution. Additionally, filter samples were collected and analyzed by liquid chromatography (LC) coupled with Orbitrap MS to determine the presence of isomeric compounds.</p><p>Consistently, online and offline Orbitrap MS analysis showed that particulate sulfate played a minor role in the formation of OSs and NOSs. In contrast, (N)OSs were rapidly formed upon addition of either gaseous SO<sub>2</sub> or particulate SO<sub>3</sub><sup>2–</sup>, suggesting S(IV) to react with organic peroxides that were formed through monoterpene oxidation. Based on these experiments, we identified specific NOS species that are formed only through either daytime or nighttime chemistry, and thus, might serve as marker molecules. Moreover, we present complete formation pathways for these species. Our study indicates that in contrast to previous work, the formation of OSs and NOSs does not require acidic sulfate particles, but rather involves the reaction of organic peroxides with S(IV) in the gas phase or the particle phase.</p>

2020 ◽  
Vol 20 (9) ◽  
pp. 5513-5526 ◽  
Author(s):  
Xiaoning Xuan ◽  
Zhongming Chen ◽  
Yiwei Gong ◽  
Hengqing Shen ◽  
Shiyi Chen

Abstract. Hydrogen peroxide (H2O2) is a vital oxidant in the atmosphere and plays critical roles in the oxidation chemistry of both liquid and aerosol phases. The partitioning of H2O2 between the gas and liquid phases, or the aerosol phase, could affect its abundance in these condensed phases and eventually the formation of secondary components. However, the partitioning processes of H2O2 in gas-liquid and gas-aerosol phases are still unclear, especially in the ambient atmosphere. In this study, field observations of gas-, liquid-, and aerosol-phase H2O2 were carried out in the urban atmosphere of Beijing during the summer and winter of 2018. The effective field-derived mean value of Henry's law constant (HAm, 2.1×105 M atm−1) was 2.5 times of the theoretical value in pure water (HAt, 8.4×104 M atm−1) at 298±2 K. The effective derived gas-aerosol partitioning coefficient (KPm, 3.8×10-3 m3 µg−1) was 4 orders of magnitude higher on average than the theoretical value (KPt, 2.8×10-7 m3 µg−1) at 270±4 K. Beyond following Henry's law or Pankow's absorptive partitioning theory, the partitioning of H2O2 in the gas-liquid and gas-aerosol phases in the ambient atmosphere was also influenced by certain physical and chemical reactions. The average concentration of liquid-phase H2O2 in rainwater during summer was 44.12±26.49 µM. In 69 % of the collected rain samples, the measured level of H2O2 was greater than the predicted value in pure water calculated by Henry's law. In these samples, 41 % of the measured H2O2 was from gas-phase partitioning, while most of the rest may be from residual H2O2 in raindrops. In winter, the level of aerosol-phase H2O2 was 0.093±0.085 ng µg−1, which was much higher than the predicted value based on Pankow's absorptive partitioning theory. The contribution of partitioning of the gas-phase H2O2 to the aerosol-phase H2O2 formation was negligible. The decomposition/hydrolysis rate of aerosol-phase organic peroxides could account for 11 %–74 % of the consumption rate of aerosol-phase H2O2, and the value depended on the composition of organic peroxides in the aerosol particles. Furthermore, the heterogeneous uptake of HO2 and H2O2 on aerosols contributed to 22 % and 2 % of the aerosol-phase H2O2 consumption, respectively.


Sensors ◽  
2019 ◽  
Vol 19 (13) ◽  
pp. 2994 ◽  
Author(s):  
Valeria Demontis ◽  
Mirko Rocci ◽  
Maurizio Donarelli ◽  
Rishi Maiti ◽  
Valentina Zannier ◽  
...  

In this work, we isolate individual wurtzite InAs nanowires and fabricate electrical contacts at both ends, exploiting the single nanostructures as building blocks to realize two different architectures of conductometric sensors: (a) the nanowire is drop-casted onto—supported by—a SiO2/Si substrate, and (b) the nanowire is suspended at approximately 250 nm from the substrate. We test the source-drain current upon changes in the concentration of humidity, ethanol, and NO2, using synthetic air as a gas carrier, moving a step forward towards mimicking operational environmental conditions. The supported architecture shows higher response in the mid humidity range (50% relative humidity), with shorter response and recovery times and lower detection limit with respect to the suspended nanowire. These experimental pieces of evidence indicate a minor role of the InAs/SiO2 contact area; hence, there is no need for suspended nanostructures to improve the sensing performance. Moreover, the sensing capability of single InAs nanowires for detection of NO2 and ethanol in the ambient atmosphere is reported and discussed.


2021 ◽  
Author(s):  
Chuan Ping Lee ◽  
Mihnea Surdu ◽  
David M. Bell ◽  
Josef Dommen ◽  
Mao Xiao ◽  
...  

Abstract. To elucidate the sources and chemical reaction pathways of organic vapors and particulate matter in the ambient atmosphere, real-time detection of both gas and particle phase is needed. State-of-the-art techniques often suffer from thermal decomposition, ionization-induced fragmentation, high cut-off size of aerosols or low time resolution. In response to all these limitations, we developed a new technique that uses extractive electrospray ionization (EESI) for online gas and particle chemical speciation, namely the dual-phase extractive electrospray ionization time-of-flight mass spectrometer (Dual-Phase-EESI-TOF or Dual-EESI in short). The Dual-EESI was designed and optimized to measure gas- and particle-phase species with saturation vapor concentrations spanning more than 10 orders of magnitude with good linearity and a measurement cycle as fast as 3 min. The gas-phase selectivity of the Dual-EESI was compared with that of nitrate chemical ionization mass spectrometry. In addition, we performed organic aerosol uptake experiments to characterize the relative gas and particle response factors. In general, the Dual-EESI is more sensitive toward gas-phase analytes as compared to their particle-phase counterparts. The real-time measurement capability of the Dual-EESI for chemically speciated gas- and particle-phase measurements can provide new insights into aerosol sources or formation mechanisms, where gas-particle partitioning behavior can be determined after absolute parameterization of the gas/particle sensitivity.


Author(s):  
Katherine Guérard ◽  
Sébastien Tremblay

In serial memory for spatial information, some studies showed that recall performance suffers when the distance between successive locations increases relatively to the size of the display in which they are presented (the path length effect; e.g., Parmentier et al., 2005) but not when distance is increased by enlarging the size of the display (e.g., Smyth & Scholey, 1994). In the present study, we examined the effect of varying the absolute and relative distance between to-be-remembered items on memory for spatial information. We manipulated path length using small (15″) and large (64″) screens within the same design. In two experiments, we showed that distance was disruptive mainly when it is varied relatively to a fixed reference frame, though increasing the size of the display also had a small deleterious effect on recall. The insertion of a retention interval did not influence these effects, suggesting that rehearsal plays a minor role in mediating the effects of distance on serial spatial memory. We discuss the potential role of perceptual organization in light of the pattern of results.


2019 ◽  
Vol 12 (4) ◽  
pp. 311-323 ◽  
Author(s):  
Salvatore Benvenga ◽  
Antonio Micali ◽  
Giovanni Pallio ◽  
Roberto Vita ◽  
Consuelo Malta ◽  
...  

Background: Cadmium (Cd) impairs gametogenesis and damages the blood-testis barrier. Objective: As the primary mechanism of Cd-induced damage is oxidative stress, the effects of two natural antioxidants, myo-inositol (MI) and seleno-L-methionine (Se), were evaluated in mice testes. Methods: Eighty-four male C57 BL/6J mice were divided into twelve groups: 0.9% NaCl (vehicle; 1 ml/kg/day i.p.); Se (0.2 mg/kg/day per os); Se (0.4 mg/kg/day per os); MI (360 mg/kg/day per os); MI plus Se (0.2 mg/kg/day); MI plus Se (0.4 mg/kg/day); CdCl2 (2 mg/kg/day i.p.) plus vehicle; CdCl2 plus MI; CdCl2 plus Se (0.2 mg/kg/day); CdCl2 plus Se (0.4 mg/kg/day); CdCl2 plus MI plus Se (0.2 mg/kg/day); and CdCl2 plus MI plus Se (0.4 mg/kg/day). After 14 days, testes were processed for biochemical, structural and immunohistochemical analyses. Results: CdCl2 increased iNOS and TNF-α expression and Malondialdehyde (MDA) levels, lowered glutathione (GSH) and testosterone, induced testicular lesions, and almost eliminated claudin-11 immunoreactivity. Se administration at 0.2 or 0.4 mg/kg significantly reduced iNOS and TNF-α expression, maintained GSH, MDA and testosterone levels, structural changes and low claudin-11 immunoreactivity. MI alone or associated with Se at 0.2 or 0.4 mg/kg significantly reduced iNOS and TNF-α expression and MDA levels, increased GSH and testosterone levels, ameliorated structural organization and increased claudin-11 patches number. Conclusion: We demonstrated a protective effect of MI, a minor role of Se and an evident positive role of the association between MI and Se on Cd-induced damages of the testis. MI alone or associated with Se might protect testes in subjects exposed to toxicants, at least to those with behavior similar to Cd.


Biomedicines ◽  
2021 ◽  
Vol 9 (3) ◽  
pp. 317
Author(s):  
Simone Mesman ◽  
Iris Wever ◽  
Marten P. Smidt

During development, mesodiencephalic dopaminergic (mdDA) neurons form into different molecular subsets. Knowledge of which factors contribute to the specification of these subsets is currently insufficient. In this study, we examined the role of Tcf4, a member of the E-box protein family, in mdDA neuronal development and subset specification. We show that Tcf4 is expressed throughout development, but is no longer detected in adult midbrain. Deletion of Tcf4 results in an initial increase in TH-expressing neurons at E11.5, but this normalizes at later embryonic stages. However, the caudal subset marker Nxph3 and rostral subset marker Ahd2 are affected at E14.5, indicating that Tcf4 is involved in correct differentiation of mdDA neuronal subsets. At P0, expression of these markers partially recovers, whereas expression of Th transcript and TH protein appears to be affected in lateral parts of the mdDA neuronal population. The initial increase in TH-expressing cells and delay in subset specification could be due to the increase in expression of the bHLH factor Ascl1, known for its role in mdDA neuronal differentiation, upon loss of Tcf4. Taken together, our data identified a minor role for Tcf4 in mdDA neuronal development and subset specification.


2020 ◽  
Vol 500 (3) ◽  
pp. 3414-3424
Author(s):  
Alec Paulive ◽  
Christopher N Shingledecker ◽  
Eric Herbst

ABSTRACT Complex organic molecules (COMs) have been detected in a variety of interstellar sources. The abundances of these COMs in warming sources can be explained by syntheses linked to increasing temperatures and densities, allowing quasi-thermal chemical reactions to occur rapidly enough to produce observable amounts of COMs, both in the gas phase, and upon dust grain ice mantles. The COMs produced on grains then become gaseous as the temperature increases sufficiently to allow their thermal desorption. The recent observation of gaseous COMs in cold sources has not been fully explained by these gas-phase and dust grain production routes. Radiolysis chemistry is a possible non-thermal method of producing COMs in cold dark clouds. This new method greatly increases the modelled abundance of selected COMs upon the ice surface and within the ice mantle due to excitation and ionization events from cosmic ray bombardment. We examine the effect of radiolysis on three C2H4O2 isomers – methyl formate (HCOOCH3), glycolaldehyde (HCOCH2OH), and acetic acid (CH3COOH) – and a chemically similar molecule, dimethyl ether (CH3OCH3), in cold dark clouds. We then compare our modelled gaseous abundances with observed abundances in TMC-1, L1689B, and B1-b.


1989 ◽  
Vol 7 (4) ◽  
pp. 527-540 ◽  
Author(s):  
E G Levine ◽  
R A King ◽  
C D Bloomfield

Heredity is generally felt to play a minor role in the development of cancer. This review critically examines this assumption. Topics discussed include evidence for heritable predisposition in animals and humans; the potential importance of genetic-environmental interactions; approaches that are being used to successfully locate genes responsible for heritable predisposition; comparability of genetic findings among heritable and corresponding sporadic malignancies; and future research directions. Breast, colon, and lung cancer are used to exemplify clinical and research activity in familial cancer; clinical phenotypes, segregation and linkage analyses, models for environmental interactions with inherited traits, and molecular mechanisms of tumor development are discussed. We conclude that the contribution of heredity to the cancer burden is greater than generally accepted, and that study of heritable predisposition will continue to reveal carcinogenic mechanisms important to the development of all cancers.


2012 ◽  
Vol 12 (2) ◽  
pp. 1083-1100 ◽  
Author(s):  
W. Trivitayanurak ◽  
P. I. Palmer ◽  
M. P. Barkley ◽  
N. H. Robinson ◽  
H. Coe ◽  
...  

Abstract. We use a nested version of the GEOS-Chem global 3-D chemistry transport model to better understand the composition and variation of aerosol over Borneo and the broader Southeast Asian region in conjunction with aircraft and satellite observations. Our focus on Southeast Asia reflects the importance of this region as a source of reactive organic gases and aerosols from natural forests, biomass burning, and food and fuel crops. We particularly focus on July 2008 when the UK BAe-146 research aircraft was deployed over northern Malaysian Borneo as part of the ACES/OP3 measurement campaign. During July 2008 we find using the model that Borneo (defined as Borneo Island and the surrounding Indonesian islands) was a net exporter of primary organic aerosol (42 kT) and black carbon aerosol (11 kT). We find only 13% of volatile organic compound oxidation products partition to secondary organic aerosol (SOA), with Borneo being a net exporter of SOA (15 kT). SOA represents approximately 19% of the total organic aerosol over the region. Sulphate is mainly from aqueous-phase oxidation (68%), with smaller contributions from gas-phase oxidation (15%) and advection into the regions (14%). We find that there is a large source of sea salt, as expected, but this largely deposits within the region; we find that dust aerosol plays only a relatively small role in the aerosol burden. In contrast to coincident surface measurements over Northern Borneo that find a pristine environment with evidence for substantial biogenic SOA formation we find that the free troposphere is influenced by biomass burning aerosol transported from the northwest of the Island and further afield. We find several transport events during July 2008 over Borneo associated with elevated aerosol concentrations, none of which coincide with the aircraft flights. We use MODIS aerosol optical depths (AOD) data and the model to put the July campaign into a longer temporal perspective. We find that Borneo is where the model has the least skill at reproducing the data, where the model has a negative bias of 76% and only captures 14% of the observed variability. This model performance reflects the small-scale island-marine environment and the mix of aerosol species, with the model showing more skill at reproducing observed AOD over larger continental regions such as China where AOD is dominated by one aerosol type. The model shows that AOD over Borneo is approximately evenly split between organic and sulphate aerosol with sea salt representing 10–20% during May–September; we find a similar breakdown over continental Southeast Asia but with less sea salt aerosol and more dust aerosol. In contrast, East China AOD is determined mainly by sulphate aerosol and a seasonal source of dust aerosol, as expected. Realistic sensitivity runs, designed to test our underlying assumptions about emissions and chemistry over Borneo, show that model AOD is most sensitive to isoprene emissions and organic gas-phase partitioning but all fail to improve significantly upon the control model calculation. This emphasises the multi-faceted dimension of the problem and the need for concurrent and coordinated development of BVOC emissions, and BVOC chemistry and organic aerosol formation mechanisms.


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