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Sample records for biogenic iron oxyhydroxide

  1. Biogenic iron oxyhydroxide formation at mid-ocean ridge hydrothermal vents: Juan de Fuca Ridge

    Energy Technology Data Exchange (ETDEWEB)

    Toner, Brandy M.; Santelli, Cara M.; Marcus, Matthew A.; Wirth, Richard; Chan, Clara S.; McCollom, Thomas; Bach, Wolfgang; Edwards, Katrina J.

    2008-05-22

    Here we examine Fe speciation within Fe-encrusted biofilms formed during 2-month seafloor incubations of sulfide mineral assemblages at the Main Endeavor Segment of the Juan de Fuca Ridge. The biofilms were distributed heterogeneously across the surface of the incubated sulfide and composed primarily of particles with a twisted stalk morphology resembling those produced by some aerobic Fe-oxidizing microorganisms. Our objectives were to determine the form of biofilm-associated Fe, and identify the sulfide minerals associated with microbial growth. We used micro-focused synchrotron-radiation X-ray fluorescence mapping (mu XRF), X-ray absorption spectroscopy (mu EXAFS), and X-ray diffraction (mu XRD) in conjunction with focused ion beam (FIB) sectioning, and highresolution transmission electron microscopy (HRTEM). The chemical and mineralogical composition of an Fe-encrusted biofilm was queried at different spatial scales, and the spatial relationship between primary sulfide and secondary oxyhydroxide minerals was resolved. The Fe-encrusted biofilms formed preferentially at pyrrhotite-rich (Fe1-xS, 0<_ x<_ 0.2) regions of the incubated chimney sulfide. At the nanometer spatial scale, particles within the biofilm exhibiting lattice fringing and diffraction patterns consistent with 2-line ferrihydrite were identified infrequently. At the micron spatial scale, Fe mu EXAFS spectroscopy and mu XRD measurements indicate that the dominant form of biofilm Fe is a short-range ordered Fe oxyhydroxide characterized by pervasive edge-sharing Fe-O6 octahedral linkages. Double corner-sharing Fe-O6 linkages, which are common to Fe oxyhydroxide mineral structures of 2-line ferrihydrite, 6-line ferrihydrite, and goethite, were not detected in the biogenic iron oxyhydroxide (BIO). The suspended development of the BIO mineral structure is consistent with Fe(III) hydrolysis and polymerization in the presence of high concentrations of Fe-complexing ligands. We hypothesize that

  2. Biogenic iron oxyhydroxide formation at mid-ocean ridge hydrothermal vents: Juan de Fuca Ridge

    International Nuclear Information System (INIS)

    Here we examine Fe speciation within Fe-encrusted biofilms formed during 2-month seafloor incubations of sulfide mineral assemblages at the Main Endeavor Segment of the Juan de Fuca Ridge. The biofilms were distributed heterogeneously across the surface of the incubated sulfide and composed primarily of particles with a twisted stalk morphology resembling those produced by some aerobic Fe-oxidizing microorganisms. Our objectives were to determine the form of biofilm-associated Fe, and identify the sulfide minerals associated with microbial growth. We used micro-focused synchrotron-radiation X-ray fluorescence mapping (mu XRF), X-ray absorption spectroscopy (mu EXAFS), and X-ray diffraction (mu XRD) in conjunction with focused ion beam (FIB) sectioning, and high-resolution transmission electron microscopy (HRTEM). The chemical and mineralogical composition of an Fe-encrusted biofilm was queried at different spatial scales, and the spatial relationship between primary sulfide and secondary oxyhydroxide minerals was resolved. The Fe-encrusted biofilms formed preferentially at pyrrhotite-rich (Fe1-xS, 0 (le) x (le) 0.2) regions of the incubated chimney sulfide. At the nanometer spatial scale, particles within the biofilm exhibiting lattice fringing and diffraction patterns consistent with 2-line ferrihydrite were identified infrequently. At the micron spatial scale, Fe mu EXAFS spectroscopy and mu XRD measurements indicate that the dominant form of biofilm Fe is a short-range ordered Fe oxyhydroxide characterized by pervasive edge-sharing Fe-O6 octahedral linkages. Double corner-sharing Fe-O6 linkages, which are common to Fe oxyhydroxide mineral structures of 2-line ferrihydrite, 6-line ferrihydrite, and goethite, were not detected in the biogenic iron oxyhydroxide (BIO). The suspended development of the BIO mineral structure is consistent with Fe(III) hydrolysis and polymerization in the presence of high concentrations of Fe-complexing ligands. We hypothesize that

  3. Mineralogy and inorganic chemistry of naturally occurring biogenic iron oxyhydroxides: Spectroscopic evidence of thermal maturation

    Science.gov (United States)

    Haddad, A.; Fakra, S.; Orcutt, B. N.; Toner, B.; Edwards, K. J.

    2011-12-01

    Microbial mats were sampled at four sites at the Lo'ihi Seamount and examined for changes in mineralogy and inorganic chemistry via synchrotron-sourced X-ray Absorption Spectroscopy (XAS). These mats are rich in iron oxyhydroxides with morphologies similar to those produced by iron oxidizing microorganisms related to Zetaproteobacteria such as Mariprofundus ferroxydans, which have been shown to be present and active in all of these mat ecosystems. The same particle morphologies are observed consistently at all four sites, which range in temperature (4 - 40°C) and hydrothermal activity (dead to very active). Fe L-edge XAS reveals no significant differences in Fe speciation between the morphologies. Mineralogy, however, as reflected in O 1s XAS measurements, appears to be a function of thermal maturation with the hottest site harboring more crystalline particles. Morphology does not factor into the changes in mineralogy. These measurements are confirmed by Fe 1s XAS spectroscopy. The C 1s XAS spectroscopy is highly variable and may be related to overall maturation (age) or undetermined factors. Elucidating the effect of thermal maturation on biogenic iron oxhydroxide particles is essential to understanding the environmental influences on their preservation in the rock record.

  4. Iron oxyhydroxide mineralization on microbial extracellular polysaccharides

    Energy Technology Data Exchange (ETDEWEB)

    Chan, Clara S.; Fakra, Sirine C.; Edwards, David C.; Emerson, David; Banfield, Jillian F.

    2010-06-22

    Iron biominerals can form in neutral pH microaerophilic environments where microbes both catalyze iron oxidation and create polymers that localize mineral precipitation. In order to classify the microbial polymers that influence FeOOH mineralogy, we studied the organic and mineral components of biominerals using scanning transmission X-ray microscopy (STXM), micro X-ray fluorescence ({mu}XRF) microscopy, and high-resolution transmission electron microscopy (HRTEM). We focused on iron microbial mat samples from a creek and abandoned mine; these samples are dominated by iron oxyhydroxide-coated structures with sheath, stalk, and filament morphologies. In addition, we characterized the mineralized products of an iron-oxidizing, stalk-forming bacterial culture isolated from the mine. In both natural and cultured samples, microbial polymers were found to be acidic polysaccharides with carboxyl functional groups, strongly spatially correlated with iron oxyhydroxide distribution patterns. Organic fibrils collect FeOOH and control its recrystallization, in some cases resulting in oriented crystals with high aspect ratios. The impact of polymers is particularly pronounced as the materials age. Synthesis experiments designed to mimic the biomineralization processes show that the polysaccharide carboxyl groups bind dissolved iron strongly but release it as mineralization proceeds. Our results suggest that carboxyl groups of acidic polysaccharides are produced by different microorganisms to create a wide range of iron oxyhydroxide biomineral structures. The intimate and potentially long-term association controls the crystal growth, phase, and reactivity of iron oxyhydroxide nanoparticles in natural systems.

  5. Magnetic birefringence of iron oxyhydroxide nanoparticles stabilised by sucrose

    International Nuclear Information System (INIS)

    Magnetically induced optical birefringence is used to investigate pharmaceutically important iron-sucrose aqueous suspensions. XRD and TEM measurements of the system of oxyhydroxide particles stabilised by sucrose have shown that this system contains iron oxyhydroxide in the form of 2-5 nm particles. The mineral form of the iron-core is suggested to be akaganeite. Anisotropy of the optical polarizability and magnetic susceptibility of akaganeite nanoparticles are calculated. The permanent dipole moment obtained for the nanoparticles studied was found to be negligible, in agreement with the characteristic superparamagnetic behaviour of the magnetic nanoparticles observed at room temperature. The Neel temperature of these nanoparticles is estimated as below 276 K. The results obtained are discussed against a background of the earlier studies of similar nanoscale systems. - Research highlights: → Polysaccharides iron complex, important in pharmaceutical applications, was studied by magnetic birefringence. → Magnetic and optical properties of the akaganeite core has been obtained. The superparamagnetic behaviour of the core has been confirmed. → The experiment suggests that the Neel temperature of these nanoparticles should be set below 276 K. The results show the importance of the magneto-optical method in recognition of magnetic properties of biologically important substances.

  6. Biogenic nitrogen and carbon in Fe-Mn-oxyhydroxides from an Archean chert, Marble Bar, Western Australia

    Science.gov (United States)

    Pinti, Daniele L.; Hashizume, Ko; Orberger, Beate; Gallien, Jean-Paul; Cloquet, Christophe; Massault, Marc

    2007-02-01

    To quantify and localize nitrogen (N) and carbon (C) in Archean rocks from the Marble Bar formation, Western Australia, and to gain insights on their origin and potential biogenicity, we conducted nuclear reaction analyses (NRA) and carbon and nitrogen isotope ratio measurements on various samples from the 3460-Myr-old Fe-rich Marble Bar chert. The Marble Bar chert formed during the alteration of basaltic volcanoclastic rocks with Fe- and Si-rich hydrothermal fluids, and the subsequent precipitation of magnetite, carbonates, massive silica, and, locally, sulfides. At a later stage, the magnetite, sulfides, and carbonates were replaced by Fe-Mn-oxyhydroxides. Nuclear reaction analyses indicate that most of the N and C resides within these Fe-Mn-oxyhydroxides, but a minor fraction is found in K-feldspars and Ba-mica dispersed in the silica matrix. The N and C isotopic composition of Fe-oxides suggests the presence of a unique biogenic source with δ 15NAIR values from +6.0 +/- 0.5‰ to 7.3 +/- 1.1‰ and a δ 13CPDB value of -19.9 +/- 0.1‰. The C and N isotope ratios are similar to those observed in Proterozoic and Phanerozoic organic matter. Diffusion-controlled fractionation of N and C released during high combustion temperatures indicates that these two elements are firmly embedded within the iron oxides, with activation energies of 18.7 +/- 3.7 kJ/mol for N and 13.0 +/- 3.8 kJ/mol for C. We propose that N and C were chemisorbed on iron and were subsequently embedded in the crystals during iron oxidation and crystal growth. The Fe-isotopic composition of the Marble Bar chert (δ 56Fe = -0.38 +/- 0.02‰) is similar to that measured in iron oxides formed by direct precipitation of iron from hydrothermal plumes in contact with oxygenated waters. To explain the N and C isotopic composition of Marble Bar chert, we propose either (1) a later addition of N and C at the end of Archean when oxygen started to rise or (2) an earlier development of localized oxygenated

  7. Iron (III) oxyhydroxide in isopropyl alcohol preparation, characterization and solvothermal treatment

    International Nuclear Information System (INIS)

    Iron (III) nitrate hydrolysis was carried out in isopropyl alcohol solution by an aqueous amonia gas stream resulting in iron (III) oxyhydroxide sol. It has been investigated in this work the solvothermal treatment of this colloidal system at 1200C and 24 hours. Iron (III) oxyhydroxide freshly obtained and solvothermally treated. Samples were dryed by lyophilization. Products obtained were characterized by the following techniques: spectrophotometric iron analysis by 1,10-orthophenantroline complexation method, powder X-ray diffraction, vibrational infrared spectra and differential thermal analysis. After solvothermal treatment resulting product was crystallized into hematite, while freshly iron (III) oxyhydroxide was non crystalline. Both of them are very active powder, showing high water adsorption

  8. Generation of hydrothermal Fe-Si oxyhydroxide deposit on the Southwest Indian Ridge and its implication for the origin of ancient banded iron formations

    Science.gov (United States)

    Sun, Zhilei; Li, Jun; Huang, Wei; Dong, Hailiang; Little, Crispin T. S.; Li, Jiwei

    2015-01-01

    hydrothermal Fe-Si oxyhydroxide deposits are now known to be analogues to ancient siliceous iron formations. In this study, samples of Fe-Si oxyhydroxide deposits were collected from hydrothermal field on the Southwest Indian Ridge. An investigation of mineralization in these deposits was carried out based on a series of mineralogical and morphological methods. X-ray diffraction and selected area electron diffraction analysis show that amorphous opal and poorly crystalline ferrihydrite are the major minerals. Furthermore, some typical filament structures detected by scanning electronic microscopy examinations, probably indicating the presence of Fe-oxidizing bacteria (FeOB), are pervasive with the main constituents being Fe, Si, P, and C. We thus believe that chemolithoautotrophic FeOB play a significant role in the formation of Fe oxyhydroxide which can effectively oxidize reduced Fe(II) sourced from hydrothermal fluids. Precipitation of amorphous silica, in contrast, is only a passive process with the Fe oxyhydroxide acting as a template. The distinct microlaminae structure alternating between the Fe-rich and Si-rich bands was observed in our samples for the first time in modern seafloor hydrothermal systems. We propose that its formation was due to the episodic temperature variation of the hydrothermal fluid which controls the biogenic Fe oxyhydroxide formation and passive precipitation of silica in this system. Our results might provide a clue for the formation mechanism of ancient banded iron formations.

  9. Removal of U(VI) from aqueous solutions by the nano-iron oxyhydroxides

    International Nuclear Information System (INIS)

    The nano-iron oxyhydroxides (α- and γ-FeOOH) were synthesized by oxidation of the various raw materials (FeSO4 and FeCl2) as iron precursors under alkaline conditions. Morphologies of nano-iron oxyhydroxides were characterized by high resolution transmission electron microscope (HRTEM), X-ray powder diffraction (XRD) and specific surface area (SSA), respectively. The removal of U(VI) from aqueous solution by nano-iron oxyhydroxides was also investigated as a function of contact time, U(VI) concentration, pH, ionic strength and temperature under ambient conditions. The occurrence of needle-like shape of nano-goethite and rod-like shape of nano- lepidocrocite were attributed to oxidization of Fe2+ under different conditions in terms of XRD analysis and HRTEM images. The sorption results indicated that the removal of U(VI) strongly depended on pH and were independent of ionic strength. Langmuir model was employed to model the sorption isotherms of U(VI) at three various temperatures of 293, 313 and 333 K. The thermodynamic parameters (ΔH , ΔS and ΔG ) computed from the temperature showed that sorption process of U(VI) on nano-iron oxyhydroxides was endothermic and spontaneous. The mechanism of U(VI) sorption on nano-iron oxyhydroxides was assumed to outer-sphere surface complexation at low pH (pH 4), whereas the uptake of U(VI) was dominated by surface precipitation at high pH conditions. Thereby nano-iron oxyhydroxides can be used as an efficient backfill materials for the in situ disposal of U(VI)-bearing contaminated groundwater. (orig.)

  10. Enhanced oxygen evolution at hydrous oxy-hydroxide modified iron electrodes in aqueous alkaline solution

    OpenAIRE

    Lyons, Michael; Doyle, Richard

    2011-01-01

    Outstanding issues regarding the film formation and the oxygen evolution reaction (OER) electrocatalytic behaviour of multicycled iron oxyhydroxide films in aqueous alkaline solution have been revisited. The oxide is grown using a repetitive poltential multicycling technique, and the mechanism of the latter hydrous oxide formation process has been discussed. A duplex layer model of the oxide/solution interphase region is proposed. The acid/base behaviour of the hydrous oxide and the microdisp...

  11. Redox switching and oxygen evolution electrocatalysis in polymeric iron oxyhydroxide films

    OpenAIRE

    LYONS, MICHAEL EDWARD

    2009-01-01

    Outstanding issues regarding the redox switching characteristics and the oxygen evolution reaction (OER) electrocatalytic behaviour of multicycled iron oxyhydroxide films in aqueous alkaline solution have been examined. Charge percolation through the hydrous layer has been quantified, using cyclic voltammetry, in terms of a charge transport diffusion coefficient DCT which admits a value of ca. 3 ? 10-10 cm2 s-1. Steady-state Tafel plot analysis and electrochemical impedance spectroscopy have ...

  12. Higher Molecular Mass Organic Matter Molecules Compete with Orthophosphate for Adsorption to Iron (Oxy)hydroxide.

    Science.gov (United States)

    Chassé, Alexander W; Ohno, Tsutomu

    2016-07-19

    The competition between orthophosphate and water-extractable organic matter (WEOM) for adsorption to iron (oxy)hydroxide mineral surfaces is an important factor in determining the plant bioavailability of P in soils. Chemical force spectroscopy was used to determine the binding force between orthophosphate and iron (oxy)hydroxide that was coated onto atomic force microscopy (AFM) tips and adsorbed with WEOM. The force measurements were conducted at pH 4.65 and 0.02 M ionic strength which are representative of typical acid soil solutions. The chemical composition of the WEOM was determined by ultrahigh resolution electrospray ionization Fourier transform ion cyclotron mass spectrometry. The results indicate a correlation between aromatic WEOM molecules that are greater than 600 Da and the reduced binding force of orthophosphate to WEOM-adsorbed iron (oxy)hydroxide AFM tips suggesting that the molecular mass of aromatic WEOM molecules plays a critical role in regulating the WEOM-P interactions with surface functional groups of minerals. Based on the results of this study, we show the importance of obtaining a detailed, molecular-scale understanding of soil processes that can help develop better management strategies to reduce waste of limited P resources and adverse environmental impacts. Specifically, soil amendments with greater content of high molecular mass aromatic components may positively affect dissolved P use efficiency in soils by maintaining P in soil solution. PMID:27362894

  13. The role of SO42- surface distribution in arsenic removal by iron oxy-hydroxides

    Science.gov (United States)

    Tresintsi, S.; Simeonidis, K.; Pliatsikas, N.; Vourlias, G.; Patsalas, P.; Mitrakas, M.

    2014-05-01

    This study investigates the contribution of chemisorbed SO42- in improving arsenic removal properties of iron oxy-hydroxides through an ion-exchange mechanism. An analytical methodology was developed for the accurate quantification of sulfate ion (SO42-) distribution onto the surface and structural compartments of iron oxy-hydroxides synthesized by FeSO4 precipitation. The procedure is based on the sequential determination of SO42- presence in the diffuse and Stern layers, and the structure of these materials as defined by the sulfate-rich environments during the reaction and the variation in acidity (pH 3-12). Physically sorbed SO42-, extracted in distilled water, and physically/chemically adsorbed ions on the oxy-hydroxide's surface leached by a 5 mM NaOH solution, were determined using ion chromatography. Total sulfate content was gravimetrically measured by precipitation as BaSO4. To validate the suggested method, results were verified by X-ray photoelectron and Fourier-transformed infrared spectroscopy. Results showed that low precipitation pH-values favor the incorporation of sulfate ions into the structure and the inner double layer, while under alkaline conditions ions shift to the diffuse layer.

  14. The investigation of iron oxyhydroxides precipitation process by potentiometric titration method

    OpenAIRE

    Abuzarova, Kamila

    2013-01-01

    It was investigated the iron oxyhydroxide precipitation process by potentiometric titration method of such systems: Fe₂(SO₄)₃-X-H₂O, Fe(NO₃)₃-X-H₂O, FeCl₃-XH₂O, where X – NH₄OH, Na₂CO₃, CO(NH₂)₂. It was determined the optimum ratio (equivalent) between the amount of a precipitator and an initial salt solution on the base of the experimental data. It was assumed previous conditions of carrying out the precipitation process for this ratio.

  15. Controls on the Fate and Speciation of Np(V) During Iron (Oxyhydr)oxide Crystallization.

    Science.gov (United States)

    Bots, Pieter; Shaw, Samuel; Law, Gareth T W; Marshall, Timothy A; Mosselmans, J Frederick W; Morris, Katherine

    2016-04-01

    The speciation and fate of neptunium as Np(V)O2(+) during the crystallization of ferrihydrite to hematite and goethite was explored in a range of systems. Adsorption of NpO2(+) to iron(III) (oxyhydr)oxide phases was reversible and, for ferrihydrite, occurred through the formation of mononuclear bidentate surface complexes. By contrast, chemical extractions and X-ray absorption spectroscopy (XAS) analyses showed the incorporation of Np(V) into the structure of hematite during its crystallization from ferrihydrite (pH 10.5). This occurred through direct replacement of octahedrally coordinated Fe(III) by Np(V) in neptunate-like coordination. Subsequent analyses on mixed goethite and hematite crystallization products (pH 9.5 and 11) showed that Np(V) was incorporated during crystallization. Conversely, there was limited evidence for Np(V) incorporation during goethite crystallization at the extreme pH of 13.3. This is likely due to the formation of a Np(V) hydroxide precipitate preventing incorporation into the goethite particles. Overall these data highlight the complex behavior of Np(V) during the crystallization of iron(III) (oxyhydr)oxides, and demonstrate clear evidence for neptunium incorporation into environmentally important mineral phases. This extends our knowledge of the range of geochemical conditions under which there is potential for long-term immobilization of radiotoxic Np in natural and engineered environments. PMID:26913955

  16. Using Magnetism to Characterize and Distinguish High Coercivity Iron Oxide and Oxyhydroxide Minerals in Atmospheric Dust

    Science.gov (United States)

    Yauk, Kimberly E.

    Natural atmospheric dust samples collected from the American southwest and globally were measured using magnetic methods in order to separate remanence attributed to the high coercivity iron oxide and oxyhydroxide minerals hematite and goethite. Dust collected from mountain snow and dust source areas in nearby arid plains were analyzed using traditional room- and low temperature methods. Additional methods were created to better examine the weak, high coercivity components. Combinations of high fields (2.5-9 T), low temperatures (10-300 K), partial AF demagnetization, and thermal demagnetization to 400 K were implemented to separate each component. Percentages of remanence attributed to magnetite, hematite, and goethite were compared to results found by HIRM (hard isothermal remanent magnetization) and Mossbauer spectroscopy with good correlation and to coercivity unmixing methods without correlation. TRM (thermoremanent magnetization) was found to be an important step in magnetizing a greater portion of the goethite fraction. Further procedures for characterizing nano grain sizes would be illuminating.

  17. The irony of iron -- biogenic iron oxides as an iron source to the ocean

    Directory of Open Access Journals (Sweden)

    David eEmerson

    2016-01-01

    Full Text Available Primary productivity in at least a third of the sunlit open ocean is thought to be iron-limited. Primary sources of dissolved iron (dFe to the ocean are hydrothermal venting, flux from the sediments along continental margins, and airborne dust. This article provides a general review of sources of hydrothermal and sedimentary iron to the ocean, and speculates upon the role that iron-cycling microbes play in controlling iron dynamics from these sources. Special attention is paid to iron-oxidizing bacteria (FeOB that live by oxidizing iron and producing biogenic iron oxides as waste products. The presence and ubiquity of FeOB both at hydrothermal systems and in sediments is only beginning to be appreciated. The biogenic oxides they produce have unique properties that could contribute significantly to the dynamics of dFe in the ocean. Changes in the physical and chemical characteristics of the ocean due to climate change and ocean acidification will undoubtedly impact the microbial iron cycle. A better understanding of the contemporary role of microbes in the iron cycle will help in predicting how these changes could ultimately influence marine primary productivity.

  18. Antagonistic effects of humic acid and iron oxyhydroxide grain-coating on biochar nanoparticle transport in saturated sand.

    Science.gov (United States)

    Wang, Dengjun; Zhang, Wei; Zhou, Dongmei

    2013-05-21

    Biochar land application may result in multiple agronomic and environmental benefits (e.g., carbon sequestration, improving soil quality, and immobilizing environmental contaminants). However, our understanding of biochar particle transport is largely unknown in natural environments with significant heterogeneity in solid (e.g., patches of iron oxyhydroxide coating) and solution chemistry (e.g., the presence of natural organic matter), which represents a critical knowledge gap in assessing the environmental impact of biochar land application. Transport and retention kinetics of nanoparticles (NPs) from wheat straw biochars produced at two pyrolysis temperatures (i.e., 350 and 550 °C) were investigated in water-saturated sand columns at environmentally relevant concentrations of dissolved humic acid (HA, 0, 1, 5, and 10 mg L(-1)) and fractional surface coverage of iron oxyhydroxide coatings on sand grains (ω, 0.16, 0.28, and 0.40). Transport of biochar NPs increased with increasing HA concentration, largely because of enhanced repulsive interaction energy between biochar NPs and sand grains. Conversely, transport of biochar NPs decreased significantly with increasing ω due to enhanced electrostatic attraction between negatively charged biochar NPs and positively charged iron oxyhydroxides. At a given ω of 0.28, biochar NPs were less retained with increasing HA concentration due to increased electrosteric repulsion between biochar NPs and sand grains. Experimental breakthrough curves and retention profiles were well described using a two-site kinetic retention model that accounted for Langmuirian blocking or random sequential adsorption at one site. Consistent with the blocking effect, the often observed flat retention profiles stemmed from decreased retention rate and/or maximum retention capacity at a higher HA concentration or smaller ω. The antagonistic effects of HA and iron oxyhydroxide grain-coating imparted on the mobility of biochar NPs suggest that

  19. Humic acid facilitates the transport of ARS-labeled hydroxyapatite nanoparticles in iron oxyhydroxide-coated sand.

    Science.gov (United States)

    Wang, Dengjun; Bradford, Scott A; Harvey, Ronald W; Gao, Bin; Cang, Long; Zhou, Dongmei

    2012-03-01

    Hydroxyapatite nanoparticles (nHAP) have been widely used to remediate soil and wastewater contaminated with metals and radionuclides. However, our understanding of nHAP transport and fate is limited in natural environments that exhibit significant variability in solid and solution chemistry. The transport and retention kinetics of Alizarin red S (ARS)-labeled nHAP were investigated in water-saturated packed columns that encompassed a range of humic acid concentrations (HA, 0-10 mg L(-1)), fractional surface coverage of iron oxyhydroxide coatings on sand grains (λ, 0-0.75), and pH (6.0-10.5). HA was found to have a marked effect on the electrokinetic properties of ARS-nHAP, and on the transport and retention of ARS-nHAP in granular media. The transport of ARS-nHAP was found to increase with increasing HA concentration because of enhanced colloidal stability and the reduced aggregate size. When HA = 10 mg L(-1), greater ARS-nHAP attachment occurred with increasing λ because of increased electrostatic attraction between negatively charged nanoparticles and positively charged iron oxyhydroxides, although alkaline conditions (pH 8.0 and 10.5) reversed the surface charge of the iron oxyhydroxides and therefore decreased deposition. The retention profiles of ARS-nHAP exhibited a hyperexponential shape for all test conditions, suggesting some unfavorable attachment conditions. Retarded breakthrough curves occurred in sands with iron oxyhydroxide coatings because of time-dependent occupation of favorable deposition sites. Consideration of the above effects is necessary to improve remediation efficiency of nHAP for metals and actinides in soils and subsurface environments. PMID:22316080

  20. Associations between iron oxyhydroxide nanoparticle growth and metal adsorption/structural incorporation

    Energy Technology Data Exchange (ETDEWEB)

    Kim, C.S.; Lentini, C.J.; Waychunas, G.A.

    2008-09-15

    The interaction of metal ions and oxyanions with nanoscale mineral phases has not yet been extensively studied despite the increased recognition of their prevalence in natural systems as a significant component of geomedia. A combination of macroscopic uptake studies to investigate the adsorption behavior of As(V), Cu(II), Hg(II), and Zn(II) onto nanoparticulate goethite ({alpha}-FeOOH) as a function of aging time at elevated temperature (75 C) and synchrotron-based X-ray studies to track changes in both the sorption mode and the rate of nanoparticle growth reveal the effects that uptake has on particle growth. Metal(loid) species which sorb quickly to the iron oxyhydroxide particles (As(V), Cu(II)) appear to passivate the particle surface, impeding the growth of the nanoparticles with progressive aging; in contrast, species that sorb more slowly (Hg(II), Zn(II)) have considerably less impact on particle growth. Progressive changes in the speciation of these particular metals with time suggest shifts in the mode of metal uptake with time, possibly indicating structural incorporation of the metal(loid) into the nanoparticle; this is supported by the continued increase in uptake concomitant with particle growth, implying that metal species may transform from surface-sorbed species to more structurally incorporated forms. This type of incorporation would have implications for the long-term fate and mobility of metals in contaminated regions, and affect the strategy for potential remediation/modeling efforts.

  1. Adsorption Mechanisms of Trivalent Gold onto Iron Oxy-Hydroxides: From the Molecular Scale to the Model

    Science.gov (United States)

    Cancès, Benjamin; Benedetti, Marc; Farges, François; Brown, Gordon E.

    2007-02-01

    Gold is a highly valuable metal that can concentrate in iron-rich exogenetic horizons such as laterites. An improved knowledge of the retention mechanisms of gold onto highly reactive soil components such as iron oxy-hydroxides is therefore needed to better understand and predict the geochemical behavior of this element. In this study, we use EXAFS information and titration experiments to provide a realistic thermochemical description of the sorption of trivalent gold onto iron oxy-hydroxides. Analysis of Au LIII-edge XAFS spectra shows that aqueous Au(III) adsorbs from chloride solutions onto goethite surfaces as inner-sphere square-planar complexes (Au(III)(OH,Cl)4), with dominantly OH ligands at pH > 6 and mixed OH/Cl ligands at lower pH values. In combination with these spectroscopic results, Reverse Monte Carlo simulations were used to constraint the possible sorption sites on the surface of goethite. Based on this structural information, we calculated sorption isotherms of Au(III) on Fe oxy-hydroxides surfaces, using the CD-MUSIC (Charge Distribution — MUlti SIte Complexation) model. The various Au(III)-sorbed species were identified as a function of pH, and the results of these EXAFS+CD-MUSIC models are compared with titration experiments. The overall good agreement between the predicted and measured structural models shows the potential of this combined approach to better model sorption processes of transition elements onto highly reactive solid surfaces such as goethite and ferrihydrite.

  2. Adsorption equilibrium of uranium on iron oxyhydroxide-PVA hydrogel spheres

    International Nuclear Information System (INIS)

    Uranium and its compounds are considered strategic mineral resources due to its usage as an energy source and war material. They are harmful to human health. Thus, liquid waste containing low uranium content (≤100 mgU/L), from the mining and/or uranium reprocessing plants or even of the research center activities require the development of methods for their treatment, in a way to reduce its content to 15 μgU/L. Adsorption is one of these methods; it requires the synthesis of preferably spherical adsorbents, chemically and physically stable and with high adsorptive capacity. The sol-gel process can synthesize adsorbents having such characteristics, prioritizing the nanostructuring of iron oxyhydroxide in a hydrophilic PVA (polyvinyl alcohol) polymer network, which had an accessible pore structure (micro-, meso- and macropores + macroholes). We successfully obtained iron-PVA hydrogel spheres with (3433 ± 63 μm) and without (2833 ± 69 μm) macroholes. Both types of spheres have good mechanical strength and chemical stability in the 2-9 pH range. Adsorptive capacity: 413.22 mgU/g (with macroholes; Freundlich model) and 249.38 mgU/g (without macroholes; Langmuir and Freundlich models), at pH 5-6, 30 °C, and 6 h. With 280 mL of with-macrohole hydrogel spheres, we can treat 1 L of liquid waste (100 mgU/L) and reduce uranium content to 20 μgU/L. (author)

  3. Adsorption equilibrium of uranium on iron oxyhydroxide-PVA hydrogel spheres

    Energy Technology Data Exchange (ETDEWEB)

    Santos, Armindo; Campos, Victor B.; Ribeiro, Luciana S.; Escanio, Camila A.; Silva, Edilaine F.; Oliveira, Felipe W., E-mail: santosa@cdtn.br, E-mail: vbc@cdtn.br, E-mail: lsr@cdtn.br, E-mail: cae@cdtn.br, E-mail: efd@cdtn.br, E-mail: fwfo@cdtn.br [Centro de Desenvolvimento da Tecnologia Nuclear (CDTN/CNEN-MG), Belo Horizonte, MG (Brazil)

    2015-07-01

    Uranium and its compounds are considered strategic mineral resources due to its usage as an energy source and war material. They are harmful to human health. Thus, liquid waste containing low uranium content (≤100 mgU/L), from the mining and/or uranium reprocessing plants or even of the research center activities require the development of methods for their treatment, in a way to reduce its content to 15 μgU/L. Adsorption is one of these methods; it requires the synthesis of preferably spherical adsorbents, chemically and physically stable and with high adsorptive capacity. The sol-gel process can synthesize adsorbents having such characteristics, prioritizing the nanostructuring of iron oxyhydroxide in a hydrophilic PVA (polyvinyl alcohol) polymer network, which had an accessible pore structure (micro-, meso- and macropores + macroholes). We successfully obtained iron-PVA hydrogel spheres with (3433 ± 63 μm) and without (2833 ± 69 μm) macroholes. Both types of spheres have good mechanical strength and chemical stability in the 2-9 pH range. Adsorptive capacity: 413.22 mgU/g (with macroholes; Freundlich model) and 249.38 mgU/g (without macroholes; Langmuir and Freundlich models), at pH 5-6, 30 °C, and 6 h. With 280 mL of with-macrohole hydrogel spheres, we can treat 1 L of liquid waste (100 mgU/L) and reduce uranium content to 20 μgU/L. (author)

  4. Effect of Transport and Aging Processes on Metal Speciation in Iron Oxyhydroxide Aggregates, Tar Creek Superfund Site, Oklahoma

    Science.gov (United States)

    Estes, E. R.; Schaider, L. A.; Shine, J. P.; Brabander, D. J.

    2010-12-01

    Following the cessation of mining activity in the late 20th century, Tar Creek Superfund Site was left highly contaminated by Pb, Zn, and Cd. Tar Creek, which flows through the site and into the Neosho River, has been studied extensively because of its potential to transport metals from the mining site to downstream communities. Previous research identified aggregated iron oxyhydroxide material, which forms when mine seepage mixes with Tar Creek surface water, as a major transport vector of metals. Frequent flooding in Tar Creek deposits aggregates on downstream floodplains, where wetting and drying processes alter the speciation of iron and other metals. This study seeks to better quantify those changes and to determine how transport and aging affects the human and ecological health risk. Sequential extractions of aggregate samples collected from the creek demonstrate that Fe is present in both amorphous (10-35% of Fe extracted) and more crystalline (8-23% of Fe extracted) phases. Substantial portions of heavy metals sorb to amorphous iron oxyhydroxide phases (accounting for 10-30% of Pb and Zn extracted) but are not associated with more crystalline iron oxide phases (representing only 1% or less of the Pb and Zn extracted). Samples have a high organic matter content (18-25% mass loss on ignition), but only Fe was significantly extracted by the oxidizing step targeting organic matter (1-2% of Pb and Zn extracted, but 10-26% of Fe extracted). The majority of metals were extracted by the soluble or residual steps. If metals and organic matter inhibit transformation of amorphous iron oxyhydroxide material to nano and crystalline iron oxides, then a steady-state volume of amorphous iron oxyhydroxide material with a high total sorption capacity may exist within Tar Creek, enhancing the metal flux accommodated by this transport mechanism. Once transported downstream and deposited on floodplains, however, it is hypothesized that repeated changes in soil matrix

  5. Influence of manganese incorporation on structure, surface and As(III)/As(V) removal capacity of iron oxy-hydroxides

    Science.gov (United States)

    Tresintsi, Sofia; Simeonidis, Konstantinos; Mitrakas, Manassis

    2013-04-01

    Iron oxy-hydroxides are well defined As(V) adsorbents dominating in water treatment market. The main drawback of these adsorbents, as well as of all commercial one, is their significantly low adsorption capacity for As(III). A breakthrough for improving As(III) adsorption of iron oxy-hydroxides may come by the MnO2incorporation. However, MnO2 decreases the total arsenic capacity proportionally to its percentage since its efficiency for As(V) is much lower than that of an iron oxy-hydroxide. It is concluded that an ideal adsorbent capable for high and simultaneous As(III) and As(V) removal should be consisted of a binary Fe(III)-Mn(IV) oxy-hydroxide both efficient for As(III) oxidation, due to Mn(IV) presence, and capture of As(V) due to a high positively surface charge density. This work studies the optimum parameters at the synthesis of single Fe and binary Fe/Mn oxy-hydroxides in a continuous flow kilogram-scale production reactor through the precipitation of FeSO4 in the pH range 3-12, under intense oxidative conditions using H2O2/KMnO4, that maximize arsenic adsorption. The evaluation of their efficiency was based on its As(III) and As(V) adsorption capacity (Q10-index) at equilibrium concentration equal to drinking water regulation limit (Ce= 10 μg/L) in NSF challenge water. The pH of synthesis was found to decisively affect, the structure, surface configuration and Q10-index. As a result, both single Fe and binary Fe/Mn oxy-hydroxides prepared at pH 4, which consist of schwertmannite and Mn(IV)-feroxyhyte respectively, were qualified according to their highest Q10-index of 13±0.5 μg As(V)/ mg for a residual arsenic concentration of 10 μg/L at an equilibrium pH 7. The high surface charge and the activation of an ion-exchange mechanism between SO42- adsorbed in the Stern layer and arsenate ions were found to significantly contribute to the increased adsorption capacity. The Q10-index for As(III) of Fe/Mn adsorbent at equilibrium pH 7 was 6.7 μg/mg, which

  6. Water determination in iron oxyhydroxides and iron ores by Karl Fischer titration

    Science.gov (United States)

    da Cunha, Camila C. R. F.; da Costa, Geraldo M.

    2016-08-01

    Protohematite (Fe2-x/3(OH) x O3-x 1 ≤ x aid of X-ray diffraction and Infrared spectroscopy. The existence of these phases in soils might have influence in redox processes, and they were considered as a possible water reservoir in Martian soils. In this study, we have used for the first time the Karl Fischer titration method to determine the amount of water released after heating several synthetic samples of goethite, hematite and natural iron ores at 105, 400, 600 and 900 °C. It was found that heating at 105 °C did not remove all moisture from the samples, and higher temperatures were necessary to completely remove all the absorbed water. The water contents determined at 400, 600 and 900 °C were found to be the same within the experimental errors, suggesting the inexistence of both protohematite and hydrohematite in the investigated samples. Therefore, the above-mentioned effects of these phases in soils might have to be reevaluated.

  7. Rapid sedimentation of iron oxyhydroxides in an active hydrothermal shallow semi-enclosed bay at Satsuma Iwo-Jima Island, Kagoshima, Japan

    Science.gov (United States)

    Kiyokawa, Shoichi; Ueshiba, Takuya

    2015-04-01

    Hydrothermal activity is common in the fishing port of Nagahama Bay, a small semi-enclosed bay located on the southwest coast of Satsuma Iwo-Jima Island (38 km south of Kyushu Island, Japan). The bay contains red-brown iron oxyhydroxides and thick deposits of sediment. In this work, the high concentration and sedimentation rates of oxyhydroxide in this bay were studied and the sedimentary history was reconstructed. Since dredging work in 1998, a thickness of ~ 1.0-1.5 m of iron oxyhydroxide-rich sediments has accumulated on the floor of the bay. To estimate the volume of iron oxyhydroxide sediments and the amount discharged from hydrothermal vents, sediment traps were operated for several years and 13 sedimentary core samples were collected to reconstruct the 10-year sedimentary history of Nagahama Bay. To confirm the timing of sedimentary events, the core data were compared with meteorological records obtained on the island, and the ages of characteristic key beds were thus identified. The sedimentation rate of iron oxyhydroxide mud was calculated, after correcting for sediment input from other sources. The sediments in the 13 cores from Nagahama Bay consist mainly of iron oxyhydroxide mud, three thick tephra beds, and a topmost thick sandy mud bed. Heavy rainfall events in 2000, 2001, 2002, and 2004-2005 coincide with tephra beds, which were reworked from Iwo-Dake ash deposits to form tephra-rich sediment. Strong typhoon events with gigantic waves transported outer-ocean-floor sediments and supplied quartz, cristobalite, tridymite, and albite sands to Nagahama Bay. These materials were redeposited together with bay sediments as the sandy mud bed. Based on the results from the sediment traps and cores, it is estimated that the iron oxyhydroxide mud accumulated in the bay at the relatively rapid rate of 33.3 cm/year (from traps) and 2.8-4.9 cm/year (from cores). The pore water contents within the sediment trap and core sediments are 73%-82% and 47

  8. Magnetically modified natural biogenic iron oxides for organic xenobiotics removal

    Czech Academy of Sciences Publication Activity Database

    Šafařík, Ivo; Filip, J.; Horská, Kateřina; Nowakova, M.; Tuček, J.; Šafaříková, Miroslava; Hashimoto, H.; Takada, J.; Zbořil, R.

    Elsevier. Roč. 24, S1 (2013), S77-S77. ISSN 0958-1669. [European Biotechnology Congress. 16.05.2013-18.05.2013, Bratislava] Institutional support: RVO:67179843 Keywords : organic xenobiotics * biogenic iron * Magnetically modified Subject RIV: EI - Biotechnology ; Bionics http://ac.els-cdn.com/S0958166913003340/1-s2.0-S0958166913003340-main.pdf?_tid=55b04b50-cbc0-11e4-8cb5-00000aab0f6c&acdnat=1426498946_517d901283c9cd0d7b198ceb605f1435

  9. Ultrafast electron and energy transfer in dye-sensitized iron oxide and oxyhydroxide nanoparticles

    DEFF Research Database (Denmark)

    Gilbert, Benjamin; Katz, Jordan E.; Huse, Nils;

    2013-01-01

    An emerging area in chemical science is the study of solid-phase redox reactions using ultrafast time-resolved spectroscopy. We have used molecules of the photoactive dye 2′,7′-dichlorofluorescein (DCF) anchored to the surface of iron(iii) oxide nanoparticles to create iron(ii) surface atoms via...

  10. Biogenic iron mineralization at Iron Mountain, CA with implications for detection with the Mars Curiosity rover

    Science.gov (United States)

    Williams, Amy J.; Sumner, Dawn Y.; Alpers, Charles N.; Campbell, Kate M.; Nordstrom, D Kirk

    2014-01-01

    (Introduction) Microbe-mineral interactions and biosignature preservation in oxidized sulfidic ore bodies (gossans) are prime candidates for astrobiological study. Such oxidized iron systems have been proposed as analogs for some Martian environments. Recent studies identified microbial fossils preserved as mineral-coated filaments. This study documents microbially-mediated mineral biosignatures in hydrous ferric oxide (HFO) and ferric oxyhydroxysulfates (FOHS) in three environments at Iron Mountain, CA. We investigated microbial community preservation via HFO and FOHS precipitation and the formation of filamentous mineral biosignatures. These environments included 1) actively precipitating (1000's yrs), naturally weathered HFO from in situ gossan, and 3) remobilized iron deposits, which contained lithified clastics and zones of HFO precipitate. We used published biogenicity criteria as guidelines to characterize the biogenicity of mineral filaments. These criteria included A) an actively precipitating environment where microbes are known to be coated in minerals, B) presence of extant microbial communities with carbon signatures, C) structures observable as a part of the host rock, and D) biological morphology, including cellular lumina, multiple member population, numerous taxa, variable and 3-D preservation, biological size ranges, uniform diameter, and evidence of flexibility. This study explores the relevance and detection of these biosignatures to possible Martian biosignatures. Similar filamentous biosignatures are resolvable by the Mars Hand Lens Imager (MAHLI) onboard the Mars Science Laboratory (MSL) rover, Curiosity, and may be identifiable as biogenic if present on Mars.

  11. Structural Basis of Uranium Incorporation In Natural Iron (Oxyhydr)oxides

    Science.gov (United States)

    Michel, F. M.; Massey, M. S.; Lezama-Pacheco, J. S.; Brown, G. E.; Fendorf, S. E.; Bargar, J.

    2009-12-01

    The development of in situ remediation strategies for uranium-contaminated groundwater at US Department of Energy (DOE) sites such as Oak Ridge, Tennessee, and Rifle, Colorado is a major DOE objective. The long-term performance, cost, and public acceptance of these approaches depend on a fundamental understanding of molecular-scale biogeochemical processes that operate in the subsurface to control the retention and stability of uranium. One important process is the interaction of U with the metastable and highly reactive solid ferrihydrite (a poorly crystalline Fe-oxyhydroxide), which is continuously precipitating in aquifers as grain coatings and subsequently transforming to more stable phases. The fate of U adsorbed to ferrihydrite remains a major question. Previous work (e.g., (1-3)) suggests that incorporation of U directly into the Fe-(oxyhydr)oxide structure may be an important process that provides a large sink capacity for subsurface uranium. Little is known about this process and the accompanying mechanisms. We have investigated the structural aspects of freshly precipitated ferrihydrite formed in the presence of varying amounts of U(VI) as UO22+ and in the absence and presence of important ground water solutes, including calcium (Ca2+) and carbonate (CO32-); these ions are also thought to play a role in U(VI) incorporation (3). In addition, we have evaluated the products formed after aging of U-sorbed ferrihydrites at ambient temperature, circum-neutral pH, and with dissolved Fe(II) present to promote redox cycling. Preliminary results indicate that during aging, the reduction of U-sorbed ferrihydrite leads to a change in the coordination of U in the reaction products, most notably the loss of uranyl cation coordination and evidence for possible structural incorporation. Additional powder diffraction, x-ray photoelectron spectroscopy, and high-energy total scattering/PDF data will be presented. This research will lead to an improved understanding of the

  12. Mineralization of Iron Oxyhydroxides in the Presence and in the Absence of Bacterial Cells

    Science.gov (United States)

    Châtellier, X.; West, M.; Rose, J.; Fortin, D.; Leppard, G. G.; Ferris, G.

    2001-12-01

    Because of their small size, iron oxides have a large surface area per unit weight ratio and are believed to play an important role as an adsorbing phase in lake sediments for various molecules, including potentially dangerous ones like heavy metals. They have been observed to form in close association with bacterial cells, by oxidation of ferrous ions. It is thus important to determine whether the presence of the bacterial cells can affect the mineralogy and the mesoscopic structure of the Fe-oxides particles, as well as their reactivity towards heavy metals. We synthesized in the lab nanoparticles of Fe-oxides by oxidation of ferrous ions. This was done in the presence and in the absence of various bacterial strains (Escherichia coli, Bacillus subtilis, Pseudomonas Aeruginosa and Bacillus licheniformis) and of inorganic ligands (sulfate, phosphate, silicate). The Fe-oxides particles were then observed by TEM on thin sections and on whole mounts. The chemical composition was estimated by wet chemistry and by EDS. The mineralogy was determined by XRD, SAED and EXAFS. Surface area was investigated by BET. And adsorption of cadmium was also measured at various pH. We observed that the size and the morphology of the particles as well as their mesoscopic spatial organization can be affected by the presence of the cells, whereas the mineralogy is controlled by the chemistry of the solution. The adsorption isotherms of cadmium on the various Fe-oxides will be discussed at the light of these observations.

  13. The Irony of IronBiogenic Iron Oxides as an Iron Source to the Ocean

    OpenAIRE

    Emerson, David

    2016-01-01

    Primary productivity in at least a third of the sunlit open ocean is thought to be iron-limited. Primary sources of dissolved iron (dFe) to the ocean are hydrothermal venting, flux from the sediments along continental margins, and airborne dust. This article provides a general review of sources of hydrothermal and sedimentary iron to the ocean, and speculates upon the role that iron-cycling microbes play in controlling iron dynamics from these sources. Special attention is paid to iron-oxidiz...

  14. Molecular-Scale Investigation with ESI-FT-ICR-MS on Fractionation of Dissolved Organic Matter Induced by Adsorption on Iron Oxyhydroxides.

    Science.gov (United States)

    Lv, Jitao; Zhang, Shuzhen; Wang, Songshan; Luo, Lei; Cao, Dong; Christie, Peter

    2016-03-01

    Adsorption by minerals is a common geochemical process of dissolved organic matter (DOM) which may induce fractionation of DOM at the mineral-water interface. Here, we examine the molecular fractionation of DOM induced by adsorption onto three common iron oxyhydroxides using electrospray ionization coupled with Fourier-transform ion cyclotron resonance mass spectrometry (ESI-FT-ICR-MS). Ferrihydrite exhibited higher affinity to DOM and induced more pronounced molecular fractionation of DOM than did goethite or lepidocrocite. High molecular weight (>500 Da) compounds and compounds high in unsaturation or rich in oxygen including polycyclic aromatics, polyphenols and carboxylic compounds had higher affinity to iron oxyhydroxides and especially to ferrihydrite. Low molecular weight compounds and compounds low in unsaturation or containing few oxygenated groups (mainly alcohols and ethers) were preferentially maintained in solution. This study confirms that the double bond equivalence and the number of oxygen atoms are valuable parameters indicating the selective fractionation of DOM at mineral and water interfaces. The results of this study provide important information for further understanding the behavior of DOM in the natural environment. PMID:26815589

  15. Magnetically-modified natural biogenic iron oxides for organic xenobiotics removal

    Czech Academy of Sciences Publication Activity Database

    Šafařík, Ivo; Filip, J.; Horská, Kateřina; Nowakova, M.; Tuček, J.; Šafaříková, Miroslava; Hashimoto, H.; Takada, J.; Zbořil, R.

    2015-01-01

    Roč. 12, č. 2 (2015), s. 673-682. ISSN 1735-1472 R&D Projects: GA MŠk(CZ) LH11111; GA MŠk LH12190 Institutional support: RVO:67179843 Keywords : Biogenic iron oxides * Leptothrix ochracea * Magnetic fluid * Magnetic adsorbents * Xenobiotics Subject RIV: EI - Biotechnology ; Bionics Impact factor: 2.190, year: 2014

  16. Chemical Force Spectroscopy Evidence Supporting the Layer-by-Layer Model of Organic Matter Binding to Iron (oxy)Hydroxide Mineral Surfaces

    KAUST Repository

    Chassé, Alexander W.

    2015-08-18

    © 2015 American Chemical Society. The adsorption of dissolved organic matter (DOM) to metal (oxy)hydroxide mineral surfaces is a critical step for C sequestration in soils. Although equilibrium studies have described some of the factors controlling this process, the molecular-scale description of the adsorption process has been more limited. Chemical force spectroscopy revealed differing adhesion strengths of DOM extracted from three soils and a reference peat soil material to an iron (oxy)hydroxide mineral surface. The DOM was characterized using ultrahigh-resolution negative ion mode electrospray ionization Fourier Transform ion cyclotron resonance mass spectrometry. The results indicate that carboxyl-rich aromatic and N-containing aliphatic molecules of DOM are correlated with high adhesion forces. Increasing molecular mass was shown to decrease the adhesion force between the mineral surface and the DOM. Kendrick mass defect analysis suggests that mechanisms involving two carboxyl groups result in the most stable bond to the mineral surface. We conceptualize these results using a layer-by-layer "onion" model of organic matter stabilization on soil mineral surfaces.

  17. Local environments and lithium adsorption on the iron oxyhydroxides lepidocrocite (gamma-FeOOH) and goethite (alpha-FeOOH): A 2H-2 and 7Li solid-state MAS NMR study

    DEFF Research Database (Denmark)

    Nielsen, Ulla Gro; Grey, Clare P.; Paik, Jonkim

    2008-01-01

    2H and 7LiMAS NMR spectroscopy techniques were applied to study the local surface and bulk environments of iron oxyhydroxide lepiclocrocite (gamma-FeOOH). 2H variable-temperature (VT) MAS NMR experiments were performed, showing the presence of short-range, strong antiferromagnetic correlations, e...

  18. Structural investigations of biogenic iron oxide samples. Preliminary results

    International Nuclear Information System (INIS)

    Some preliminary results on morphology and structure of iron oxide particles formed inside Klebsiella oxytoca bacteria are presented. In particular, by means of optical microscopy, scanning electron microscopy and small-angle X-ray scattering the effect of the bacteria age (the duration of growth) on the nanoparticles properties is studied

  19. INVESTIGATION OF THE TRANSFORMATION OF URANIUM UNDER IRON-REDUCING CONDITIONS: REDUCTION OF UVI BY BIOGENIC FEII/FEIII HYDROXIDE (GREEN RUST)

    Energy Technology Data Exchange (ETDEWEB)

    O' Loughlin, Edward J.; Scherer, Michelle M.; Kemner, Kenneth M.

    2006-12-31

    The recent identification of green rusts (GRs) as products of the reduction of FeIII oxyhydroxides by dissimilatory iron-reducing bacteria, coupled with the ability of synthetic (GR) to reduce UVI species to insoluble UO2, suggests that biogenic green rusts (BioGRs) may play an important role in the speciation (and thus mobility) of U in FeIII-reducing environments. The objective of our research was to examine the potential for BioGR to affect the speciation of U under FeIII-reducing conditions. To meet this objective, we designed and executed a hypothesis-driven experimental program to identify key factors leading to the formation of BioGRs as products of dissimilatory FeIII reduction, to determine the key factors controlling the reduction of UVI to UIV by GRs, and to identify the resulting U-bearing mineral phases. The results of this research significantly increase our understanding of the coupling of biotic and abiotic processes with respect to the speciation of U in iron-reducing environments. In particular, the reduction of UVI to UIV by BioGR with the subsequent formation of U-bearing mineral phases may be effective for immobilizing U in suboxic subsurface environments. This information has direct applications to contaminant transport modeling and bioremediation engineering for natural or enhanced in situ remediation of subsurface contamination.

  20. Deposition of Biogenic Iron Minerals in a Methane Oxidizing Microbial Mat

    Directory of Open Access Journals (Sweden)

    Christoph Wrede

    2013-01-01

    Full Text Available The syntrophic community between anaerobic methanotrophic archaea and sulfate reducing bacteria forms thick, black layers within multi-layered microbial mats in chimney-like carbonate concretions of methane seeps located in the Black Sea Crimean shelf. The microbial consortium conducts anaerobic oxidation of methane, which leads to the formation of mainly two biomineral by-products, calcium carbonates and iron sulfides, building up these chimneys. Iron sulfides are generated by the microbial reduction of oxidized sulfur compounds in the microbial mats. Here we show that sulfate reducing bacteria deposit biogenic iron sulfides extra- and intracellularly, the latter in magnetosome-like chains. These chains appear to be stable after cell lysis and tend to attach to cell debris within the microbial mat. The particles may be important nuclei for larger iron sulfide mineral aggregates.

  1. The effect of the synthetic route on the structural, textural, morphological and catalytic properties of iron(iii) oxides and oxyhydroxides.

    Science.gov (United States)

    Oulego, Paula; Villa-García, María A; Laca, Adriana; Diaz, Mario

    2016-06-21

    A variety of iron(iii) oxides and oxyhydroxides were synthesised and characterised using three distinct methods of preparation: microemulsion, precipitation and sol-gel. The results clearly showed that the structure, textural properties, crystal morphology and catalytic performance of the phases obtained were highly dependent on the chemical routes used for the synthesis. Precipitation and microemulsion methods allowed obtaining mesoporous nanostructured iron(iii) oxides with mean particle sizes of 4 nm (amorphous hematite) and 7 nm (ferrihydrite), which exhibited a high surface area (291.4 m(2) g(-1) and 192.3 m(2) g(-1), respectively) and a very good catalytic behaviour in the advanced oxidation of highly non-biodegradable wastewaters. The different conditions employed in the synthesis of these materials through the sol-gel method yielded two goethites with practically the same catalytic properties, but dissimilar morphologies and texture. When soft agitation and slow addition of the precipitating agent were used, the resulting material (G1) was made up of shorter and finer particles, markedly acicular, with an average length of 400 ± 50 nm and width of 15 ± 5 nm. However, vigorous agitation and rapid addition of the precipitating agent led to the formation of longer and coarser particles, moderately acicular, the average length and width being 950 ± 100 nm and 140 ± 20 nm, respectively. The use of the sol-gel technique also resulted in the formation of a solid consisting of a mixture of hematite as the main crystalline phase and goethite particles dispersed among the hematite particles. This solid presented a low specific surface area (13.2 m(2) g(-1)) and lower catalytic activity. Therefore, precipitation and microemulsion proved to be the most suitable techniques to synthesise catalytically active disordered iron(iii) oxide nanoparticles, due to the presence of highly reactive non-stoichiometric iron(iii) ions, a higher surface area and smaller particle

  2. Biogenic oxides from neutrophilic iron bacteria and possibilities for application in the nanotechnology

    International Nuclear Information System (INIS)

    The aim of this study is to obtain and characterize the ferric oxides/(oxy)hydroxides formed after cultivation of bacteria under laboratory conditions. The pure cultures of these bacteria isolated from natural habitats are identified by the methods of classical and molecular taxonomy as strains of the Leptothrix genus. Adler (AM) and Silicon iron glucose peptone (SIGP) media are the most appropriate ones for obtaining the iron oxides. The characterization of the oxides and sheaths is performed by different physical methods. The sheaths are formed in a SIGP medium. Light micrograph images and SEM revealed the average size and diameter of the sheaths. The XRD measurements showed the composition of the oxides obtained, as well as the average size of the iron particles (up to 30 nm). The TEM micrographs showed the shape of the biogenic nanoparticles, while the magnetic measurements demonstrated the superparamagnetic character of the magnetic part of the biomaterials. The new biogenic materials are promising for application in magneto electronic for building biosensors

  3. Simulated atmospheric processing of iron oxyhydroxide minerals at low pH: Roles of particle size and acid anion in iron dissolution

    OpenAIRE

    Rubasinghege, Gayan; Lentz, Robert W.; Scherer, Michelle M.; Grassian, Vicki H.

    2010-01-01

    A number of recent studies have shown that iron dissolution in Fe-containing dust aerosol can be linked to source material (mineral or anthropogenic), mineralogy, and iron speciation. All of these factors need to be incorporated into atmospheric chemistry models if these models are to accurately predict the impact of Fe-containing dusts into open ocean waters. In this report, we combine dissolution measurements along with spectroscopy and microscopy to focus on nanoscale size effects in the d...

  4. Microbial reduction of ferric iron oxyhydroxides as a way for remediation of grey forest soils heavily polluted with toxic metals by infiltration of acid mine drainage

    Science.gov (United States)

    Georgiev, Plamen; Groudev, Stoyan; Spasova, Irena; Nicolova, Marina

    2015-04-01

    The abandoned uranium mine Curilo is a permanent source of acid mine drainage (AMD) which steadily contaminated grey forest soils in the area. As a result, the soil pH was highly acidic and the concentration of copper, lead, arsenic, and uranium in the topsoil was higher than the relevant Maximum Admissible Concentration (MAC) for soils. The leaching test revealed that approximately half of each pollutant was presented as a reducible fraction as well as the ferric iron in horizon A was presented mainly as minerals with amorphous structure. So, the approach for remediation of the AMD-affected soils was based on the process of redoxolysis carried out by iron-reducing bacteria. Ferric iron hydroxides reduction and the heavy metals released into soil solutions was studied in the dependence on the source of organic (fresh or silage hay) which was used for growth and activity of soil microflora, initial soil pH (3.65; 4.2; and 5.1), and the ion content of irrigation solutions. The combination of limestone (2.0 g/ kg soil), silage addition (at rate of 45 g dry weight/ kg soil) in the beginning and reiterated at 6 month since the start of soil remediation, and periodical soil irrigation with slightly acidic solutions containing CaCl2 was sufficient the content of lead and arsenic in horizon A to be decreased to concentrations similar to the relevant MAC. The reducible, exchangeable, and carbonate mobile fractions were phases from which the pollutants was leached during the applied soil remediation. It determined the higher reduction of the pollutants bioavailability also as well as the process of ferric iron reduction was combined with neutralization of the soil acidity to pH (H2O) 6.2.

  5. A comparison of biogenic iron quotas during a diatom spring bloom using multiple approaches

    Directory of Open Access Journals (Sweden)

    A. L. King

    2012-02-01

    Full Text Available Biogenic Fe quotas were determined using three distinct techniques on samples collected concurrently in the subtropical Pacific Ocean east of New Zealand. Fe quotas were measured using radioisotope uptake experiments (24 h incubation, bulk filtration and analysis by inductively-coupled plasma mass spectrometer (ICPMS, and single-cell synchrotron x-ray fluorescence (SXRF analysis over a sixteen-day period (year days 263 to 278 of 2008 during a quasi-Lagrangian drifter experiment that tracked the evolution of the annual spring diatom bloom within a counter-clockwise open-ocean eddy. Overall, radioisotope uptake-determined Fe quotas (washed with oxalate reagent to remove extracellular Fe were the lowest (0.5–1.0 mmol Fe:mol P; 4–8 μmol Fe:mol C, followed by single-cell Fe quotas (2.3–7.5 mmol Fe:mol P; 17–57 μmol Fe:mol C, and the highest and most variable quotas were from the bulk filtration ICPMS approach that used the oxalate reagent wash, corrected for lithogenic Fe using Al (0.8–21 mmol Fe:mol P; 4–136 μmol Fe:mol C. During the evolution of the spring bloom within the eddy (year days 263 to 272, the surface mixed layer inventories of particulate biogenic elements (C, N, P, Si and chlorophyll increased while Fe quotas estimated from all three approaches exhibited a general decline. After the onset of the bloom decline, the drogued buoys exited the eddy center (days 273 to 277. Fe quotas returned to pre-bloom values during this part of the study. Our standardized and coordinated sampling protocols reveal the general observed trend in Fe quotas: ICPMS > SXRF > radioisotope uptake. We discuss the inherent differences between the techniques and argue that each technique has its individual merits and uniquely contributes to the characterization of the oceanic particulate Fe pool.

  6. Biogenic nano-magnetite and nano-zero valent iron treatment of alkaline Cr(VI) leachate and chromite ore processing residue

    OpenAIRE

    Watts, Mathew P.; Coker, Victoria S.; Parry, Stephen A.; Pattrick, Richard A.D.; Thomas, Russell A.P.; Kalin, Robert; Lloyd, Jonathan R.

    2015-01-01

    Highly reactive nano-scale biogenic magnetite (BnM), synthesized by the Fe(III)-reducing bacterium Geobacter sulfurreducens, was tested for the potential to remediate alkaline Cr(VI) contaminated waters associated with chromite ore processing residue (COPR). The performance of this biomaterial, targeting aqueous Cr(VI) removal, was compared to a synthetic alternative, nano-scale zero valent iron (nZVI). Samples of highly contaminated alkaline groundwater and COPR solid waste were obtained fro...

  7. Relationship between P and the most reactive fraction of Fe(III) oxyhydroxide in various aquatic and sedimentary environments

    Science.gov (United States)

    Anschutz, Pierre

    2014-05-01

    Phosphorus can experience a series of biogeochemical pathways. Primary P has an igneous origin and occurs mostly as apatite in bedrocks. Once P is dissolved as phosphate ion, it can incorporate organic matter or become adsorbed onto inorganic particles. The liberation of P from organic matter through bacterial respiration produces a subsequent flux back to the biota or a storage in Fe and Al oxyhydroxides, or in authigenic or biogenic phosphate minerals. The adsorption of phosphate on Fe- and Al-oxide and oxyhydroxide has been extensively studied in soil science because phosphorus is a limiting nutrient in terrestrial ecosystems, and sorptive removal of natural or fertilizer phosphorus impacts the production level of crops and forests. Fe(III) oxides/oxyhydroxides are subject to reductive dissolution, and consequently redox conditions play an important role in soil P-bioavailability. The main process of phosphorus removal from the aquatic systems is burial with sediments. Exchange between sediment and overlying water takes place through benthic biogeochemical processes, including organic-P mineralization, redox-driven Fe-P cycling, and benthic phosphorus efflux from sediments. A portion of the pore-water phosphate derived from organic matter mineralization may be adsorbed onto detrital or authigenic iron oxyhydroxides in the oxidized zone of the sediment. Once advected in the reduced zone of sediments through burial or bioturbation, the most reducible fraction of Fe(III) phase can be reduced and solubilized, leading to a release of phosphate. Eventually, P can be buried over long period as relict organic-P, P associated with refractory iron oxides, and apatite. Therefore, Fe-bound P is often the initial sink of P supplied by organic matter, but not the major final sink. Several techniques have been developed to extract P bound to Fe(III) phases. The citrate-dithionite buffered (CDB) solution is one of the most often used solution to measure Fe(III)-bound P. CDB

  8. Effect of nitrate enrichment and diatoms on the bioavailability of Fe(III) oxyhydroxide colloids in seawater.

    Science.gov (United States)

    Liu, Feng-Jiao; Huang, Bang-Qin; Li, Shun-Xing; Zheng, Feng-Ying; Huang, Xu-Guang

    2016-03-01

    The photoconversion of colloidal iron oxyhydroxides was a significant source of bioavailable iron in coastal systems. Diatoms dominate phytoplankton communities in coastal and upwelling regions. Diatoms are often exposed to eutrophication. We investigated the effects of different species of diatom, cell density, illumination period, and nitrate additions on the bioavailability of Fe(III) oxy-hydroxide colloids in seawaters. With the increase of illumination period from 1 to 4 h, the ratios of concentrations of total dissolved Fe (DFe) to colloidal iron oxyhydroxides and Fe(II) to DFe increased up to 24.3% and 23.9% for seawater without coastal diatoms, 45.6% and 30.2% for Skeletonema costatum, 44.3% and 29.7% for Thalassiosira weissflogii, respectively. The photochemical activity of coastal diatoms themselves (excluding the dissolved organic matter secreted by algae) on the species transformation of iron in seawater (including the light-induced dissolution of Fe(III) oxyhydroxide colloids and the photo-reduction of Fe(III) into Fe(II)) was confirmed for the first time. There was no significant difference of the ability of S. costatum and Thalassiosira weissflogii on the photoconversion of colloidal iron oxyhydroxides. The photoproduction of dissolved Fe(II) and DFe in the seawater with or without diatoms could be depressed by the nitrate addition. PMID:26766021

  9. Binding of heavy metal ions in aggregates of microbial cells, EPS and biogenic iron minerals measured in-situ using metal- and glycoconjugates-specific fluorophores

    Science.gov (United States)

    Hao, Likai; Guo, Yuan; Byrne, James M.; Zeitvogel, Fabian; Schmid, Gregor; Ingino, Pablo; Li, Jianli; Neu, Thomas R.; Swanner, Elizabeth D.; Kappler, Andreas; Obst, Martin

    2016-05-01

    Aggregates consisting of bacterial cells, extracellular polymeric substances (EPS) and Fe(III) minerals formed by Fe(II)-oxidizing bacteria are common at bulk or microscale chemical interfaces where Fe cycling occurs. The high sorption capacity and binding capacity of cells, EPS, and minerals controls the mobility and fate of heavy metals. However, it remains unclear to which of these component(s) the metals will bind in complex aggregates. To clarify this question, the present study focuses on 3D mapping of heavy metals sorbed to cells, glycoconjugates that comprise the majority of EPS constituents, and Fe(III) mineral aggregates formed by the phototrophic Fe(II)-oxidizing bacteria Rhodobacter ferrooxidans SW2 using confocal laser scanning microscopy (CLSM) in combination with metal- and glycoconjugates-specific fluorophores. The present study evaluated the influence of glycoconjugates, microbial cell surfaces, and (biogenic) Fe(III) minerals, and the availability of ferrous and ferric iron on heavy metal sorption. Analyses in this study provide detailed knowledge on the spatial distribution of metal ions in the aggregates at the sub-μm scale, which is essential to understand the underlying mechanisms of microbe-mineral-metal interactions. The heavy metals (Au3+, Cd2+, Cr3+, CrO42-, Cu2+, Hg2+, Ni2+, Pd2+, tributyltin (TBT) and Zn2+) were found mainly sorbed to cell surfaces, present within the glycoconjugates matrix, and bound to the mineral surfaces, but not incorporated into the biogenic Fe(III) minerals. Statistical analysis revealed that all ten heavy metals tested showed relatively similar sorption behavior that was affected by the presence of sorbed ferrous and ferric iron. Results in this study showed that in addition to the mineral surfaces, both bacterial cell surfaces and the glycoconjugates provided most of sorption sites for heavy metals. Simultaneously, ferrous and ferric iron ions competed with the heavy metals for sorption sites on the organic

  10. 2-Nitrophenol reduction promoted by S. putrefaciens 200 and biogenic ferrous iron: The role of different size-fractions of dissolved organic matter

    International Nuclear Information System (INIS)

    Graphical abstract: - Highlights: • Dissolved organic matter (DOM) act as electron shuttle in redox reactions. • Different molecular weight DOM fractions have different electron transfer capacity. • A higher electron transfer capacities value indicates a higher reduction rate. • DOM transfer electron from S. putrefaciens 200 to 2-nitrophenol (2-NP) and Fe(III). • DOM and biogenic Fe(II) synergistically enhanced the 2-NP reductive transformation. - Abstract: The reduction of nitroaromatic compounds (listed as a priority pollutant) in natural subsurface environments typically coexists with dissimilatory reduction of iron oxides effected by dissolved organic matter (DOM). Investigating the impact of the DOM that influences those reduction processes is crucial for understanding and predicting the geochemical fate of these environmental species. This study investigated the impact of different molecular weight DOM fractions (DMWDs) on the 2-nitrophenol (2-NP) reduction by S. putrefaciens 200 (SP200) and α-Fe2O3 with lactate (excluding electron donor interference). Kinetic measurements demonstrated that 2-NP reduction rates were affected by the redox reactivity of active species under DMWDs (denoted as L-DOM, M-DOM, and H-DOM). The enhanced reduction rates are consistent with the negative shifts in peak oxidation potential values, the increases in HA-like/FA-like values, aromaticity index values and electron transfer capacity values. L-DOM acted mainly as ligands to complex Fe(II), whereas the significant role of H-DOM in reductive reactions should be acting as an electron shuttle, transferring electrons from SP200 to Fe(III) and 2-NP and from biogenic Fe(II) to 2-NP, further accelerating the 2-NP reductions. Those observations provide valuable insights into the role of DOM in the biogeochemical redox processes and the remediation of contaminated soil in a natural environment

  11. Carbon-13 magnetic relaxation rates or iron (III) complexes of some biogenic amines and parent compounds in aqueous solutions

    International Nuclear Information System (INIS)

    Spin-lattice relaxation rates (R1) from naturally occuring C-13 F.T. N.M.R. spectra of some catecholamines and parent compounds with Iron(III) at pD = 4 were determined in order to elucidate the molecular mechanism underlying their association in aqueous solutions. Complexation was observed only for catecholic ligands. The R1 values were used to calculate iron-carbon scaled distances, and two complexation models were proposed where the catecholic function binds Fe(III) in the first and second coordination spheres respectively. The latter case was shown to be the consistent with the molecular geometries. (orig.)

  12. Cerium Oxyhydroxide Clusters: Formation, Structure and Reactivity

    Energy Technology Data Exchange (ETDEWEB)

    Frederic Aubriet; Jean-Jacques Gaumet; Wibe A de Jong; Groenewold, Gary S (058000); Gianotto, Anita K (057404); McIlwain, Michael E (051783); Michael J. Van Stipdonk; Christopher M. Leavitt

    2009-06-01

    Cerium oxyhydroxide cluster anions were produced by irradiating ceric oxide particles using 355 nm laser pulses that were synchronized with pulses of nitrogen gas admitted to the irradiation chamber. The gas pulse stabilized the nascent clusters that are largely anhydrous [CexOy] ions and neutrals. These initially-formed species react with water, principally forming closed-shell (c-s) oxohydroxy species that are described by the general formula [CexOy(OH)z]-. In general, the extent of hydroxylation varies from a value of 3 OH per Ce atom when x = 1 to a value slightly greater than 1 for x > 8. The Ce3 and Ce6 species deviate significantly from this trend: the x = 3 cluster accommodates more hydroxyl moieties compared to neighboring congeners at x = 2 and x = 4. Conversely, the x = 6 cluster is significantly less hydroxylated. Density functional theory (DFT) modeling of the cluster structures show that the hydrated clusters are hydrolyzed, and contain one-to-multiple hydroxide moieties, but not datively bound water. DFT also predicts an energetic preference for formation of highly symmetric structures as the size of the clusters increases. The calculated structures indicate that the ability of the Ce3 oxyhydroxide to accommodate more extensive hydroxylation is due to a more open, hexagonal structure in which the Ce atoms can participate in multiple hydrolysis reactions. Conversely the Ce6 oxyhydroxide has an octahedral structure that is not conducive to hydrolysis. In addition to the c-s clusters, open-shell (o-s) oxyhydroxides and superoxides are also formed, and they become more prominent as the size of the clusters increases, suggesting that the larger ceria clusters have an increased ability to stabilize a non-bonding electron. The overall intensity of the clusters tends to monotonically decrease as the cluster size increases, however this trend is interrupted at Ce13, which is significantly more stable compared to neighboring congeners, suggesting formation of

  13. Cerium Oxyhydroxide Clusters: Formation, Structure and Reactivity

    Energy Technology Data Exchange (ETDEWEB)

    Aubriet, F.; Gaumet, Jean-Jacques; De Jong, Wibe A.; Groenewold, G. S.; Gianotto, Anita K.; McIIwain, Michael E.; Van Stipdonk, Michael J.; Leavitt, Christopher M.

    2009-05-11

    Cerium oxyhydroxide cluster anions were produced by irradiating ceric oxide particles using 355 nm laser pulses that were synchronized with pulses of nitrogen gas admitted to the irradiation chamber. The gas pulse stabilized the nascent clusters that are largely anhydrous [CexOy] ions and neutrals. These initially-formed species react with water, principally forming closed-shell (c-s) oxohydroxy species that are described by the general formula [CexOy(OH)z]-. In general, the extent of hydroxylation varies from a value of 3 OH per Ce atom when x = 1 to a value slightly greater than 1 for x > 8. The Ce3 and Ce6 species deviate significantly from this trend: the x = 3 cluster accommodates more hydroxyl moieties compared to neighboring congeners at x = 2 and x = 4. Conversely, the x = 6 cluster is significantly less hydroxylated. Density functional theory (DFT) modeling of the cluster structures show that the hydrated clusters are hydrolyzed, and contain one-to-multiple hydroxide moieties, but not datively bound water. DFT also predicts an energetic preference for formation of highly symmetric structures as the size of the clusters increases. The calculated structures indicate that the ability of the Ce3 oxyhydroxide to accommodate more extensive hydroxylation is due to a more open, hexagonal structure in which the Ce atoms can participate in multiple hydrolysis reactions. Conversely the Ce6 oxyhydroxide has an octahedral structure that is not conducive to hydrolysis. In addition to the c-s clusters, open-shell (o-s) oxyhydroxides and superoxides are also formed, and they become more prominent as the size of the clusters increases, suggesting that the larger ceria clusters have an increased ability to stabilize a non-bonding electron. The overall intensity of the clusters tends to monotonically decrease as the cluster size increases, however this trend is interrupted at Ce13, which is significantly more stable compared to neighboring congeners, suggesting formation of

  14. Biogenic nano-magnetite and nano-zero valent iron treatment of alkaline Cr(VI) leachate and chromite ore processing residue

    International Nuclear Information System (INIS)

    Highlights: • Remediation of high pH Cr(VI) contamination related to COPR and its groundwater. • Extensive characterization of COPR and its related groundwater. • Cr(VI) reduction to Cr(III) by biogenic nano-magnetite and nano-zero valent iron. • Critical assessment of reactivity and passivation using spectroscopy and imaging. • Stabilization of the COPR Cr(VI) source by addition of nanoparticles. - Abstract: Highly reactive nano-scale biogenic magnetite (BnM), synthesized by the Fe(III)-reducing bacterium Geobacter sulfurreducens, was tested for the potential to remediate alkaline Cr(VI) contaminated waters associated with chromite ore processing residue (COPR). The performance of this biomaterial, targeting aqueous Cr(VI) removal, was compared to a synthetic alternative, nano-scale zero valent iron (nZVI). Samples of highly contaminated alkaline groundwater and COPR solid waste were obtained from a contaminated site in Glasgow, UK. During batch reactivity tests, Cr(VI) removal from groundwater was inhibited by ∼25% (BnM) and ∼50% (nZVI) when compared to the treatment of less chemically complex model pH 12 Cr(VI) solutions. In both the model Cr(VI) solutions and contaminated groundwater experiments the surface of the nanoparticles became passivated, preventing complete coupling of their available electrons to Cr(VI) reduction. To investigate this process, the surfaces of the reacted samples were analyzed by TEM-EDX, XAS and XPS, confirming Cr(VI) reduction to the less soluble Cr(III) on the nanoparticle surface. In groundwater reacted samples the presence of Ca, Si and S was also noted on the surface of the nanoparticles, and is likely responsible for earlier onset of passivation. Treatment of the solid COPR material in contact with water, by addition of increasing weight % of the nanoparticles, resulted in a decrease in aqueous Cr(VI) concentrations to below detection limits, via the addition of ⩾5% w/w BnM or ⩾1% w/w nZVI. XANES analysis of the

  15. Microbial and hydrothermal aspects of ferric oxyhydroxides and ferrosic hydroxides: the example of Franklin Seamount, Western Woodlark Basin, Papua New Guinea

    Directory of Open Access Journals (Sweden)

    Boyd TD

    2001-09-01

    Full Text Available Deposits of Fe-Si-Mn oxyhydroxides are commonly found on the seafloor on seamounts and mid-ocean spreading centers. At Franklin Seamount located near the western extremity of Woodlark Basin, Papua New Guinea, Fe-Si-Mn oxyhydroxides are being precipitated as chimneys and mounds upon a substrate of mafic lava. Previous studies have shown that the vent fluids have a low temperature (20–30°C and are characterized by a total dissolved iron concentration of 0.038 mM kg-1, neutral pH (6.26 and no measurable H2S. The chimneys have a yellowish appearance with mottled red–orange patches when observed in situ from a submersible, but collected samples become redder within a few hours of being removed from the sea. The amorphous iron oxyhydroxides, obtained from active and inactive vents, commonly possess filamentous textures similar in appearance to sheaths and stalks excreted by the iron-oxidizing bacteria Leptothrix and Gallionella; however, formless agglomerates are also common. Textural relationships between apparent bacterial and non-bacterial iron suggest that the filaments are coeval with and/or growing outwards from the agglomerates. The amorphous iron oxyhydroxides are suggested to precipitate hydrothermally as ferrosic hydroxide, a mixed-valence (Fe2+-Fe3+ green–yellow iron hydroxide compound. Consideration of the thermodynamics and kinetics of iron in the vent fluid, suggest that the precipitation is largely pH controlled and that large amounts of amorphous iron oxyhydroxides are capable of being precipitated by a combination of abiotic hydrothermal processes. Some biologically induced precipitation of primary ferric oxyhydroxides (two-XRD-line ferrihydrite may have occurred directly from the fluid, but most of the filamentous iron micro-textures in the samples appear to have a diagenetic origin. They may have formed as a result of the interaction between the iron-oxidizing bacteria and the initially precipitated ferrosic hydroxide that

  16. Van Vleck paramagnetism of europium oxyhydroxide

    Institute of Scientific and Technical Information of China (English)

    Hiroaki Samata; Naoki Wada; Tadashi C Ozawa

    2015-01-01

    Europium oxyhydroxide crystals were synthesized by the flux method. The as-grown crystals were transparent and had a plate-like shape with natural flat surfaces. The powder XRD data were refined by assuming a monoclinic structure of the space group P21/m and lattice parameters of a=0.4346 nm, b=0.3744 nm, c=0.6107 nm, and β=108.62°. The magnetic susceptibility of the EuOOH crystals exhibited typical Van Vleck temperature-independent paramagnetism below 120 K. The calculated susceptibility, based on Van Vleck’s theory, agreed with the experimental data to some extent, with the coupling constantλ=458±10 K. The ex-perimental results were in close agreement with the results calculated using a modified formula withλ=505±2 K and a constant term C=4.6×10−4 emu/(mol·Oe).

  17. Mechanism of pyrrhotite formation from ferric oxyhydroxide catalyst; Kokoritsu sekitan ekika shokubai no kaihatsu (Okishi suisankatetsu shokubai karano pyrrhotite seisei kyodo)

    Energy Technology Data Exchange (ETDEWEB)

    Tazawa, K.; Koyama, T.; Kaneko, T.; Shimasaki, K. [Nippon Brown Coal Liquefaction Co. Ltd., Tokyo (Japan)

    1996-10-28

    It is thought that iron-based catalysts for coal liquefaction exercise their catalytic activity by forming pyrrhotite (Fe(1-x)S). However, there are still a lot of unknown problems remained concerning the formation and agglomeration behaviors of pyrrhotite. These make a difficulty for improving the activity of iron-based catalysts. In this study, sulfiding behaviors of {alpha}-iron oxyhydroxide ({alpha}-FeOOH) and {gamma}-iron oxyhydroxide ({gamma}-FeOOH) were investigated to reveal the formation and agglomeration behaviors of pyrrhotite. It was found that pyrrhotite was easily converted from ferric oxyhydroxide catalysts having large specific surface areas at the sulfiding temperature below 250{degree}C, and fine crystallites of pyrrhotite were formed at the initial stage of sulfiding. Crystal growth of pyrrhotite at the sulfiding temperature over 350{degree}C depended on the catalyst forms. It was also found that smaller crystallites of pyrrhotite were formed from {gamma}-FeOOH than from {alpha}-FeOOH and amorphous iron oxyhydroxide. 5 refs., 7 figs., 1 tab.

  18. Water vapor diffusion into a nanostructured iron oxyhydroxide.

    Science.gov (United States)

    Song, Xiaowei; Boily, Jean-François

    2013-06-17

    Water diffusion through 0.4 nm × 0.4 nm wide tunnels of synthesized akaganéite (β-FeOOH) nanoparticles was studied by a coupled experimental-molecular modeling approach. A sorption isotherm model obtained from quartz crystal microbalance measurements suggests that the akaganéite bulk can accommodate a maximum of 22.4 mg of water/g (44% bulk site occupancy) when exposed to atmospheres of up to 16 Torr water vapor. Fourier transform infrared spectroscopy also showed that water molecules interact with (hydr)oxo groups on both the akaganéite bulk and surface. Diffusion reactions through the akaganéite bulk were confirmed through important changes in the hydrogen-bonding environment of bulk hydroxyl groups. Molecular dynamics simulations showed that water molecules are localized in cavities that are bound by eight hydroxyl groups, forming short-lived (tunnel openings are exposed, revealed sluggish rates of incorporation between interfacial water species and their tunnel counterparts. The presence of defects in the synthesized particles are suspected to contribute to different diffusion rates in the laboratory when compared to those observed in pristine crystalline materials, as studied by molecular modeling. PMID:23701490

  19. Phase transition of iron oxyhydroxides by mechanical activation

    International Nuclear Information System (INIS)

    The grinding kinetics of α-FeOOH and β-FeOOH was investigated in dependence on decreasing particle size. Samples were ground for various periods at room temperature and subsequently investigated by Moessbauer spectrometry. The Moessbauer parameters and spectra of α-FeOOH and β-FeOOH for various activation times are given. (Z.S.)

  20. The adsorption of arsenic oxyacids to iron oxyhydroxide columns

    OpenAIRE

    Mähler, Johan

    2013-01-01

    The fundamental side of this project includes determination of ionic radii and plausible hydration numbers for the weakly hydrated alkali metal ions in solution, as well as an investigation of the intramolecular bond lengths of arsenic oxyacid species and orthotelluric acid. Experimental methods such as EXAFS, XANES and LAXS have been used for these purposes, as well as thorough screening for relevant structures in crystal structure databases. The improved ionic radius for the sodium ion in s...

  1. Iron

    Science.gov (United States)

    Iron is a mineral that our bodies need for many functions. For example, iron is part of hemoglobin, a protein which carries ... It helps our muscles store and use oxygen. Iron is also part of many other proteins and ...

  2. Iron

    Science.gov (United States)

    ... seafood, and foods that contain vitamin C , like citrus fruits, strawberries, sweet peppers, tomatoes, and broccoli. What ... diets. What are some effects of iron on health? Scientists are studying iron to understand how it ...

  3. Iron

    DEFF Research Database (Denmark)

    Hansen, Jakob Bondo; Moen, I W; Mandrup-Poulsen, T

    2014-01-01

    The interest in the role of ferrous iron in diabetes pathophysiology has been revived by recent evidence of iron as an important determinant of pancreatic islet inflammation and as a biomarker of diabetes risk and mortality. The iron metabolism in the β-cell is complex. Excess free iron is toxic......, but at the same time, iron is required for normal β-cell function and thereby glucose homeostasis. In the pathogenesis of diabetes, iron generates reactive oxygen species (ROS) by participating in the Fenton chemistry, which can induce oxidative damage and apoptosis. The aim of this review is to...... present and discuss recent evidence, suggesting that iron is a key pathogenic factor in both type 1 and type 2 diabetes with a focus on inflammatory pathways. Pro-inflammatory cytokine-induced β-cell death is not fully understood, but may include iron-induced ROS formation resulting in dedifferentiation...

  4. Studies of the surface reactivity of metal oxyhydroxides and sulfides with relevance to environmental chemistry

    Science.gov (United States)

    Pierre-Louis, Andro-Marc

    With the benefits of an ever increasing advance of industrialization around the globe come formidable environmental problems. Three environmental problems that have relevance to the research described in this thesis are the 1) buildup of atmospheric CO2 gas through the burning of fossil fuels, 2) eutrophication of aquatic systems, and 3) the acidification of environments from acid mine drainage (AMD) resulting from coal-mining activities. In particular research is presented in this thesis that investigated the surface chemistry of CO2 and phosphate (PO43-) on a suite of environmentally relevant iron oxyhydroxide materials and the chemistry of phospholipid molecules on environmentally relevant iron sulfide surfaces to suppress AMD. To develop a microscopic understanding of the surface chemistry of the different systems, an array of experimental and computational techniques were used in the research. Techniques included X-ray photoelectron spectroscopy, atomic adsorption, X-ray diffraction, scanning transmission microscopy with electron dispersive X-ray spectroscopy (STEM/EDS), ion chromatography (IC), and attenuated total reflectance Fourier transform Infrared (ATR-FTIR). Results from the latter technique were interpreted with the aid of density function theory (DFT) calculations. Iron oxyhydroxides, which consisted of ferrihydrite (FeOOH), goethite (α-FeOOH), ferrimagnetic ferrihydrite (FerriFh), and aluminum-doped iron oxyhydroxide (content from 0-100 mol%) were synthesized and studied before and after exposure to gaseous CO2, CO32-, and PO43- species. FeOOH and mixed Al/Fe oxyhydroxide surfaces showed high affinities for the formation of carbonate and bicarbonate species upon exposure to gaseous CO2. Within the Al/Fe oxyhydroxide circumstance, a low Al level of incorporation in the iron oxyhydroxide structure caused a slight increase in surface area and increase in the amount of oxyanion (e.g., CO32- or PO43-) adsorption up to an Al level of 30 mol%. Significant

  5. Biogenic green synthesis of monodispersed gum kondagogu (Cochlospermum gossypium) iron nanocomposite material and its application in germination and growth of mung bean (Vigna radiata) as a plant model.

    Science.gov (United States)

    Raju, Dugyala; Mehta, Urmil J; Beedu, Sashidhar Rao

    2016-06-01

    An eco-friendly green and one-pot synthesis of highly monodispersed iron (Fe) nanoparticles (NPs) by using a natural biopolymer, gum kondagogu (GK) as reducing and capping agent is proposed. The NPs synthesised were characterised by ultra-violet-visible spectroscopy, transmission electron microscopy, scanning electron microscopy and X-ray diffraction. As the concentration of gum and time increases, the intensity of NPs formation increased. The NPs were highly monodispersed with uniform circular shapes of 2-6 nm in size. The formed NPs were crystalline in nature which was confirmed by diffraction analysis. The conversion ratio of Fe ionic form to NPs was 21% which was quantified by inductively coupled plasma mass spectroscopy (ICP-MS). Fe is essential for plant growth and development. A study was conducted to examine the effect of these NPs on the growth of mung bean (Vigna radiata). The radical length and biomass was increased in seeds exposed to Fe NPs than the ions. The uptake of Fe NPs by the sprouts was also quantified by ICP-MS, in which Fe was more in mung bean seeds exposed to NPs. The α-amylase activity was increased in the seeds exposed to NPs. The observed increase in the biomass by Fe NPs and seed germination may facilitate its application in the agriculture as an important cost-effective method for plant growth. PMID:27256894

  6. Aluminum oxyhydroxide based separator/electrolyte and battery system, and a method of making the same

    Science.gov (United States)

    Gerald, II; Rex E.; Klingler, Robert J.; Rathke, Jerome W.

    2011-02-15

    The instant invention relates a solid-state electrochemical cell and a novel separator/electrolyte incorporated therein. The invented electrochemical cell generally comprising: a unique metal oxyhydroxide based (i.e. AlOOH) separator/electrolyte membrane sandwiched between a first electrode and a second electrode. The novel separator/electrolyte comprises a nanoparticulate metal oxyhydroxide, preferably AlOOH and a salt which are mixed and then pressed together to form a monolithic metal oxyhydroxide-salt membrane.

  7. BIO-1211 (Biogen).

    Science.gov (United States)

    Bolger, G T

    2000-05-01

    Biogen, in collaboration with Merck & Co, is developing late activator VLA-4 (alpha4beta1) integrin antagonists for the potential treatment of inflammatory conditions [271194]. Merck has begun phase II trials with the lead compound, BIO-1211, for asthma, Biogen is still conducting preclinical research for its designated indications [317648,319225]. Under the collaborative agreement, each company has worldwide rights to certain indications; Merck has rights for asthma and Biogen retains the rights to a number of smaller indications, including multiple sclerosis, inflammatory bowel disease, renal indications and most diseases in which the US patient population is less than 200,000 [271194]. VLA-4 inhibitors show anti-inflammatory action by inhibition of binding between adhesion factors and leukocytes, but with no loss of basophil function, and they have the advantage of specificity not seen with existing drugs [273417]. In February 1999, Lehman Brothers predicted 40% probabilities that the compound would reach the US and ex-US markets for the asthma indication (Merck), and launch onto these markets by 2003. Peak annual sales of US dollar 500 million (US) and US dollar 500 million (outside US) are predicted, both in 2010 [319225]. PMID:16100687

  8. Arsenic species in weathering mine tailings and biogenic solids at the Lava Cap Mine Superfund Site, Nevada City, CA

    Science.gov (United States)

    2011-01-01

    linear combination, least-squares fits totals of several samples deviate by more than ± 20% from 100%, suggesting that additional phases may be present that were not identified or evaluated in this study. Conclusions Sub- to anoxic conditions minimize dissolution of arsenopyrite at the LCMS site, but may accelerate the dissolution of As-bearing secondary iron phases such as Fe3+-oxyhydroxides and arseniosiderite, if sufficient organic matter is present to spur anaerobic microbial activity. Oxidizing, dry conditions favor the stabilization of secondary phases, while promoting oxidative breakdown of the primary sulfides. The stability of both primary and secondary As phases is likely to be at a minimum under cyclic wet-dry conditions. Biogenic iron (hydr)oxide flocs can sequester significant amounts of arsenic; this property may be useful for treatment of perpetual sources of As such as mine adit water, but the fate of As associated with natural accumulations of floc material needs to be assessed. PMID:21261983

  9. Arsenic species in weathering mine tailings and biogenic solids at the Lava Cap Mine Superfund Site, Nevada City, CA

    Directory of Open Access Journals (Sweden)

    Ashley Roger P

    2011-01-01

    less certain. The linear combination, least-squares fits totals of several samples deviate by more than ± 20% from 100%, suggesting that additional phases may be present that were not identified or evaluated in this study. Conclusions Sub- to anoxic conditions minimize dissolution of arsenopyrite at the LCMS site, but may accelerate the dissolution of As-bearing secondary iron phases such as Fe3+-oxyhydroxides and arseniosiderite, if sufficient organic matter is present to spur anaerobic microbial activity. Oxidizing, dry conditions favor the stabilization of secondary phases, while promoting oxidative breakdown of the primary sulfides. The stability of both primary and secondary As phases is likely to be at a minimum under cyclic wet-dry conditions. Biogenic iron (hydroxide flocs can sequester significant amounts of arsenic; this property may be useful for treatment of perpetual sources of As such as mine adit water, but the fate of As associated with natural accumulations of floc material needs to be assessed.

  10. Determination of the stable iron isotopic composition of sequentially leached iron phases in marine sediments

    OpenAIRE

    Henkel, Susann; Kasten, Sabine; Poulton, Simon W.; Michael STAUBWASSER

    2016-01-01

    Reactive iron (oxyhydr)oxide minerals preferentially undergo early diagenetic redox cycling which can result in the production of dissolved Fe(II), the adsorption of Fe(II) onto particle surfaces, and the formation of authigenic Fe minerals. The partitioning of iron in sediments has traditionally been studied by applying sequential extractions that target operationally-defined iron phases. Here, we complement an existing sequential leaching method by developing a sample processing protocol fo...

  11. Biogenic magnetite in the nematode caenorhabditis elegans.

    Science.gov (United States)

    Cranfield, Charles G; Dawe, Adam; Karloukovski, Vassil; Dunin-Borkowski, Rafal E; de Pomerai, David; Dobson, Jon

    2004-01-01

    The nematode Caenorhabditis elegans is widely used as a model system in biological research. Recently, examination of the production of heat-shock proteins in this organism in response to mobile phone-type electromagnetic field exposure produced the most robust demonstration to date of a non-thermal, deleterious biological effect. Though these results appear to be a sound demonstration of non-thermal bioeffects, to our knowledge, no mechanism has been proposed to explain them. We show, apparently for the first time, that biogenic magnetite, a ferrimagnetic iron oxide, is present in C. elegans. Its presence may have confounding effects on experiments involving electromagnetic fields as well as implications for the use of this nematode as a model system for iron biomineralization in multi-cellular organisms. PMID:15801597

  12. Aluminum oxyhydroxide based separator/electrolyte and battery system, and a method making the same

    Science.gov (United States)

    Gerald, II, Rex E.; Klingler, Robert J.; Rathke, Jerome W.

    2011-03-08

    The instant invention relates a solid-state electrochemical cell and a novel separator/electrolyte incorporated therein. A preferred embodiment of the invented electrochemical cell generally comprises a unique metal oxyhydroxide based (i.e. AlOOH) separator/electrolyte membrane sandwiched between a first electrode and a second electrode. A preferred novel separator/electrolyte comprises a nanoparticulate metal oxyhydroxide, preferably AlOOH and a salt which are mixed and then pressed together to form a monolithic metal oxyhydroxide-salt membrane.

  13. Biogenic Impact on Materials

    Science.gov (United States)

    Stephan, Ina; Askew, Peter; Gorbushina, Anna; Grinda, Manfred; Hertel, Horst; Krumbein, Wolfgang; Müller, Rolf-Joachim; Pantke, Michael; Plarre, Rüdiger (Rudy); Schmitt, Guenter; Schwibbert, Karin

    Materials as constituents of products or components of technical systems rarely exist in isolation and many must cope with exposure in the natural world. This chapter describes methods that simulate how a material is influenced through contact with living systems such as microorganisms and arthropods. Both unwanted and desirable interactions are considered. This biogenic impact on materials is intimately associated with the environment to which the material is exposed (Materials-Environment Interaction, Chap. 15). Factors such as moisture, temperature and availability of food sources all have a significant influence on biological systems. Corrosion (Chap. 12) and wear (Chap. 13) can also be induced or enhanced in the presence of microorganisms. Section 14.1 introduces the categories between desired (biodegradation) and undesired (biodeterioration) biological effects on materials. It also introduces the role of biocides for the protection of materials. Section 14.2 describes the testing of wood as a building material especially against microorganisms and insects. Section 14.3 characterizes the test methodologies for two other groups of organic materials, namely polymers (Sect. 14.3.1) and paper and textiles (Sect. 14.3.2). Section 14.4 deals with the susceptibility of inorganic materials such as metals (Sect. 14.4.1), concrete (Sect. 14.4.2) and ceramics (Sect. 14.4.3) to biogenic impact. Section 14.5 treats the testing methodology concerned with the performance of coatings and coating materials. In many of these tests specific strains of organisms are employed. It is vital that these strains retain their ability to utilize/attack the substrate from which they were isolated, even when kept for many years in the laboratory. Section 14.6 therefore considers the importance of maintaining robust and representative test organisms that are as capable of utilizing a substrate as their counterparts in nature such that realistic predictions of performance can be made.

  14. The biogenic approach to cognition.

    Science.gov (United States)

    Lyon, Pamela

    2006-03-01

    After half a century of cognitive revolution we remain far from agreement about what cognition is and what cognition does. It was once thought that these questions could wait until the data were in. Today there is a mountain of data, but no way of making sense of it. The time for tackling the fundamental issues has arrived. The biogenic approach to cognition is introduced not as a solution but as a means of approaching the issues. The traditional, and still predominant, methodological stance in cognitive inquiry is what I call the anthropogenic approach: assume human cognition as the paradigm and work 'down' to a more general explanatory concept. The biogenic approach, on the other hand, starts with the facts of biology as the basis for theorizing and works 'up' to the human case by asking psychological questions as if they were biological questions. Biogenic explanations of cognition are currently clustered around two main frameworks for understanding biology: self-organizing complex systems and autopoiesis. The paper describes the frameworks and infers from them ten empirical principles--the biogenic 'family traits'--that constitute constraints on biogenic theorizing. Because the anthropogenic approach to cognition is not constrained empirically to the same degree, I argue that the biogenic approach is superior for approaching a general theory of cognition as a natural phenomenon. PMID:16628463

  15. Ferrite grade iron oxides from ore rejects

    Indian Academy of Sciences (India)

    K S Rane; V M S Verenkar; P Y Sawant

    2001-06-01

    Iron oxyhydroxides and hydroxides were synthesized from chemically beneficiated high SiO2/Al2O3 low-grade iron ore (57.49% Fe2O3) rejects and heated to get iron oxides of 96–99.73% purity. The infrared band positions, isothermal weight loss and thermogravimetric and chemical analysis established the chemical formulas of iron-oxyhydroxides as -FeOOH.0.3H2O; -FeOOH.0.2H2O and amorphous FeOOH. The thermal products of all these were -Fe2O3 excepting that of -FeOOH.0.3H2O which gave mainly -Fe2O3 and some admixture of -Fe2O3. The hydrazinated iron hydroxides and oxyhydroxides, on the other hand, decomposed autocatalytically to mainly -Fe2O3. Hydrazine method modifies the thermal decomposition path of the hydroxides. The saturation magnetization, s, values were found to be in the range 60–71 emu g–1 which are close to the reported values for -Fe2O3. Mechanism of the -Fe2O3 formation by hydrazine method is discussed.

  16. Iron dynamics in the rhizosphere as a case study for analyzing interactions between soils, plants and microbes

    OpenAIRE

    Lemanceau, Philippe; Bauer, Petra; Kraemer, Stephan; Briat, Jean-Francois

    2010-01-01

    Iron is an essential element for plants and microbes. However, in most cultivated soils, the concentration of iron available for these living organisms is very low because its solubility is controlled by stable hydroxides, oxyhydroxides and oxides. In the rhizosphere, there is a high demand of iron because of the iron uptake by plants, and microorganisms which density and activity are promoted by the release of root exudates. Plants and microbes have evolved active strategies of iron uptake. ...

  17. Facile synthesis of iron phosphide nanorods for efficient and durable electrochemical oxygen evolution.

    Science.gov (United States)

    Xiong, Dehua; Wang, Xiaoguang; Li, Wei; Liu, Lifeng

    2016-07-01

    Iron phosphide (FeP) nanorods have been fabricated by a facile hydrothermal synthesis of iron oxyhydroxide precursors, followed by a convenient phosphorization process. The FeP nanorods dispersed on carbon fiber paper current collectors exhibit outstanding catalytic activity and excellent long-term stability toward the oxygen evolution reaction (OER). PMID:27333123

  18. Thermochemistry of Ruthenium Oxyhydroxide Species and Their Impact on Volatile Speciations in Severe Nuclear Accident Conditions.

    Science.gov (United States)

    Miradji, Faoulat; Virot, François; Souvi, Sidi; Cantrel, Laurent; Louis, Florent; Vallet, Valérie

    2016-02-01

    Literature thermodynamic data of ruthenium oxyhydroxides reveal large uncertainties in some of the standard enthalpies of formation, motivating the use of high-level relativistic correlated quantum chemical methods to reduce the level of discrepancies. Reaction energies leading to the formation of all possible oxyhydroxide species RuOx(OH)y(H2O)z have been calculated for a series of reactions combining DFT (TPSSh-5%HF) geometries and partition functions, CCSD(T) energies extrapolated to the complete basis set limits. The highly accurate ab initio thermodynamic data were used as input data of thermodynamic equilibrium computations to derive the speciation of gaseous ruthenium species in the temperature, pressure and concentration conditions of severe nuclear accidents occurring in pressurized water reactors. At temperatures lower than 1000 K, gaseous ruthenium tetraoxide is the dominating species, between 1000 and 2000 K ruthenium trioxide becomes preponderant, whereas at higher temperatures gaseous ruthenium oxide, dioxide and even Ru in gaseous phase are formed. Although earlier studies predicted the formation of oxyhydroxides in significant quantities, the use of highly accurate ab initio thermodynamic data for ruthenium gaseous species leads to a more reliable inventory of gaseous ruthenium species in which gaseous oxyhydroxide ruthenium molecules are formed only in negligible amounts. PMID:26789932

  19. Synthesis of aluminum oxy-hydroxide nanofibers from porous anodic alumina.

    Science.gov (United States)

    Jha, Himendra; Kikuchi, Tatsuya; Sakairi, Masatoshi; Takahashi, Hideaki

    2008-10-01

    A novel method for the synthesis of aluminum oxy-hydroxide nanofibers from a porous anodic oxide film of aluminum is demonstrated. In the present method, the porous anodic alumina not only acts as a template, but also serves as the starting material for the synthesis. The porous anodic alumina film is hydrothermally treated for pore-sealing, which forms aluminum oxy-hydroxide inside the pores of the oxide film as well as on the surface of the film. The hydrothermally sealed porous oxide film is immersed in the sodium citrate solution, which selectively etches the porous aluminum oxide from the film, leaving the oxy-hydroxide intact. The method is simple and gives highly uniform aluminum oxy-hydroxide nanofibers. Moreover, the diameter of the nanofibers can be controlled by controlling the pore size of the porous anodic alumina film, which depends on the anodizing conditions. Nanofibers with diameters of about 38-85 nm, having uniform shape and size, were successfully synthesized using the present method. PMID:21832599

  20. Synthesis of aluminum oxy-hydroxide nanofibers from porous anodic alumina

    Energy Technology Data Exchange (ETDEWEB)

    Jha, Himendra; Kikuchi, Tatsuya; Sakairi, Masatoshi; Takahashi, Hideaki [Laboratory of Interface Microstructure Analysis (LIMSA), Division of Materials Science and Engineering, Graduate School of Engineering, Hokkaido University, Sapporo 060-8628 (Japan)], E-mail: himendra@eng.hokudai.ac.jp

    2008-10-01

    A novel method for the synthesis of aluminum oxy-hydroxide nanofibers from a porous anodic oxide film of aluminum is demonstrated. In the present method, the porous anodic alumina not only acts as a template, but also serves as the starting material for the synthesis. The porous anodic alumina film is hydrothermally treated for pore-sealing, which forms aluminum oxy-hydroxide inside the pores of the oxide film as well as on the surface of the film. The hydrothermally sealed porous oxide film is immersed in the sodium citrate solution, which selectively etches the porous aluminum oxide from the film, leaving the oxy-hydroxide intact. The method is simple and gives highly uniform aluminum oxy-hydroxide nanofibers. Moreover, the diameter of the nanofibers can be controlled by controlling the pore size of the porous anodic alumina film, which depends on the anodizing conditions. Nanofibers with diameters of about 38-85 nm, having uniform shape and size, were successfully synthesized using the present method.

  1. Biogenic amines in dairy products

    OpenAIRE

    Linares, Daniel M.; Martín, M. Cruz; Ladero Losada, Víctor Manuel; Álvarez González, Miguel Ángel; Fernández García, María

    2011-01-01

    Biogenic amines (BA) are organic, basic, nitrogenous compounds with biological activity, mainly formed by the decarboxylation of amino acids. BA are present in a wide range of foods, including dairy products, and can accumulate in high concentrations. In some cheeses more than 1000 mg of BA have been detected per kilogram of cheese. The consumption of food containing large amounts of these amines can have toxicological consequences. Although there is no specific legislation regarding the BA c...

  2. Biogenic amines in seafood: a review.

    Science.gov (United States)

    Biji, K B; Ravishankar, C N; Venkateswarlu, R; Mohan, C O; Gopal, T K Srinivasa

    2016-05-01

    The biogenic amines are low molecular weight organic bases present normally in the body with biological activity influencing important physiological functions. The physiological functions of these molecules are achieved by very low concentrations in the tissues. However, significantly high amounts of biogenic amines are produced during processing and storage of seafood as a result of microbial contamination and inadequate storage conditions. Microorganisms having decarboxylase enzyme activity convert amino acids to their respective biogenic amines. Biogenic amines in seafood have been implicated as a major causative agent of food borne illness, where intoxication results from the ingestion of foods containing higher amount of biogenic amines. Hence its identification, quantitation and awareness of this food borne toxin are important in relation to food safety and spoilage. The aim of this paper is to review the basic concepts of seafood quality and safety in relation to biogenic amines along with its control measures and future areas for research. PMID:27407186

  3. BIOGENIC AMINES CONTENT IN DIFFERENT WINE SAMPLES

    OpenAIRE

    Attila Kántor; Miroslava Kačániová; Vendula Pachlová

    2015-01-01

    Twenty-five samples of different Slovak wines before and after filtration were analysed in order to determine the content of eight biogenic amines (tryptamine, phenylalanine, putrescine, cadaverine, histamine, tyramine, spermidine and spermine). The method involves extraction of biogenic amines from wine samples with used dansyl chloride. Ultra-high performance liquid chromatography (UHPLC) was used for determination of biogenic amines equipped with a Rapid Resolution High Definition (RRHD), ...

  4. Synthesis and characterisation of new MO(OH)2 (M = Zr, Hf) oxyhydroxides and related Li2MO3 salts.

    Science.gov (United States)

    Baklanova, Yana V; Denisova, Tatyana A; Maksimova, Lidiya G; Tyutyunnik, Alexander P; Baklanova, Inna V; Shein, Igor R; Neder, Reinhard B; Tarakina, Nadezda V

    2014-02-21

    Two new solid MO(OH)2 (M = Zr, Hf) oxyhydroxides have been synthesised by an ion-exchange reaction from Li2MO3 (M = Zr, Hf) precursors obtained by a citrate combustion technique. The crystal structure of the oxyhydroxides has been solved by direct methods and refined using Rietveld full profile fitting based on X-ray powder diffraction data. Both oxyhydroxides crystallize in a P2(1)/c monoclinic unit cell and have a structure resembling that of the related salts. Detailed characterisation of the fine-structure features and chemical bonding in precursors and oxyhydroxide powders has been performed using vibrational spectroscopy, nuclear magnetic resonance spectroscopy, scanning electron microscopy, pair distribution function analysis and quantum-chemical modelling. PMID:24343584

  5. Effects of phosphate and silicate on the transformation of hydroxycarbonate green rust to ferric oxyhydroxides

    Science.gov (United States)

    Feng, Xionghan; Wang, Xiaoming; Zhu, Mengqiang; Koopal, Luuk K.; Xu, Huanhuan; Wang, Yan; Liu, Fan

    2015-12-01

    transformation of the γ-FeOOH-like phase to goethite is catalyzed by the adsorbed Fe(II). For the P system, the released Fe(II) forms ternary surface complexes with P on the mineral surfaces without any catalytic role, leading to the formation of lepidocrocite at low P concentrations. Clearly, the oxidative transformation of green rust to various crystalline iron oxyhydroxides depends on the type and concentration (Fe/anion molar ratio) of co-existing anions. This study also suggests that the natural goethite formed by Fe(II) oxidation in the form of plate-like or isodimensional particles is most likely related to the ubiquitous presence of silicates in soil environments.

  6. The associations of heavy metals with crystalline iron oxides in the polluted soils around the mining areas in Guangdong Province, China.

    Science.gov (United States)

    Yin, Hui; Tan, Nianhao; Liu, Chuanping; Wang, Juju; Liang, Xiaoliang; Qu, Mingkai; Feng, Xionghan; Qiu, Guohong; Tan, Wenfeng; Liu, Fan

    2016-10-01

    In current selective sequential extraction (SSE) methods, heavy metals associated well-crystallized iron oxyhydroxides are not well defined and considered, and usually fall into residual forms, which actually make their mobility and environmental risk underestimated. This study compared various fractions of heavy metals in samples of mining tailings and nearby soils under different land uses in Guangdong Province of China. Iron oxides in these soils were mainly Al-substituted goethites and/or hematites. Independent of the land uses, the percentages of various Cd fractions in the soils decrease in the order of well-crystallized iron oxyhydroxides-associated (27.2-91.2%) > residual (2.1-37.0%) > reducible FeMn oxides (3.2-45.7%) > exchangeable (1.0-28.2%) > organic-associated form (0-5.1%). Pb mainly existes in the residual fraction (25.9-74.5%), followed by crystalline iron oxyhydroxides-associated (0.4-69.0%) and reducible fractions (2.4-40.4%). Zn mainly exists in the residual fraction (25.4-85.9%), followed by the well-crystallized iron oxyhydroxides-associated fraction (6.4-55.0%). However, Cu mainly existes in the residual form and the fractionation of Cu varies obviously between samples. The association of these metals with crystalline iron oxyhydroxides in the soils decreases in the sequence of Cd > Pb > Zn > Cu. These results suggest that in heavy-metal-polluted weathered soils in tropical and subtropical areas enriched with iron oxides, it is essential to assess potential bioavailability and toxicity of heavy metals bound to well-crystallized iron oxyhydroxides with appropriate procedures in the fractionation measurement. The modified Tessier method present here can be used to quantify the fractions of heavy metals in such areas. PMID:27427775

  7. Iron and Iron Metabolism

    OpenAIRE

    Melike Sezgin Evim; Birol Baytan; Adalet Meral Güneş

    2012-01-01

    Iron is an essential element for almost all living organisms except some bacteria. A great number of new articles related to the iron metabolism have been published in recent years explaining new findings. Hepsidine, a peptide hormon, that is recently found, regulates iron methabolism by effecting iron absorbsion from gut, secreting iron from hepatic store and flows iron from macrophages. Hepsidin blockes to effluxe iron from cells by bounding to ferroportin and by inducing ferroportin destru...

  8. Improved dewatering of CEPT sludge by biogenic flocculant from Acidithiobacillus ferrooxidans.

    Science.gov (United States)

    Wong, Jonathan W C; Murugesan, Kumarasamy; Yu, Shuk Man; Kurade, Mayur B; Selvam, Ammaiyappan

    2016-01-01

    Bioleaching using an iron-oxidizing bacterium, Acidithiobacillus ferrooxidans, and its biogenic flocculants was evaluated to improve the dewaterability of chemically enhanced primary treatment (CEPT) sewage sludge. CEPT sludge in flasks was inoculated with A. ferrooxidans culture, medium-free cells and the cell-free culture filtrate with and without the energy substance Fe(2+), and periodically the sludge samples were analysed for the dewaterability. This investigation proves that bioleaching effectively improved the sludge dewaterability as evidenced from drastic reduction in capillary suction time (≤20 seconds) and specific resistance to filtration (≥90%); however, it requires an adaptability period of 1-2 days. On the other hand, the biogenic flocculant produced by A. ferrooxidans greatly decreased the time-to-filtration and facilitated the dewaterability within 4 h. Results indicate that rapid dewatering of CEPT sludge by biogenic flocculants provides an opportunity to replace the synthetic organic polymer for dewatering. PMID:26901727

  9. A comparison between acoustic properties and heat effects in biogenic (magnetosomes) and abiotic magnetite nanoparticle suspensions

    Science.gov (United States)

    Józefczak, A.; Leszczyński, B.; Skumiel, A.; Hornowski, T.

    2016-06-01

    Magnetic nanoparticles show unique properties and find many applications because of the possibility to control their properties using magnetic field. Magnetic nanoparticles are usually synthesized chemically and modification of the particle surface is necessary. Another source of magnetic nanoparticles are various magnetotactic bacteria. These biogenic nanoparticles (magnetosomes) represent an attractive alternative to chemically synthesized iron oxide particles because of their unique characteristics and a high potential for biotechnological and biomedical applications. This work presents a comparison between acoustic properties of biogenic and abiotic magnetite nanoparticle suspensions. Experimental studies have shown the influence of a biological membrane on the ultrasound properties of magnetosomes suspension. Finally the heat effect in synthetic and biogenic magnetite nanoparticles is also discussed. The experimental study shows that magnetosomes present good heating efficiency.

  10. The role of biogenic structures on the biogeochemical functioning of mangrove constructed wetlands sediments - A mesocosm approach

    International Nuclear Information System (INIS)

    Benthic metabolism (measured as CO2 production) and carbon oxidation pathways were evaluated in 4 mangrove mesocosms subjected daily to seawater or 60% sewage in the absence or presence of mangrove trees and biogenic structures (pneumatophores and crab burrows). Total CO2 emission from darkened sediments devoid of biogenic structures at pristine conditions was comparable during inundation (immersion) and air exposure (emersion), although increased 2-7 times in sewage contaminated mesocosms. Biogenic structures increased low tide carbon gas emissions at contaminated (30%) and particularly pristine conditions (60%). When sewage was loaded into the mesocosms under unvegetated and planted conditions, iron reduction was substituted by sulfate reduction and contribution of aerobic respiration to total metabolism remained above 50%. Our results clearly show impacts of sewage on the partitioning of electron acceptors in mangrove sediment and confirm the importance of biogenic structures for biogeochemical functioning but also on greenhouse gases emission.

  11. Interactions of silica with iron oxides: Effects on oxide transformations and sorption properties

    International Nuclear Information System (INIS)

    This report is a review of the literature on the adsorption of silica species on iron oxides and oxyhydroxides, and its effects on the adsorption of other species and on oxide interconversion reactions. The information is discussed briefly in the contexts of nuclear waste disposal and boiler-water chemistry. (author). 76 refs

  12. Structural incorporation of iron into Ge-imogolite nanotubes: a promising step for innovative nanomaterials

    OpenAIRE

    Avellan, A.; Levard, C.; Kumar, N; Rose, J.; L. Olivi; Thill, A.; Chaurand, P.; Borschneck, D.; Masion, A.

    2014-01-01

    Novel iron-doped aluminogermanate nanotubes were obtained using a single step, aqueous phase synthesis protocol. These nanotubes are isostructural with imogolite, a natural occurring nanofiber, but are obtained by-product free in substantially larger quantities with aluminum substitution levels around 1%. Increasing the Fe concentrations led to higher substitution levels but also to the co-precipitation of Fe (oxy)hydroxides.

  13. Multifunctional Silver Coated E-33/Iron Oxide Water Filters: Inhibition of Biofilm Growth and Arsenic Removal

    Science.gov (United States)

    Bayoxide® E33 (E-33, Goethite) is a widely used commercial material for arsenic adsorption. It is a mixture of iron oxyhydroxide and oxides. E-33 is primarily used to remove arsenic from water and to a lesser extent, other anions, but generally lacks multifunctuality. It is a non...

  14. Metallic iron for environmental remediation: learning from electrocoagulation.

    OpenAIRE

    Noubactep, C.; Schöner, A.

    2010-01-01

    The interpretation of processes yielding aqueous contaminant removal in the presence of elemental iron (e.g. in Fe(0)/H(2)O systems) is subject to numerous complications. Reductive transformations by Fe(0) and its primary corrosion products (Fe(II) and H/H(2)) as well as adsorption onto and co-precipitation with secondary and tertiary iron corrosion products (iron hydroxides, oxyhydroxides, and mixed valence Fe(II)/Fe(III) green rusts) are considered the main removal mechanisms on a case-to-c...

  15. FeII induced mineralogical transformations of ferric oxyhydroxides into magnetite of variable stoichiometry and morphology

    OpenAIRE

    Usman, Muhammad; Abdelmoula, Mustapha; Hanna, Khalil; Grégoire, Brian; Faure, Pierre; Ruby, Christian

    2012-01-01

    The Mössbauer spectroscopy was used to monitor the mineralogical transformations of ferrihydrite (F), lepidocrocite (L) and goethite (G) into magnetite as a function of aging time. Ferric oxyhydroxides were reacted with soluble FeII and OH- in stoichiometric amounts to form magnetite at an initial pH of  9.7. Observed transformation extent into magnetite followed the order: F > L > G with almost 30 % of untransformed G after 1 month. The departure from stoichiometry, δ, of magnetite (Fe3-δO4...

  16. A comparative study of nitrite reduction by synthetic and biogenic Fe(II-III) hydroxysalts green rusts: Evidence for hydroxyl-nitrite green rust formation as an intermediate reaction product.

    Science.gov (United States)

    Ona-Nguema, G.; Guerbois, D.; Morin, G.; Zhang, Y.; Noel, V.; Brest, J.

    2013-12-01

    The occurrence of high nitrite concentrations as a result of anthropogenic activities is an important water quality concern as it is highly toxic to human and fauna, and it is used as a nitrogen source for the assimilation process. The toxicity of nitrite is related to its transformation into carcinogenic N-nitroso compounds, which are suspected to be responsible for some gastric cancers, and to its ability to convert the hemoglobin to methaemoglobin what is then unable to fix oxygen and to transport it to the tissues, involving hypoxia and the blue-baby syndrome [1]. To reduce the adverse effect of nitrite on human health and on macroalgal blooms, any process enhancing the transformation of nitrite ions to nitrogen gas is of interest for the remediation of natural environments. To achieve this purpose the use of processes involving Fe(II)-containing minerals could be considered as one of the best options. Green-rusts are mixed Fe(II-III) layered double hydroxides commonly found in anoxic zones of natural environments such as sediments and hydromorphic soils. In such anoxic environments, green rust minerals play an important role in the biogeochemical redox cycling of iron and nitrogen, and can affect the speciation and mobility of many organic and inorganic contaminants. The present study investigates the reduction of nitrite by two synthetic and two biogenic green rusts. On the one hand, Fe(II-III) hydroxychloride and Fe(II-III) hydroxycarbonate green rusts were used as synthetic interlayer forms of GR, which are referred to as ';syn-GR(CO3)' and ';syn-GR(Cl)', respectively. On the other hand, the study was performed with biogenic Fe(II-III) hydroxycarbonate green rusts obtained from the bioreduction of two ferric precursors, either Fe(III)-oxyhydroxycarbonate or lepidocrocite; these biogenic green rusts are referred to as ';bio-GR(CO3)F' and ';bio-GR(CO3)L', respectively. For synthetic green rusts, results showed that the oxidation of both syn-GR(CO3) and syn

  17. The gas phase oxide and oxyhydroxide chemistry of trace amounts of rhenium

    International Nuclear Information System (INIS)

    In preparation of experiments to investigate the chemical properties of bohrium (Bh, element 107) the behaviour of Re, its lighter homologue in group 7, was studied in different oxidizing chemical systems. The adsorption data of Re oxide and oxyhydroxide compounds on quartz surfaces were evaluated from results of thermochromatography experiments and confirmed in isothermal gas chromatography experiments applying 1 cm as standard state for the simple gas adsorption process: X(g) ↔ X(ads) (X = ReO3, HReO4) ΔHads(ReO3) = -190 ± 10 kJ/mol; ΔSads(ReO3) = -179±30 J/mol K; ΔHads(HReO4) = -77 ± 5 kJ/mol; ΔSads(HReO4) = -187±50 J/mol K. An on-line separation method for oxides and oxyhydroxides of short lived Re isotopes using isothermal high temperature gas-solid adsorption chromatography was developed. Separation yields and times of group 7 elements from lanthanides (model for actinides), polonium and bismuth were determined using the model isotopes 169,170,174,176Re, 152-155Er, 151-154Ho, 218Po, and 214Bi. An updated correlation function between the microscopic adsorption enthalpy and the macroscopic sublimation enthalpy was calculated from the experimental adsorption data of this work and literature data. (orig.)

  18. The gas phase oxide and oxyhydroxide chemistry of trace amounts of rhenium

    Energy Technology Data Exchange (ETDEWEB)

    Eichler, R. [Dept. of Chemistry and Biochemistry, Univ. of Bern (Switzerland); Eichler, B.; Jost, D.T.; Dressler, R.; Tuerler, A. [Paul-Scherrer-Inst., Villigen (Switzerland); Gaeggeler, H.W. [Dept. of Chemistry and Biochemistry, Univ. of Bern (Switzerland); Paul-Scherrer-Inst., Villigen (Switzerland)

    1999-07-01

    In preparation of experiments to investigate the chemical properties of bohrium (Bh, element 107) the behaviour of Re, its lighter homologue in group 7, was studied in different oxidizing chemical systems. The adsorption data of Re oxide and oxyhydroxide compounds on quartz surfaces were evaluated from results of thermochromatography experiments and confirmed in isothermal gas chromatography experiments applying 1 cm as standard state for the simple gas adsorption process: X(g) {r_reversible} X(ads) (X = ReO{sub 3}, HReO{sub 4}) {delta}H{sub ads}(ReO{sub 3}) = -190 {+-} 10 kJ/mol; {delta}S{sub ads}(ReO{sub 3}) = -179{+-}30 J/mol K; {delta}H{sub ads}(HReO{sub 4}) = -77 {+-} 5 kJ/mol; {delta}S{sub ads}(HReO{sub 4}) = -187{+-}50 J/mol K. An on-line separation method for oxides and oxyhydroxides of short lived Re isotopes using isothermal high temperature gas-solid adsorption chromatography was developed. Separation yields and times of group 7 elements from lanthanides (model for actinides), polonium and bismuth were determined using the model isotopes {sup 169,170,174,176}Re, {sup 152-155}Er, {sup 151-154}Ho, {sup 218}Po, and {sup 214}Bi. An updated correlation function between the microscopic adsorption enthalpy and the macroscopic sublimation enthalpy was calculated from the experimental adsorption data of this work and literature data. (orig.)

  19. SPATIAL VARIATIONS IN BIOGENIC EMISSIONS FOR LITHUANIA

    OpenAIRE

    Ulevičius, Vidmantas; Byčenkien, Svetlana; Senuta, Kestas

    2008-01-01

    Abstract: The numerical modelling of biogenic volatile organic compounds (BVOCs) monoterpene and isoprene was carried out using three-dimensional (3D) mesoscale meteorological and photochemical atmospheric models. Emission factors, combined with land cover data represented by the appropriate 11 Biogenic Emission Inventory System (BEIS) vegetation categories, along with environmental correction factors were used to derive emission fluxes of isoprene, monoterpene and other VOCs for Lit...

  20. Formation temperatures of thermogenic and biogenic methane

    OpenAIRE

    Stolper, D. A.; Lawson, M.; Davis, C. L.; Ferreira, A. A.; Santos Neto, E. V.; Ellis, G.S.; Lewan, M.D.; Martini, A. M.; Tang, Y.; Schoell, M.; Sessions, A.L.; Eiler, J. M.

    2014-01-01

    Methane is an important greenhouse gas and energy resource generated dominantly by methanogens at low temperatures and through the breakdown of organic molecules at high temperatures. However, methane-formation temperatures in nature are often poorly constrained. We measured formation temperatures of thermogenic and biogenic methane using a “clumped isotope” technique. Thermogenic gases yield formation temperatures between 157° and 221°C, within the nominal gas window, and biogenic gases yiel...

  1. Biogenic amines in raw and processed seafood

    OpenAIRE

    Pierina eVisciano; Maria eSchirone; Rosanna eTofalo; Giovanna eSuzzi

    2012-01-01

    The presence of biogenic amines in raw and processed seafood, associated with either time/temperature conditions or food technologies is discussed in the present paper from a safety and prevention point of view. In particular, storage temperature, handling practices, presence of microbial populations with decarboxylase activity and availability of free amino acids are considered the most important factors affecting the production of biogenic amines in raw seafood. On the other hand, some foo...

  2. Observations and assessment of iron oxide nanoparticles in metal-polluted mine drainage within a steep redox gradient, and a comparison to synthetic analogs

    OpenAIRE

    Johnson, Carol A.

    2014-01-01

    The complex interactions at the interfaces of minerals, microbes, and metals drive the cycling of iron and the fate and transport of metal(loid)s in contaminated systems. The former uranium mine near Ronneburg, Germany is one such system, where slightly acidic mine drainage crossing a steep redox gradient (groundwater outflow into a stream) forms and transforms iron (oxy)hydroxide nanoparticles. These particles interact with toxic metal(loid)s in water and sediments. Iron oxidizing and reduci...

  3. Effect of thermal treatment and ageing on IR transmission and visible photoluminescence of nanostructured aluminum oxyhydroxide

    International Nuclear Information System (INIS)

    IR transmission and visible photoluminescence (PL) were studied in raw nanoporous aluminum oxyhydroxide (NOA) and in samples after thermal treatment at different temperatures. Structural and chemical modifications of the NOA sample were related to the water content and adsorption/desorption process at the surface. The differences observed in the FTIR spectra in vacuum and after ageing of the samples can be explained by the effects of molecular water and OH- groups on the stability of the low-temperature phases of NOA. A considerable increase in PL intensity and spectrum expansion to longer wavelengths were observed in all NOA samples after water desorption. This was accompanied by strong changes in the PL decay kinetics. Quenching of the fast luminescent decay and low-energy transitions in aged samples were observed after ageing of the samples. Partial passivation of the NOA surface and defective sites under ambient conditions is discussed.

  4. Arsenic removal from acidic solutions with biogenic ferric precipitates.

    Science.gov (United States)

    Ahoranta, Sarita H; Kokko, Marika E; Papirio, Stefano; Özkaya, Bestamin; Puhakka, Jaakko A

    2016-04-01

    Treatment of acidic solution containing 5g/L of Fe(II) and 10mg/L of As(III) was studied in a system consisting of a biological fluidized-bed reactor (FBR) for iron oxidation, and a gravity settler for iron precipitation and separation of the ferric precipitates. At pH 3.0 and FBR retention time of 5.7h, 96-98% of the added Fe(II) precipitated (99.1% of which was jarosite). The highest iron oxidation and precipitation rates were 1070 and 28mg/L/h, respectively, and were achieved at pH 3.0. Subsequently, the effect of pH on arsenic removal through sorption and/or co-precipitation was examined by gradually decreasing solution pH from 3.0 to 1.6 (feed pH). At pH 3.0, 2.4 and 1.6, the highest arsenic removal efficiencies obtained were 99.5%, 80.1% and 7.1%, respectively. As the system had ferric precipitates in excess, decreased arsenic removal was likely due to reduced co-precipitation at pH<2.4. As(III) was partially oxidized to As(V) in the system. In shake flask experiments, As(V) sorbed onto jarosite better than As(III). Moreover, the sorption capacity of biogenic jarosite was significantly higher than that of synthetic jarosite. The developed bioprocess simultaneously and efficiently removes iron and arsenic from acidic solutions, indicating potential for mining wastewater treatment. PMID:26705889

  5. BIOGENIC AMINES CONTENT IN DIFFERENT WINE SAMPLES

    Directory of Open Access Journals (Sweden)

    Attila Kántor

    2015-02-01

    Full Text Available Twenty-five samples of different Slovak wines before and after filtration were analysed in order to determine the content of eight biogenic amines (tryptamine, phenylalanine, putrescine, cadaverine, histamine, tyramine, spermidine and spermine. The method involves extraction of biogenic amines from wine samples with used dansyl chloride. Ultra-high performance liquid chromatography (UHPLC was used for determination of biogenic amines equipped with a Rapid Resolution High Definition (RRHD, DAD detectors and Extend-C18 LC column (50 mm x 3.0 mm ID, 1.8 μm particle size. In this study the highest level of biogenic amine in all wine samples represent tryptamine (TRM with the highest content 170.9±5.3 mg/L in Pinot Blanc wine. Phenylalanine (PHE cadaverine (CAD, histamine (HIS and spermidine (SPD were not detected in all wines; mainly SPD was not detected in 16 wines, HIS not detected in 14 wines, PHE and CAD not detected in 2 wines. Tyramine (TYR, spermine (SPN and putrescine (PUT were detected in all wines, but PUT and SPN in very low concentration. The worst wine samples with high biogenic amine content were Saint Laurent (BF, Pinot Blanc (S and Pinot Noir (AF.

  6. Biogenic amines in raw and processed seafood

    Directory of Open Access Journals (Sweden)

    Pierina eVisciano

    2012-06-01

    Full Text Available The presence of biogenic amines in raw and processed seafood, associated with either time/temperature conditions or food technologies is discussed in the present paper from a safety and prevention point of view. In particular, storage temperature, handling practices, presence of microbial populations with decarboxylase activity and availability of free amino acids are considered the most important factors affecting the production of biogenic amines in raw seafood. On the other hand, some food technological treatments such as salting, ripening, fermentation or marination can increase the levels of biogenic amines in processed seafood. The consumption of high amount of biogenic amines, above all histamine, can result in food borne poisoning which is a worldwide problem. The European Regulation established as maximum limits for histamine, in fishery products from fish species associated with high histidine amounts, values ranging from 100 to 200 mg/kg, while for products which have undergone enzyme maturation treatment in brine, the aforementioned limits rise to 200 and 400 mg/kg. Preventive measures and emerging methods aiming at controlling the production of biogenic amines are also reported for potential application in seafood industries.

  7. FeII induced mineralogical transformations of ferric oxyhydroxides into magnetite of variable stoichiometry and morphology

    International Nuclear Information System (INIS)

    The Mössbauer spectroscopy was used to monitor the mineralogical transformations of ferrihydrite (F), lepidocrocite (L) and goethite (G) into magnetite as a function of aging time. Ferric oxyhydroxides were reacted with soluble FeII and OH– in stoichiometric amounts to form magnetite at an initial pH of ∼9.7. Observed transformation extent into magnetite followed the order: F>L>G with almost 30% of untransformed G after 1 month. The departure from stoichiometry, δ, of magnetite (Fe3−δO4) generated from F (δ∼0.04) and L (δ∼0.05) was relatively low as compared to that in magnetite from G (δ∼0.08). The analysis by transmission electron microscopy and BET revealed that generated magnetite was also different in terms of morphology, particle size and surface area depending on the nature of initial ferric oxyhydroxide. This method of preparation is a possible way to form nano-sized magnetite. - Graphical abstract: Mössbauer spectrum of the early stage of magnetite formation formed from the interaction of adsorbed FeII species with goethite. Highlights: ► Ferric oxides were reacted with hydroxylated FeII to form magnetite. ► Magnetite formation was quantified as a function of aging time. ► Complete transformation of ferrihydrite and lepidocrocite was achieved. ► Almost 70% of initial goethite was transformed. ► Resulting magnetites have differences in stoichiometry and morphological properties.

  8. Biogenic crust dynamics on sand dunes

    CERN Document Server

    Kinast, Shai; Yizhaq, Hezi; Ashkenazy, Yosef

    2012-01-01

    Sand dunes are often covered by vegetation and biogenic crusts. Despite their significant role in dune stabilization, biogenic crusts have rarely been considered in studies of dune dynamics. Using a simple model, we study the existence and stability ranges of different dune-cover states along gradients of rainfall and wind power. Two ranges of alternative stable states are identified: fixed crusted dunes and fixed vegetated dunes at low wind power, and fixed vegetated dunes and active dunes at high wind power. These results suggest a cross-over between two different forms of desertification.

  9. Biogenic amines and radiosensitivity of solitary cells

    International Nuclear Information System (INIS)

    Different stability of cells to ionizing radiation is considered from a position of the ''elevated biochemical radioresistance background'' concept. Experimental evidence presented indicates an important role of endogenic amines (serotonin and histamine) possessing radioprotector properties in the cell radioresistance formation. The concept about their effect as being solely a result of circulatory hypoxia is critically discussed. The experimental results favor the existence of a ''cellular'' component, along with the ''hypoxic'' one, in the mechanism of action of biogenic amines. These compounds can affect the initial stages of peroxide oxidation of lipids, thereby favoring a less intensive oxidation induced by radiation. Biogenic amines can also exert influence on the cyclic nucleotide system

  10. Factors influencing biogenic amines accumulation in dairy products

    OpenAIRE

    Daniel M. eLinares; Beatriz edel Río; Victor eLadero; Noelia eMartínez; María eFernández; María Cruz eMartín; Miguel A. eAlvarez

    2012-01-01

    Fermented foods are within the food products more often complained of having caused biogenic amines poisoning. Concerning milk-based fermented foods, cheese is the main product likely to contain significant levels of biogenic amines, specially tyramine, histamine and putrescine. Prompted by the increasing awareness of the risks related to dietary uptake of high biogenic amine loads, in this review we report about cheese elaboration and processing technological aspects affecting biogenic amine...

  11. Humic acid facilitates the transport of ARS-labeled hydroxyapatite nanoparticles in iron oxyhydroxide-coated sand

    Science.gov (United States)

    Hydroxyapatite nanoparticles (nHAP) have been widely used to remediate soil and wastewater contaminated with metals and radionuclides. However, our understanding of nHAP transport and fate is limited in natural environments that exhibit significant variability in solid and solution chemistry. The tr...

  12. A survey of biogenic amines in vinegars.

    Science.gov (United States)

    Ordóñez, J L; Callejón, R M; Morales, M L; García-Parrilla, M C

    2013-12-01

    This paper reports the determination of biogenic amines by high-performance liquid chromatography (HPLC) and fluorescence detection after derivatization with 6-aminoquinolyl-N-hydroxysuccinimidyl carbamate (AQC) in balsamic, apple, and red, white, and Sherry wine vinegars. A solid-phase extraction (SPE) with mixed-mode resins method was used before analysis. The method was successfully validated obtaining adequate values of selectivity, response linearity, precision, accuracy, and low detection and quantification limits. The total content of biogenic amines in vinegars ranged from 23.35 to 1445.2 μg/L, being lower than those reported in wines. Putrescine was the amine that showed the highest concentrations in most samples. Methylamine and phenylethylamine were not determined in any vinegar. Balsamic and "Pedro Ximénez" Sherry vinegars reached the highest amounts of biogenic amines, while apple, white and Sherry wine vinegars had the lowest concentrations. Principal component analysis using the biogenic amines as variables, allowed to separate the different kind of vinegars, excepting red vinegars. PMID:23871015

  13. Biogenic UO2 Characterization and Surface Reactivity

    International Nuclear Information System (INIS)

    Nano-scale biogenic UO2 is easier to oxidize and more reactive to aqueous metal ions than bulk UO2. In an attempt to understand these differences in properties, we have used a suite of bulk and surface characterization techniques to examine differences in the reactivity of biogenic UO2 versus bulk UO2 with respect to aqueous Zn(II). Precipitation of biogenic UO2 was mediated by Shewanella putrefaciens CN32, and the precipitates were washed using two protocols: (1) 5% NaOH, followed by 4 mM KHCO3/KCl (NA-wash; ''NAUO2'', to remove surface organic matter), and (2) 4 mM KHCO3-KCl (BI-wash; ''BIUO2'', to remove soluble uranyl species). BET surface areas of biogenic-UO2 prepared using the two protocols are 128.63 m2g-1 and 92.56 m2g-1, respectively; particle sizes range from 2-10 nm as determined by FEG-SEM. Surface composition was probed using XPS, which showed a strong carbon 1s signal for the BI-washed samples; surface uranium is > 90% U(IV) for both washing protocols. U LIII-edge XANES spectra also indicate that U(IV) is the dominant oxidation state in the biogenic UO2 samples. Fits of the EXAFS spectra of these samples yielded half the number of uranium second-shell neighbors relative to bulk UO2, and no detectable oxygen neighbors beyond the first shell. At pH 7, the sorption of Zn(II) onto both biogenic and bulk UO2 is independent of electrolyte concentration, suggesting that Zn(II) sorption complexes are dominantly inner-sphere. Fits of Zn K-edge EXAFS spectra for biogenic UO2 indicate that Zn(II) sorption is dependent on the washing protocol. Zn-U pair correlations are observed for the NA-washed samples, but not for the BI-washed ones, suggesting that Zn(II) sorbs directly to the UO2 surface in the first case, and possibly to organic matter in the latter. Further work is required to elucidate the binding mechanism of Zn(II) to bulk UO2

  14. Soil flushing, iron coprecipitation, and ceramic membrane filtration: Innovative technologies for remediating arsenic-contaminated soil and groundwater

    Energy Technology Data Exchange (ETDEWEB)

    Redwine, J.C. [Southern Company Services, Inc., Birmingham, AL (United States)

    1995-12-31

    This paper provides a brief description and case study of soil flushing to treat contaminated groundwater. Selected reagents may be added to the flushing water to enhance contaminant removal. In the iron coprecipitation process, and iron salt is added to the contaminated water and the pH is adjusted to induce precipitation of iron oxyhydroxides. During floc formation, trace elements adsorb onto the iron floc. Cross-flow ceramic membrane filtration can be used to remove any remaining contaminant in the feed stream. In field tests, an arsenic plume flushed with citric acid was reduced by 73 percent after 6 months of treatment.

  15. Improved Aeration Process - Catalytic Role Of The Iron Oxides In Arsenic Oxidation And Coprecipitation

    DEFF Research Database (Denmark)

    Kowalski, Krysztof; Søgaard, Erik Gydesen

    2013-01-01

    improved aeration process that can also help in developing better arsenic removal treatment. The results present advantages of arsenic oxidation in an aeration process in the presence of ferrihydrite surface that have been shown to adsorb arsenic simultaneously to its oxidation. The presence of...... aeration. Moreover, it was found that the adsorption rate was limited by an excess of dissolved iron, due to competition between arsenic and iron compounds for adsorption sites on iron oxyhydroxide surface. The results were obtained both in lab and pilot scale experiments, which enabled to illustrate...

  16. The Morphology, Phase Composition and Effect of Corrosion Product on Simulated Archaeological Iron%仿古铸铁腐蚀产物的形貌、结构的演化历程及其危害性研究

    Institute of Scientific and Technical Information of China (English)

    王紫色; 许淳淳; 曹霞; 徐奔

    2007-01-01

    The immersion corrosion of archaeological iron in solution (0.06mol·L-1 NaCl+0.03mol·L-1 Na2SO4+ 0.01mol·L-1 NaHCO3) simulating soil water composition was presented.The evolution of archaeological iron from iron to iron oxide and to iron oxy-hydroxides compounds was investigated by scanning electron microscope (SEM) and X-ray diffraction (XRD) analysis.According to the morphology, phase composition, and transformation process, the contributions of each corrosion product to archaeological iron were discussed.

  17. Dietary iron-loaded rat liver haemosiderin and ferritin: in situ measurement of iron core nanoparticle size and cluster structure using anomalous small-angle x-ray scattering

    Energy Technology Data Exchange (ETDEWEB)

    Bovell, Eliza; Buckley, Craig E.; Chua-anusorn, Wanida; Cookson, David; Kirby, Nigel; Saunders, Martin; St. Pierre, Timothy G. ((UWA)); ((Curtin U.)); ((ASRP))

    2009-03-16

    The morphology, particle size distribution and cluster structure of the hydrated iron(III) oxyhydroxide particles associated with haemosiderin and ferritin in dietary iron-loaded rat liver tissue have been investigated using transmission electron microscopy (TEM) and anomalous small-angle x-ray scattering (ASAXS). Rat liver tissue was removed from a series of female Porton rats which had been fed an iron-rich diet until sacrifice at various ages from 2-24 months. Hepatic iron concentrations ranged from 1 to 65 mg Fe g{sup -1} dry tissue. TEM studies showed both dispersed and clustered iron-containing nanoparticles. The dispersed particles were found to have mean sizes ({+-}standard deviation) of 54 {+-} 8 {angstrom} for the iron-loaded animals and 55 {+-} 7 {angstrom} for the controls. Superposition of particles in TEM images prevented direct measurement of nanoparticulate size in the clusters. The ASAXS data were modelled to provide a quantitative estimate of both the size and spacing of iron oxyhydroxide particles in the bulk samples. The modelling yielded close-packed particles with sizes of 60 to 78 {angstrom} which when corrected for anomalous scattering suggests sizes from 54 to 70 {angstrom}. Particle size distributions are of particular importance since they determine the surface iron to core iron ratios, which in turn are expected to be related to the molar toxicity of iron deposits in cells.

  18. Composite ferric oxyhydroxide-containing phases formed in neutral aqueous solutions of tryptophan and indole-3-acetic acid

    International Nuclear Information System (INIS)

    Moessbauer, FTIR and XRD analyses showed that in aqueous medium in air in the presence of L-tryptophan (Trp) or indole-3-acetic acid (IAA) the ambient-temperature ageing of the precipitates formed from ferrous sulphate at pH ∼ 7 gave composite phases with varying proportions of γ-FeOOH (a dominating crystalline phase), α-FeOOH (both fine-grained, showing superparamagnetic behaviour at 298 K, and relatively better crystallized) and amorphous ferric hydroxide. The experimental data suggested a competition for adsorption sites at the oxyhydroxide surface in the suspension during phase transformations, as well as the transformation of γ-FeOOH (and/or amorphous ferric hydroxide) to α-FeOOH via the dissolution-reprecipitation mechanism. The formation of certain ferric oxyhydroxide phases in the presence of Trp and IAA - released e.g., in the course of bacterial and plant metabolism - can contribute to the regulation of soil mineral composition. (author)

  19. Mercury transformations and exchanges in a high turbidity estuary: The role of organic matter and amorphous oxyhydroxides

    OpenAIRE

    Laurier, Fabien; Cossa, Daniel; Gonzalez, Jean-Louis; Breviere, Emily; Sarazin, G

    2003-01-01

    The speciation and partition of mercury in a macrotidal estuary (Seine estuary, France) was studied in order to explore the role of the high turbidity zone (HTZ) in mercury transfer to the adjacent coastal waters. Water and particles were analyzed to determine the concentrations of various mercury species, including monomethylmercury and the inorganic fraction. The exchangeable particulate mercury, which varies with salinity, and the mercury fraction associated with the amorphous oxyhydroxide...

  20. Sonochemical intercalation synthesis of nano γ-nickel oxyhydroxide: Structure and electrochemical properties

    International Nuclear Information System (INIS)

    Nano γ-nickel oxyhydroxide (nano γ-NiOOH), intended as a new positive electrode material for alkaline Zn/Ni batteries, was synthesized by a sonochemical intercalation method. Using NaClO as oxidant, 5 M NiCl2 solution was added dropwise to a concentrated alkaline solution of NaClO + NaOH, which allows all four elementary reactions (precipitation, oxidation, cation exchange, and water molecule intercalation) to proceed simultaneously under low-frequency ultrasonic irradiation. XRD, SAXS, TEM, SEM, AAS, IR, TG, CT (complexometric titration), cyclic voltammetry (CV), and a charge-discharge test of imitative cell have been used to characterize the microstructural characteristics, composition and electrochemical properties of the synthesized material. The results showed that the lattice parameters of nano γ-NiOOH are a = 2.8256 A and c = 20.7938 A. The average oxidation state of Ni in the sample is 3.65 as measured by an indirect iodine method. The alkali metallic Na+ ions and water molecules have been inserted into sites between NiO2 layers. The cyclic voltammogram of nano γ-NiOOH exhibited two cathodic peaks and two anodic peaks, which is in accord with the redox reaction between the various phases of Ni(OH)2 and NiOOH. The charge-discharge test of imitative cells revealed that nano γ-NiOOH exhibited a higher discharge capacity than spherical β-NiOOH

  1. The Specific Capacitive Performances of the Manganese Oxyhydroxide/Carbon microcoil Electrodes for Supercapacitors

    International Nuclear Information System (INIS)

    Highlights: • MnOOH@carbon microcoil composites are successfully prepared. • The pseudo-capacitive behaviors are extensively studied. • The composites show good electrochemical performance. • Energy storge mechanism of the electrode material is discussed. - Abstract: Manganese oxyhydroxide (MnOOH)/carbon microcoil (CMC) composites are fabricated by micro-wave deposition. Then, their structures are characterized by scanning, transmission electron microscopy and X-ray diffraction. This work presents an extensive study of the pseudocapacitive performances of the as−prepared MnOOH@CMC electrodes in mild Na2SO4 electrolyte. It shows a specific capacitance of 396 F g−1 at a scan rate of 2 mV s−1. Moreover, these binary composites exhibit a good rate capability and cycling stability, retaining 137.6 F g−1 at current density of 2 A g−1 after 10,000 cycles. The good electrochemical performances of the composites are attributed to the ions from the electrolyte can easily diffusing into almost all pores of the electrode, leading to a complete insertion reaction

  2. Cobalt oxyhydroxide nanoflake based fluorescence sensing platform for label-free detection of DNA.

    Science.gov (United States)

    Chang, Yaqing; Zhang, Zhe; Liu, Huiqing; Wang, Nan; Tang, Jilin

    2016-08-01

    Detection of specific DNA sequences is critical in life science. In this study, we investigated the interaction of cobalt oxyhydroxide (CoOOH) nanoflakes with DNA and their fluorescence quenching mechanism of a FAM-labeled single-stranded DNA (ssDNA) probe. ssDNA could adsorb on the CoOOH surface via electrostatic interactions and therefore the fluorescence of FAM was quenched. However, upon addition of targets, ssDNA was hybridized with target DNA and the formed double-stranded DNA (dsDNA) had much weaker affinity to CoOOH, resulting in the retaining of fluorescence. Based on the affinity difference of CoOOH nanoflakes to ssDNA and dsDNA and fluorescence resonance energy transfer based fluorescence quenching, a mix-and-detect method was proposed for homogeneous detection of DNA. The proposed method is simple and can be finished in a few minutes with high sensitivity. Furthermore, it displays a wide linear range from 1 to 50 nM with a detection limit of 0.5 nM and is capable of detecting DNA in real biological samples. PMID:27251111

  3. High Temperature Transformation of Iron Minerals in Bauxite

    International Nuclear Information System (INIS)

    Moessbauer hyperfine and X-ray diffraction studies have been carried on original bauxite sample and thermally treated (between 200 and 1200 deg. C) samples. Moessbauer spectrum of original bauxite shows the dominance of hematite (α-Fe2O3) along with Al-substituted hematite and goethite (α-FeOOH) of fine particle size. Moessbauer parameters for thermally treated samples indicate transformation of almost all of iron oxy-hydroxides into hematite up to 350 deg. C. Around 800 deg. C the formation of a new iron phase, assigned as iron substituted mullite (3Al2O3 2SiO3), occurs and its intensity increases with the rise in temperature and reaches a saturation around 1200 deg. C. Furthermore, our studies confirm that HCl leaching is quite effective for the iron oxide removal.

  4. Formation temperatures of thermogenic and biogenic methane

    Science.gov (United States)

    Stolper, D.A.; Lawson, M.; Davis, C.L.; Ferreira, A.A.; Santos Neto, E. V.; Ellis, G.S.; Lewan, M.D.; Martini, A.M.; Tang, Y.; Schoell, M.; Sessions, A.L.; Eiler, J.M.

    2014-01-01

    Methane is an important greenhouse gas and energy resource generated dominantly by methanogens at low temperatures and through the breakdown of organic molecules at high temperatures. However, methane-formation temperatures in nature are often poorly constrained. We measured formation temperatures of thermogenic and biogenic methane using a “clumped isotope” technique. Thermogenic gases yield formation temperatures between 157° and 221°C, within the nominal gas window, and biogenic gases yield formation temperatures consistent with their comparatively lower-temperature formational environments (<50°C). In systems where gases have migrated and other proxies for gas-generation temperature yield ambiguous results, methane clumped-isotope temperatures distinguish among and allow for independent tests of possible gas-formation models.

  5. Structural investigation of biogenic ferrihydrite nanoparticles dispersion

    International Nuclear Information System (INIS)

    Structural properties of biogenic ferrihydrite nanoparticles produced by bacteria Klebsiella oxytoca are investigated. Investigations of morphology and size of particles dispersed in water by means of high-resolution transmission electron microscopy and small angle X-ray scattering measurements were performed. By model calculations followed by fitting procedure the structural parameters of a cylinder of radius R = (4.87 ± 0.02) nm and height L = (2.12 ± 0.04) nm are obtained

  6. Biogenic Amines in Raw and Processed Seafood

    OpenAIRE

    Visciano, Pierina; Schirone, Maria; Tofalo, Rosanna; Suzzi, Giovanna

    2012-01-01

    The presence of biogenic amines (BAs) in raw and processed seafood, associated with either time/temperature conditions or food technologies is discussed in the present paper from a safety and prevention point of view. In particular, storage temperature, handling practices, presence of microbial populations with decarboxylase activity and availability of free amino acids are considered the most important factors affecting the production of BAs in raw seafood. On the other hand, some food techn...

  7. Biogenic Magnetite in Martian Meteorite ALH84001

    Science.gov (United States)

    Thomas-Keprta, K. L.; Bazylinski, Dennis; Wentworth, Susan J.; McKay, David S.; Kirschvink, Joseph L.; Clemett, SImon J.; Bell, Mary Sue; Golden, D. C.; Gibson, Everett K., Jr.

    1999-01-01

    Fine-grained magnetite (Fe3O4) in martian meteorite ALH84001, generally less than 200 nm in size, is located primarily in the rims that surround the carbonate globules. There are two populations of ALH84001 magnetites, which are likely formed at low temperature by inorganic and biogenic processes. Nearly 27% of ALH84001 magnetite particles, also called elongated prisms, have characteristics which make them uniquely identifiable as biological precipitates. Additional information is contained in the original extended abstract.

  8. Nanophase iron oxides as a key ultraviolet sunscreen for ancient photosynthetic microbes

    Science.gov (United States)

    Bishop, Janice L.; Louris, Stephanie K.; Rogoff, Dana A.; Rothschild, Lynn J.

    2006-07-01

    We propose that nanophase iron-oxide-bearing materials provided important niches for ancient photosynthetic microbes on the Earth that ultimately led to the oxygenation of the Earth's atmosphere and the formation of iron-oxide deposits. Atmospheric oxygen and ozone attenuate ultraviolet radiation on the Earth today providing substantial protection for photosynthetic organisms. With ultraviolet radiation fluxes likely to have been even higher on the early Earth than today, accessing solar radiation was particularly risky for early organisms. Yet, we know that photosynthesis arose early and played a critical role in subsequent evolution. Of primary importance was protection below 290 nm, where peak nucleic acid (~260 nm) and protein (~280 nm) absorptions occur. Nanophase ferric oxide/oxyhydroxide minerals absorb, and thus block, the lethal ultraviolet radiation, while transmitting light through much of the visible and near-infrared regions of interest to photosynthesis (400 to 1100 nm). Furthermore, they were available in early environments, and are synthesized by many organisms. Based on experiments using nanophase ferric oxide/oxyhydroxide minerals as a sunscreen for photosynthetic microbes, we suggest that iron, an abundant element widely used in biological mechanisms, may have provided the protection that early organisms needed in order to be able to use photosynthetically active radiation while being protected from ultraviolet-induced damage. The results of this study are broadly applicable to astrobiology because of the abundance of iron in other potentially habitable bodies and the evolutionary pressure to utilize solar radiation when available as an energy source. This model could apply to a potential life form on Mars or other bodies where liquid water and ultraviolet radiation could have been present at significant levels. Based on ferric oxide/oxyhydroxide spectral properties, likely geologic processes, and the results of experiments with the

  9. Discrimination of abiogenic and biogenic alkane gases

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    We have combined the analytical data of the carbon isotope distribution pattern, R/Ra and CH4/3He values of abiogenic and biogenic (referring to the thermogenic and bacterial or microbial) alkane gases in China with those of alkane gases from USA, Russia, Germany, Australia and other countries. Four discrimination criteria are derived from this comparative study: 1) Carbon isotopic composition is generally greater than -30‰ for abiogenic methane and less than -30‰ for biogenic methane; 2) Abiogenic alkane gases have a carbon isotopic reversal trend (δ 13C1> δ 13C2> δ 13C3> δ 13C4) with δ 13C1>-30‰ in general; 3) Gases with R/Ra >0.5 and δ 13C11 δ 13C2>0 are of abiogenic origin; 4) Gases (meth- ane) with CH4/3He≤106 are of abiogenic origin, whereas gases with CH4/3He≥1011 are of biogenic origin.

  10. Cytotoxicity and genotoxicity of biogenic silver nanoparticles

    Science.gov (United States)

    Lima, R.; Feitosa, L. O.; Ballottin, D.; Marcato, P. D.; Tasic, L.; Durán, N.

    2013-04-01

    Biogenic silver nanoparticles with 40.3 ± 3.5 nm size and negative surface charge (- 40 mV) were prepared with Fusarium oxysporum. The cytotoxicity of 3T3 cell and human lymphocyte were studied by a TaliTM image-based cytometer and the genotoxicity through Allium cepa and comet assay. The results of BioAg-w (washed) and BioAg-nw (unwashed) biogenic silver nanoparticles showed cytotoxicity exceeding 50 μg/mL with no significant differences of response in 5 and 10 μg/mL regarding viability. Results of genotoxicity at concentrations 5.0 and 10.0 ug/mL show some response, but at concentrations 0.5 and 1.0 μg/mL the washed and unwashed silver nanoparticles did not present any effect. This in an important result since in tests with different bacteria species and strains, including resistant, MIC (minimal inhibitory concentration) had good answers at concentrations less than 1.9 μg/mL. This work concludes that biogenic silver nanoparticles may be a promising option for antimicrobial use in the range where no cyto or genotoxic effect were observed. Furthermore, human cells were found to have a greater resistance to the toxic effects of silver nanoparticles in comparison with other cells.

  11. Rett syndrome - Stimulation of endogenous biogenic amines

    Science.gov (United States)

    Pelligra, R.; Norton, R. D.; Wilkinson, R.; Leon, H. A.; Matson, W. R.

    1992-01-01

    Transient hypercapnic hyperoxemia was induced in two Rett syndrome children by the administration of a gaseous mixture of 80 percent O2 and 20 percent CO2. Time course studies of neurotransmitters and their metabolites showed an immediate and marked increase in central biogenic amine turnover following inhalation of the gas mixture. The increased turnover of biogenic amines was associated with improved clinical changes. This suggests a coupled relationship and provides further support for an etiological role of neurotransmitter dysfunction in Rett syndrome. In a complementary study, elevation of pulmonary CO2 by application of a simple rebreathing device resulted in improvement of abnormal blood gases and elimination of the Cheyne-Stokes-like respiratory pattern of the Rett syndrome. Near normalization of the EEG occurred when a normal respiratory pattern was imposed by means of a respirator. Taken together, these results lead to the preliminary conclusion that cerebral hypoxemia secondary to abnormal respiratory function may contribute to diminished production of biogenic amines in Rett syndrome.

  12. biogenic aerosol precursors: volatile amines from agriculture

    Science.gov (United States)

    Kuhn, Uwe; Sintermann, Jörg; Spirig, Christoph; Ammann, Christof; Neftel, Albrecht

    2010-05-01

    Information on the occurrence of volatile biogenic amines in the atmosphere is marginal. This group of N-bearing organic compounds are assumed to be a small, though significant component of the atmospheric N-cycle, but are not accounted for in global assessments due to the scarceness of available data. There is increasing evidence for an important role of biogenic amines in the formation of new particulate matter, as well as for aerosol secondary growth. Volatile amines are ubiquitously formed by biodegradation of organic matter, and agriculture is assumed to dominantly contribute to their atmospheric burden. Here we show that the mixing ratios of volatile amines within livestock buildings scale about 2 orders of magnitude lower than NH3, confirming the few literature data available (e.g., Schade and Crutzen, J. Atm. Chem. 22, 319-346, 1995). Flux measurements after manure application in the field, mixing ratios in the headspace of manure storage pools, and concentrations in distilled manure all indicate major depletion of amines relative to NH3 during manure processing. We conclude that the agricultural source distribution of NH3 and amines is not similar. While for NH3 the spreading of manure in the field dominates agricultural emissions, the direct release from livestock buildings dominates the budget of volatile biogenic amines.

  13. Evidence for the biogenic origin of manganese-enriched layers in Lake Superior sediments.

    Science.gov (United States)

    Palermo, Christine; Dittrich, Maria

    2016-04-01

    Manganese (Mn) and iron (Fe)-enriched sediment layers were discovered in Lake Superior within, above and below the oxic-anoxic interface. While the role of bacteria in redox reactions with Mn is known to be significant, little information exists about indigenous microbial communities in many freshwater environments. This study examined the bacterial communities of Mn-enriched layers in Lake Superior to identify the potential Mn(II) oxidizers responsible for the formation of Mn oxides. Anaerobic Mn(II) oxidation occurring in the Mn-enriched layers at the oxic-anoxic interface was investigated using Mn(II)-enriched cultures. High-resolution microscopic and spectroscopic investigations provided evidence of the biogenic formation of Mn oxides on cell surfaces. Spectroscopic mapping confirmed high levels of Mn in structures resembling biogenic Mn oxides. These structures were observed in enrichment cultures and in Mn-enriched layer sediment samples, indicating the significance of biogenic Mn oxidation occurring in situ. 16S ribosomal DNA pyrosequencing was used to identify the bacteria potentially responsible for Mnoxide formation in the enrichment cultures and Mn-enriched layers, revealing that the Mn-enriched layer contains classes with known Mn(II)-oxidizing members. Pyrosequencing of bacterial cultures suggested that these bacteria may be Bacillus strains, and that anaerobic microbial-mediated Mn(II) oxidation contributes to the formation of the layers. PMID:26636960

  14. Iron overdose

    Science.gov (United States)

    Iron is a mineral found in many over-the-counter supplements. Iron overdose occurs when someone takes more than the ... This can be by accident or on purpose. Iron overdose is especially dangerous for children. A severe ...

  15. Oxidatively Electrodeposited Thin-Film Transition Metal (Oxy)hydroxides as Oxygen Evolution Catalysts.

    Science.gov (United States)

    Morales-Guio, Carlos G; Liardet, Laurent; Hu, Xile

    2016-07-20

    The electrolysis of water to produce hydrogen and oxygen is a simple and attractive approach to store renewable energies in the form of chemical fuels. The oxygen evolution reaction (OER) is a complex four-electron process that constitutes the most energy-inefficient step in water electrolysis. Here we describe a novel electrochemical method for the deposition of a family of thin-film transition metal (oxy)hydroxides as OER catalysts. The thin films have nanodomains of crystallinity with lattice spacing similar to those of double-layered hydroxides. The loadings of these thin-film catalysts were accurately determined with a resolution of below 1 μg cm(-2) using an electrochemical quartz microcrystal balance. The loading-activity relations for various catalysts were established using voltammetry and impedance spectroscopy. The thin-film catalysts have up to four types of loading-activity dependence due to film nucleation and growth as well as the resistance of the films. A zone of intrinsic activity has been identified for all of the catalysts where the mass-averaged activity remains constant while the loading is increased. According to their intrinsic activities, the metal oxides can be classified into three categories: NiOx, MnOx, and FeOx belong to category I, which is the least active; CoOx and CoNiOx belong to category II, which has medium activity; and FeNiOx, CoFeOx, and CoFeNiOx belong to category III, which is the most active. The high turnover frequencies of CoFeOx and CoFeNiOx at low overpotentials and the simple deposition method allow the fabrication of high-performance anode electrodes coated with these catalysts. In 1 M KOH and with the most active electrode, overpotentials as low as 240 and 270 mV are required to reach 10 and 100 mA cm(-2), respectively. PMID:27344954

  16. Biosafety of the application of biogenic nanometal powders in husbandry

    Science.gov (United States)

    Anatolievna Nazarova, Anna; Dmitrievna Polischuk, Svetlana; Anatolievna Stepanova, Irina; Ivanovich Churilov, Gennady; Chau Nguyen, Hoai; Buu Ngo, Quoc

    2014-03-01

    Effects of iron and copper nanopowders (particle size of 20-40 nm) were investigated on rabbits of 1 month age and heifers of 6 months. For introduction of nanometals into the animal's ration, the mixed fodder was treated with the nanometal powder suspension in such a way: 0.08 mg of nanoiron per kg of animal's body weight and 0.04 mg kg-1 for nanocopper. The weight gain of the heifers who received nanoiron and nanocopper after 8 months was 22.4 and 10.7% higher than that of the control, respectively. For the rabbits who received nano Fe and Cu after 3 months, the weight gain was 11.7 and 7.3% compared to the control, respectively. Under the action of metal nanopowders morphological indices of blood were changed in comparison with the control: after 8 months the quantity of erythrocytes increased by 19.6%, hemoglobin by 17.1% and leukocytes by 7.6%. There was a realignment in leukocytic formula: the quantity of lymphocytes increased by 9% compared to the control. Biogenic metals in superdispersive state were able to stimulate immune, enzymatic and humoral systems of the animal's organism, promoting metabolism. Adding Co and Cu metal nanopowders to the bull-calves’ fodder rations increased content of Ca by 31.8 and 0%, Fe by 38.8 and 37.5%, K by 19.2 and 15.3%, Mg by 17.6 and 23.5%, Mn by 9.8 and 45% and Na by 20.5 and 8.8%, respectively, compared to control. Metal nanopowders improved the quality indices and meat productivity of black-white bull-calves, expressed in intensive growth of muscle, tissue and more nutritious meat. The conducted veterinary-sanitary expertise showed that the supplements based on iron, cobalt and copper nanopowders can be used as safe bioactive supplements in animal husbandry.

  17. XENOBIOTICS AND BIOGENIC ELEMENTS IN RAW COW'S MILK

    Directory of Open Access Journals (Sweden)

    Agnieszka Greń

    2012-12-01

    Full Text Available Normal 0 21 false false false SK X-NONE X-NONE This paper presents the concentration some toxic and biogenic elements in milk from Nitra region. The aim of this investigation was to evaluate 30 samples of raw milk with fat contents 3.8% obtained from milk machine in the Nitra region. Samples were analyzed for metal contents using atomic absorption spectrophotometry (AAS. In comparison with maximum acceptable concentration for milk in the food codex of the Slovak republic, the level of contamination with cadmium was exceeded and reached the value 0.221 µg.ml-1. The copper content ranged from 1.201 µg.ml-1 to 5.810 µg.ml-1 and the average concentration reached 3.793 µg.ml-1.  Iron had an average of 1.824 µg.ml-1. Overall in all milk samples high correlations were found. Between positive correlation (0.7019 and negative correlation between of nickel and potassium concentration in raw milk (-0.72 was found. doi:10.5219/246

  18. In situ, high-resolution evidence for iron-coupled mobilization of phosphorus in sediments.

    Science.gov (United States)

    Ding, Shiming; Wang, Yan; Wang, Dan; Li, Yang Yang; Gong, Mengdan; Zhang, Chaosheng

    2016-01-01

    Reductive dissolution of phosphorus-bearing iron (Fe) (oxyhydr)oxides has been regarded as a primary mechanism responsible for the mobilization of phosphorus (P) in sediments for over 70 years. However, to date there is little in situ evidence to support this hypothesis. In this study, a total of 16 sites in the large eutrophic Lake Taihu were selected for investigation. Newly-developed diffusive gradients in thin films (ZrO-Chelex DGT) probes were deployed to simultaneously measure labile Fe and P mainly released from sediment solids at millimeter spatial resolution. Significantly positive correlations were observed between DGT-labile Fe and P at 14 sites, implying a release of P following reductive dissolution of Fe (oxyhydr)oxides. A coincident resupply of Fe(II) and P was observed from sediment solids to buffer their releases from DGT perturbance, further verifying the mechanism of Fe-coupled mobilization of P. The ratio of DGT-labile Fe/P was found to be positively correlated with the ratio of easily reducible (oxyhydr)oxide Fe to its associated P, indicating that this solid phase should retain P prior to its release. The results provide direct evidence for the coupling between Fe and P in sediments and further identify the easily reducible Fe (oxyhydr)oxide species involved in the coupling process. PMID:27087199

  19. Biogenic amine metabolism in juvenile neurocardiogenic syncope with dysautonomia

    OpenAIRE

    Butler, Ian J.; Lankford, Jeremy E; Hashmi, Syed Shahrukh; Numan, Mohammed T

    2014-01-01

    Objective Biogenic amine brain levels and their cerebral metabolism are frequently studied by quantitation of biogenic amine metabolites in cerebrospinal fluid (CSF) compared to age-matched controls. There is a paucity of studies in adolescents and young adults investigating the potential role of disordered cerebral biogenic amine metabolism in young patients who have dysautonomia based on abnormal head-up tilt table (HUTT). Methods In a cohort of juvenile patients with neurocardiogenic synco...

  20. Status of research on biogenic coalbed gas generation mechanisms

    Institute of Scientific and Technical Information of China (English)

    2010-01-01

    Biogenic coalbed gas,how it is generated and the geochemical characteristics of the gas are gaining global attention.The ways coalbed gas is generated,the status of research on the generation mechanism and the methods of differentiating between biogenic gasses are discussed.The generation of biogenic coalbed methane is consistent with anaerobic fermentation theory.Commercial biogenic coalbed gas reservoirs are mainly generated by the process of CO2 reduction.The substrates used by the microbes living in the...

  1. Geochemical study of evaporite and clay mineral-oxyhydroxide samples from the Waste Isolation Pilot Plant site

    International Nuclear Information System (INIS)

    Samples of clay minerals, insoluble oxyhydroxides, and their host evaporites from the WIPP site have been studied for their major and minor elements abundances, x-ray diffraction characteristics, K-Ar ages, and Rb-Sr ages. This study was undertaken to determine their overall geochemical characteristics and to investigate possible interactions between evaporates and insoluble constituents. The evaporite host material is water-soluble, having Cl/Br ratios typical of marine evaporites, although the Br content is low. Insoluble material (usually a mixture of clay minerals and oxyhydroxide phases) yields very high Cl/Br ratios, possibly because of Cl from admixed halide minerals. This same material yields K/Rb and Th/U ratios in the normal range for shales; suggesting little, if any, effect of evaporite-induced remobilization of U, K, or Rb in the insoluble material. The rare-earth element (REE) data also show normal REE/chondrite (REE/CHON) distribution patterns, supporting the K/Rb and Th/U data. Clay minerals yield K-Ar dates in the range 365 to 390 Ma and a Rb-Sr isochron age of 428 ± 7 Ma. These ages are well in excess of the 220- to 230-Ma formational age of the evaporites, and confirm the detrital origin of the clays. The ages also show that any evaporite or clay mineral reactions that might have occurred at or near the time of sedimentation and diagenesis were not sufficient to reset the K-Ar and Rb-Sr systematics of the clay minerals. Further, x-ray data indicate a normal evaporitic assemblage of clay minerals and Fe-rich oxyhydroxide phases. The clay minerals and other insoluble material appear to be resistant to the destructive effects of their entrapment in the evaporites, which suggests that these insoluble materials would be good getters for any radionuclides (hypothetically) released from the storage of radioactive wastes in the area

  2. Intravenous ferric carboxymaltose for the treatment of iron deficiency anemia

    Directory of Open Access Journals (Sweden)

    João Ricardo Friedrisch

    2015-12-01

    Full Text Available ABSTRACT Nutritional iron deficiency anemia is the most common deficiency disorder, affecting more than two billion people worldwide. Oral iron supplementation is usually the first choice for the treatment of iron deficiency anemia, but in many conditions, oral iron is less than ideal mainly because of gastrointestinal adverse events and the long course needed to treat the disease and replenish body iron stores. Intravenous iron compounds consist of an iron oxyhydroxide core, which is surrounded by a carbohydrate shell made of polymers such as dextran, sucrose or gluconate. The first iron product for intravenous use was the high molecular weight iron dextran. However, dextran-containing intravenous iron preparations are associated with an elevated risk of anaphylactic reactions, which made physicians reluctant to use intravenous iron for the treatment of iron deficiency anemia over many years. Intravenous ferric carboxymaltose is a stable complex with the advantage of being non- dextran-containing and a very low immunogenic potential and therefore not predisposed to anaphylactic reactions. Its properties permit the administration of large doses (15 mg/kg; maximum of 1000 mg/infusion in a single and rapid session (15-minute infusion without the requirement of a test dose. The purpose of this review is to discuss some pertinent issues in relation to the history, pharmacology, administration, efficacy, and safety profile of ferric carboxymaltose in the treatment of patients with iron deficiency anemia.

  3. The effect of initial iron concentration and pH on the radiolytic formation of γ-FeOOH nanoparticles

    International Nuclear Information System (INIS)

    The formation of iron oxyhydroxide nanoparticles under gamma irradiation is a process in the infancy of its understanding. Herein we present work to describe how initial iron concentration and pH impact the growth of radiolytically formed nanoparticles. These results can be used to better understand the activity transport processes occurring within a reactor environment which may pose both environmental and safety concerns. Preliminary results suggest that the final particle size is proportional to the initial dissolved iron concentration, while experiments probing the effect of solution pH are ongoing. (author)

  4. Structure-composition-activity relationships in transition-metal oxide and oxyhydroxide oxygen-evolution electrocatalysts

    Science.gov (United States)

    Trotochaud, Lena

    Solar water-splitting is a potentially transformative renewable energy technology. Slow kinetics of the oxygen evolution reaction (OER) limit the efficiency of solar-watersplitting devices, thus constituting a hurdle to widespread implementation of this technology. Catalysts must be stable under highly oxidizing conditions in aqueous electrolyte and minimally absorb light. A grand goal of OER catalysis research is the design of new materials with higher efficiencies enabled by comprehensive understanding of the fundamental chemistry behind catalyst activity. However, little progress has been made towards this goal to date. This dissertation details work addressing major challenges in the field of OER catalysis. Chapter I introduces the current state-of-the-art and challenges in the field. Chapter II highlights work using ultra-thin films as a platform for fundamental study and comparison of catalyst activity. Key results of this work are (1) the identification of a Ni0.9Fe0.1OOH catalyst displaying the highest OER activity in base to date and (2) that in base, many transition-metal oxides transform to layered oxyhydroxide materials which are the active catalysts. The latter result is critical in the context of understanding structure-activity relationships in OER catalysts. Chapter III explores the optical properties of these catalysts, using in situ spectroelectrochemistry to quantify their optical absorption. A new figure-of-merit for catalyst performance is developed which considers both optical and kinetic losses due to the catalyst and describes how these factors together affect the efficiency of composite semiconductor/catalyst photoanodes. In Chapter IV, the fundamental structure-composition-activity relationships in Ni1--xFexOOH catalysts are systematically investigated. This work shows that nearly all previous studies of Ni-based catalysts were likely affected by the presence of Fe impurities, a realization which holds significant weight for future study

  5. SUICIDAL IDEATION AND BIOGENIC AMINES IN DEPRESSION*

    OpenAIRE

    Palaniappan, V.; V. Ramachandran; Somasundaram, O.

    1983-01-01

    SUMMARY This report is based on the study of 40 depressives in an attempt to explore the possible association between the suicidal ideas and the biogenic amines. The severity of suicidal ideas was measured on Hamilton Depressive Rating Scale and their amine metabolites were measured (MHFG, HVA and 5 HIAA) in urine and C.S.F. It was observed that the level of 5 HIAA, and Serotonin (5 HT) was more related to suicidal ideas and was inversely related. The probable associations between these are d...

  6. Effect of ferric oxyhydroxide grain coatings on the transport of bacteriophage PRD1 and Cryptosporidium parvum oocysts in saturated porous media

    Science.gov (United States)

    Abudalo, R.A.; Bogatsu, Y.G.; Ryan, J.N.; Harvey, R.W.; Metge, D.W.; Elimelech, M.

    2005-01-01

    To test the effect of geochemical heterogeneity on microorganism transport in saturated porous media, we measured the removal of two microorganisms, the bacteriophage PRD1 and oocysts of the protozoan parasite Cryptosporidium parvum, in flow-through columns of quartz sand coated by different amounts of a ferric oxyhydroxide. The experiments were conducted over ranges of ferric oxyhydroxide coating fraction of ?? = 0-0.12 for PRD1 and from ?? = 0-0.32 for the oocysts at pH 5.6-5.8 and 10-4 M ionic strength. To determine the effect of pH on the transport of the oocysts, experiments were also conducted over a pH range of 5.7-10.0 at a coating fraction of ?? = 0.04. Collision (attachment) efficiencies increased as the fraction of ferric oxyhydroxide coated quartz sand increased, from ?? = 0.0071 to 0.13 over ?? = 0-0.12 for PRD1 and from ?? = 0.059 to 0.75 over ?? = 0-0.32 for the oocysts. Increasing the pH from 5.7 to 10.0 resulted in a decrease in the oocyst collision efficiency as the pH exceeded the expected point of zero charge of the ferric oxyhydroxide coatings. The collision efficiencies correlated very well with the fraction of quartz sand coated by the ferric oxyhydroxide for PRD1 but not as well for the oocysts. ?? 2005 American Chemical Society.

  7. Hard X-ray total scattering study on the structure of Si-dopped ferric oxyhydroxides and products of their transformation

    Science.gov (United States)

    Pieczara, Gabriela; Borkiewicz, Olaf; Manecki, Maciej; Rzepa, Grzegorz

    2016-04-01

    Here we report the results of a detailed structural investigation, using synchrotron-based pair distribution function analyses (PDF) and high-resolution X-ray diffraction (HR-XRD), on a series of Si-bearing synthetic analogues of ferrihydrite with a range of Si/Fe ratio relevant to geological environments and on products of their thermal transformation. Hard X-ray total scattering data suitable for PDF analyses have been collected at the PDF-dedicated beamline 11-ID-B and the HR-XRD data at beamline 11-BM of the Advanced Photon Source (APS) at Argonne National Laboratory (ANL). Ferrihydrite is a poorly crystalline, nano-sized hydrous ferric oxyhydroxide with a nominal/ideal formula Fe5HO8•4H2O. Its chemical composition however, can vary significantly and the atomic structure is yet to be fully understood despite multitude of structural studies undertaken over the past two decades (Michel et al., 2007; Manceau, 2009). One of the most commonly discussed and still unsettled contention points regarding the structural arrangements of ferrihydrite is related to the presence or absence of tetraherdally coordinated iron(III) within its structure. The majority of experimental work carried out to date focused on pure, synthetic ferrihydrite analogues with chemical composition close to ideal/nominal. This approach is clearly a significant oversimplification of natural ferrihydrite which always contains substantial amounts of admixtures, with Si, C, P, As, Ca, S and Al being the most common. One of the most important and the most commonly encountered impurities is Si, in the form of silicate ion that has strong affinity for ferrihydrite. SiO2content in natural ferrihydrites can vary substantially but generally falls with the range of 2.6-31.5 wt% (Cismasu et al., 2011). In certain environments however, such as modern seafloor hydrothermal vents, higher Si/Fe ratios (up to ca. 3) have been reported (Sun et al., 2013). The results of previous reports indicate that silicate

  8. Determination of Biogenic Amines with HPLC-APCI-MS

    Science.gov (United States)

    Determination of biogenic amines in fish samples can be used as a quality attribute and are commonly performed using a derivatization step followed by high pressure liquid chromatography (HPLC) and UV detection. Over estimation and misidentification of biogenic amines can occur when interfering comp...

  9. Biogenic amines in submicron marine aerosol (Invited)

    Science.gov (United States)

    Facchini, M.

    2010-12-01

    Ammonium salts of dimethyl and diethyl amine (DMA+ and DEA+) have been detected in size segregated marine samples collected in the North Atlantic over open ocean and at a coastal site. DMA+ and DEA+ peak in the accumulation mode range while very low concentration, close to detection limit, are observed in the coarse size fractions, as well as in sea spray aerosol artificially generated in the laboratory using sea water. These results indicate a secondary formation pathway. DMA+ and DEA+ represent up to 20% of secondary organic aerosol (SOA) in our samples , and to our knowledge they are the most abundant organic species besides MSA ever detected in clean marine aerosol . Maximum concentrations have been observed during spring and summer when the biological activity is high and in clean marine air masses, thus indicating biogenic sources. Total organic nitrogen (ON) concentration also peaks in the accumulation mode range and represents in our samples a fraction from 32 to 54 % of the total SOA. Ammonium salt formation from biogenic amines might be an important source of marine SOA and atmospheric nitrogen at the global scale with a seasonal variation connected to the oceanic biological productivity and an atmospheric cycle parallel to that of the organosulfur species.

  10. Production and Early Preservation of Lipid Biomarkers in Iron Hot Springs

    OpenAIRE

    Parenteau, Mary N.; Jahnke, Linda L; Farmer, Jack D.; Cady, Sherry L.

    2014-01-01

    The bicarbonate-buffered anoxic vent waters at Chocolate Pots hot springs in Yellowstone National Park are 51–54°C, pH 5.5–6.0, and are very high in dissolved Fe(II) at 5.8–5.9 mg/L. The aqueous Fe(II) is oxidized by a combination of biotic and abiotic mechanisms and precipitated as primary siliceous nanophase iron oxyhydroxides (ferrihydrite). Four distinct prokaryotic photosynthetic microbial mat types grow on top of these iron deposits. Lipids were used to characterize the community compos...

  11. Factors influencing biogenic amines accumulation in dairy products

    Directory of Open Access Journals (Sweden)

    Daniel M. eLinares

    2012-05-01

    Full Text Available Fermented foods are within the food products more often complained of having caused biogenic amines poisoning. Concerning milk-based fermented foods, cheese is the main product likely to contain significant levels of biogenic amines, specially tyramine, histamine and putrescine. Prompted by the increasing awareness of the risks related to dietary uptake of high biogenic amine loads, in this review we report about cheese elaboration and processing technological aspects affecting biogenic amines levels. Synthesis of biogenic amines is possible only when three conditions converge: i availability of the substrate amino acids; ii presence of microorganisms with the appropriate catabolic pathway activated; and iii environmental conditions favorable to the decarboxilation activity. These conditions depend on several factors such as milk treatment (pasteurization, use of starter cultures, NaCl concentration, time and temperature of ripening and preservation, pH… which will be discussed in this chapter.

  12. Fractionation of Cu and Zn isotopes during adsorption onto amorphous Fe(III) oxyhydroxide: Experimental mixing of acid rock drainage and ambient river water

    Science.gov (United States)

    Balistrieri, L.S.; Borrok, D.M.; Wanty, R.B.; Ridley, W.I.

    2008-01-01

    Fractionation of Cu and Zn isotopes during adsorption onto amorphous ferric oxyhydroxide is examined in experimental mixtures of metal-rich acid rock drainage and relatively pure river water and during batch adsorption experiments using synthetic ferrihydrite. A diverse set of Cu- and Zn-bearing solutions was examined, including natural waters, complex synthetic acid rock drainage, and simple NaNO3 electrolyte. Metal adsorption data are combined with isotopic measurements of dissolved Cu (65Cu/63Cu) and Zn (66Zn/64Zn) in each of the experiments. Fractionation of Cu and Zn isotopes occurs during adsorption of the metal onto amorphous ferric oxyhydroxide. The adsorption data are modeled successfully using the diffuse double layer model in PHREEQC. The isotopic data are best described by a closed system, equilibrium exchange model. The fractionation factors (??soln-solid) are 0.99927 ?? 0.00008 for Cu and 0.99948 ?? 0.00004 for Zn or, alternately, the separation factors (??soln-solid) are -0.73 ?? 0.08??? for Cu and -0.52 ?? 0.04??? for Zn. These factors indicate that the heavier isotope preferentially adsorbs onto the oxyhydroxide surface, which is consistent with shorter metal-oxygen bonds and lower coordination number for the metal at the surface relative to the aqueous ion. Fractionation of Cu isotopes also is greater than that for Zn isotopes. Limited isotopic data for adsorption of Cu, Fe(II), and Zn onto amorphous ferric oxyhydroxide suggest that isotopic fractionation is related to the intrinsic equilibrium constants that define aqueous metal interactions with oxyhydroxide surface sites. Greater isotopic fractionation occurs with stronger metal binding by the oxyhydroxide with Cu > Zn > Fe(II).

  13. Title: Biogenic Magnetite Prevails in Oxic Pelagic Red Clay Core in the South Pacific Gyre

    Science.gov (United States)

    Shimono, T.; Yamazaki, T.

    2012-12-01

    Magnetotactic bacteria have been observed in wide variety of environments, including soils, freshwater lakes, and marine sediments, since Blakemore (1975) first described in 1975. Magnetotactic bacteria, which most commonly live within the oxic-anoxic transition zone (OATZ) of aquatic environments, produce intracellular crystals of magnetic minerals, specifically magnetite or greigite. It is considered that the magnetite/greigite crystals facilitate the bacteria's search for optimal conditions within the sharp chemical gradients of the OATZ. Petermann and Bleil (1993) reported living magnetotactic bacteria in pelagic and hemipelagic sediments near OATZ in the eastern South Atlantic at water depths to about 3,000 m, but they couldn't find actively swimming magnetotactic bacteria in sediments of deeper water depths. The South Pacific Gyre (SPG) is far from continents and the lowest productivity region on Earth. IODP site U1365 (water depth ~5,700 m) cored pelagic red clay of 75.5 m thick above ~100 Ma basement (except for the chart layer from ~42 to 63.5 m) in the western edge of the SPG. The core mainly consists of iron rich clay. The color is dark reddish and/or dark brown throughout the core. We conducted a paleomagnetic and environmental rock magnetic study of the pelagic clay core. The magnetostratigraphy revealed the top 5 m sediments cover the last 5 My, and sedimentation rate decreases downward from 1.7 to 0.6 m/m.y. Geochemical measurements of pore water indicate that dissolved oxygen was present throughout the core (>50 μM). Thus oxygen penetrates through the entire sediment column to the sediment/basalt interface, and there is no OATZ. Magnetic mineral assemblage of this core is dominated by biogenic magnetite despite no OATZ. First-order reversal curve (FORC) diagrams of all specimens have a narrow central ridge along the Hc axis with very small vertical spread. This indicates very weak magnetostatic interaction (Roberts et al., 2000), and is the

  14. Total balance of biogenic fuels for thermal uses; Ganzheitliche Bilanzierung verschiedener biogener Festbrennstoffe zur thermischen Nutzung

    Energy Technology Data Exchange (ETDEWEB)

    Becher, S.; Kaltschmitt, M. [Stuttgart Univ. (Germany). Inst. fuer Energiewirtschaft und Rationelle Energieanwendung (IER)

    1996-12-31

    In this situation of unfavourable energy price levels, the use of biogenic fuels for power supply can be recommended only if it serves to reduce environmental pollution. Against this background and on the basis of a primary energy balance, the authors attempted a total balance of selected enfironmental effects (global heating and acidification potential) of biomass use as compared to fossil fuel combustion. (orig) [Deutsch] ie Nutzung biogener Festbrennstoffe zur Energienachfragedeckung ist bei dem gegenwaertigen unguenstigen Energiepreisniveau nur dann zu rechtfertigen, wenn es durch die Biomassenutzung zu einer Reduzierung der energiebedingten Umwelteffekte kommt. Vor disem Hintergrund werden ausgehend von der Primaerenergiebilanz ausgewaehlte Umwelteffekte (d.h. das Treibhaus- und das Versauerungspotential) einer Biomassenutzung im Vergleich zu einer Nutzung fossiler Energietraeger ganzheitlich bilanziert. Die wesentlichen Ergebnisse werden zusammengefasst und interpretiert. (orig)

  15. Iron Overload

    Science.gov (United States)

    ... drug called an iron chelator to remove excess iron from your body because of transfusion-dependent anemias. Be sure to talk with your doctor about the potential benefits and risks of using these drugs. Previous Article ...

  16. Laboratory and field evaluation of municipal compost/limestone/iron mixtures as filling material for permeable reactive barriers for in-situ acid mine drainage treatment

    Energy Technology Data Exchange (ETDEWEB)

    Gibert, O. [Univ. Politecnica de Catalunya, Barcelona (Spain). Dept. d' Enginyeria Quimica]|[Univ. Politecnica de Catalunya, Barcelona (Spain). Centre Tecnologic de Manresa; Cortina, J.-L. [Univ. Politecnica de Catalunya, Barcelona (Spain). Dept. d' Enginyeria Quimica; Ayora, C. [Institut de Ciencies de la Terra Jaume Almera, Barcelona (Spain); Bolzicco, J.; Carrera, J. [Univ. Politecnica de Catalunya, Barcelona (Spain). Dept. d' Enginyeria del Terreny

    2003-07-01

    The objective of the present study was to assess the potential of municipal compost as a carbon provider to sulphate reducing bacteria (SRB) for AMD bio-remediation for use in PRB at high flow rates (>0.1 m/d). Different mixtures where municipal compost was accompanied by limestone and optionally by zero-valent iron were assessed in batch and column experiments to treat acidic waters with high contents of sulphates and eventually of metals. A check of the treated wate was carried out throughout the experiments. At the end of the column experiments, precipitates were withdrawn for SEM, EDS and XRD examination and, for one of the columns, solid digestion and sequential extraction were carried out for chemical analysis. Results showed that waters were cleaned of metals and acidity, but when no supplementation of simple organic carbon compounds was carried out it does not seem from chemical and morphology analysis that mechanisms whereby metal removal occurs was due predominantly to biogenic sulphide generation but to the pH increase, i.e. metal (oxy)hydroxides and carbonates precipitation. These precipitates could sorb other metals onto the surface. Sorption to organic matter could also contribute to some extent to metal removal. When zero-valent iron was present, cementation of copper also occurred. It can be concluded that, as applied in this study, municipal compost assessed under high flow rates was a poorly effective carbon source to support a continuous SRB activity. Then selection of reactive materials for permeable reactive barriers is a critical issue on the step of barrier design and construction. Optimisation of such treatments is very laborious, still being studied up to date and often empirical. In the present laboratory study the municipal compost assessed (typically selected as carbon organic source for PRB treating acid mine drainage) under our experimental conditions was too poor a carbon source to support a continuous SRB activity, due to the high

  17. 76 FR 80368 - Notification of Teleconferences of the Science Advisory Board Biogenic Carbon Emissions Panel

    Science.gov (United States)

    2011-12-23

    ... draft report and accounting framework. As noticed in 76 FR 61100-61101, the SAB Biogenic Carbon... AGENCY Notification of Teleconferences of the Science Advisory Board Biogenic Carbon Emissions Panel... Biogenic Carbon Emissions Panel to review EPA's draft Accounting Framework for Biogenic CO2 Emissions...

  18. Iron Homeostasis and Nutritional Iron Deficiency123

    OpenAIRE

    Theil, Elizabeth C.

    2011-01-01

    Nonheme food ferritin (FTN) iron minerals, nonheme iron complexes, and heme iron contribute to the balance between food iron absorption and body iron homeostasis. Iron absorption depends on membrane transporter proteins DMT1, PCP/HCP1, ferroportin (FPN), TRF2, and matriptase 2. Mutations in DMT1 and matriptase-2 cause iron deficiency; mutations in FPN, HFE, and TRF2 cause iron excess. Intracellular iron homeostasis depends on coordinated regulation of iron trafficking and storage proteins enc...

  19. The ultrasound assisted extraction of matrix elements and heavy metal fractions associated with Fe, Al and Mn oxyhydroxides from soil

    Directory of Open Access Journals (Sweden)

    Stanišić Svetlana M.

    2012-01-01

    Full Text Available The single agent extractions of major and trace metals from soil sample were conducted by means of rotary mixer and ultrasonic bath with sonication time of 10, 20, 30, 40 and 50 min. The sequential extraction according to the BCR scheme was undertaken. The obtained soil extracts were analyzed by ICP-OES and according to the results the rotary mixer assisted extraction was more efficient in the case of alkaline-earth elements. However, by the use of ultrasound several times higher amounts of matrix elements (Fe, Al and Mn and heavy metals predominantly associated with Fe, Al and Mn oxyhydroxides were extracted. The increase of the sonication time failed to improve extraction yields. The changes of the conductivity, pH, oxidoreduction potential, particle size diameter and zeta potential of colloid particles, with the sonication time increase were measured. The extraction mechanism and expressed selectivity of ultrasound is discussed and explanation is suggested.

  20. Biogenic amines in meat and fermented meat products

    Directory of Open Access Journals (Sweden)

    Joanna Stadnik

    2010-09-01

    Full Text Available Recent trends in food quality and safety promote an increasing search for trace compounds that can affect human health. Biogenic amines belong to this group of substances. They can cause distinctive pharmacological, physiological and toxic effects in organisms. Their amounts are usually increasing as a consequence of the use of poor quality raw materials, during controlled or spontaneous microbial fermentation or in the course of food spoilage. The origin of biogenic amines makes them suitable as chemical indicators of the hygienic quality and freshness of some foods being associated to the degree of food fermentation or degradation. The development of appropriate manufacturing technologies to obtain products free or nearly free from biogenic amines is a challenge for the meat industry. This review briefly summarises current knowledge on the biological implications of biogenic amines on human health and collects data on the factors affecting their formation in meat and fermented meat products.

  1. A molecular probe for the optical detection of biogenic amines

    OpenAIRE

    Lee, Boram; Scopelliti, Rosario; Severin, Kay

    2011-01-01

    A coumarin derivative was employed for the detection of biogenic amines in buffered aqueous solution by UV-Vis or fluorescence spectroscopy. Incorporated in a polymeric matrix, the dye can also be used for the optical detection of gaseous amines.

  2. Biogenic silica in surficial sediments of Prydz Bay, Antarctica

    Institute of Scientific and Technical Information of China (English)

    Hu Chuanyu; Xue Bin; Yu Peisong; Pan Jianming

    2008-01-01

    The content and distribution of biogenic silica were investigated in sediment cores from Prydz Bay,Antarctica,during the CHINARE 18/21 cruise.The results show that the content of biogenic silica(BSiO 2 )is ranged from 4.89% to 85.41%,and the average content of biogenic silica is 30.90%,the highest valueoccurred at the IV 10 station.The profile of BSiO 2 in sediment is contrast to that of silicate in the interstitial water.The content of biogenic silica and organic carbon in the surface sediments in the central area of Prydz Bay gyre were much higher than those in other area,and closely related to the Chla content and primary productivity of phytoplankton in the surface water column.

  3. Biogenic Silver for Disinfection of Water Contaminated with Viruses▿

    OpenAIRE

    De Gusseme, Bart; Sintubin, Liesje; Baert, Leen; Thibo, Ellen; Hennebel, Tom; Vermeulen, Griet; Uyttendaele, Mieke; Verstraete, Willy; Boon, Nico

    2009-01-01

    The presence of enteric viruses in drinking water is a potential health risk. Growing interest has arisen in nanometals for water disinfection, in particular the use of silver-based nanotechnology. In this study, Lactobacillus fermentum served as a reducing agent and bacterial carrier matrix for zerovalent silver nanoparticles, referred to as biogenic Ag0. The antiviral action of biogenic Ag0 was examined in water spiked with an Enterobacter aerogenes-infecting bacteriophage (UZ1). Addition o...

  4. Factors Influencing Biogenic Amines Accumulation in Dairy Products

    OpenAIRE

    Linares, Daniel M.; del Río, Beatriz; Ladero, Victor; Martínez, Noelia; Fernández, María; Martín, María Cruz; Álvarez, Miguel A.

    2012-01-01

    Fermented foods are among the food products more often complained of having caused episodes of biogenic amines (BA) poisoning. Concerning milk-based fermented foods, cheese is the main product likely to contain potentially harmful levels of BA, specially tyramine, histamine, and putrescine. Prompted by the increasing awareness of the risks related to dietary uptake of high biogenic amine loads, in this review we report all those elaboration and processing technological aspects affecting BA bi...

  5. Factors influencing biogenic amines accumulation in dairy products

    OpenAIRE

    Alvarez, Miguel A.

    2012-01-01

    Fermented foods are among the food products more often complained of having caused episodes of biogenic amines (BA) poisoning. Concerning milk-based fermented foods, cheese is the main product likely to contain potentially harmful levels of BA, specially tyramine, histamine, and putrescine. Prompted by the increasing awareness of the risks related to dietary uptake of high biogenic amine loads, in this review we report all those elaboration and processing technological aspects affecting BA bi...

  6. Quantification of biogenic amines by microchip electrophoresis with chemiluminescence detection

    OpenAIRE

    Zhao, Shulin; Yong HUANG; Shi, Ming; Liu, Yi-Ming

    2009-01-01

    A highly sensitive microchip electrophoresis (MCE) method with chemiluminescence (CL) detection was developed for the determination of biogenic amines including agmatine, epinephrine, dopamine, tyramine, and histamine in human urine samples. To achieve a high assay sensitivity, the targeted analytes were pre-column labeled by a CL tagging reagent, N-(4-aminobutyl)-N-ethylisoluminol (ABEI). ABEI-tagged biogenic amines after MCE separation reacted with hydrogen peroxide in the presence of horse...

  7. Biogenic amines in meat and fermented meat products

    OpenAIRE

    Joanna Stadnik; Zbigniew J. Dolatowski

    2010-01-01

    Recent trends in food quality and safety promote an increasing search for trace compounds that can affect human health. Biogenic amines belong to this group of substances. They can cause distinctive pharmacological, physiological and toxic effects in organisms. Their amounts are usually increasing as a consequence of the use of poor quality raw materials, during controlled or spontaneous microbial fermentation or in the course of food spoilage. The origin of biogenic amines makes them suitabl...

  8. BIOGENIC AMINES CONTENT IN SELECTED WINES DURING WINEMAKING

    OpenAIRE

    Radka Flasarová; Leona Buňková; Barbora Ivičičová; František Buňka; Stanislav Kráčmar

    2012-01-01

    The aim of this study was to describe the development of selected biogenic amines (histamine; tyramine; phenylethylamine; putrescine; agmatine; and cadaverine) during the winemaking in 10 selected species grown in Central Europe in 2008. The analysis was performed using ion-exchange chromatography by the sodium-citrate buffers with the post-column ninhydrin derivatization and photometric detection. A comparison of the content of biogenic amines in red and wine varieties showed that red wines ...

  9. Biogenic silver for disinfection of water contaminated with viruses.

    Science.gov (United States)

    De Gusseme, Bart; Sintubin, Liesje; Baert, Leen; Thibo, Ellen; Hennebel, Tom; Vermeulen, Griet; Uyttendaele, Mieke; Verstraete, Willy; Boon, Nico

    2010-02-01

    The presence of enteric viruses in drinking water is a potential health risk. Growing interest has arisen in nanometals for water disinfection, in particular the use of silver-based nanotechnology. In this study, Lactobacillus fermentum served as a reducing agent and bacterial carrier matrix for zerovalent silver nanoparticles, referred to as biogenic Ag(0). The antiviral action of biogenic Ag(0) was examined in water spiked with an Enterobacter aerogenes-infecting bacteriophage (UZ1). Addition of 5.4 mg liter(-1) biogenic Ag(0) caused a 4.0-log decrease of the phage after 1 h, whereas the use of chemically produced silver nanoparticles (nAg(0)) showed no inactivation within the same time frame. A control experiment with 5.4 mg liter(-1) ionic Ag+ resulted in a similar inactivation after 5 h only. The antiviral properties of biogenic Ag(0) were also demonstrated on the murine norovirus 1 (MNV-1), a model organism for human noroviruses. Biogenic Ag(0) was applied to an electropositive cartridge filter (NanoCeram) to evaluate its capacity for continuous disinfection. Addition of 31.25 mg biogenic Ag(0) m(-2) on the filter (135 mg biogenic Ag(0) kg(-1) filter medium) caused a 3.8-log decline of the virus. In contrast, only a 1.5-log decrease could be obtained with the original filter. This is the first report to demonstrate the antiviral efficacy of extracellular biogenic Ag(0) and its promising opportunities for continuous water disinfection. PMID:20038697

  10. Biogenic Silver for Disinfection of Water Contaminated with Viruses▿

    Science.gov (United States)

    De Gusseme, Bart; Sintubin, Liesje; Baert, Leen; Thibo, Ellen; Hennebel, Tom; Vermeulen, Griet; Uyttendaele, Mieke; Verstraete, Willy; Boon, Nico

    2010-01-01

    The presence of enteric viruses in drinking water is a potential health risk. Growing interest has arisen in nanometals for water disinfection, in particular the use of silver-based nanotechnology. In this study, Lactobacillus fermentum served as a reducing agent and bacterial carrier matrix for zerovalent silver nanoparticles, referred to as biogenic Ag0. The antiviral action of biogenic Ag0 was examined in water spiked with an Enterobacter aerogenes-infecting bacteriophage (UZ1). Addition of 5.4 mg liter−1 biogenic Ag0 caused a 4.0-log decrease of the phage after 1 h, whereas the use of chemically produced silver nanoparticles (nAg0) showed no inactivation within the same time frame. A control experiment with 5.4 mg liter−1 ionic Ag+ resulted in a similar inactivation after 5 h only. The antiviral properties of biogenic Ag0 were also demonstrated on the murine norovirus 1 (MNV-1), a model organism for human noroviruses. Biogenic Ag0 was applied to an electropositive cartridge filter (NanoCeram) to evaluate its capacity for continuous disinfection. Addition of 31.25 mg biogenic Ag0 m−2 on the filter (135 mg biogenic Ag0 kg−1 filter medium) caused a 3.8-log decline of the virus. In contrast, only a 1.5-log decrease could be obtained with the original filter. This is the first report to demonstrate the antiviral efficacy of extracellular biogenic Ag0 and its promising opportunities for continuous water disinfection. PMID:20038697

  11. The Molecular Mechanism of Iron(III) Oxide Nucleation.

    Science.gov (United States)

    Scheck, Johanna; Wu, Baohu; Drechsler, Markus; Rosenberg, Rose; Van Driessche, Alexander E S; Stawski, Tomasz M; Gebauer, Denis

    2016-08-18

    A molecular understanding of the formation of solid phases from solution would be beneficial for various scientific fields. However, nucleation pathways are still not fully understood, whereby the case of iron (oxyhydr)oxides poses a prime example. We show that in the prenucleation regime, thermodynamically stable solute species up to a few nanometers in size are observed, which meet the definition of prenucleation clusters. Nucleation then is not governed by a critical size, but rather by the dynamics of the clusters that are forming at the distinct nucleation stages, based on the chemistry of the linkages within the clusters. This resolves a longstanding debate in the field of iron oxide nucleation, and the results may generally apply to oxides forming via hydrolysis and condensation. The (molecular) understanding of the chemical basis of phase separation is paramount for, e.g., tailoring size, shape and structure of novel nanocrystalline materials. PMID:27466739

  12. Survival and viability of cells from iron depositing bacterial strains in pretests for the EXPOSE-R2-Experiment

    OpenAIRE

    Feyh, N.; de Vera, J.P.; Szewzyk, U

    2014-01-01

    Five environmental isolates (Pseudomonas sp. BS1, Hyphomonas sp. BS2, Tetrasphaera sp. FL1, Pedomicrobium sp. FL6 and Leptothrix sp. OT_B_406) were chosen for EXPOSE-R2 including pretests (EVT1/2, SVT) due to their ability to form Fe(III)-oxyhydroxide-containing biofilms as observed for natural communities of iron depositing bacteria. Samples were produced by drying iron-containing cell aggregates on Mars regolith simulant mixtures (S-/P-MRS) (Böttger et al., 2012). Different Mars- and ...

  13. Shelf-to-basin iron shuttling enhances vivianite formation in deep Baltic Sea sediments

    Science.gov (United States)

    Reed, Daniel C.; Gustafsson, Bo G.; Slomp, Caroline P.

    2016-01-01

    Coastal hypoxia is a growing and persistent problem largely attributable to enhanced terrestrial nutrient (i.e., nitrogen and phosphorus) loading. Recent studies suggest phosphorus removal through burial of iron (II) phosphates, putatively vivianite, plays an important role in nutrient cycling in the Baltic Sea - the world's largest anthropogenic dead zone - yet the dynamics of iron (II) phosphate formation are poorly constrained. To address this, a reactive-transport model was used to reconstruct the diagenetic and depositional history of sediments in the Fårö basin, a deep anoxic and sulphidic region of the Baltic Sea where iron (II) phosphates have been observed. Simulations demonstrate that transport of iron from shelf sediments to deep basins enhances vivianite formation while sulphide concentrations are low, but that pyrite forms preferentially over vivianite when sulphate reduction intensifies due to elevated organic loading. Episodic reoxygenation events, associated with major inflows of oxic waters, encourage the retention of iron oxyhydroxides and iron-bound phosphorus in sediments, increasing vivianite precipitation as a result. Results suggest that artificial reoxygenation of the Baltic Sea bottom waters could sequester up to 3% of the annual external phosphorus loads as iron (II) phosphates, but this is negligible when compared to potential internal phosphorus loads due to dissolution of iron oxyhydroxides when low oxygen conditions prevail. Thus, enhancing vivianite formation through artificial reoxygenation of deep waters is not a viable engineering solution to eutrophication in the Baltic Sea. Finally, simulations suggest that regions with limited sulphate reduction and hypoxic intervals, such as eutrophic estuaries, could act as important phosphorus sinks by sequestering vivianite. This could potentially alleviate eutrophication in shelf and slope environments.

  14. Iron load

    Directory of Open Access Journals (Sweden)

    Filippo Cassarà

    2013-03-01

    Full Text Available Recent research addressed the main role of hepcidin in the regulation of iron metabolism. However, while this mechanism could be relevant in causing iron load in Thalassemia Intermedia and Sickle-Cell Anemia, its role in Thalassemia Major (TM is marginal. This is mainly due to the high impact of transfusional requirement into the severe increase of body iron. Moreover, the damage of iron load may be worsened by infections, as HCV hepatitis, or liver and endocrinological damage. One of the most relevant associations was found between splenectomy and increase of risk for mortality due,probably, to more severe iron load. These issues suggest as morbidity and mortality of this group of patients they do not depend only by our ability in controlling heart damage but even in preventing or treating particular infections and complications. This finding is supported by the impairment of survival curves in patients with complications different from heart damage. However, because, during recent years different direct and indirect methods to detect iron overload in patients affected by secondary hemochromatosis have been implemented, our ability to maintain under control iron load is significantly improved. Anyway, the future in iron load management remains to be able to have an iron load map of our body for targeting chelation and other medical treatment according to the single organ damage.

  15. Adsorption and transformation of selected human-used macrolide antibacterial agents with iron(III) and manganese(IV) oxides

    Energy Technology Data Exchange (ETDEWEB)

    Feitosa-Felizzola, Juliana [Laboratoire Chimie Provence, Aix-Marseille Universites-CNRS (UMR 6264), 3 place Victor Hugo, 13331 Marseille Cedex 3 (France); Hanna, Khalil [Laboratoire de Chimie Physique et Microbiologie pour l' Environnement, CNRS-Universite Henri Poincare-Nancy 1 (UMR 7564), 405 rue de Vandoeuvre, 54600 Villers-les-Nancy (France); Chiron, Serge [Laboratoire Chimie Provence, Aix-Marseille Universites-CNRS (UMR 6264), 3 place Victor Hugo, 13331 Marseille Cedex 3 (France)], E-mail: serge.chiron@univ-provence.fr

    2009-04-15

    The adsorption/transformation of two members (clarithromycin and roxithromycin) of the macrolide (ML) antibacterial agents on the surface of three environmental subsurface sorbents (clay, iron(III) and manganese(IV) oxy-hydroxides) was investigated. The adsorption fitted well to the Freundlich model with a high sorption capacity. Adsorption probably occurred through a surface complexation mechanism and was accompanied by slow degradation of the selected MLs. Transformation proceeded through two parallel pathways: a major pathway was the hydrolysis of the cladinose sugar, and to a lesser extent the hydrolysis of the lactone ring. A minor pathway was the N-dealkylation of the amino sugar. This study indicates that Fe(III) and Mn(IV) oxy-hydroxides in aquatic sediments may play an important role in the natural attenuation of MLs. Such an attenuation route yields a range of intermediates that might retain some of their biological activity. - Iron(III) and manganese(IV) oxy-hydroxides in aquatic sediments may play an important role in the natural attenuation of macrolide antibacterial agents.

  16. Biogenic and non-biogenic Si pools in terrestrial ecosystems: results from a novel analysis method

    Science.gov (United States)

    Barao, Lucia; Vandevenne, Floor; Clymans, Wim; Meire, Patrick; Frings, Patrick; Conley, Daniel; Struyf, Eric

    2015-04-01

    Silicon (Si) is a chemical element frequently associated with highly abundant silicate minerals in the Earth crust. Over millions of years, the interaction of such minerals with the atmosphere and hydrosphere produces a myriad of processed compounds, and the mineral weathering consumes CO2 during the process. The weathering of minerals also triggers the export of dissolved Si (DSi) to coastal waters and the ocean. Here, DSi is deposited in diatom frustules, in an amorphous biogenic form (BSi). Diatoms account for 50% of the primary production and are crucial for the export of carbon into the deep sea. In recent years, it was acknowledged that terrestrial systems filter the Si transition from the terrestrial mineral to the marine and coastal biological pool, by the incorporation of DSi into plants. In this process, DSi is taken up by roots together with other nutrients and precipitates in plant cells in amorphous structures named phytoliths. After dead, plant tissues become mixed in the top soil, where BSi is available for dissolution and will control the DSi availability in short time scales. Additionally, Si originated from soil forming processes can also significantly interfere with the global cycle. The Si cycle in terrestrial ecosystems is a key factor to coastal ecology, plant ecology, biogeochemistry and agro-sciences, but the high variability of different biogenic and non-biogenic Si pools remains as an obstacle to obtain accurate measurements. The traditional methods, developed to isolate diatoms in ocean sediments, only account for simple mineral corrections. In this dissertation we have adapted a novel continuous analysis method (during alkaline extraction) that uses Si-Al ratios and reactivity to differ biogenic from non-biogenic fractions. The method was originally used in marine sediments, but we have developed it to be applicable in a wide range of terrestrial, aquatic and coastal ecosystems. We first focused on soils under strong human impact in

  17. Iron deficiency

    DEFF Research Database (Denmark)

    Schou, Morten; Bosselmann, Helle; Gaborit, Freja;

    2015-01-01

    BACKGROUND: Both iron deficiency (ID) and cardiovascular biomarkers are associated with a poor outcome in heart failure (HF). The relationship between different cardiovascular biomarkers and ID is unknown, and the true prevalence of ID in an outpatient HF clinic is probably overlooked. OBJECTIVES...... understand iron metabolism in elderly HF patients....

  18. Biogenic amines in Italian Pecorino cheese

    Directory of Open Access Journals (Sweden)

    Maria eSchirone

    2012-05-01

    Full Text Available The quality of distinctive artisanal cheeses is closely associated with the territory of production and its traditions. Pedoclimatic characteristics, genetic autochthonous variations and anthropic components create an environment so specific that it would be extremely difficult to reproduce elsewhere. Pecorino cheese is included in this sector of the market and is widely diffused in Italy (approximately 53.727t of production. Pecorino is a common name given to indicate Italian cheeses made exclusively from pure ewes' milk characterized by a high content of fat matter and it is mainly produced in the middle and south of Italy by traditional procedures from raw or thermized milk. The microbiota plays a major role in the development of the organoleptic characteristics of the cheese but it can also be responsible for the accumulation of undesirable substances, such as biogenic amines (BA. Several factors can contribute to the qualitative and quantitative profiles of BA’s in Pecorino cheese such as environmental hygienic conditions, pH, salt concentration, aw, fat content, pasteurization of milk, decarboxylase microorganisms, starter cultures, temperature and time of ripening, storage, part of the cheese (core, edge and the presence of cofactor. Generally, the total content of BA’s can range from about 100-2400 mg/kg, with a prevalence of toxicologically important BA’s, tyramine and histamine. The presence of BA in Pecorino cheeses is becoming increasingly important to consumers and cheese-maker alike, due to the potential threats of toxicity to humans and consequent trade implications.

  19. A cobalt oxyhydroxide-modified upconversion nanosystem for sensitive fluorescence sensing of ascorbic acid in human plasma

    Science.gov (United States)

    Cen, Yao; Tang, Jun; Kong, Xiang-Juan; Wu, Shuang; Yuan, Jing; Yu, Ru-Qin; Chu, Xia

    2015-08-01

    Ascorbic acid (AA), a potent antioxidant readily scavenging reactive species, is a crucial micronutrient involved in many biochemical processes. Here, we have developed a cobalt oxyhydroxide (CoOOH)-modified upconversion nanosystem for fluorescence sensing of AA activity in human plasma. The nanosystem consists of upconversion nanoparticles (UCNPs) NaYF4:30% Yb,0.5% Tm@NaYF4, which serve as energy donors, and CoOOH nanoflakes formed on the surface of UCNPs, which act as efficient energy acceptors. The fluorescence resonance energy transfer (FRET) process from the UCNPs to the absorbance of the CoOOH nanoflakes occurs in the nanosystem. The AA-mediated specific redox reaction reduces CoOOH into Co2+, leading to the inhibition of FRET, and resulting in the recovery of upconversion emission spectra. On the basis of these features, the nanosystem can be used for sensing AA activity with sensitivity and selectivity. Moreover, due to the minimizing background interference provided by UCNPs, the nanosystem has been applied to monitoring AA levels in human plasma sample with satisfactory results. The proposed approach may potentially provide an analytical platform for research and clinical diagnosis of AA related diseases.Ascorbic acid (AA), a potent antioxidant readily scavenging reactive species, is a crucial micronutrient involved in many biochemical processes. Here, we have developed a cobalt oxyhydroxide (CoOOH)-modified upconversion nanosystem for fluorescence sensing of AA activity in human plasma. The nanosystem consists of upconversion nanoparticles (UCNPs) NaYF4:30% Yb,0.5% Tm@NaYF4, which serve as energy donors, and CoOOH nanoflakes formed on the surface of UCNPs, which act as efficient energy acceptors. The fluorescence resonance energy transfer (FRET) process from the UCNPs to the absorbance of the CoOOH nanoflakes occurs in the nanosystem. The AA-mediated specific redox reaction reduces CoOOH into Co2+, leading to the inhibition of FRET, and resulting in the

  20. Redox switching and oxygen evolution at hydrous oxyhydroxide modified nickel electrodes in aqueous alkaline solution: effect of hydrous oxide thickness and base concentration

    OpenAIRE

    Lyons, Michael

    2012-01-01

    Outstanding issues regarding the film formation, the redox switching reaction and the oxygen evolution reaction (OER) electrocatalytic behaviour of multi-cycled nickel oxy-hydroxide films in aqueous alkaline solution have been discussed. The oxide is grown using a repetitive potential multi-cycling technique, and the mechanism of the latter hydrous oxide formation process has been discussed. A duplex layer model of the oxide/solution interphase region is proposed. The acid/base behaviour of t...

  1. Copper isotope fractionation during its interaction with soil and aquatic microorganisms and metal oxy(hydr)oxides: Possible structural control

    Science.gov (United States)

    Pokrovsky, O. S.; Viers, J.; Emnova, E. E.; Kompantseva, E. I.; Freydier, R.

    2008-04-01

    This work is aimed at quantifying the main environmental factors controlling isotope fractionation of Cu during its adsorption from aqueous solutions onto common organic (bacteria, algae) and inorganic (oxy(hydr)oxide) surfaces. Adsorption of Cu on aerobic rhizospheric ( Pseudomonas aureofaciens CNMN PsB-03) and phototrophic aquatic ( Rhodobacter sp. f-7bl, Gloeocapsa sp. f-6gl) bacteria, uptake of Cu by marine ( Skeletonema costatum) and freshwater ( Navicula minima, Achnanthidium minutissimum and Melosira varians) diatoms, and Cu adsorption onto goethite (FeOOH) and gibbsite (AlOOH) were studied using a batch reaction as a function of pH, copper concentration in solution and time of exposure. Stable isotopes of copper in selected filtrates were measured using Neptune multicollector ICP-MS. Irreversible incorporation of Cu in cultured diatom cells at pH 7.5-8.0 did not produce any isotopic shift between the cell and solution (Δ 65/63Cu(solid-solution)) within ±0.2‰. Accordingly, no systematic variation was observed during Cu adsorption on anoxygenic phototrophic bacteria ( Rhodobacter sp.), cyanobacteria ( Gloeocapsa sp.) or soil aerobic exopolysaccharide (EPS)-producing bacteria ( P. aureofaciens) in circumneutral pH (4-6.5) and various exposure times (3 min to 48 h): Δ 65Cu(solid-solution) = 0.0 ± 0.4‰. In contrast, when Cu was adsorbed at pH 1.8-3.5 on the cell surface of soil the bacterium P. aureofacienshaving abundant or poor EPS depending on medium composition, yielded a significant enrichment of the cell surface in the light isotope (Δ 65Cu (solid-solution) = -1.2 ± 0.5‰). Inorganic reactions of Cu adsorption at pH 4-6 produced the opposite isotopic offset: enrichment of the oxy(hydr)oxide surface in the heavy isotope with Δ 65Cu(solid-solution) equals 1.0 ± 0.25‰ and 0.78 ± 0.2‰ for gibbsite and goethite, respectively. The last result corroborates the recent works of Mathur et al. [Mathur R., Ruiz J., Titley S., Liermann L., Buss H. and

  2. The nanostructured Au-doped cobalt oxyhydroxide based carbon monoxide sensor for fire detection at its earlier stages

    International Nuclear Information System (INIS)

    Two nanostructures of cobalt oxyhydroxide (CoOOH) and Au-loaded CoOOH with amount of Au (0.05, 0.5 and 1 mass%), respectively, were investigated for gas sensing properties to combustion by-product pollutants, which are typical for early stages of fire. The nanostructured p-type semiconductor films have shown good sensitivity to carbon monoxide (CO) in the temperature range 50–110 °C with the maximum sensitivity to CO at 80 °C. As the amount of Au-load increased to 0.5 mass%, the improvement in both CO sensitivity and response/recovery rates has been established. The additional increase of the Au-load up to 1 mass% degraded the CO sensing properties of the device. Cross-sensitivity investigation of the sensor to various gases co-existing at the earlier stages of fire revealed that CO sensitivity of nanostructured Au-loaded CoOOH is the highest among other gases. The morphologies of the prepared Au-doped CoOOH samples have been studied by x-ray diffraction (XRD), energy-dispersive x-ray diffraction (EDX) and scanning electron microscopy (SEM) techniques. The promoting effects of Au loads were discussed. The results of this work may be applicable for further development of carbon monoxide sensors for fire detection at its earlier stages

  3. Synthesis of Nanosized Zinc-Doped Cobalt Oxyhydroxide Parties by a Dropping Method and Their Carbon Monoxide Gas Sensing Properties

    Directory of Open Access Journals (Sweden)

    Jian-Wen Wang

    2013-01-01

    Full Text Available Two nanostructures of cobalt oxyhydroxide (CoOOH and Zinc-(Zn- doped CoOOH (1–4% Zn are prepared from Co(NO32 solution via microtitration with NaOH and oxidation in air. The X-ray diffraction (XRD analysis results show that a pure state of nano-CoOOH can be obtained at an alkalinity (OH−/Co+ of 5 with 40°C heat treatment after 6 h. The Zn ions preferentially substitute Co ions in the CoOOH structure, resulting in a decrease of its crystallinity. The disc-like CoOOH nanostructure exhibits good sensitivity to carbon monoxide (CO in a temperature range of 40–110°C with maximum sensitivity to CO at around 70–80°C. When CoOOH nanostructure is doped with 1% Zn, its sensitivity and selectivity for CO gas are improved at 70–80°C; further Zn doping to 2% degraded the CO sensing properties of nano-CoOOH. The results of a cross-sensitivity investigation of the sensor to various gases coexisting at early stages of a fire show that the sensitivity of Zn-doped nano-CoOOH is the highest toward CO. Zn-doped nano-CoOOH film exhibits a high sensitivity to CO at room temperature, making it a promising sensor for early-stage fire detection.

  4. Non-native Co-, Mn-, and Ti-oxyhydroxide nanocrystals in ferritin for high efficiency solar energy conversion.

    Science.gov (United States)

    Erickson, S D; Smith, T J; Moses, L M; Watt, R K; Colton, J S

    2015-01-01

    Quantum dot solar cells seek to surpass the solar energy conversion efficiencies achieved by bulk semiconductors. This new field requires a broad selection of materials to achieve its full potential. The 12 nm spherical protein ferritin can be used as a template for uniform and controlled nanocrystal growth, and to then house the nanocrystals for use in solar energy conversion. In this study, precise band gaps of titanium, cobalt, and manganese oxyhydroxide nanocrystals within ferritin were measured, and a change in band gap due to quantum confinement effects was observed. The range of band gaps obtainable from these three types of nanocrystals is 2.19-2.29 eV, 1.93-2.15 eV, and 1.60-1.65 eV respectively. From these measured band gaps, theoretical efficiency limits for a multi-junction solar cell using these ferritin-enclosed nanocrystals are calculated and found to be 38.0% for unconcentrated sunlight and 44.9% for maximally concentrated sunlight. If a ferritin-based nanocrystal with a band gap similar to silicon can be found (i.e. 1.12 eV), the theoretical efficiency limits are raised to 51.3% and 63.1%, respectively. For a current matched cell, these latter efficiencies become 41.6% (with an operating voltage of 5.49 V), and 50.0% (with an operating voltage of 6.59 V), for unconcentrated and maximally concentrated sunlight respectively. PMID:25490522

  5. Technologies for the utilisation of biogenic waste in the bioeconomy.

    Science.gov (United States)

    O'Callaghan, Kenneth

    2016-05-01

    A brief review has been done of technologies involved in the exploitation of biogenic wastes, in order to provide an introduction to the subject from the technological perspective. Biogenic waste materials and biomass have historically been utilised for thousands of years, but a new conversation is emerging on the role of these materials in modern bioeconomies. Due to the nature of the products and commodities now required, a modern bioeconomy is not simply a rerun of former ones. This new dialogue needs to help us understand how technologies for managing and processing biogenic wastes--both established and novel--should be deployed and integrated (or not) to meet the requirements of the sustainability, closed-loop and resource-security agendas that evidently sit behind the bioeconomy aspirations now being voiced in many countries and regions of the world. PMID:26769498

  6. Measuring biogenic silica in marine sediments and suspended matter

    Science.gov (United States)

    DeMaster, David J.

    Measuring the biogenic silica content of marine sediments and suspended matter is essential for a variety of geochemical, biological, and sedimentological studies. Biota forming siliceous skeletal material account for as much as one third of the primary productivity in the ocean [Lisitzin, 1972] and a significant portion (2 to 70% by weight) of open-ocean sediments. Biogenic silica measurements reveal important information concerning the bulk chemistry of suspended material or sediment and are essential in any type of silica flux study in the water column or seabed. Analyses of this biogenic phase in marine plankton are useful in characterizing the basic types of biota present and in comparing the distributions of particulate and dissolved silicate when evaluating nutrient dynamics [Nelson and Smith, 1986]. In the marine environment, diatoms, radiolaria, sponges, and silicoflagellates are the common types of siliceous biota.

  7. Seasonal trends of biogenic terpene emissions.

    Science.gov (United States)

    Helmig, Detlev; Daly, Ryan Woodfin; Milford, Jana; Guenther, Alex

    2013-09-01

    Biogenic volatile organic compound (BVOC) emissions from six coniferous tree species, i.e. Pinus ponderosa (Ponderosa Pine), Picea pungens (Blue Spruce), Pseudotsuga menziesii (Rocky Mountain Douglas Fir) and Pinus longaeva (Bristlecone Pine), as well as from two deciduous species, Quercus gambelii (Gamble Oak) and Betula occidentalis (Western River Birch) were studied over a full annual growing cycle. Monoterpene (MT) and sesquiterpene (SQT) emissions rates were quantified in a total of 1236 individual branch enclosure samples. MT dominated coniferous emissions, producing greater than 95% of BVOC emissions. MT and SQT demonstrated short-term emission dependence with temperature. Two oxygenated MT, 1,8-cineol and piperitone, were both light and temperature dependent. Basal emission rates (BER, normalized to 1000μmolm(-2)s(-1) and 30°C) were generally higher in spring and summer than in winter; MT seasonal BER from the coniferous trees maximized between 1.5 and 6.0μgg(-1)h(-1), while seasonal lows were near 0.1μgg(-1)h(-1). The fractional contribution of individual MT to total emissions was found to fluctuate with season. SQT BER measured from the coniferous trees ranged from <0.01 to 0.15μgg(-1)h(-1). BER of up to 1.2μgg(-1)h(-1) of the SQT germacrene B were found from Q. gambelii, peaking in late summer. The β-factor, used to define temperature dependence in emissions modeling, was not found to exhibit discernible growth season trends. A seasonal correction factor proposed by others in previous work to account for a sinusoidal shaped emission pattern was applied to the data. Varying levels of agreement were found between the data and model results for the different plant species seasonal data sets using this correction. Consequently, the analyses on this extensive data set suggest that it is not feasible to apply a universal seasonal correction factor across different vegetation species. A modeling exercise comparing two case scenarios, (1) without and (2

  8. Biogenic emissions from Citrus species in California

    Science.gov (United States)

    Fares, Silvano; Gentner, Drew R.; Park, Jeong-Hoo; Ormeno, Elena; Karlik, John; Goldstein, Allen H.

    2011-09-01

    Biogenic Volatile Organic Compounds (BVOC) emitted from plants are the dominant source of reduced carbon chemicals to the atmosphere and are important precursors to the photochemical production of ozone and secondary organic aerosols. Considering the extensive land used for agriculture, cultivated Citrus plantations may play an important role in the chemistry of the atmosphere especially in regions such as the Central Valley of California. Moreover, the BVOC emissions from Citrus species have not been characterized in detail and more species-specific inputs for regional models of BVOC emissions are needed. In this study, we measured the physiological parameters and emissions of the most relevant BVOC (oxygenated compounds, monoterpenes, and sesquiterpenes) for four predominant Citrus species planted in California ( Citrus sinensis var. 'Parent Navel', Citrus limon var. 'Meyer', Citrus reticulata var. 'W. Murcott' and 'Clementine'). We used two analytical techniques to measure a full range of BVOC emitted: Proton Transfer Reaction Mass Spectrometry (PTR-MS) and gas chromatography with mass spectrometry. Methanol, followed by acetone and acetaldehyde, were the dominant BVOC emitted from lemon and mandarin trees (basal emission rates up to 300 ng(C) g(DW) -1 h -1), while oxygenated monoterpenes, monoterpenes, and sesquiterpenes were the main BVOC emitted from orange trees (basal emission rates up to = 2500 ng(C) g(DW) -1 h -1). Light and temperature-dependent algorithms were better predictors of methanol, acetaldehyde, acetone, isoprene and monoterpenes for all the Citrus species. Whereas, temperature-dependent algorithms were better predictors of oxygenated monoterpenes, and sesquiterpenes. We observed that flowering increased emissions from orange trees by an order of magnitude with the bulk of BVOC emissions being comprised of monoterpenes, sesquiterpenes, and oxygenated monoterpenes. Chemical speciation of BVOC emissions show that the various classes of terpene

  9. Biogenic amines in dry fermented sausages: a review.

    Science.gov (United States)

    Suzzi, Giovanna; Gardini, Fausto

    2003-11-15

    Biogenic amines are compounds commonly present in living organisms in which they are responsible for many essential functions. They can be naturally present in many foods such as fruits and vegetables, meat, fish, chocolate and milk, but they can also be produced in high amounts by microorganisms through the activity of amino acid decarboxylases. Excessive consumption of these amines can be of health concern because their not equilibrate assumption in human organism can generate different degrees of diseases determined by their action on nervous, gastric and intestinal systems and blood pressure. High microbial counts, which characterise fermented foods, often unavoidably lead to considerable accumulation of biogenic amines, especially tyramine, 2-phenylethylamine, tryptamine, cadaverine, putrescine and histamine. However, great fluctuations of amine content are reported in the same type of product. These differences depend on many variables: the quali-quantitative composition of microbial microflora, the chemico-physical variables, the hygienic procedure adopted during production, and the availability of precursors. Dry fermented sausages are worldwide diffused fermented meat products that can be a source of biogenic amines. Even in the absence of specific rules and regulations regarding the presence of these compounds in sausages and other fermented products, an increasing attention is given to biogenic amines, especially in relation to the higher number of consumers with enhanced sensitivity to biogenic amines determined by the inhibition of the action of amino oxidases, the enzymes involved in the detoxification of these substances. The aim of this paper is to give an overview on the presence of these compounds in dry fermented sausages and to discuss the most important factors influencing their accumulation. These include process and implicit factors as well as the role of starter and nonstarter microflora growing in the different steps of sausage production

  10. Biogenic methane potential of marine sediments. Application of chemical thermodynamics

    Energy Technology Data Exchange (ETDEWEB)

    Arning, E.T.; Schulz, H.M. [Helmholtz Centre Potsdam GFZ, Potsdam (Germany); Berk, W. van [Technical Univ. of Clausthal (Germany). Dept. of Hydrogeology

    2013-08-01

    Accumulations of biogenic methane-dominated gas are widespread and occur in a variety of depositional settings and rock types. However, the potential of biogenic methane remains underexplored. This is mainly due to the fact that quantitative assessments applying numerical modeling techniques for exploration purposes are generally lacking to date. Biogenic methane formation starts in relatively shallow marine sediments below the sulfate reduction zone. When sulfate is exhausted, methanogenesis via the CO{sub 2} reduction pathway is often the dominant biogenic methane formation process in marine sediments (Claypool and Kaplan, 1974). The process can be simplified by the reaction: 2CH{sub 2}O + Ca{sup 2+} + H{sub 2}O {yields} CH{sub 4} + CaCO{sub 3} + 2H{sup +}. The products of early diagenetic reactions initiate coupled equilibrium reactions that induce a new state of chemical equilibrium among minerals, pore water and gas. The driving force of the complex biogeochemical reactions in sedimentary environments during early diagenesis is the irreversible redox-conversion of organic matter. Early diagenetic formation of biogenic methane shortly after deposition ('early diagenesis') was retraced using PHREEQC computer code that is applied to calculate homogenous and heterogeneous mass-action equations in combination with one-dimensional diffusion driven transport (Parkhurst and Appelo, 1999). Our modeling approach incorporates interdependent diagenetic reactions evolving into a diffusive multi-component and multiphase system by means of thermodynamic equilibrium calculations of species distribution (Arning et al., 2011, 2012, 2013). Reaction kinetics of organic carbon conversion is integrated into the set of equilibrium reactions by defining type and amount of converted organic matter in a certain time step. It is the aim (1) to calculate quantitatively thermodynamic equilibrium conditions (composition of pore water, mineral phase and gas phase assemblage) in

  11. Corrosion-Resistant Amorphous Alloy Ribbons for Electromagnetic Filtration of Iron Rusts from Water

    OpenAIRE

    Kawashima, Asahi; Asami, Katsuhiko; Sato, Takeaki; Hashimoto, Koji

    1985-01-01

    An attempt was made to use corrosion-resistant amorphous Fe-9Cr-13P-7C alloy ribbons as an electromagnetic filter material for trapping various iron rusts suspended in water at 40℃. The ferrimagnetic Fe_3O_4 rust was trapped with the 100% efficiency and paramagnetic rusts such as α-Fe_2O_3, α-FeOOH and amorphous ferric oxyhydroxide were trapped with certain efficiencies at the magnetic field strength of 0.5-10 kOe. The regeneration of the filter by back-washing was easy. The trapping capacity...

  12. The iron-encrusted microbial community of Urothoe poseidonis (Crustacea, Amphipoda)

    Science.gov (United States)

    Gillan, David C.; Ribesse, Jérôme; de Ridder, Chantal

    2004-06-01

    A rust-coloured coating frequently covers the appendages and sternites of Urothoe poseidonis, an amphipod living in the burrow of the echinoid Echinocardium cordatum. Up to 80% of the collected amphipods were coated. In winter, coated amphipods were always more abundant than uncoated ones. In summer, uncoated specimens predominated. The aspect, location and development of the coating are similar in juveniles and adults. EDAX analyses and Prussian blue testing indicate that the rust-coloured coating contains iron oxyhydroxide minerals with trace metals and phosphorus. Scanning electron microscopy shows that the iron coating harbours bacterial filaments related to Beggiatoaceae (3 morphotypes were observed). Protozoans, possibly Peritrichia of the families Rovinjellidae or Vaginicolidae (one morphotype), were also observed on pereopods VI and VII. The formation of the iron coating and its potential role in the biology of the amphipod are discussed.

  13. Ratios of biogenic elements for distinguishing recent from fossil microorganisms

    Science.gov (United States)

    Hoover, Richard B.

    2007-09-01

    The ability to distinguish possible microfossils from recent biological contaminants is of great importance to Astrobiology. In this paper we discuss the application of the ratios of life critical biogenic elements (C/O; C/N; and C/S) as determined by Energy Dispersive X-ray Spectroscopy (EDS) to this problem. Biogenic element ratios are provided for a wide variety of living cyanobacteria and other microbial extremophiles, preserved herbarium materials, and ancient biota from the Antarctic Ice Cores and Siberian and Alaskan Permafrost for comparison with macrofossils and microfossils in ancient terrestrial rocks and carbonaceous meteorites.

  14. Ratios of Biogenic Elements for Distinguishing Recent from Fossil Microorganisms

    Science.gov (United States)

    Hoover, Richard B.

    2007-01-01

    The ability to distinguish possible microfossils from recent biological contaminants is of great importance to Astrobiology. In this paper we discuss the application of the ratios of life critical biogenic elements (C/O; C/N; and C/S) as determined by Energy Dispersive X-ray Spectroscopy (EDS) to this problem. Biogenic element ratios will be provided for a wide variety of living cyanobacteria and other microbial extremophiles, preserved herbarium materials, and ancient biota from the Antarctic Ice Cores and Siberian and Alaskan Permafrost for comparison with megafossils and microfossils in ancient terrestrial rocks and carbonaceous meteorites.

  15. Influence of beer storage for the selected biogenic amines content

    OpenAIRE

    Brýdlová, Nikola

    2012-01-01

    This thesis does not only changes in the content of biogenic amines during storage of bottled beer, but beer in general. The production of beer in the world is gradually increasing. In 2010, produced a 811,4 million hectoliters of beer. Czech Republic in 2010 produced 17,1 million hectoliters in 2011 and ceased production decline. Average consumption in the Czech Republic was in 2010, 144 liters/person/year. Another chapter is devoted to biogenic amines. They are nitrogen compounds, in which ...

  16. Determination of Biogenic Amines in Different Shrimp Species for Export

    International Nuclear Information System (INIS)

    This study is part of the project on the ''Quality Assurance of Different Shrimp Species for Export''. Local shrimp samples were collected from Ministry of Livestock and Fisheries and various private enterprises. Contents of biogenic amines were determined by using benzoyl chloride derivatization method with HPLC (reverse phase high performance liquid chromatography). Based on the biogenic amines, quality index of shrimps were correlated with freshness index so that the grade of shrimp samples can be classified as excellent, good, and acceptable. All sizes of shrimps such as extra large, large, medium were found to excceptable respectively

  17. Native iron

    DEFF Research Database (Denmark)

    Brooks, Charles Kent

    2015-01-01

    We live in an oxidized world: oxygen makes up 22 percent of the atmosphere and by reacting with organic matter produces most of our energy, including the energy our bodies use to function: breathe, think, move, etc. It has not always been thus. Originally the Earth, in common with most of the Solar...... System, was reduced. The oxidized outer layers of the Earth have formed by two processes. Firstly, water is decomposed to oxygen and hydrogen by solar radiation in the upper parts of the atmosphere, the light hydrogen diffusing to space, leaving oxygen behind. Secondly, plants, over the course of...... situation unique in the Solar System. In such a world, iron metal is unstable and, as we all know, oxidizes to the ferric iron compounds we call 'rust'. If we require iron metal it must be produced at high temperatures by reacting iron ore, usually a mixture of ferrous (Fe2+) and ferric (Fe3+) oxides (Fe2O3...

  18. Influence of the immobilized yeast cells technology on the presence of biogenic amines in wine

    OpenAIRE

    Miličević, Borislav; Šubarić, Drago; Babić, Jurislav; Ačkar, Đurđica; Jozinović, Antun; Petošić, Emil; Matijević, Anita

    2014-01-01

    Biogenic amines are basic nitrogenous low molecular weight compounds with biological activity. Biogenic amines are important because they contain a health risk for sensitive humans. Biogenic amines in the wine can be formed from their precursors by various microorganisms present in the wine, at any stage of production. The aim of the present work was to study the changes of the content of biogenic amines in wines made from grape variety Frankovka and Pinot noir (Vitis vinifera L.) from Kutjev...

  19. The Potential of the Yeast Debaryomyces hansenii H525 to Degrade Biogenic Amines in Food

    OpenAIRE

    Mathias Bäumlisberger; Urs Moellecken; Helmut König; Harald Claus

    2015-01-01

    Twenty-six yeasts from different genera were investigated for their ability to metabolize biogenic amines. About half of the yeast strains produced one or more different biogenic amines, but some strains of Debaryomyces hansenii and Yarrowia lipolytica were also able to degrade such compounds. The most effective strain D. hanseniii H525 metabolized a broad spectrum of biogenic amines by growing and resting cells. Degradation of biogenic amines by this yeast isolate could be attributed to a pe...

  20. METABOLISM OF IRON STORES

    OpenAIRE

    Saito, Hiroshi

    2014-01-01

    ABSTRACT Remarkable progress was recently achieved in the studies on molecular regulators of iron metabolism. Among the main regulators, storage iron, iron absorption, erythropoiesis and hepcidin interact in keeping iron homeostasis. Diseases with gene-mutations resulting in iron overload, iron deficiency, and local iron deposition have been introduced in relation to the regulators of storage iron metabolism. On the other hand, the research on storage iron metabolism has not advanced since th...

  1. Biogenic volatile organic compounds - small is beautiful

    Science.gov (United States)

    Owen, S. M.; Asensio, D.; Li, Q.; Penuelas, J.

    2012-12-01

    While canopy and regional scale flux measurements of biogenic volatile organic compounds (bVOCs) are essential to obtain an integrated picture of total compound reaching the atmosphere, many fascinating and important emission details are waiting to be discovered at smaller scales, in different ecological and functional compartments. We concentrate on bVOCs below ground to pollination of flowers. Although bVOC emissions from soil surfaces are small, bVOCs are exuded by roots of some plant species, and can be extracted from decaying litter. Naturally occurring monoterpenes in the rhizosphere provide a specialised carbon source for micro-organisms, helping to define the micro-organism community structure, and impacting on nutrient cycles which are partly controlled by microorganisms. Naturally occurring monoterpenes in the soil system could also affect the aboveground structure of ecosystems because of their role in plant defence strategies and as mediating chemicals in allelopathy. A gradient of monoterpene concentration was found in soil around Pinus sylvestris and Pinus halepensis, decreasing with distance from the tree. Some compounds (α-pinene, sabinene, humulene and caryophyllene) in mineral soil were linearly correlated with the total amount of each compound in the overlying litter, indicating that litter might be the dominant source of these compounds. However, α-pinene did not fall within the correlation, indicating a source other than litter, probably root exudates. We also show that rhizosphere bVOCs can be a carbon source for soil microbes. In a horizontal gradient from Populus tremula trees, microbes closest to the tree trunk were better enzymatically equipped to metabolise labeled monoterpene substrate. Monoterpenes can also increase the degradation rate in soil of the persistant organic pollutants, likely acting as analogues for the cometabo-lism of polychlorinated biphenyls (PCBs) Flowers of a ginger species (Alpinia kwangsiensis) and a fig species

  2. Biogenic gases in tropical floodplain river

    Directory of Open Access Journals (Sweden)

    Maria Victória Ramos Ballester

    2001-06-01

    Full Text Available Analysis of the distribution of biogenic gases in the floodplain of the Mogi-Guaçu River (São Paulo, Brazil enabled the establishment of a "redox hierarchy", in which the main channel was the most oxidizing environment, followed by Diogo Lake, with Infernão Lake having the most reducing conditions of the subsystems evaluated. Diogo Lake exported about 853.4 g C.m-2.year-1, of which, 14.6% was generated from methanogenesis and 36.7% by aerobic respiration. For Infernão Lake, these values were 2016 g C.m-2.year-1, 1.8 % and 41.5 %, respectively. Carbon export by these systems was predominantly in the form of CO2, which was responsible for the release of 728.78 g C.m-2.year-1 at Diogo Lake and 1979.72 g C.m-2. year-1 at Infernão Lake. Such patterns may result from the nature of the hydrological conditions, the action of the hydroperiod, and morphological characteristics of the environment.A análise da distribuição de gases biogênicos na planície de inundação do Rio Mogi Guaçu (São Paulo, Brasil possibilitou o estabelecimento de um gradiente redox para os sistemas aquáticos avaliados, em que o canal principal do rio apresentou-se como o ambiente mais oxidado, seguido da Lagoa do Diogo, e a Lagoa do Infernão apresentando as condições mais redutoras entre os ambientes em questão. A Lagoa do Diogo exporta um total de 853,4 g C.m-2.ano-1, do qual 14,6% é produzido pela metanogênese e 36,7% pela respiração aeróbia. Para a Lagoa do Infernão estes valores foram respectivamente de 2.016 g C.m-2.ano-1, 1,8% e de 41,5%. A exportação de carbono por estes sistemas é realizada, predominantemente na forma de CO2, nos valores de 728,78 g C.m-2.ano-1 para a Lagoa do Diogo e 1.979,72 g C.m-2.ano-1 para a Lagoa do Infernão. Estes padrões parecem estar relacionados com a natureza das condições hidrológicas, com a ação do hidroperíodo e com as características morfológicas do ambiente.

  3. A cobalt oxyhydroxide nanoflake-based nanoprobe for the sensitive fluorescence detection of T4 polynucleotide kinase activity and inhibition

    Science.gov (United States)

    Cen, Yao; Yang, Yuan; Yu, Ru-Qin; Chen, Ting-Ting; Chu, Xia

    2016-04-01

    Phosphorylation of nucleic acids with 5'-OH termini catalyzed by polynucleotide kinase (PNK) is an inevitable process and has been implicated in many important cellular events. Here, we found for the first time that there was a significant difference in the adsorbent ability of cobalt oxyhydroxide (CoOOH) nanoflakes between single-stranded DNA (ssDNA) and double-stranded DNA (dsDNA), which resulted in the fluorescent dye-labeled dsDNA still retaining strong fluorescence emission, while the fluorescence signal of ssDNA was significantly quenched by CoOOH nanoflakes. Based on this discovery, we developed a CoOOH nanoflake-based nanoprobe for the fluorescence sensing of T4 PNK activity and its inhibition by combining it with λ exonuclease cleavage reaction. In the presence of T4 PNK, dye-labeled dsDNA was phosphorylated and then cleaved by λ exonuclease to generate ssDNA, which could adsorb on the CoOOH nanoflakes and whose fluorescence was quenched by CoOOH nanoflakes. Due to the high quenching property of CoOOH nanoflakes as an efficient energy acceptor, a sensitive and selective sensing approach with satisfactory performance for T4 PNK sensing in a complex biological matrix has been successfully constructed and applied to the screening of inhibitors. The developed approach may potentially provide a new platform for further research, clinical diagnosis, and drug discovery of nucleotide kinase related diseases.Phosphorylation of nucleic acids with 5'-OH termini catalyzed by polynucleotide kinase (PNK) is an inevitable process and has been implicated in many important cellular events. Here, we found for the first time that there was a significant difference in the adsorbent ability of cobalt oxyhydroxide (CoOOH) nanoflakes between single-stranded DNA (ssDNA) and double-stranded DNA (dsDNA), which resulted in the fluorescent dye-labeled dsDNA still retaining strong fluorescence emission, while the fluorescence signal of ssDNA was significantly quenched by Co

  4. Non-native Co-, Mn-, and Ti-oxyhydroxide nanocrystals in ferritin for high efficiency solar energy conversion

    International Nuclear Information System (INIS)

    Quantum dot solar cells seek to surpass the solar energy conversion efficiencies achieved by bulk semiconductors. This new field requires a broad selection of materials to achieve its full potential. The 12 nm spherical protein ferritin can be used as a template for uniform and controlled nanocrystal growth, and to then house the nanocrystals for use in solar energy conversion. In this study, precise band gaps of titanium, cobalt, and manganese oxyhydroxide nanocrystals within ferritin were measured, and a change in band gap due to quantum confinement effects was observed. The range of band gaps obtainable from these three types of nanocrystals is 2.19–2.29 eV, 1.93–2.15 eV, and 1.60–1.65 eV respectively. From these measured band gaps, theoretical efficiency limits for a multi-junction solar cell using these ferritin-enclosed nanocrystals are calculated and found to be 38.0% for unconcentrated sunlight and 44.9% for maximally concentrated sunlight. If a ferritin-based nanocrystal with a band gap similar to silicon can be found (i.e. 1.12 eV), the theoretical efficiency limits are raised to 51.3% and 63.1%, respectively. For a current matched cell, these latter efficiencies become 41.6% (with an operating voltage of 5.49 V), and 50.0% (with an operating voltage of 6.59 V), for unconcentrated and maximally concentrated sunlight respectively. (paper)

  5. Enzymatic Sensor of Biogenic Amines with Optical Oxygen Transducer

    Czech Academy of Sciences Publication Activity Database

    Maixnerová, Lucie; Horvitz, Alexandar; Kuncová, Gabriela; Přibyl, M.; Šebela, M.; Koštejn, Martin

    Brno: Masarykova Universita, 2014, s. 173. ISBN 978-80-210-7159-9. [CEITEC Annual Conference. Brno (CZ), 21.10.2014-24.10.2014] R&D Projects: GA TA ČR TA03010544 Institutional support: RVO:67985858 Keywords : optical enzymatic biosensor * biogenic amines * mathematical model Subject RIV: CB - Analytical Chemistry, Separation

  6. Azo dye decolorization assisted by chemical and biogenic sulfide

    Energy Technology Data Exchange (ETDEWEB)

    Prato-Garcia, Dorian [Laboratory for Research on Advanced Processes for Water Treatment, Unidad Académica Juriquilla, Instituto de Ingeniería, Universidad Nacional Autónoma de México, Blvd. Juriquilla 3001, Querétaro 76230 (Mexico); Cervantes, Francisco J. [División de Ciencias Ambientales, Instituto Potosino de Investigación Científica y Tecnológica, Camino a la Presa de San José 2055, San Luis Potosí 78216 (Mexico); Buitrón, Germán, E-mail: gbuitronm@ii.unam.mx [Laboratory for Research on Advanced Processes for Water Treatment, Unidad Académica Juriquilla, Instituto de Ingeniería, Universidad Nacional Autónoma de México, Blvd. Juriquilla 3001, Querétaro 76230 (Mexico)

    2013-04-15

    Highlights: ► Azo dyes were reduced efficiently by chemical and biogenic sulfide. ► Biogenic sulfide was more efficient than chemical sulfide. ► There was no competition between dyes and sulfate for reducing equivalents. ► Aromatic amines barely affected the sulfate-reducing process. -- Abstract: The effectiveness of chemical and biogenic sulfide in decolorizing three sulfonated azo dyes and the robustness of a sulfate-reducing process for simultaneous decolorization and sulfate removal were evaluated. The results demonstrated that decolorization of azo dyes assisted by chemical sulfide and anthraquinone-2,6-disulfonate (AQDS) was effective. In the absence of AQDS, biogenic sulfide was more efficient than chemical sulfide for decolorizing the azo dyes. The performance of sulfate-reducing bacteria in attached-growth sequencing batch reactors suggested the absence of competition between the studied azo dyes and the sulfate-reducing process for the reducing equivalents. Additionally, the presence of chemical reduction by-products had an almost negligible effect on the sulfate removal rate, which was nearly constant (94%) after azo dye injection.

  7. Azo dye decolorization assisted by chemical and biogenic sulfide

    International Nuclear Information System (INIS)

    Highlights: ► Azo dyes were reduced efficiently by chemical and biogenic sulfide. ► Biogenic sulfide was more efficient than chemical sulfide. ► There was no competition between dyes and sulfate for reducing equivalents. ► Aromatic amines barely affected the sulfate-reducing process. -- Abstract: The effectiveness of chemical and biogenic sulfide in decolorizing three sulfonated azo dyes and the robustness of a sulfate-reducing process for simultaneous decolorization and sulfate removal were evaluated. The results demonstrated that decolorization of azo dyes assisted by chemical sulfide and anthraquinone-2,6-disulfonate (AQDS) was effective. In the absence of AQDS, biogenic sulfide was more efficient than chemical sulfide for decolorizing the azo dyes. The performance of sulfate-reducing bacteria in attached-growth sequencing batch reactors suggested the absence of competition between the studied azo dyes and the sulfate-reducing process for the reducing equivalents. Additionally, the presence of chemical reduction by-products had an almost negligible effect on the sulfate removal rate, which was nearly constant (94%) after azo dye injection

  8. Advances in Biochemical Screening for Phaeochromocytoma using Biogenic Amines

    OpenAIRE

    Whiting, Malcolm J; Doogue, Matthew P

    2009-01-01

    Biochemical testing for phaeochromocytoma is performed in diagnostic laboratories using a variety of tests with plasma, serum or 24-hour urine collections. These tests include catecholamines and their methylated metabolites - the metanephrines, either individually or in combination with their sulfated metabolites. High-performance liquid chromatography (HPLC) continues to be the dominant analytical method for biogenic amine quantitation. Chromatographic techniques are changing, with improveme...

  9. Biogenic Isoprene Emission Mechanism from 13CO2 Exposure Experiments

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    Biogenic isoprene emissions have been believed to be from only photosynthesis processes in plant. However nocturnal isoprene emission from pine is detected. And by feeding 13CO2 to plants, it is found that both photosynthesis pathway and light independent processes contribute to isoprene emissions.

  10. Emission of Biogenic Volatile Organic Compounds in the Arctic

    DEFF Research Database (Denmark)

    Lindwall, Frida

    Emissions of biogenic volatile organic compounds (BVOCs) from arctic ecosystems are scarcely studied and the effect of climate change on BVOC emissions even less so. BVOCs are emitted from all living organisms and play a role for atmospheric chemistry. The major part of BVOCs derives from plants...

  11. Biogenic Magnetite Formation through Anaerobic Biooxidation of Fe(II)

    OpenAIRE

    Chaudhuri, Swades K.; Lack, Joseph G.; Coates, John D.

    2001-01-01

    The presence of isotopically light carbonates in association with fine-grained magnetite is considered to be primarily due to the reduction of Fe(III) by Fe(III)-reducing bacteria in the environment. Here, we report on magnetite formation by biooxidation of Fe(II) coupled to denitrification. This metabolism offers an alternative environmental source of biogenic magnetite.

  12. Iron Fertilization in the Southern Ocean Deduced From Environmental Magnetism of Sediment Cores

    Science.gov (United States)

    Yamazaki, T.; Ikehara, M.

    2012-12-01

    With rock-magnetic technique, biogenic magnetites in sediments can be detected utilizing the characteristics of almost no magnetostatic interactions and narrow coercivity distribution, reflecting occurrence of single-domain magnetites in a chain (e.g., Egli et al., 2010; Roberts et al., 2011). Magnetic mineral assemblages in pelagic sediments of Pacific and Indian Oceans often have two distinctive constituents; the first is characterized by non-interacting on first-order reversal curve (FORC) diagrams and low-coercivity (~40 mT) with small dispersion on isothermal remanent magnetization (IRM) component analyses, and the second is characterized by interacting and middle-coercivity (~100 mT). The former is interpreted as biogenic magnetites and the latter is terrigenous maghemites (Yamazaki, 2009; 2012). The ratio of anhysteretic remanent magnetization susceptibility to saturation IRM reflects relative abundance of the biogenic and terrigenous components. In the Southern Ocean, magnetic mineral concentration increases in glacial periods. The variation pattern closely resembles eolian dust flux records from Antarctic ice cores, but the cause of the linkage was unclear, as the dust flux is too small for the source of terrigenous materials in the Southern Ocean. Our environmental magnetic study of late Pleistocene sediments from the south Indian Ocean revealed that biogenic magnetites are a dominant constituent of the magnetic minerals. In glacials, the abundance of both biogenic and terrigenous components increased with increased proportions of the latter. Increased ocean productivity in glacials is suggested from increased proportions of biogenic magnetites with elongated morphologies, indicative of less-oxic conditions, and increased sedimentation rates. These observations suggest that the increased magnetic concentration in glacials in the Southern Ocean may be explained by iron fertilization; the production of biogenic magnetites was enhanced associated with

  13. Seasonal variations of coastal sedimentary trace metals cycling: Insight on the effect of manganese and iron (oxy)hydroxides, sulphide and organic matter

    International Nuclear Information System (INIS)

    Highlights: • Multivariate statistic treatment (PCA) classified main elements and samples groups. • Trace metals mobility in porewater showed seasonal variations. • Strong control of Fe and Mn on metals dynamics at surface sediments. • Influence of dissolved organic matter on metal-sulphide equilibrium. - Abstract: The combination of analysis, multivariate treatment (PCA) and chemical speciation calculation confirmed the control of Fe, Mn, sulphide and organic matter on metals dynamics in coastal sediments (0–5 cm surface sediments and sediments cores) of Toulon Bay (NW Mediterranean). The temporal monitoring of the physic-chemical parameters as well as the dissolved/particulate minor (Fe/Mn) and trace elements (i.e. Ag, Cd, Co, Cu, Ni, Pb, Zn, …) concentrations in porewaters and sediments were assessed. Multivariate treatment revealed different behaviours for marine elements, terrestrial ones and contaminants. Seasonal variations of metals mobilization in porewater were observed, related to diagenesis activity. Element mobility was studied by selective extractions (ascorbate, acid and alkaline) on sediments. Thermodynamic simulation (PHREEQC) was performed to calculate the elemental dissolved speciation, the mineral saturation index and then to simulate the solid/liquid interaction through precipitation processes, studying the contrasted influence of dissolved organic matter and sulphide

  14. Investigating sorption on iron-oxyhydroxide soil minerals by solid-state NMR spectroscopy: a 6Li MAS NMR study of adsorption and absorption on goethite

    DEFF Research Database (Denmark)

    Nielsen, Ulla Gro; Paik, Younkee; Julmis, Keinia;

    2005-01-01

    system representing an ideal model system for NMR studies. 6Li resonances with large hyperfine shifts (approximately 145 ppm) were observed above the goethite point of zero charge, providing clear evidence for the presence of Li-O-Fe connectivities, and thus the formation of an inner sphere Li+ complex...... on the goethite surface. Even larger Li hyperfine shifts (289 ppm) were observed for Li+-exchanged goethite, which contains lithium ions in the tunnels of the goethite structure, confirming the Li assignment of the 145 ppm Li resonance to the surface sites. Udgivelsesdato: 2005-Oct-6...

  15. The Potential of the Yeast Debaryomyces hansenii H525 to Degrade Biogenic Amines in Food

    Directory of Open Access Journals (Sweden)

    Mathias Bäumlisberger

    2015-11-01

    Full Text Available Twenty-six yeasts from different genera were investigated for their ability to metabolize biogenic amines. About half of the yeast strains produced one or more different biogenic amines, but some strains of Debaryomyces hansenii and Yarrowia lipolytica were also able to degrade such compounds. The most effective strain D. hanseniii H525 metabolized a broad spectrum of biogenic amines by growing and resting cells. Degradation of biogenic amines by this yeast isolate could be attributed to a peroxisomal amine oxidase activity. Strain H525 may be useful as a starter culture to reduce biogenic amines in fermented food.

  16. Iron and Your Child

    Science.gov (United States)

    ... Story" 5 Things to Know About Zika & Pregnancy Iron and Your Child KidsHealth > For Parents > Iron and ... enough iron in their daily diets. How Much Iron Do Kids Need? Kids require different amounts of ...

  17. Iron-Deficiency Anemia

    Medline Plus

    Full Text Available ... have enough iron in your body. Low iron levels usually are due to blood loss, poor diet, ... iron supplements and multivitamins to improve her iron levels. Susan also made changes to her diet, such ...

  18. Iron homeostasis and nutritional iron deficiency.

    Science.gov (United States)

    Theil, Elizabeth C

    2011-04-01

    Nonheme food ferritin (FTN) iron minerals, nonheme iron complexes, and heme iron contribute to the balance between food iron absorption and body iron homeostasis. Iron absorption depends on membrane transporter proteins DMT1, PCP/HCP1, ferroportin (FPN), TRF2, and matriptase 2. Mutations in DMT1 and matriptase-2 cause iron deficiency; mutations in FPN, HFE, and TRF2 cause iron excess. Intracellular iron homeostasis depends on coordinated regulation of iron trafficking and storage proteins encoded in iron responsive element (IRE)-mRNA. The noncoding IRE-mRNA structures bind protein repressors, IRP1 or 2, during iron deficiency. Integration of the IRE-RNA in translation regulators (near the cap) or turnover elements (after the coding region) increases iron uptake (DMT1/TRF1) or decreases iron storage/efflux (FTN/FPN) when IRP binds. An antioxidant response element in FTN DNA binds Bach1, a heme-sensitive transcription factor that coordinates expression among antioxidant response proteins like FTN, thioredoxin reductase, and quinone reductase. FTN, an antioxidant because Fe(2+) and O(2) (reactive oxygen species generators) are consumed to make iron mineral, is also a nutritional iron concentrate that is an efficiently absorbed, nonheme source of iron from whole legumes. FTN protein cages contain thousands of mineralized iron atoms and enter cells by receptor-mediated endocytosis, an absorption mechanism distinct from transport of nonheme iron salts (ferrous sulfate), iron chelators (ferric-EDTA), or heme. Recognition of 2 nutritional nonheme iron sources, small and large (FTN), will aid the solution of iron deficiency, a major public health problem, and the development of new policies on iron nutrition. PMID:21346101

  19. An in situ study of the role of surface films on granular iron in the permeable iron wall technology

    Science.gov (United States)

    Ritter, K.; Odziemkowski, M. S.; Gillham, R. W.

    2002-03-01

    Permeable walls of granular iron are a new technology developed for the treatment of groundwater contaminated with dissolved chlorinated solvents. Degradation of the chlorinated solvents involves a charge transfer process in which they are reductively dechlorinated, and the iron is oxidized. The iron used in the walls is an impure commercial material that is covered with a passive layer of Fe 2O 3, formed as a result of a high-temperature oxidation process used in the production of iron. Understanding the behaviour of this layer upon contact with solution is important, because Fe 2O 3 inhibits mechanisms involved in contaminant reduction, including electron transfer and catalytic hydrogenation. Using a glass column specially designed to allow for in situ Raman spectroscopic and open circuit potential measurements, the passive layer of Fe 2O 3 was observed to be largely removed from the commercial product, Connelly iron, upon contact with Millipore water and with a solution of Millipore water containing 1.5 mg/l trichloroethylene (TCE). It has been previously shown that Fe 2O 3 is removed from iron surfaces upon contact with solution by an autoreduction reaction; however, prior to this work, the reaction has not been shown to occur on the impure commercial iron products used in permeable granular iron walls. The rate of removal was sufficiently rapid such that the initial presence of Fe 2O 3 at the iron surface would have no consequence with respect to the performance of an in situ wall. Subsequent to the removal of Fe 2O 3 layer, magnetite and green rust formed at the iron surface as a result of corrosion in both the Millipore water and the solution containing TCE. The formation of these two species, rather than higher valency iron oxides and oxyhydroxides, is significant for the technology. The former can interfere with contaminant degradation because they inhibit electron transfer and catalytic hydrogenation. Magnetite and green rust, in contrast, will not

  20. Iron and iron derived radicals

    International Nuclear Information System (INIS)

    We have discussed some reactions of iron and iron-derived oxygen radicals that may be important in the production or treatment of tissue injury. Our conclusions challenge, to some extent, the usual lines of thought in this field of research. Insofar as they are born out by subsequent developments, the lessons they teach are two: Think fast! Think small! In other words, think of the many fast reactions that can rapidly alter the production and fate of highly reactive intermediates, and when considering the impact of competitive reactions on such species, think how they affect the microenvironment (on the molecular scale) ''seen'' by each reactive molecule. 21 refs., 3 figs., 1 tab

  1. Quantifying Rates of Complete Microbial Iron Redox Cycling in Acidic Hot Springs

    Science.gov (United States)

    St Clair, B.; Pottenger, J. W.; Shock, E.

    2013-12-01

    Large accumulations of iron oxide commonly occur in shallow outflows of acidic hot springs, and culturing, molecular techniques, and microscopy by others indicate that this iron oxide (often ferrihydrite) is largely biogenic in Yellowstone National Park. The hot springs that support iron mats have several consistent geochemical features including combinations of pH, temperature, sulfide, dissolved oxygen, depth and ferrous iron concentration appropriate to support iron oxidation. These springs nearly always have a point source leading to a large shallow outflow apron. Microbial zones often, but not always, include a small clear zone near the source, followed by a sulfide oxidation zone, iron mat, and finally photosynthesis. The yellow sulfide oxidation zone is separated from the red iron mat by a sharp transition resulting from increasing dissolved oxygen from atmospheric contact and microbial depletion of sulfide. The iron mat is typically the largest microbial zone in the feature by area. Further down the outflow, iron oxidation appears to be outcompeted by phototrophs as the temperature cools. Occasionally there is overlap in these zones, but one metabolism always appears dominant. Our experiments at diverse hot springs indicate that microbial reduction is less geochemically restricted than oxidation, requiring only organic carbon, ferric minerals and an anoxic environment. With iron oxidizers fixing carbon and producing layers of ferric minerals that become rapidly anoxic with depth, iron reduction is invariably proximal to where biogenic iron oxides are forming. To characterize the interplay of oxidation and reduction rates that permit oxide accumulation, we conducted rate experiments at geochemically diverse Yellowstone hot springs featuring visible iron oxides in thermal areas throughout the park. These experiments were performed during two summer field seasons to determine in situ and maximum rates of iron oxidation and reduction by measuring changing

  2. Preserved filamentous microbial biosignatures in the Brick Flat gossan, Iron Mountain, California

    Science.gov (United States)

    Williams, Amy J.; Sumner, Dawn Y.; Alpers, Charles N.; Karunatillake, Suniti; Hofmann, Beda A

    2015-01-01

    A variety of actively precipitating mineral environments preserve morphological evidence of microbial biosignatures. One such environment with preserved microbial biosignatures is the oxidized portion of a massive sulfide deposit, or gossan, such as that at Iron Mountain, California. This gossan may serve as a mineralogical analogue to some ancient martian environments due to the presence of oxidized iron and sulfate species, and minerals that only form in acidic aqueous conditions, in both environments. Evaluating the potential biogenicity of cryptic textures in such martian gossans requires an understanding of how microbial textures form biosignatures on Earth. The iron-oxide-dominated composition and morphology of terrestrial, nonbranching filamentous microbial biosignatures may be distinctive of the underlying formation and preservation processes. The Iron Mountain gossan consists primarily of ferric oxide (hematite), hydrous ferric oxide (HFO, predominantly goethite), and jarosite group minerals, categorized into in situ gossan, and remobilized iron deposits. We interpret HFO filaments, found in both gossan types, as HFO-mineralized microbial filaments based in part on (1) the presence of preserved central filament lumina in smooth HFO mineral filaments that are likely molds of microbial filaments, (2) mineral filament formation in actively precipitating iron-oxide environments, (3) high degrees of mineral filament bending consistent with a flexible microbial filament template, and (4) the presence of bare microbial filaments on gossan rocks. Individual HFO filaments are below the resolution of the Mars Curiosity and Mars 2020 rover cameras, but sinuous filaments forming macroscopic matlike textures are resolvable. If present on Mars, available cameras may resolve these features identified as similar to terrestrial HFO filaments and allow subsequent evaluation for their biogenicity by synthesizing geochemical, mineralogical, and morphological analyses. Sinuous

  3. Preserved Filamentous Microbial Biosignatures in the Brick Flat Gossan, Iron Mountain, California.

    Science.gov (United States)

    Williams, Amy J; Sumner, Dawn Y; Alpers, Charles N; Karunatillake, Suniti; Hofmann, Beda A

    2015-08-01

    A variety of actively precipitating mineral environments preserve morphological evidence of microbial biosignatures. One such environment with preserved microbial biosignatures is the oxidized portion of a massive sulfide deposit, or gossan, such as that at Iron Mountain, California. This gossan may serve as a mineralogical analogue to some ancient martian environments due to the presence of oxidized iron and sulfate species, and minerals that only form in acidic aqueous conditions, in both environments. Evaluating the potential biogenicity of cryptic textures in such martian gossans requires an understanding of how microbial textures form biosignatures on Earth. The iron-oxide-dominated composition and morphology of terrestrial, nonbranching filamentous microbial biosignatures may be distinctive of the underlying formation and preservation processes. The Iron Mountain gossan consists primarily of ferric oxide (hematite), hydrous ferric oxide (HFO, predominantly goethite), and jarosite group minerals, categorized into in situ gossan, and remobilized iron deposits. We interpret HFO filaments, found in both gossan types, as HFO-mineralized microbial filaments based in part on (1) the presence of preserved central filament lumina in smooth HFO mineral filaments that are likely molds of microbial filaments, (2) mineral filament formation in actively precipitating iron-oxide environments, (3) high degrees of mineral filament bending consistent with a flexible microbial filament template, and (4) the presence of bare microbial filaments on gossan rocks. Individual HFO filaments are below the resolution of the Mars Curiosity and Mars 2020 rover cameras, but sinuous filaments forming macroscopic matlike textures are resolvable. If present on Mars, available cameras may resolve these features identified as similar to terrestrial HFO filaments and allow subsequent evaluation for their biogenicity by synthesizing geochemical, mineralogical, and morphological analyses. Sinuous

  4. Biogenic emission measurement and inventories determination of biogenic emissions in the eastern United States and Texas and comparison with biogenic emission inventories

    OpenAIRE

    Warneke, C.; De Gouw, JA; Del Negro, L; J. Brioude; Mckeen, S.; H. Stark; Kuster, WC; Goldan, PD; Trainer, M.; Fehsenfeld, FC; Wiedinmyer, C.; Guenther, AB; Hansel, A.; A. Wisthaler; Atlas, E.

    2010-01-01

    During the NOAA Southern Oxidant Study 1999 (SOS1999), Texas Air Quality Study 2000 (TexAQS2000), International Consortium for Atmospheric Research on Transport and Transformation (ICARTT2004), and Texas Air Quality Study 2006 (TexAQS2006) campaigns, airborne measurements of isoprene and monoterpenes were made in the eastern United States and in Texas, and the results are used to evaluate the biogenic emission inventories BEIS3.12, BEIS3.13, MEGAN2, and WM2001. Two methods are used for the ev...

  5. Biomass burning: Combustion emissions, satellite imagery, and biogenic emissions

    International Nuclear Information System (INIS)

    This chapter deals with two different, but related, aspects of biomass burning. The first part of the chapter deals with a technique to estimate the instantaneous emissions of trace gases produced by biomass burning using satellite imagery. The second part of the chapter concerns the recent discovery that burning results in significantly enhanced biogenic emissions of N2O, NO, and CH4. Hence, biomass burning has both an immediate and long-term impact on the production of trace gases to the atmosphere. The objective of this research is to better assess and quantify the role of this research is to better assess and quantify the role and impact of biomass as a driver for global change. It will be demonstrated that satellite imagery of fires may be used to estimate combustion emissions and may in the future be used to estimate the long-term postburn biogenic emissions of trace gases to the atmosphere

  6. Gas formation. Formation temperatures of thermogenic and biogenic methane.

    Science.gov (United States)

    Stolper, D A; Lawson, M; Davis, C L; Ferreira, A A; Santos Neto, E V; Ellis, G S; Lewan, M D; Martini, A M; Tang, Y; Schoell, M; Sessions, A L; Eiler, J M

    2014-06-27

    Methane is an important greenhouse gas and energy resource generated dominantly by methanogens at low temperatures and through the breakdown of organic molecules at high temperatures. However, methane-formation temperatures in nature are often poorly constrained. We measured formation temperatures of thermogenic and biogenic methane using a "clumped isotope" technique. Thermogenic gases yield formation temperatures between 157° and 221°C, within the nominal gas window, and biogenic gases yield formation temperatures consistent with their comparatively lower-temperature formational environments (<50°C). In systems where gases have migrated and other proxies for gas-generation temperature yield ambiguous results, methane clumped-isotope temperatures distinguish among and allow for independent tests of possible gas-formation models. PMID:24970083

  7. Manganese in biogenic magnetite crystals from magnetotactic bacteria.

    Science.gov (United States)

    Keim, Carolina N; Lins, Ulysses; Farina, Marcos

    2009-03-01

    Magnetotactic bacteria produce either magnetite (Fe(3)O(4)) or greigite (Fe(3)S(4)) crystals in cytoplasmic organelles called magnetosomes. Whereas greigite magnetosomes can contain up to 10 atom% copper, magnetite produced by magnetotactic bacteria was considered chemically pure for a long time and this characteristic was used to distinguish between biogenic and abiogenic crystals. Recently, it was shown that magnetosomes containing cobalt could be produced by three strains of Magnetospirillum. Here we show that magnetite crystals produced by uncultured magnetotactic bacteria can incorporate manganese up to 2.8 atom% of the total metal content (Fe+Mn) when manganese chloride is added to microcosms. Thus, chemical purity can no longer be taken as a strict prerequisite to consider magnetite crystals to be of biogenic origin. PMID:19187208

  8. Hauterivian shallow marine calcareous biogenic mounds: S.E. Spain

    OpenAIRE

    Arias, Consuelo; Masse, Jean Pierre; Vilas Minondo, Lorenzo

    1995-01-01

    Hauterivian biogenic deposits from the Prebetic northern margin near Caudete (Albacete Province, southeastern Spain) are represented by low domed bodies, less than 10 m thick, surrounded by bioclastic sediments and capped by siliciclastics. They consist of a coral, stromatoporoid and microbial framework with cavities filled by mud, rapidly lithified. Intermound bioclastics, derived from the mound organic community, reflect high energy conditions and shallow water settings. Mound g...

  9. Biogenic amines in smear and mould-ripened cheeses

    OpenAIRE

    Pavel Pleva; Leona Buňková; Eva Theimrová; Vendula Bartošáková; František Buňka; Khatantuul Purevdorj

    2014-01-01

    The aim of the study was the monitoring of six biogenic amines (histamine, tyramine, phenylethylamine, tryptamine, putrescine, and cadaverine) and two polyamines (spermidine and spermine) in 30 samples of dairy products purchased in the Czech Republic, namely in 15 samples of mould-ripened cheeses and in 15 samples of smear-ripened cheeses. A further goal was the microbiological analysis of the individual samples of cheeses (total count of microorganisms, number of enterobacteria, enterococci...

  10. Analysis of Some Biogenic Amines by Micellar Liquid Chromatography

    OpenAIRE

    Irena Malinowska; Katarzyna E. Stępnik

    2012-01-01

    Micellar liquid chromatography (MLC) with the use of high performance liquid chromatography (HPLC) was used to determine some physicochemical parameters of six biogenic amines: adrenaline, dopamine, octopamine, histamine, 2-phenylethylamine, and tyramine. In this paper, an influence of surfactant’s concentration and pH of the micellar mobile phase on the retention of the tested substances was examined. To determine the influence of surfactant’s concentration on the retention of the tested ami...

  11. Biogenic calcite structures in Green Lake, James Ross Island, Antarctica

    Czech Academy of Sciences Publication Activity Database

    Elster, Josef; Nedbalová, Linda; Komárek, Jiří; Vodrážka, R.

    Brno: Masarykova Univerzita, 2009 - (Barták, M.; Hájek, J.; Váczi, P.), s. 38-40 ISBN 978-80-210-4987-1. [Electronic Conference on Interactions between Antarctic Life and Environmental Factors. Brno (CZ), 22.10.2009-23.10.2009] R&D Projects: GA MŠk(CZ) ME 945 Institutional research plan: CEZ:AV0Z60050516 Keywords : Green Lake * James Ross * Biogenic calcite structures Subject RIV: EF - Botanics

  12. BAECC Biogenic Aerosols - Effects on Clouds and Climate

    Energy Technology Data Exchange (ETDEWEB)

    Petäjä, Tuukka [Univ. of Helsinki (Finland); Moisseev, Dmitri [Univ. of Helsinki (Finland); Sinclair, Victoria [Univ. of Helsinki (Finland); O' Connor, Ewan J. [Finnish Meteorological Institute, Helsinki (Finland); Manninen, Antti J. [Univ. of Helsinki (Finland); Levula, Janne [Univ. of Helsinki (Finland); Väänänen, Riikka [Univ. of Helsinki (Finland); Heikkinen, Liine [Univ. of Helsinki (Finland); Äijälä, Mikko [Univ. of Helsinki (Finland); Aalto, Juho [Univ. of Helsinki (Finland); Bäck, Jaana [University of Helsinki, Finland

    2015-11-01

    Biogenic Aerosols - Effects on Clouds and Climate (BAECC)”, featured the U.S. Department of Energy’s Atmospheric Radiation Measurement (ARM) Program’s 2nd Mobile Facility (AMF2) in Hyytiälä, Finland. It operated for an 8-month intensive measurement campaign from February to September 2014. The main research goal was to understand the role of biogenic aerosols in cloud formation. One of the reasons to perform BAECC study in Hyytiälä was the fact that it hosts SMEAR-II (Station for Measuring Forest Ecosystem-Atmosphere Relations), which is one of the world’s most comprehensive surface in-situ observation sites in a boreal forest environment. The station has been measuring atmospheric aerosols, biogenic emissions and an extensive suite of parameters relevant to atmosphere-biosphere interactions continuously since 1996. The BAECC enables combining vertical profiles from AMF2 with surface-based in-situ SMEAR-II observations and allows the processes at the surface to be directly related to processes occurring throughout the entire tropospheric column. With the inclusion of extensive surface precipitation measurements, and intensive observation periods involving aircraft flights and novel radiosonde launches, the complementary observations of AMF2 and SMEAR-II provide a unique opportunity for investigating aerosol-cloud interactions, and cloud-to-precipitation processes. The BAECC dataset will initiate new opportunities for evaluating and improving models of aerosol sources and transport, cloud microphysical processes, and boundary-layer structures.

  13. Human iron transporters

    OpenAIRE

    Garrick, Michael D.

    2010-01-01

    Human iron transporters manage iron carefully because tissues need iron for critical functions, but too much iron increases the risk of reactive oxygen species. Iron acquisition occurs in the duodenum via divalent metal transporter (DMT1) and ferroportin. Iron trafficking depends largely on the transferrin cycle. Nevertheless, non-digestive tissues have a variety of other iron transporters that may render DMT1 modestly redundant, and DMT1 levels exceed those needed for the just-mentioned task...

  14. Iron bioavailability from commercially available iron supplements

    OpenAIRE

    Christides, Tatiana; Wray, David; McBride, Richard; Fairweather, Rose; Sharp, Paul

    2015-01-01

    Purpose Iron deficiency anaemia (IDA) is a global public health problem. Treatment with the standard of care ferrous iron salts may be poorly tolerated, leading to non-compliance and ineffective correction of IDA. Employing supplements with higher bioavailability might permit lower doses of iron to be used with fewer side effects, thus improving treatment efficacy. Here, we compared the iron bioavailability of ferrous sulphate tablets with alternative commercial iron products, including th...

  15. Stabilization of biosolids with nanoscale zero-valent iron (nZVI)

    International Nuclear Information System (INIS)

    Biosolids are the treated organic residuals, also known as sludge, that are generated from domestic wastewater treatment plants. According to the USEPA, over 7 millions tons (dry weight) of biosolids are generated every year in the US by more than the 16,000 wastewater treatment plants and a large portion of these biosolids is disposed on land. Nuisance odors, the potential of pathogen transmission, and presence of toxic and persistent organic chemicals and metals in biosolids have for the most part limited the use of land applications. This paper presents zero-valent iron nanoparticles (1-100 nm) for the treatment and stabilization of biosolids. Iron nanoparticles have been shown to form stable and nonvolatile surface complexes with malodorous sulfur compounds such as hydrogen sulfide and methyl sulfides, degrade persistent organic pollutants such as PCBs and chlorinated pesticides, and sequestrate toxic metal ions such as mercury and lead. The end products from the nanoparticle reactions are iron oxides and oxyhydroxides, similar to the ubiquitous iron minerals in the environment. Due to the large surface area and high surface reactivity, only a relatively low dose (<0.1% wt) of iron nanoparticles is needed for effective biosolids stabilization. The iron nanoparticle technology may thus offer an economically and environmentally sustainable and unique solution to one of the most vexing environmental problems

  16. Global Biogenic Emission of Carbon Dioxide from Landfills

    Science.gov (United States)

    Lima, R.; Nolasco, D.; Meneses, W.; Salazar, J.; Hernández, P.; Pérez, N.

    2002-12-01

    Human-induced increases in the atmospheric concentrations of greenhouse gas components have been underway over the past century and are expected to drive climate change in the coming decades. Carbon dioxide was responsible for an estimated 55 % of the antropogenically driven radiactive forcing of the atmosphere in the 1980s and is predicted to have even greater importance over the next century (Houghton et al., 1990). A highly resolved understanding of the sources and sinks of atmospheric CO2, and how they are affected by climate and land use, is essential in the analysis of the global carbon cycle and how it may be impacted by human activities. Landfills are biochemical reactors that produce CH4 and CO2 emissions due to anaerobic digestion of solid urban wastes. Estimated global CH4 emission from landfills is about 44 millions tons per year and account for a 7.4 % of all CH4 sources (Whiticar, 1989). Observed CO2/CH4 molar ratios from landfill gases lie within the range of 0.7-1.0; therefore, an estimated global biogenic emission of CO2 from landfills could reach levels of 11.2-16 millions tons per year. Since biogas extraction systems are installed for extracting, purifying and burning the landfill gases, most of the biogenic gas emission to the atmosphere from landfills occurs through the surface environment in a diffuse and disperse form, also known as non-controlled biogenic emission. Several studies of non-controlled biogenic gas emission from landfills showed that CO2/CH4 weight ratios of surface landfill gases, which are directly injected into the atmosphere, are about 200-300 times higher than those observed in the landfill wells, which are usually collected and burned by gas extraction systems. This difference between surface and well landfill gases is mainly due to bacterial oxidation of the CH4 to CO2 inducing higher CO2/CH4 ratios for surface landfill gases than those well landfill gases. Taking into consideration this observation, the global biogenic

  17. Magnetotactic bacteria form magnetite from a phosphate-rich ferric hydroxide via nanometric ferric (oxyhydr)oxide intermediates

    OpenAIRE

    J. Baumgartner; Morin, G.; Menguy, N.; Perez Gonzalez, T.; Widdrat, M.; Cosmidis, J.; Faivre, D.

    2013-01-01

    The iron oxide mineral magnetite (Fe3O4) is produced by various organisms to exploit magnetic and mechanical properties. Magnetotactic bacteria have become one of the best model organisms for studying magnetite biomineralization, as their genomes are sequenced and tools are available for their genetic manipulation. However, the chemical route by which magnetite is formed intracellularly within the so-called magnetosomes has remained a matter of debate. Here we used X-ray absorption spectrosco...

  18. 40K in the Black Sea: a proxy to estimate biogenic sedimentation

    International Nuclear Information System (INIS)

    An approach to estimate the rate of biogenic sedimentation in the Black Sea using the naturally occurring radionuclide 40K has been considered. It allows assessment of the contribution of suspended matter of biological origin to the overall sediment accumulation in the Black Sea coastal, shelf and deep-water areas. Based upon this method, a relationship between the biogenic fraction of the seabed sediments and the water depth has been established with a view to differentiating the contributions of allochthonous and autochthonous suspended matter to the sedimentation rate. Overall, 40K can be considered as an easily applicable proxy to assess sedimentation rate of biogenic fraction of particulate matter in marine environments. - Highlights: • 40K-based approach was developed to assess biogenic sedimentation in the Black Sea. • 40K-derived relationship between biogenic sedimentation and water depth was traced. • 40K is an easily applicable proxy to estimate rate of biogenic sedimentation in sea

  19. Biogenic amines in commercially produced Yulu, a Chinese fermented fish sauce.

    Science.gov (United States)

    Jiang, Wei; Xu, Ying; Li, Chunsheng; Dong, Xiaoyan; Wang, Dongfeng

    2014-01-01

    Seven biogenic amines were determined in 35 commercially produced Yulu samples from three provinces of China by pre-column derivatisation with dansyl chloride (Dns-Cl) and high-performance liquid chromatography with fluorescence detection (HPLC-FLD). Putrescine, cadaverine, histamine and tyramine were the major biogenic amines (more than 100 mg kg(-1)), while tryptamine, spermidine and spermine were regarded as minor biogenic amines (less than 25 mg kg(-1)). Twenty samples contained more than 50 mg kg(-1) histamine (the limit for histamine in seafood products as suggested by the Food and Drug Administration). Twenty-one samples contained more than 100 mg kg(-1) tyramine and 10 contained more than 1000 mg kg(-1) total biogenic amines. This study provided data on biogenic amine levels in Chinese fermented fish sauce. The results suggested that biogenic amine content should be monitored in commercially produced Yulu. PMID:24779975

  20. Biogenic Mn oxides for effective adsorption of Cd from aquatic environment

    International Nuclear Information System (INIS)

    Biogenic Mn oxides exert important controls on trace metal cycling in aquatic and soil environments. A Mn-oxidizing bacterium Bacillus sp. WH4 was isolated from Fe-Mn nodules of an agrudalf in central China. The biogenic Mn oxides formed by mediation of this Mn oxidizing microorganism were identified as short-ranged and nano-sized Mn oxides. Cd adsorption isotherms, pH effect on adsorption and kinetics were investigated in comparison with an abiotic Mn oxide todorokite. Maximum adsorption of Cd to the biogenic Mn oxides and todorokite was 2.04 and 0.69 mmol g-1 sorbent, respectively. Thus, the biogenic Mn oxides were more effective Cd adsorbents than the abiotic Mn oxide in the aquatic environment. The findings could improve our knowledge of biogenic Mn oxides formation in the environment and their important roles in the biogeochemical cycles of heavy metals. - Biogenic Mn oxides effectively adsorb Cd from aquatic environments.

  1. Biogenic Mn oxides for effective adsorption of Cd from aquatic environment

    Energy Technology Data Exchange (ETDEWEB)

    Meng Youting [State Key Laboratory of Urban and Regional Ecology, Research Center for Eco-environmental Sciences, Chinese Academy of Sciences, Beijing 100085 (China); Graduate School, Chinese Academy of Sciences, Beijing 100039 (China); Zheng Yuanming; Zhang Limei [State Key Laboratory of Urban and Regional Ecology, Research Center for Eco-environmental Sciences, Chinese Academy of Sciences, Beijing 100085 (China); He Jizheng, E-mail: jzhe@rcees.ac.c [State Key Laboratory of Urban and Regional Ecology, Research Center for Eco-environmental Sciences, Chinese Academy of Sciences, Beijing 100085 (China)

    2009-08-15

    Biogenic Mn oxides exert important controls on trace metal cycling in aquatic and soil environments. A Mn-oxidizing bacterium Bacillus sp. WH4 was isolated from Fe-Mn nodules of an agrudalf in central China. The biogenic Mn oxides formed by mediation of this Mn oxidizing microorganism were identified as short-ranged and nano-sized Mn oxides. Cd adsorption isotherms, pH effect on adsorption and kinetics were investigated in comparison with an abiotic Mn oxide todorokite. Maximum adsorption of Cd to the biogenic Mn oxides and todorokite was 2.04 and 0.69 mmol g{sup -1} sorbent, respectively. Thus, the biogenic Mn oxides were more effective Cd adsorbents than the abiotic Mn oxide in the aquatic environment. The findings could improve our knowledge of biogenic Mn oxides formation in the environment and their important roles in the biogeochemical cycles of heavy metals. - Biogenic Mn oxides effectively adsorb Cd from aquatic environments.

  2. Iron and iron derived radicals

    Energy Technology Data Exchange (ETDEWEB)

    Borg, D.C.; Schaich, K.M.

    1987-04-01

    We have discussed some reactions of iron and iron-derived oxygen radicals that may be important in the production or treatment of tissue injury. Our conclusions challenge, to some extent, the usual lines of thought in this field of research. Insofar as they are born out by subsequent developments, the lessons they teach are two: Think fastexclamation Think smallexclamation In other words, think of the many fast reactions that can rapidly alter the production and fate of highly reactive intermediates, and when considering the impact of competitive reactions on such species, think how they affect the microenvironment (on the molecular scale) ''seen'' by each reactive molecule. 21 refs., 3 figs., 1 tab.

  3. Microbial iron mats at the Mid-Atlantic Ridge and evidence that Zetaproteobacteria may be restricted to iron-oxidizing marine systems.

    Directory of Open Access Journals (Sweden)

    Jarrod J Scott

    Full Text Available Chemolithoautotrophic iron-oxidizing bacteria play an essential role in the global iron cycle. Thus far, the majority of marine iron-oxidizing bacteria have been identified as Zetaproteobacteria, a novel class within the phylum Proteobacteria. Marine iron-oxidizing microbial communities have been found associated with volcanically active seamounts, crustal spreading centers, and coastal waters. However, little is known about the presence and diversity of iron-oxidizing communities at hydrothermal systems along the slow crustal spreading center of the Mid-Atlantic Ridge. From October to November 2012, samples were collected from rust-colored mats at three well-known hydrothermal vent systems on the Mid-Atlantic Ridge (Rainbow, Trans-Atlantic Geotraverse, and Snake Pit using the ROV Jason II. The goal of these efforts was to determine if iron-oxidizing Zetaproteobacteria were present at sites proximal to black smoker vent fields. Small, diffuse flow venting areas with high iron(II concentrations and rust-colored microbial mats were observed at all three sites proximal to black smoker chimneys. A novel, syringe-based precision sampler was used to collect discrete microbial iron mat samples at the three sites. The presence of Zetaproteobacteria was confirmed using a combination of 16S rRNA pyrosequencing and single-cell sorting, while light micros-copy revealed a variety of iron-oxyhydroxide structures, indicating that active iron-oxidizing communities exist along the Mid-Atlantic Ridge. Sequencing analysis suggests that these iron mats contain cosmopolitan representatives of Zetaproteobacteria, but also exhibit diversity that may be uncommon at other iron-rich marine sites studied to date. A meta-analysis of publically available data encompassing a variety of aquatic habitats indicates that Zetaproteobacteria are rare if an iron source is not readily available. This work adds to the growing understanding of Zetaproteobacteria ecology and suggests

  4. Molecular methods for the detection of biogenic amine-producing bacteria on foods

    OpenAIRE

    Landete, José María; Rivas, Blanca de las; Marcobal, Angela; Muñoz, Rosario

    2007-01-01

    Biogenic amines are low molecular weight organic bases that can be detected in raw and processed foods. Several toxicological problems resulting from the ingestion of food containing biogenic amines have been described. Biogenic amines are mainly produced by the decarboxylation of certain amino acids by microbial action. Since the ability of microorganisms to decarboxylate amino acid is highly variable, being in most cases strain-specific, the detection of bacteria possessing amino a...

  5. Formation of biogenic amines and vitamin K contents in the Norwegian autochthonous cheese Gamalost during ripening

    OpenAIRE

    Qureshi, Tahir; Vermeer, Cees; Vegarud, Gerd; Abrahamsen, Roger; Skeie, Siv

    2013-01-01

    Gamalost, a Norwegian mould (Mucor mucedo) ripened autochthonous cheese, is a potential functional food due to a high content of peptides that might reduce hypertension, however it has a high content of free amino acids which may be precursors for biogenic amines. This study aimed to investigate if Gamalost might have further health benefits or risks by determination of the formation of vitamin K and biogenic amines. The development of biogenic amines and vitamin K was analysed during ripenin...

  6. Improved multiplex-PCR method for the simultaneous detection of food bacteria producing biogenic amines

    OpenAIRE

    Marcobal, Ángela; Rivas, Blanca de las; Muñoz, Rosario

    2006-01-01

    The presence of biogenic amines in foods is of considerable public concern for the food industry and the regulatory agencies, since given the potential health hazard, there is a growing demand from consumers and control authorities to reduce the allowable limits of biogenic amines in foods and beverages. Rapid and simple methods are needed for the analysis of the ability to form biogenic amines by bacteria in order to evaluate the potential risk of bacterial occurring in ...

  7. Biogenic amines degradation by malolactic bacteria: towards a potential application in wine

    OpenAIRE

    GiuseppeSpano; VittorioCapozzi; Alvarez, Miguel A.; DanielaFiocco; FrancescoGrieco

    2012-01-01

    Biogenic amines in wine represent a toxicological risk for the health of the consumer, with several trade implications. In this study 26 strains of Lactobacillus plantarum were analysed for their ability to degrade biogenic amines commonly found during wine fermentation. Two strains of L. plantarum were selected in reason of their ability to degrade putrescine and tyramine. The degradation was assessed in vitro, both in presence of the biogenic amines and in presence of the specific chemical ...

  8. Biogenic amines degradation by Lactobacillus plantarum: toward a potential application in wine

    OpenAIRE

    Capozzi, Vittorio; Russo, Pasquale; Ladero, Victor; Fernández, María; Fiocco, Daniela; Alvarez, Miguel A.; Grieco, Francesco; Spano, Giuseppe

    2012-01-01

    Biogenic amines in wine represent a toxicological risk for the health of the consumer, with several trade implications. In this study 26 strains of Lactobacillus plantarum were analysed for their ability to degrade biogenic amines commonly found during wine fermentation. Two strains of L. plantarum were selected in reason of their ability to degrade putrescine and tyramine. The degradation was assessed in vitro, both in presence of the biogenic amines and in presence of the specific chemical ...

  9. Control of biogenic amines in fermented sausages: role of starter cultures

    OpenAIRE

    MariluzLatorre-Moratalla; SaraBover-Cid

    2012-01-01

    Biogenic amines show biological activity and exert undesirable physiological effects when absorbed at high concentrations. Biogenic amines are mainly formed by microbial decarboxylation of amino acids and thus are usually present in a wide range of foods, fermented sausages being one of the major biogenic amine sources. The use of selected starter cultures is one of the best technological measures to control aminogenesis during meat fermentation. Although with variable effectiveness, several ...

  10. Control of Biogenic Amines in Fermented Sausages: Role of Starter Cultures

    OpenAIRE

    Latorre-Moratalla, M.L.; Bover-Cid, Sara; Veciana-Nogués, M.T.; Vidal-Carou, M.C.

    2012-01-01

    Biogenic amines show biological activity and exert undesirable physiological effects when absorbed at high concentrations. Biogenic amines are mainly formed by microbial decarboxylation of amino acids and thus are usually present in a wide range of foods, fermented sausages being one of the major biogenic amine sources. The use of selected starter cultures is one of the best technological measures to control aminogenesis during meat fermentation. Although with variable effectiveness, several ...

  11. Significant Biogenic Silica Retention from Reverse Weathering in Non-deltaic Sediments

    Science.gov (United States)

    Krause, J. W.; Larson, A. M.; Darrow, E. S.; Carmichael, R. H.

    2014-12-01

    Coastal biogeochemical processes exert important controls on the net delivery of silicon to the ocean. Reverse weathering of biogenic silica by authigenic transformation has been suggested to be an important processes for silicon retention in coastal sediments. Many reported sediment biogenic silica measurements may underestimate this authigenically-transformed fraction; for example, the incorporation of metal hydroxides with the biogenic silica matrix suppresses the ability to distinguish it from mineral silica when using a traditional alkaline leach. Most studies demonstrating the importance of reverse weathering on biogenic silica have examined deltaic sediments in river dominated systems (e.g. Mississippi, Amazon), but this has not been examined in sediments which lack strong fluvial input. Using sediment cores from the outside the Mississippi River plume, we adapted a method which lessens the interference of metal hydroxides on biogenic silica by using an initial acid leach. The addition of this step increased the measured biogenic silica up to five-fold above that detected using a traditional alkaline digestion method. The magnitude of authigenically-altered biogenic silica in these cores was significant, representing a majority of the sediment biogenic silica pool at most depths. These findings confirm the importance of reverse-weathered biogenic silica as a mechanism for silicon retention and suggest the significance of this process may be more widespread.

  12. Effect of radioprotective biogenic amines on peroxide oxidation of lipids in rat small intestine mucosa microsomes

    International Nuclear Information System (INIS)

    The radioprotective biogenic amines, dopamine, histamine, and serotonin inhibited lipid peroxidation in rat small intestine mucosal microsomes. Possible mechanisms of these inhibitory effects are discussed

  13. Distribution and accumulation of biogenic silica in the intertidal sediments of the Yangtze Estuary

    Institute of Scientific and Technical Information of China (English)

    HOU Lijun; LIU Min; XU Shiyuan; YAN Huimin; OU Dongni; CHENG Shubo; LIN Xiao

    2008-01-01

    Sedimentary biogenic silica is known to be all important parameter to understand biogeochemical processes and paleoenviromental records in estuarine and coastal ecosystems. Consequently, it is of great significance to investigate accumulation and distribution of biogenic silica in sediments. The two-step mild acid-mild alkaline extraction procedure was used to leach biogenic silica and its early diagenetic products in intertidal sediments of the Yangtze Estuary. The results showed that total biogenic silica(t-BSi)in the intertidal sediments varied from 237. 7-419. 4 μmol Si/g. while the mild acid leachable silica(Si-HCl)and the mild alkaline leachable silica(Si-Alk)were in the range of 25. 1-72. 9μmol Si/g and 208. 1-350. 4 μmol Si/g. respectively. Significant correlations were observed for the grain size distributions of sediments and different biogenic silica pools in intertidal sediments. This confirms that grain size distribution Can significantly affect biogenic silica contents in sediments. Close relationships of biogenic silica with organic carbon and nitrogen Were also found, reflecting that there is a strong coupling between biogenic silica and organic matter biogeochemical cycles in the intertidal system of the Yangtze Estuary. Additionally, the early diagenetic changes of biogenic silica in sediments are discussed in the present study.

  14. Iron Sucrose Injection

    Science.gov (United States)

    ... is in a class of medications called iron replacement products. It works by replenishing iron stores so ... ferumoxytol (Feraheme), iron dextran (Dexferrum, Infed, Proferdex), or sodium ferric gluconate (Ferrlecit); any other medications; or any ...

  15. Iron Dextran Injection

    Science.gov (United States)

    ... is in a class of medications called iron replacement products. It works by replenishing iron stores so ... carboxymaltose (Injectafer), ferumoxytol (Feraheme), iron sucrose (Venofer), or sodium ferric gluconate (Ferrlecit);any other medications; or any ...

  16. Iron-Deficiency Anemia

    Medline Plus

    Full Text Available ... refers to a condition in which your blood has a lower than normal number of red blood ... iron, your body starts using the iron it has stored. Soon, the stored iron gets used up. ...

  17. Taking iron supplements

    Science.gov (United States)

    ... medlineplus.gov/ency/article/007478.htm Taking iron supplements To use the sharing features on this page, ... levels. You may also need to take iron supplements as well to rebuild iron stores in your ...

  18. Iron deficiency anemia

    Science.gov (United States)

    ... Iron-rich foods include: Chicken and turkey Dried lentils, peas, and beans Fish Meats (liver is the ... and egg yolks are high sources of iron. Flour, bread, and some cereals are fortified with iron. ...

  19. Pharmacology of Iron Transport

    OpenAIRE

    Byrne, Shaina L.; Krishnamurthy, Divya; Wessling-Resnick, Marianne

    2012-01-01

    Elucidating the molecular basis for the regulation of iron uptake, storage, and distribution is necessary to understand iron homeostasis. Pharmacological tools are emerging to identify and distinguish among different iron transport pathways. Stimulatory or inhibitory small molecules with effects on iron uptake can help characterize the mechanistic elements of iron transport and the roles of the transporters involved in these processes. In particular, iron chelators can serve as potential phar...

  20. Biogenic Emissions of Light Alkenes from a Coniferous Forest

    Science.gov (United States)

    Rhew, R. C.; Turnipseed, A. A.; Martinez, L.; Shen, S.; De Gouw, J. A.; Warneke, C.; Koss, A.; Lerner, B. M.; Miller, B. R.; Smith, J. N.; Guenther, A. B.

    2014-12-01

    Alkenes are reactive hydrocarbons that play important roles in the photochemical production of tropospheric ozone and in the formation of secondary organic aerosols. The light alkenes (C2-C4) originate from both biogenic and anthropogenic sources and include C2H4 (ethene), C3H6 (propene) and C4H8 (1-butene, 2-butene, 2-methylpropene). Light alkenes are used widely as chemical feedstocks because their double bond makes them versatile for industrial reactions. Their biogenic sources are poorly characterized, with most global emissions estimates relying on laboratory-based studies; net ecosystem emissions have been measured at only one site thus far. Here we report net ecosystem fluxes of light alkenes and isoprene from a semi-arid ponderosa pine forest in the Rocky Mountains of Colorado, USA. Canopy scale fluxes were measured using relaxed eddy accumulation (REA) techniques on the 28-meter NCAR tower in the Manitou Experimental Forest Observatory. Updrafts and downdrafts were determined by sonic anemometry and segregated into 'up' and 'down' reservoirs over the course of an hour. Samples were then measured on two separate automated gas chromatographs (GCs). The first GC measured light hydrocarbons (C2-C6 alkanes and C2-C5 alkenes) by flame ionization detection (FID). The second GC measured halocarbons (methyl chloride, CFC-12, and HCFC-22) by electron capture detection (ECD). Additional air measurements from the top of the tower included hydrocarbons and their oxidation products by Proton Transfer Reaction Mass Spectrometry (PTR-MS). Three field intensives were conducted during the summer of 2014. The REA flux measurements showed that ethene, propene and the butene emissions have significant diurnal cycles, with maximum emissions at midday. The light alkenes contribute significantly to the overall biogenic source of reactive hydrocarbons and have a temporal variability that may be associated with physical and biological parameters. These ecosystem scale measurements

  1. Biogenic influence on cloud microphysics over the global ocean

    Directory of Open Access Journals (Sweden)

    A. Lana

    2012-02-01

    Full Text Available Aerosols have a large potential to influence climate through their effects on the microphysics and optical properties of clouds and, hence, on the Earth's radiation budget. Aerosol-cloud interactions have been intensively studied in polluted air, but the possibility that the marine biosphere plays a role in regulating cloud brightness in the pristine oceanic atmosphere remains largely unexplored. We used 9 yr of global satellite data and ocean climatologies to derive parameterizations of (a production fluxes of sulfur aerosols formed by the oxidation of the biogenic gas dimethylsulfide emitted from the sea surface; (b production fluxes of secondary organic aerosols from biogenic organic volatiles; (c emission fluxes of biogenic primary organic aerosols ejected by wind action on sea surface; and (d emission fluxes of sea salt also lifted by the wind upon bubble bursting. Series of global weekly estimates of these fluxes were correlated to series of cloud droplet effective radius data derived from satellite (MODIS. Similar analyses were conducted in more detail at 6 locations spread among polluted and clean regions of the oceanic atmosphere. The outcome of the statistical analysis was that negative correlation was common at mid and high latitude for sulfur and organic secondary aerosols, indicating both might be important in seeding cloud droplet activation. Conversely, primary aerosols (organic and sea salt showed more variable, non-significant or positive correlations, indicating that, despite contributing to large shares of the marine aerosol mass, they are not major drivers of the variability of cloud microphysics. Uncertainties and synergisms are discussed, and recommendations of research needs are given.

  2. Post-speleogenetic biogenic modification of Gomantong Caves, Sabah, Borneo

    Science.gov (United States)

    Lundberg, Joyce; McFarlane, Donald A.

    2012-07-01

    The Gomantong cave system of eastern Sabah, Malaysia, is well-known as an important site for harvesting edible bird-nests and, more recently, as a tourist attraction. Although the biology of the Gomantong system has been repeatedly studied, very little attention has been given to the geomorphology. Here, we report on the impact of geobiological modification in the development of the modern aspect of the cave, an important but little recognized feature of tropical caves. Basic modeling of the metabolic outputs from bats and birds (CO2, H2O, heat) reveals that post-speleogenetic biogenic corrosion can erode bedrock by between ~ 3.0 mm/ka (1 m/~300 ka) and ~ 4.6 mm/ka (1 m/~200 ka). Modeling at high densities of bats yields rates of corrosion of ~ 34 mm/ka (or 1 m/~30 ka). Sub-aerial corrosion creates a previously undescribed speleological feature, the apse-flute, which is semicircular in cross-section and ~ 80 cm wide. It is vertical regardless of rock properties, developing in parallel but apparently completely independently, and often unbroken from roof to floor. They end at a blind hemi-spherical top with no extraneous water source. Half-dome ceiling conch pockets are remnants of previous apse-fluting. Sub-cutaneous corrosion creates the floor-level guano notch formed by organic acid dissolution of bedrock in contact with guano. Speleogenetic assessment suggests that as much as 70-95% of the total volume of the modern cave may have been opened by direct subaerial biogenic dissolution and biogenically-induced collapse, and by sub-cutaneous removal of limestone, over a timescale of 1-2 Ma.

  3. Genetics Home Reference: iron-refractory iron deficiency anemia

    Science.gov (United States)

    ... refractory iron deficiency anemia iron-refractory iron deficiency anemia Enable Javascript to view the expand/collapse boxes. ... All Close All Description Iron-refractory iron deficiency anemia is one of many types of anemia , which ...

  4. Microwave sintering of biogenic hydroxyapatite ceramics for reconstructive surgery

    Directory of Open Access Journals (Sweden)

    Hanna Tovstonoh

    2014-03-01

    Full Text Available Ceramics based on biogenic hydroxyapatite have been produced via a microwave sintering at 1000 °C for 5, 10, 15, 20 and 30 min. It was shown that all of the ceramics studied exhibit volumetric shrinkage (2.3–4.6 %, which increases with increasing sintering time at maximum temperature. It was established that the total porosity did not depend on sintering time at 1000 °C and was equal to 38–40 %. Moreover, in all of the materials an open porosity dominated. The ultimate compression strength was in the range 35–40 MPa.

  5. Diel Variation of Biogenic Volatile Organic Compound Emissions

    DEFF Research Database (Denmark)

    Lindwall, Frida; Faubert, Patrick; Rinnan, Riikka

    2015-01-01

    Many hours of sunlight in the midnight sun period suggest that significant amounts of biogenic volatile organic compounds (BVOCs) may be released from arctic ecosystems during night-time. However, the emissions from these ecosystems are rarely studied and limited to point measurements during...... the same range as those during the day. These results warn against overlooking the night period when considering arctic emissions. During the day, the quantity of BVOCs and the number of different compounds emitted was higher under ambient light than in darkness. The monoterpenes α-fenchene, α...

  6. Studies in biogenic amine metabolism by mass spectrometry

    International Nuclear Information System (INIS)

    Two areas of mass spectral study related to biogenic amine metabolism are presented: The use of electron capture negative ion chemical ionization mass spectrometry for the quantitation of melatonin and other indole amines, and general synthetic procedures useful for the synthesis of deuterated diazomethane and deuteromethylated catechols. The factors determining instrumental sensitivity in negative ion chemical ionization are discussed, and the enhancement of the primary ion beam using magnetic fields is described. Quantitation of human plasma melatonin at the parts per trillion or pg/ml level has been demonstrated and is routinely performed as a selected ion monitoring assay. (Auth.)

  7. Biogenic amines and acute thermal stress in the rat

    Science.gov (United States)

    Williams, B. A.; Moberg, G. P.

    1975-01-01

    A study is summarized which demonstrates that depletion of the biogenic amines 5-hydroxytryptamine (5-HT) or norepinephrine (NE) alters the normal thermoregulatory responses to acute temperature stress. Specifically, NE depletion caused a significant depression in equilibrium rectal temperature at 22 C and a greater depression in rectal temperature than controls in response to cold (6 C) stress; NE depletion also resulted in a significantly higher rectal temperature response to acute heat (38 C) stress. Depletion of 5-HT had less severe effects. It remains unclear whether the primary site of action of these agents is central or peripheral.

  8. Pulmonary extraction of biogenic amines during septic shock

    International Nuclear Information System (INIS)

    The effect of live Escherichia coli on the pulmonary extraction of the biogenic amines 14C 5-hydroxytryptamine, (5-HT) and 3H-epinephrine was investigated. The labeled isotopes were injected into a central venous catheter and collected from an aortic catheter. One hundred per cent of the labeled epinephrine was recovered in the control and septic state. Only 32.8 +/- 3.6% SEM of the 5-hydroxytryptamine was recovered before sepsis and 42.5 +/- 4.9% SEM after sepsis. During sepsis, mean arterial pressure fell to 58 mm Hg from 121 mm Hg. Pulmonary shunt increased from .7 +/- .05 SEM to .33 +/- .09 SEM

  9. The influence of marine biogenic particles on ice phase initiation

    Science.gov (United States)

    Alpert, P. A.; Radway, J.; Aller, J. Y.; Knopf, D. A.

    2011-12-01

    Aerosol particles vary in composition with many being biogenic and of terrestrial or marine origin. Efficient ice forming biogenic particles are typically thought to be of terrestrial origin; however, recent data demonstrate that marine biogenic particles can act as ice nuclei (IN) in both immersion and deposition modes, with and without association of NaCl. These results are significant given that ocean derived particles including phytoplankton, microorganisms, transparent exopolymers, and colloidal gels become aerosolized from the sea surface microlayer through wave breaking and bubble bursting. Such particles typically include sea salt, but in situ observations of air masses associated with phytoplankton blooms have identified organic compounds as significant mass contributors to aerosol loading. Here we present results from experiments with Thalassiosira pseudonana, Emiliania huxleyi, and Nanochloris atomus, phytoplankton with distinctly different cell walls: silica, calcite, and cellulose fibrils, respectively, as efficient IN in immersion and deposition modes at typical tropospheric conditions. In a separate set of experiments, submicron size particles with and without organics are generated through bubble bursting in a custom built seawater tank. Subsequently collected, these particles are observed using a coupled cooling stage/optical microscope, for their ice nucleation potential as a function of particle temperature (T), water activity (aw), relative humidity with respect to ice (RHice), droplet volume, and particle surface area. In the immersion mode, fragmented and intact cells of T. pseudonana and N. atomus enhance ice nucleation in aqueous NaCl solution droplets by ~10-30 K and 10-20 K above the homogeneous freezing limit, and for a range of aw of 1.0-0.8, while E. huxleyi do not enhance freezing temperatures. In the deposition mode, all three species nucleate ice for RHice as low as ~120%, however, for each, different nucleation modes occur at warmer

  10. Carbon nanomaterial based electrochemical sensors for biogenic amines

    International Nuclear Information System (INIS)

    This review describes recent advances in the use of carbon nanomaterials for electroanalytical detection of biogenic amines (BAs). It starts with a short introduction into carbon nanomaterials such as carbon nanotubes, graphene, nanodiamonds, carbon nanofibers, fullerenes, and their composites. Next, electrochemical sensing schemes are discussed for various BAs including dopamine, serotonin, epinephrine, norepinephrine, tyramine, histamine and putrescine. Examples are then given for methods for simultaneous detection of various BAs. Finally, we discuss the current and future challenges of carbon nanomaterial-based electrochemical sensors for BAs. The review contains 175 references. (author)

  11. Extracellular proteins limit the dispersal of biogenic nanoparticles

    Science.gov (United States)

    Moreau, J.W.; Weber, P.K.; Martin, M.C.; Gilbert, B.; Hutcheon, I.D.; Banfield, J.F.

    2007-01-01

    High-spatial-resolution secondary ion microprobe spectrometry, synchrotron radiation-based Fourier-transform infrared spectroscopy, and polyacrylamide gel analysis demonstrated the intimate association of proteins with spheroidal aggregates of biogenic zinc sulfide nanocrystals, an example of extracellular biomineralization. Experiments involving synthetic zinc sulfide nanoparticles and representative amino acids indicated a driving role for cysteine in rapid nanoparticle aggregation. These findings suggest that microbially derived extracellular proteins can limit the dispersal of nanoparticulate metal-bearing phases, such as the mineral products of bioremediation, that may otherwise be transported away from their source by subsurface fluid flow.

  12. Extracellular Proteins Limit the Dispersal of BiogenicNanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Moreau, John W.; Weber, Peter K.; Martin, Michael C.; Gilbert,Benjamin; Hutcheon, Ian D.; Banfield, Jillian F.

    2007-04-27

    High spatial-resolution secondaryion microprobespectrometry, synchrotron radiation Fourier-transform infraredspectroscopy and polyacrylamide gel analysis demonstrate the intimateassociation of proteins with spheroidal aggregates of biogenic zincsulfide nanocrystals, an example of extracellular biomineralization.Experiments involving synthetic ZnS nanoparticles and representativeamino acids indicate a driving role for cysteine in rapid nanoparticleaggregation. These findings suggest that microbially-derivedextracellular proteins can limit dispersal of nanoparticulatemetal-bearing phases, such as the mineral products of bioremediation,that may otherwise be transported away from their source by subsurfacefluid flow.

  13. Iron and stony-iron meteorites

    DEFF Research Database (Denmark)

    Benedix, Gretchen K.; Haack, Henning; McCoy, T.J.

    2014-01-01

    Without iron and stony-iron meteorites, our chances of ever sampling the deep interior of a differentiated planetary object would be next to nil. Although we live on a planet with a very substantial core, we will never be able to sample it. Fortunately, asteroid collisions provide us with a rich...... sampling of the deep interiors of differentiated asteroids. Iron and stony-iron meteorites are fragments of a large number of asteroids that underwent significant geological processing in the early solar system. Parent bodies of iron and some stony-iron meteorites completed a geological evolution similar...... to that continuing on Earth – although on much smaller length- and timescales – with melting of the metal and silicates; differentiation into core, mantle, and crust; and probably extensive volcanism. Iron and stony-iron meteorites are our only available analogues to materials found in the deep...

  14. Mineralogy of iron microbial mats from Loihi Seamount

    Directory of Open Access Journals (Sweden)

    Brandy Marie Toner

    2012-04-01

    Full Text Available Extensive mats of Fe oxyhydroxides and associated Fe-oxidizing microbial organisms form in diverse geochemical settings – freshwater seeps to deep-sea vents – where ever opposing Fe(II-oxygen gradients prevail. The mineralogy, reactivity, and structural transformations of Fe oxyhydroxides precipitated from submarine hydrothermal fluids within microbial mats remains elusive in active and fossil systems. In response, a study of Fe microbial mat formation at the Loihi Seamount was conducted to describe the physical and chemical characteristics of Fe-phases using extended X-ray absorption fine structure spectroscopy, powder X-ray diffraction, synchrotron radiation X-ray total scattering, low-temperature magnetic measurements, and Mössbauer spectroscopy. Particle sizes of 3.5-4.6 nm were estimated from magnetism data, and coherent scattering domain sizes as small as 1.6 nm are indicated by pair distribution function (PDF analysis. Disorder in the nanostructured Fe-bearing phases results in limited intermediate-range structural order: less than that of standard 2-line ferrihydrite (Fh, except for the Pohaku site. The short-range ordered natural Fh (FhSRO phases were stable at 4 °C in the presence of oxygen for at least 1 year and during 400 oC treatment. The observed stability of the FhSRO is consistent with magnetic observations that point to non-interacting nanoparticles. PDF analyses of total scattering data provide further evidence for FhSRO particles with a poorly ordered silica coating. The presence of coated particles explains the small coherent scattering domain for the mat minerals, as well as the stability of the minerals over time and against heating. The mineral properties observed here provide a starting point from which progressively older and more extensively altered iron deposits may be examined, with the ultimate goal of improved interpretation of past biogeochemical conditions and diagenetic processes.

  15. An in situ corrosion study of Middle Ages wrought iron bar chains in the Amiens Cathedral

    Science.gov (United States)

    Grassini, S.; Angelini, E.; Parvis, M.; Bouchar, M.; Dillmann, P.; Neff, D.

    2013-12-01

    The corrosion behaviour of Middle Ages wrought iron bar chains exposed to indoor atmospheric corrosion for hundred of years in the Notre Dame Cathedral of Amiens (France) has been evaluated by means of Electrochemical Impedance Spectroscopy (EIS), a well-established electrochemical technique extensively used for testing anticorrosive properties of metal coatings. The measurements have been performed in situ with a portable EIS instrument designed to work as a standalone device, in six different areas of the wrought iron bar chains characterized by different aesthetical appearance. Moreover, a properly designed electrochemical cell has been employed to carry out the impedance measurements without affecting the artefacts surfaces. The wrought iron bar chains, as evidenced by μ-Raman and microscopic analyses, are covered by corrosion products constituted by iron oxides and oxyhydroxides, such as goethite, lepidocrocite, maghemite, akaganeite, organized in complex layered structures. In situ EIS allows one to investigate the phenomena involved at the electrochemical interfaces among the various corrosion products and to assess and predict their corrosion behaviour. From the analysis of the experimental findings of this monitoring campaign, EIS measurements can be proposed to restorers/conservators as a reliable indicator of dangerous situations on which they must act for the preservation of the iron artefacts.

  16. Iron from Zealandic bog iron ore -

    DEFF Research Database (Denmark)

    Lyngstrøm, Henriette Syrach

    2011-01-01

    og geologiske materiale, metallurgiske analyser og eksperimentel arkæologiske forsøg - konturerne af en jernproduktion med udgangspunkt i den sjællandske myremalm. The frequent application by archaeologists of Werner Christensen’s distribution map for the occurrence of bog iron ore in Denmark (1966...... contours are sketched of iron production based on bog iron ore from Zealand....

  17. Biogenic emissions of isoprenoids and NO in China and comparison to anthropogenic emissions

    International Nuclear Information System (INIS)

    In this study, a regional dynamical model (WRF) is used to drive biogenic emission models to calculate high resolution (10 x 10 km) biogenic emissions of isoprene (C5H8), monoterpenes (C1H16), and nitric oxide (NO) in China. This high resolution biogenic inventory will be available for the community to study the effect of biogenic emissions on photochemical oxidants in China. The biogenic emissions are compared to anthropogenic emissions to gain insight on the potential impact of the biogenic emissions on tropospheric chemistry, especially ozone production in this region. The results show that the biogenic emissions in China exhibit strongly diurnal, seasonal, and spatial variations. The isoprenoid (including both isoprene and monoterpenes) emissions are closely correlated to tree density and strongly vary with season and local time. During winter (January), the biogenic isoprenoid emissions are the lowest, resulting from lower temperature and solar radiation, and highest in summer (July) due to higher temperature and solar radiation. The biogenic NO emissions are also higher during summer and lower during winter, but the magnitude of the seasonal variation is smaller than the emissions of isoprene and monoterpenes. The biogenic emissions of NO are widely spread out in the northern, eastern, and southern China regions, where high-density agricultural soil lands are located. Both biogenic NO and isoprenoid emissions are very small in western China. The calculated total biogenic emission budget is smaller than the total anthropogenic VOC emission budget in China. The biogenic isoprenoid and anthropogenic VOC emissions are 10.9 and 15.1 Tg year-1, respectively. The total biogenic and anthropogenic emissions of NO are 5.9 and 11.5 Tg(NO) year-1, respectively. The study shows that in central eastern China, the estimated biogenic emissions of isoprenoids are very small, and the anthropogenic emissions of VOCs are dominant in this region. However, in northeastern and

  18. Liver iron transport

    Institute of Scientific and Technical Information of China (English)

    Ross M Graham; Anita CG Chua; Carly E Herbison; John K Olynyk; Debbie Trinder

    2007-01-01

    The liver plays a central role in iron metabolism. It is the major storage site for iron and also expresses a complex range of molecules which are involved in iron transport and regulation of iron homeostasis. An increasing number of genes associated with hepatic iron transport or regulation have been identified. These include transferrin receptors (TFR1 and 2), a ferrireductase (STEAP3), the transporters divalent metal transporter-1 (DMT1) and ferroportin (FPN) as well as the haemochromatosis protein, HFE and haemojuvelin (HJV),which are signalling molecules. Many of these genes also participate in iron regulatory pathways which focus on the hepatic peptide hepcidin. However, we are still only beginning to understand the complex interactions between liver iron transport and iron homeostasis. This review outlines our current knowledge of molecules of iron metabolism and their roles in iron transport and regulation of iron homeostasis.

  19. Synergistic effects of pCO2 and iron availability on nutrient consumption ratio of the Bering Sea phytoplankton community

    Science.gov (United States)

    Sugie, K.; Endo, H.; Suzuki, K.; Nishioka, J.; Kiyosawa, H.; Yoshimura, T.

    2013-10-01

    Little is known concerning the effect of CO2 on phytoplankton ecophysiological processes under nutrient and trace element-limited conditions, because most CO2 manipulation experiments have been conducted under elements-replete conditions. To investigate the effects of CO2 and iron availability on phytoplankton ecophysiology, we conducted an experiment in September 2009 using a phytoplankton community in the iron limited, high-nutrient, low-chlorophyll (HNLC) region of the Bering Sea basin . Carbonate chemistry was controlled by the bubbling of the several levels of CO2 concentration (180, 380, 600, and 1000 ppm) controlled air, and two iron conditions were established, one with and one without the addition of inorganic iron. We demonstrated that in the iron-limited control conditions, the specific growth rate and the maximum photochemical quantum efficiency (Fv/Fm) of photosystem (PS) II decreased with increasing CO2 levels, suggesting a further decrease in iron bioavailability under the high-CO2 conditions. In addition, biogenic silica to particulate nitrogen and biogenic silica to particulate organic carbon ratios increased from 2.65 to 3.75 and 0.39 to 0.50, respectively, with an increase in the CO2 level in the iron-limited controls. By contrast, the specific growth rate, Fv/Fm values and elemental compositions in the iron-added treatments did not change in response to the CO2 variations, indicating that the addition of iron canceled out the effect of the modulation of iron bioavailability due to the change in carbonate chemistry. Our results suggest that high-CO2 conditions can alter the biogeochemical cycling of nutrients through decreasing iron bioavailability in the iron-limited HNLC regions in the future.

  20. Synergistic effects of pCO2 and iron availability on nutrient consumption ratio of the Bering Sea phytoplankton community

    Directory of Open Access Journals (Sweden)

    K. Sugie

    2013-10-01

    Full Text Available Little is known concerning the effect of CO2 on phytoplankton ecophysiological processes under nutrient and trace element-limited conditions, because most CO2 manipulation experiments have been conducted under elements-replete conditions. To investigate the effects of CO2 and iron availability on phytoplankton ecophysiology, we conducted an experiment in September 2009 using a phytoplankton community in the iron limited, high-nutrient, low-chlorophyll (HNLC region of the Bering Sea basin . Carbonate chemistry was controlled by the bubbling of the several levels of CO2 concentration (180, 380, 600, and 1000 ppm controlled air, and two iron conditions were established, one with and one without the addition of inorganic iron. We demonstrated that in the iron-limited control conditions, the specific growth rate and the maximum photochemical quantum efficiency (Fv/Fm of photosystem (PS II decreased with increasing CO2 levels, suggesting a further decrease in iron bioavailability under the high-CO2 conditions. In addition, biogenic silica to particulate nitrogen and biogenic silica to particulate organic carbon ratios increased from 2.65 to 3.75 and 0.39 to 0.50, respectively, with an increase in the CO2 level in the iron-limited controls. By contrast, the specific growth rate, Fv/Fm values and elemental compositions in the iron-added treatments did not change in response to the CO2 variations, indicating that the addition of iron canceled out the effect of the modulation of iron bioavailability due to the change in carbonate chemistry. Our results suggest that high-CO2 conditions can alter the biogeochemical cycling of nutrients through decreasing iron bioavailability in the iron-limited HNLC regions in the future.

  1. 78 FR 50135 - Soil Biogenics Ltd., File No. 500-1; Order of Suspension of Trading

    Science.gov (United States)

    2013-08-16

    ... From the Federal Register Online via the Government Publishing Office SECURITIES AND EXCHANGE COMMISSION Soil Biogenics Ltd., File No. 500-1; Order of Suspension of Trading August 14, 2013. It appears to... concerning the securities of Soil Biogenics Ltd. because it has not filed ] any periodic reports since...

  2. Concentration of Biogenic Amines in ‘Pinot Noir’ Wines Produced in Croatia

    Directory of Open Access Journals (Sweden)

    Ana Jeromel

    2012-03-01

    Full Text Available The origins of biogenic amines are sound grapes, alcoholic fermentations, malolactic fermentation and microbial activities during wine storage. These biologically produced amines are essential at low concentrations for optimal metabolic and physiological functions in animals, plants and micro-organisms. During alcoholic fermentation the degree of maceration is the first factor that affects the extraction of compounds present in the grape skin, among them aminoacids, precursors of biogenic amines. The aim of the present work was to study the changes of the concentration of biogenic amines in wines made from Vitis vinifera ‘Pinot noir’ from Plešivica (vintage 2009 produced with classical maceration, cold maceration and use of sur lie method. Biogenic amines were quantified using a reversed-phase high performance liquid chromatography (HPLC with fluorescence detection after pre-column derivatization with o-phthalaldehyde (OPA. In ‘Pinot noir’ wines tested, histamine was the most abundant biogenic amine followed by tryptamine and 2-Phenylethylamine. Total amount of biogenic amines ranged from 8.72 mg/L in wines made with classical maceration up to 9.34 mg/L in sur lie wines. In summary, from the results obtained in this study, it can be concluded that sur lie technology can influence the formation of biogenic acids since the release of amino acids is probably more pronounced in wines aged with lees and stirred weekly. No significant differences were found in the concentration of biogenic amines in relation to the used maceration process.

  3. Genome Sequence Analysis of the Biogenic Amine-Degrading Strain Lactobacillus casei 5b

    OpenAIRE

    Ladero Losada, Víctor Manuel; Herrero, Ana; Martínez Álvarez, Noelia; Río Lagar, Beatriz del; Linares, Daniel M.; Fernández García, María; Martín, M. Cruz; Álvarez González, Miguel Ángel

    2014-01-01

    We here report a 3.02-Mbp annotated draft assembly of the Lactobacillus casei 5b genome. The sequence of this biogenic amine-degrading dairy isolate may help identify the mechanisms involved in the catabolism of biogenic amines and perhaps shed light on ways to reduce the presence of these toxic compounds in food.

  4. Concentration of Biogenic Amines in ‘Pinot Noir’ Wines Produced in Croatia

    Directory of Open Access Journals (Sweden)

    Ana Jeromel

    2014-02-01

    Full Text Available The origins of biogenic amines are sound grapes, alcoholic fermentations, malolactic fermentation and microbial activities during wine storage. These biologically produced amines are essential at low concentrations for optimal metabolic and physiological functions in animals, plants and micro-organisms. During alcoholic fermentation the degree of maceration is the first factor that affects the extraction of compounds present in the grape skin, among them aminoacids, precursors of biogenic amines. The aim of the present work was to study the changes of the concentration of biogenic amines in wines made from Vitis vinifera ‘Pinot noir’ from Plešivica (vintage 2009 produced with classical maceration, cold maceration and use of sur lie method. Biogenic amines were quantified using a reversed-phase high performance liquid chromatography (HPLC with fluorescence detection after pre-column derivatization with o-phthalaldehyde (OPA. In ‘Pinot noir’ wines tested, histamine was the most abundant biogenic amine followed by tryptamine and 2-Phenylethylamine. Total amount of biogenic amines ranged from 8.72 mg/L in wines made with classical maceration up to 9.34 mg/L in sur lie wines. In summary, from the results obtained in this study, it can be concluded that sur lie technology can influence the formation of biogenic acids since the release of amino acids is probably more pronounced in wines aged with lees and stirred weekly. No significant differences were found in the concentration of biogenic amines in relation to the used maceration process.

  5. A biogenic volatile organic compounds emission inventory for Yunnan Province

    Institute of Scientific and Technical Information of China (English)

    WANG Zhi-hui; BAI Yu-hua; ZHANG Shu-yu

    2005-01-01

    The first detailed inventory for volatile organic compounds(VOC) emissions from vegetation over Yunnan Province, China was presented. The spatially and temporally resolved inventory was developed based on a geographic information system (GIS), remote sensing(RS) data and field measurement data, such as digitized land-use data, normalized difference vegetation index (NDVl) and temperature data from direct real-time measurement. The inventory has a spatial resolution of 5 km × 5 km and a time resolution of 1 h.Urban, agriculture, and natural land-use distributions in Yunnan Province were combined with biomass factors for each land-use category to produce a spatially resolved biomass inventory. A biogenic emission inventory was developed by combining the biomass inventory with hourly emission rates for tree, shrub and ground cover species of the study area. Correcting for environmental factors, including light intensity and temperature, a value of 1.1 × 1012 gC for total annual biogenic VOC emissions from Yunnan Province, including 6.1 × 1011 gCfor isoprene, 2.1 × 1011 gC for monoterpenes, and 2.6 × 1011 gC for OVOC was obtained. The highest VOC emissions occurred in the northwestern, southwestern and north region of Yunnan Province. Some uncertainties were also discussed in this study.

  6. Factors influencing biogenic amines accumulation in dairy products.

    Science.gov (United States)

    Linares, Daniel M; Del Río, Beatriz; Ladero, Victor; Martínez, Noelia; Fernández, María; Martín, María Cruz; Alvarez, Miguel A

    2012-01-01

    Fermented foods are among the food products more often complained of having caused episodes of biogenic amines (BA) poisoning. Concerning milk-based fermented foods, cheese is the main product likely to contain potentially harmful levels of BA, specially tyramine, histamine, and putrescine. Prompted by the increasing awareness of the risks related to dietary uptake of high biogenic amine loads, in this review we report all those elaboration and processing technological aspects affecting BA biosynthesis and accumulation in dairy foods. Improved knowledge of the factors involved in the synthesis and accumulation of BA should lead to a reduction in their incidence in milk products. Synthesis of BA is possible only when three conditions converge: (i) availability of the substrate amino acids; (ii) presence of microorganisms with the appropriate catabolic pathway activated; and (iii) environmental conditions favorable to the decarboxylation activity. These conditions depend on several factors such as milk treatment (pasteurization), use of starter cultures, NaCl concentration, time, and temperature of ripening and preservation, pH, temperature, or post-ripening technological processes, which will be discussed in this chapter. PMID:22783233

  7. Analysis of biogenic amines using corona discharge ion mobility spectrometry.

    Science.gov (United States)

    Hashemian, Z; Mardihallaj, A; Khayamian, T

    2010-05-15

    A new method based on corona discharge ion mobility spectrometry (CD-IMS) was developed for the analysis of biogenic amines including spermidine, spermine, putrescine, and cadaverine. The ion mobility spectra of the compounds were obtained with and without n-Nonylamine used as the reagent gas. The high proton affinity of n-Nonylamine prevented ion formation from compounds with a proton affinity lower than that of n-Nonylamine and, therefore, enhanced its selectivity. It was also realized that the ion mobility spectrum of n-Nonylamine varied with its concentration. A sample injection port of a gas chromatograph was modified and used as the sample introduction system into the CD-IMS. The detection limits, dynamic ranges, and analytical parameters of the compounds with and without using the reagent gas were obtained. The detection limits and dynamic ranges of the compounds were about 2ng and 2 orders of magnitude, respectively. The wide dynamic range of CD-IMS originates from the high current of the corona discharge. The results revealed the high capability of the CD-IMS for the analysis of biogenic amines. PMID:20298897

  8. Carbon and hydrogen isotopic composition and generation pathway of biogenic gas in China

    Institute of Scientific and Technical Information of China (English)

    SHEN Ping; WANG Xiaofeng; XU Yin; SHI Baoguang; XU Yongchang

    2009-01-01

    The carbon and hydrogen isotopic composition of biogenic gas is of great importance for the study of its generation pathway and reservoiring characteristics. In this paper, the formation pathways and reservoiring characteristics of biogenic gas reservoirs in China are described in terms of the carbon and hydrogen isotopic compositions of 31 gas samples from 10 biogenic gas reservoirs. The study shows that the hydrogen isotopic compositions of these biogenic gas reservoirs can be divided into three intervals:δDCH4>-200‰,-250‰<δDCH4<-200‰ and δDCH4<-250‰. The forerunners believed that the main generation pathway of biogenic gas under the condition of continental fresh water is acetic fermentation. Our research results showed that the generation pathway of biogenic gas under the condition of marine facies is typical CO2- reduction, the biogenic gas has heavy hydrogen isotopic composition: its δDCH4 values are higher than -200‰; that the biogenic gas under the condition of continental facies also was generated by the same way, but its hydrogen isotopic composition is lighter than that of biogenetic gas generated under typical marine facies condition: -250‰<δDCH4<-200‰, the δDCH4 values may be related to the salinity of the water medium in ancient lakes. From the relevant data of the Qaidam Basin, it can be seen that the hydrogen isotopic composition of biogenic methane has the same variation trend with increasing salinity of water medium. There are biogenic gas reservoirs formed in transitional regions under the condition of continental facies. These gas reservoirs resulted from both CO2- reduction and acetic fermentation, the formation of which may be related to the non-variant salinity of ancient water medium and the relatively high geothermal gradient, as is the case encountered in the Baoshan Basin. The biogenic gas generating in these regions has light hydrogen isotopic composition: δDCH4<-250‰, and relatively heavy carbon isotopic

  9. Green Rusts and Their Relationship to Iron Corrosion; a Key Role in Microbially Influenced Corrosion

    International Nuclear Information System (INIS)

    Moessbauer spectroscopy (MS) has often been used to characterise double-layered hydroxysalts usually named green rusts (GR) and to follow their Fe(II)/Fe(III) ratio during the oxidation process of Fe(OH)2 in the presence of aggressive anions such as Cl-, SO42-, CO32-,.... They are intermediate compounds between the initial metal Fe(0) via the Fe(II) and the final Fe(III) (oxyhydr)oxides constituting the usual rusts. E-pH Pourbaix diagrams of iron for predicting the aqueous corrosion conditions of iron-based materials are determined by monitoring the electrode potential Eh and pH vs. time. The crystal structure of GRs, in any case constituted of layers of [FeII(1-x)FeIIIx (OH)2]x+ that alternate with interlayers [(x/n)An-.(mx/n)H2O]x- made of An- anions and water molecules, are presented. Several examples of the role of GRs are discussed, from chloride pitting of concrete reinforcing bars to bacterial corrosion of cast iron in water pipes or steel sheet piles in harbours. The efficiency of corrosion inhibitors like phosphate and their relationship to the oxidation of GRs are presented from basic MS studies. But most importantly, the evidence by MS of the dissimilatory reduction of a common ferric oxyhydroxide, γ-FeOOH lepidocrocite, into a GR by the action of a bacterium, Shewanella putrefaciens, opens the path through which microbially influenced corrosion (MIC) operates. A cycling of aerobic and anaerobic conditions is necessary where GRs but also magnetite play likely the key role.

  10. Green Rusts and Their Relationship to Iron Corrosion; a Key Role in Microbially Influenced Corrosion

    Energy Technology Data Exchange (ETDEWEB)

    Genin, J.-M. R.; Refait, Ph.; Abdelmoula, M. [Universite Henri Poincare, Laboratoire de Chimie Physique et Microbiologie pour l' Environnement, UMR 7564, CNRS-Universite Henri Poincare-Nancy 1, Equipe Microbiologie et Physique and Departement Materiaux et Structures, ESSTIN (France)

    2002-03-15

    Moessbauer spectroscopy (MS) has often been used to characterise double-layered hydroxysalts usually named green rusts (GR) and to follow their Fe(II)/Fe(III) ratio during the oxidation process of Fe(OH){sub 2} in the presence of aggressive anions such as Cl{sup -}, SO{sub 4}{sup 2-}, CO{sub 3}{sup 2-},.... They are intermediate compounds between the initial metal Fe(0) via the Fe(II) and the final Fe(III) (oxyhydr)oxides constituting the usual rusts. E-pH Pourbaix diagrams of iron for predicting the aqueous corrosion conditions of iron-based materials are determined by monitoring the electrode potential E{sub h} and pH vs. time. The crystal structure of GRs, in any case constituted of layers of [Fe{sup II}{sub (1-x)}Fe{sup III}{sub x} (OH){sub 2}]{sup x+} that alternate with interlayers [(x/n)A{sup n-}.(mx/n)H{sub 2}O]{sup x-} made of A{sup n-} anions and water molecules, are presented. Several examples of the role of GRs are discussed, from chloride pitting of concrete reinforcing bars to bacterial corrosion of cast iron in water pipes or steel sheet piles in harbours. The efficiency of corrosion inhibitors like phosphate and their relationship to the oxidation of GRs are presented from basic MS studies. But most importantly, the evidence by MS of the dissimilatory reduction of a common ferric oxyhydroxide, {gamma}-FeOOH lepidocrocite, into a GR by the action of a bacterium, Shewanella putrefaciens, opens the path through which microbially influenced corrosion (MIC) operates. A cycling of aerobic and anaerobic conditions is necessary where GRs but also magnetite play likely the key role.

  11. [Iron-refractory iron deficiency anemia].

    Science.gov (United States)

    Kawabata, Hiroshi

    2016-02-01

    The major causes of iron deficiency anemia (IDA) include iron loss due to bleeding, increased iron requirements, and decreased iron absorption by the intestine. The most common cause of IDA in Japanese women is iron loss during menstruation. Autoimmune atrophic gastritis and Helicobacter pylori infection can also cause IDA by reducing intestinal iron absorption. In addition to these common etiologies, germline mutations of TMPRSS6 can cause iron-refractory IDA (IRIDA). TMPRSS6 encodes matriptase-2, a membrane-bound serine protease primarily expressed in the liver. Functional loss of matriptase-2 due to homozygous mutations results in an increase in the expression of hepcidin, which is the key regulator of systemic iron homeostasis. The serum hepcidin increase in turn leads to a decrease in iron supply from the intestine and macrophages to erythropoietic cells. IRIDA is microcytic and hypochromic, but decreased serum ferritin is not observed as in IDA. IRIDA is refractory to oral iron supplementation, but does respond to intravenous iron supplementation to some extent. Because genetic testing is required for the diagnoses of IRIDA, a considerable number of cases may go undiagnosed and may thus be overlooked. PMID:26935626

  12. Special thermite cast irons

    OpenAIRE

    Yu. Zhiguts; I. Kurytnik

    2008-01-01

    The given paper deals with the problems of the synthesis of cast iron by metallothermy synthesis. On the basis of investigated method of calculations structures of charges have been arranged and cast iron has been synthesized further. Peculiarities metallothermic smelting were found, mechanical properties and structure of received cast iron were investigated and different technologies for cast iron receiving were worked out.

  13. Iron deficiency anemia

    Science.gov (United States)

    Anemia - iron deficiency ... iron from old red blood cells. Iron deficiency anemia develops when your body's iron stores run low. ... You may have no symptoms if the anemia is mild. Most of the time, ... slowly. Symptoms may include: Feeling weak or tired more often ...

  14. Nutritional iron deficiency

    NARCIS (Netherlands)

    Zimmermann, M.B.; Hurrell, R.F.

    2007-01-01

    Iron deficiency is one of the leading risk factors for disability and death worldwide, affecting an estimated 2 billion people. Nutritional iron deficiency arises when physiological requirements cannot be met by iron absorption from diet. Dietary iron bioavailability is low in populations consuming

  15. Urinary iron excretion test in iron deficiency anemia.

    OpenAIRE

    Kimura,Ikuro; Yamana,Masatoshi; NNishishita,Akira; Sugiyama,Motoharu; Miyata, Akira

    1980-01-01

    A urinary iron excretion test was carried out in 22 patients with iron deficiency anemia. The iron excretion index was significantly higher in patients with intractable iron deficiency anemia compared with normal subjects and anemic patients who were responsive to iron therapy. The findings suggest that iron excretion may be a factor that modulates the response of patients to iron therapy.

  16. Mammalian iron transport.

    Science.gov (United States)

    Anderson, Gregory Jon; Vulpe, Christopher D

    2009-10-01

    Iron is essential for basic cellular processes but is toxic when present in excess. Consequently, iron transport into and out of cells is tightly regulated. Most iron is delivered to cells bound to plasma transferrin via a process that involves transferrin receptor 1, divalent metal-ion transporter 1 and several other proteins. Non-transferrin-bound iron can also be taken up efficiently by cells, although the mechanism is poorly understood. Cells can divest themselves of iron via the iron export protein ferroportin in conjunction with an iron oxidase. The linking of an oxidoreductase to a membrane permease is a common theme in membrane iron transport. At the systemic level, iron transport is regulated by the liver-derived peptide hepcidin which acts on ferroportin to control iron release to the plasma. PMID:19484405

  17. Photoemission study of metallic iron nanoparticles surface aging in biological fluids. Influence on biomolecules adsorption

    Energy Technology Data Exchange (ETDEWEB)

    Canivet, L.; Denayer, F.O. [Université de Lille 2, Droit et Santé, 42 rue P. Duez, 59000 Lille (France); Champion, Y.; Cenedese, P. [CNRS-ICMPE, 2 rue H. Dunant, 94320 Thiais (France); Dubot, P., E-mail: pdubot@icmpe.cnrs.fr [CNRS-ICMPE, 2 rue H. Dunant, 94320 Thiais (France)

    2014-07-01

    Iron nanoparticles (nFe) prepared by vaporization and cryogenic condensation process (10–100 nm) has been exposed to Hank's balanced salt solution (HBSS) and the B-Ali cell growth fluids. These media can be used for cellular growth to study nFe penetration through cell membrane and its induced cytotoxicity. Surface chemistry of nFe exposed to such complex fluids has been characterized as the nanoparticles surface can be strongly changed by adsorption or corrosion processes before reaching intracellular medium. Particle size and surface chemistry have been characterized by scanning electron microscopy (SEM) and high-resolution X-ray photoelectron spectroscopy (HR-XPS). Exposition of nFe particles to growth and differentiation media leads to the formation of an oxy-hydroxide layer containing chlorinated species. We found that the passivated Fe{sub 2}O{sub 3} layer of the bare nFe particles is rapidly transformed into a thicker oxy-hydroxide layer that has a greater ability to adsorb molecular ions or ionic biomolecules like proteins or DNA.

  18. Iron metabolism and iron supplementation in cancer patients

    OpenAIRE

    Ludwig, Heinz; Evstatiev, Rayko; Kornek, Gabriela; Aapro, Matti; Bauernhofer, Thomas; Buxhofer-Ausch, Veronika; Fridrik, Michael; Geissler, Dietmar; Geissler, Klaus; Gisslinger, Heinz; Koller, Elisabeth; Kopetzky, Gerhard; Lang, Alois; Rumpold, Holger; Steurer, Michael

    2015-01-01

    Summary Iron deficiency and iron deficiency-associated anemia are common complications in cancer patients. Most iron deficient cancer patients present with functional iron deficiency (FID), a status with adequate storage iron, but insufficient iron supply for erythroblasts and other iron dependent tissues. FID is the consequence of the cancer-associated cytokine release, while in absolute iron deficiency iron stores are depleted resulting in similar but often more severe symptoms of insuffici...

  19. Monitoring biogenic volatile compounds emitted by Eucalyptus citriodora using SPME.

    Science.gov (United States)

    Zini, C A; Augusto, F; Christensen, T E; Smith, B P; Caramão, E B; Pawliszy, J

    2001-10-01

    A procedure to monitor BVOC emitted by living plants using SPME technique is presented. For this purpose, a glass sampling chamber was designed. This device was employed for the characterization of biogenic volatile compounds emitted by leaves of Eucalyptus citriodora. After extraction with SPME fibers coated with PDMS/ DVB, it was possible to identify or detect 33 compounds emitted by this plant. A semiquantitative approach was applied to monitor the behavior of the emitted BVOC during 9 days. Circadian profiles of the variation in the concentration of isoprene were plotted. Using diffusion-based SPME quantitation, a recently introduced analytical approach, with extraction times as short as 15 s, it was possible to quantify subparts-per-billion amounts of isoprene emitted by this plant. PMID:11605854

  20. Ion-induced nucleation of pure biogenic particles

    CERN Document Server

    Kirkby, Jasper; Sengupta, Kamalika; Frege, Carla; Gordon, Hamish; Williamson, Christina; Heinritzi, Martin; Simon, Mario; Yan, Chao; Almeida, João; Tröstl, Jasmin; Nieminen, Tuomo; Ortega, Ismael K; Wagner, Robert; Adamov, Alexey; Amorim, Antonio; Bernhammer, Anne-Kathrin; Bianchi, Federico; Breitenlechner, Martin; Brilke, Sophia; Chen, Xuemeng; Craven, Jill; Dias, antonio; Ehrhart, Sebastian; Flagan, Richard C; Franchin, Alessandro; Fuchs, Claudia; Guida, Roberto; Hakala, Jani; Hoyle, Christopher R; Jokinen, Tuija; Junninen, Heikki; Kangasluoma, Juha; Kim, Jaeseok; Krapf, Manuel; Kürten, andreas; Laaksonen, Ari; Lehtipalo, Katrianne; Makhmutov, Vladimir; Mathot, Serge; Molteni, Ugo; Onnela, antti; Peräkylä, Otso; Piel, Felix; Petäjä, Tuukka; Praplan, Arnaud P; Pringle, Kirsty; Rap, Alexandru; Richards, Nigel A D; Riipinen, Ilona; Rissanen, Matti P; Rondo, Linda; Sarnela, Nina; Schobesberger, Siegfried; Scott, Catherine E; Seinfeld, John H; Sipilä, Mikko; Steiner, Gerhard; Stozhkov, Yuri; Stratmann, Frank; Tomé, Antonio; Virtanen, Annele; Vogel, Alexander L; Wagner, Andrea C; Wagner, Paul E; Weingartner, Ernest; Wimmer, Daniela; Winkler, Paul M; Ye, Penglin; Zhang, Xuan; Hansel, Armin; Dommen, Josef; Donahue, Neil M; Worsnop, Douglas R; Baltensperger, Urs; Kulmala, Markku; Carslaw, Kenneth S; Curtius, Joachim

    2016-01-01

    Atmospheric aerosols and their effect on clouds are thought to be important for anthropogenic radiative forcing of the climate, yet remain poorly understood. Globally, around half of cloud condensation nuclei originate from nucleation of atmospheric vapours. It is thought that sulfuric acid is essential to initiate most particle formation in the atmosphere and that ions have a relatively minor role. Some laboratory studies, however, have reported organic particle formation without the intentional addition of sulfuric acid, although contamination could not be excluded. Here we present evidence for the formation of aerosol particles from highly oxidized biogenic vapours in the absence of sulfuric acid in a large chamber under atmospheric conditions. The highly oxygenated molecules (HOMs) are produced by ozonolysis of $\\alpha$-pinene. We find that ions from Galactic cosmic rays increase the nucleation rate by one to two orders of magnitude compared with neutral nucleation. Our experimental findings are supported...

  1. Fungal spores overwhelm biogenic organic aerosols in a midlatitudinal forest

    Science.gov (United States)

    Zhu, Chunmao; Kawamura, Kimitaka; Fukuda, Yasuro; Mochida, Michihiro; Iwamoto, Yoko

    2016-06-01

    Both primary biological aerosol particles (PBAPs) and oxidation products of biogenic volatile organic compounds (BVOCs) contribute significantly to organic aerosols (OAs) in forested regions. However, little is known about their relative importance in diurnal timescales. Here, we report biomarkers of PBAP and secondary organic aerosols (SOAs) for their diurnal variability in a temperate coniferous forest in Wakayama, Japan. Tracers of fungal spores, trehalose, arabitol and mannitol, showed significantly higher levels in nighttime than daytime (p SOA formation. Using tracer-based methods, we estimated that fungal spores account for 45 % of organic carbon (OC) in nighttime and 22 % in daytime, whereas BVOC oxidation products account for 15 and 19 %, respectively. To our knowledge, we present for the first time highly time-resolved results that fungal spores overwhelmed BVOC oxidation products in contributing to OA especially in nighttime. This study emphasizes the importance of both PBAPs and SOAs in forming forest organic aerosols.

  2. Magnetic properties of iron minerals produced by natural iron- and manganese-reducing groundwater bacteria

    Science.gov (United States)

    Abrajevitch, Alexandra; Kondratyeva, Lubov M.; Golubeva, Evgeniya M.; Kodama, Kazuto; Hori, Rie S.

    2016-08-01

    Understanding the contribution of biogenic magnetic particles into sedimentary assemblages is a current challenge in palaeomagnetism. It has been demonstrated recently that magnetic particles produced through biologically controlled mineralization processes, such as magnetosomes from magnetotactic bacteria, contribute to the recording of natural remanent magnetization in marine and lacustrian sediments. Contributions from other, biologically induced, mineralization types, which are known from multiple laboratory experiments to include magnetic minerals, remain largely unknown. Here, we report magnetic properties of iron minerals formed by a community of iron- and manganese-reducing bacteria isolated from a natural groundwater deposit during a 2 yr long incubation experiment. The main iron phases of the biomineralized mass are lepidocrocite, goethite and magnetite, each of which has environmental significance. Unlike the majority of the previous studies that reported superparamagnetic grain size, and thus no remanence carrying capacity of biologically induced magnetite, hysteresis and first-order reversal curves measurements in our study have not detected significant superparamagnetic contribution. The biomineralized mass, instead, contains a mixture of single-domain to pseudo-single-domain and multidomain magnetite particles that are capable of carrying a stable chemical remanent magnetization. Isothermal remanent magnetization acquisition parameters and first-order reversal curves signatures of the biomineralized samples deviate from previously proposed criteria for the distinction of extracellular (biologically induced) magnetic particles in mixtures. Given its potential significance as a carrier of natural remanent magnetization, environmental requirements, distribution in nature and the efficiency in the geomagnetic field recording by biologically induced mineralization need comprehensive investigation.

  3. Magnetic properties of iron minerals produced by natural iron- and manganese-reducing groundwater bacteria

    Science.gov (United States)

    Abrajevitch, Alexandra; Kondratyeva, Lubov M.; Golubeva, Evgeniya M.; Kodama, Kazuto; Hori, Rie S.

    2016-06-01

    Understanding the contribution of biogenic magnetic particles into sedimentary assemblages is a current challenge in paleomagnetism. It has been demonstrated recently that magnetic particles produced through biologically controlled mineralization processes, such as magnetosomes from magnetotactic bacteria, contribute to the recording of natural remanent magnetization in marine and lacustrian sediments. Contributions from other, biologically induced, mineralization types, which are known from multiple laboratory experiments to include magnetic minerals, remain largely unknown. Here, we report magnetic properties of iron minerals formed by a community of iron- and manganese-reducing bacteria isolated from a natural groundwater deposit during a two year long incubation experiment. The main iron phases of the biomineralized mass are lepidocrocite, goethite and magnetite, each of which has environmental significance. Unlike the majority of the previous studies that reported superparamagnetic grain size, and thus no remanence carrying capacity of biologically induced magnetite, hysteresis and first order reversal curves measurements in our study have not detected significant superparamagnetic contribution. The biomineralized mass, instead, contains a mixture of single-domain to pseudo-single-domain and multi-domain magnetite particles that are capable of carrying a stable chemical remanent magnetization. Isothermal remanent magnetization acquisition parameters and first order reversal curves signatures of the biomineralized samples deviate from previously proposed criteria for the distinction of extracellular (biologically induced) magnetic particles in mixtures. Given its potential significance as a carrier of natural remanent magnetization, environmental requirements, distribution in nature and the efficiency in the geomagnetic field recording by biologically induced mineralization need comprehensive investigation.

  4. Iron and stony-iron meteorites

    DEFF Research Database (Denmark)

    Benedix, Gretchen K.; Haack, Henning; McCoy, T. J.

    2014-01-01

    interiors of Earth and other terrestrial planets. This chapter deals with our current knowledge of these meteorites. How did they form? What can they tell us about the early evolution of the solar system and its solid bodies? How closely do they resemble the materials from planetary interiors? What do and...... sampling of the deep interiors of differentiated asteroids. Iron and stony-iron meteorites are fragments of a large number of asteroids that underwent significant geological processing in the early solar system. Parent bodies of iron and some stony-iron meteorites completed a geological evolution similar......Without iron and stony-iron meteorites, our chances of ever sampling the deep interior of a differentiated planetary object would be next to nil. Although we live on a planet with a very substantial core, we will never be able to sample it. Fortunately, asteroid collisions provide us with a rich...

  5. Rapid Detection and Identification of Biogenic Aerosol Releases and Sources

    Science.gov (United States)

    Wagner, J.; Macher, J.; Ghosal, S.; Ahmed, K.; Hemati, K.; Wall, S.; Kumagai, K.

    2011-12-01

    Biogenic aerosols can be important contributors to aerosol chemistry, cloud droplet and ice nucleation, absorption and scattering of radiation, human health and comfort, and plant, animal, and microbial ecology. Many types of bioaerosols, e.g., fungal spores, are released into the atmosphere in response to specific climatological and meteorological conditions. The rapid identification of bioaerosol releases is thus important for better characterization of the above phenomena, as well as enabling public officials to respond quickly and appropriately to releases of infectious agents or biological toxins. One approach to rapid and accurate bioaerosol detection is to employ sequential, automated samples that can be fed directly into an image acquisition and data analysis device. Raman spectroscopy-based identification of bioaerosols, automated analysis of microscopy images, and automated detection of near-monodisperse peaks in aerosol size-distribution data were investigated as complementary approaches to traditional, manual methods for the identification and counting of fungal and actinomycete spores. Manual light microscopy is a widely used analytical technique that is compatible with a number of air sample formats and requires minimal sample preparation. However, a major drawback is its dependence on a human analyst's ability to distinguish particles and accurately count, size, and identify them. Therefore, automated methods, such as those evaluated in this study, have the potential to provide cost-effective and rapid alternatives if demonstrated to be accurate and reliable. An exploratory examination of individual spores for several macro- and microfungi (those with and without large fruiting bodies) by Raman microspectroscopy found unique spectral features that were used to identify fungi to the genus level. Automated analyses of digital spore images accurately recognized and counted single fungal spores and clusters. An automated procedure to discriminate near

  6. CO2 Biogenic vs Anthropogenic Sectoral Contribution for INFLUX

    Science.gov (United States)

    Lopez-Coto, I.; Prasad, K.; Hu, H.; Whetstone, J. R.; Miles, N. L.; Richardson, S.; Lauvaux, T.; Davis, K. J.; Turnbull, J. C.; Karion, A.; Sweeney, C.; Brewer, A.; Hardesty, M.; Cambaliza, M. O. L.; Shepson, P. B.; Patarasuk, R.; Gurney, K. R.

    2014-12-01

    The Indianapolis Flux Experiment (INFLUX) aims to use a top-down inversion methodology to quantify sources of Greenhouse Gas (GHG) emissions over an urban domain with high spatial and temporal resolution. This project is an experimental test bed which is intended to establish reliable methods for quantifying and validating GHG emissions independently of the inventory methods typically used for Measurement, Reporting and Verification (MRV) of pollution sources. Analyzing the contribution of different source types or sectors is a fundamental step in order to achieve an accuracy level desired for such MRV applications. This is especially challenging when attempting to determine anthropogenic emissions during the growing season since biological GHG fluxes reach a maximum at this time. To this end, the Weather Research and Forecasting Model (WRF-ARW) version 3.5.1 was used along with a modified version of the Green House Gases chemistry module for simulating the CO2 mole fraction transport during September and October 2013. Sectoral anthropogenic CO2 emissions were obtained from Hestia 2012 and from Vulcan 2002 beyond the spatial coverage of Hestia. Biogenic CO2 emissions were simulated by using an augmented version of the "Vegetation Photosynthesis and Respiration Model" (VPRM) included in WRF-CHEM. An implementation of the unconstrained nonlinear global optimization method of Nelder and Mead was employed to find the optimum values for the VPRM parameters for each vegetation category by using data from Ameriflux eddy covariance flux towers. Here we present a preliminary assessment of the relative contribution of biological vs sectoral anthropogenic CO2 fluxes on the INFLUX measurements network. The simulations are compared to tower and aircraft measurements that include trace gases with the capacity to distinguish observationally anthropogenic and biogenic CO2 sources and sinks. In addition, an evaluation of the sensitivity of the sectoral attribution to meteorological

  7. Anthropogenic impact on biogenic Si pools in temperate soils

    Science.gov (United States)

    Clymans, W.; Struyf, E.; Govers, G.; Vandevenne, F.; Conley, D. J.

    2011-05-01

    Human land use changes directly affect silica (Si) mobilisation and Si storage in terrestrial ecosystems and influence Si export from the continents, although the magnitudes of the impact are unknown. Yet biogenic silica (BSi) in soils is an understudied aspect. We have quantified and compared total biogenic (PSia) and easily soluble (PSie) Si pools at four sites along a gradient of disturbance in southern Sweden. An estimate of the magnitude of change in temperate continental BSi pools due to human disturbance is provided. Land use clearly affects BSi pools and their distribution. Total PSia and PSie for a continuous forested site at Siggaboda Nature Reserve (66 900 ± 22 800 kg SiO2 ha-1 and 952 ± 16 kg SiO2 ha-1) are significantly higher than disturbed land use types from the Råshult Culture Reserve including arable land (28 800 ± 7200 kg SiO2 ha-1 and 239 ± 91 kg SiO2 ha-1), pasture sites (27 300 ± 5980 kg SiO2 ha-1 and 370 ± 129 kg SiO2 ha-1) and grazed forest (23 600 ± 6370 kg SiO2 ha-1 and 346 ± 123 kg SiO2 ha-1). Vertical PSia and PSie profiles show significant (pexport of 1.1 ± 0.8 Tmol Si yr-1, leading to an annual contribution of ca. 20 % to the global land-ocean Si flux carried by rivers. Human activities clearly exert a long-term influence on Si cycling in soils and contribute significantly to the land-ocean Si flux.

  8. Role of mesoscale eddies on the variability of biogenic flux in the northern and central Bay of Bengal

    Digital Repository Service at National Institute of Oceanography (India)

    Vidya, P.J.; PrasannaKumar, S.

    15 m with spatial resolution of 1o x 1o [Bonjean and Lagerloef, 2002]. 3 Results 3.1 Biogenic flux The time-series of biogenic flux at NBBT during the period 1994 February to 1998 November is presented in Figure 2a (black line). Biogenic flux... with low SSHA (Figure 2, black line). Interestingly, at both the locations, all the peaks in the biogenic flux showed an inverse relation with SSHA (negative). This indicates that biogenic flux at both the locations is someway related to negative SSHA...

  9. Benthic phosphorus and iron budgets for three NW African slope sediments: a balance approach

    Directory of Open Access Journals (Sweden)

    K. Küster-Heins

    2010-02-01

    Full Text Available Despite intensive research on the different domains of the marine phosphorus (P cycle during the last decades, frequently discussed open questions still exist especially on controlling factors for the benthic behaviour of P and its general distribution in sediment-pore water systems. Steady state or the internal balance of all relevant physical and (biogeochemical processes are amongst the key issues. In this study we present and discuss an extended data set from surface sediments recovered from three locations on the NW African continental slope. Pore water data and results from sequential sediment extractions give clear evidence to the well-known close relationship between the benthic cycles of P and iron. Accordingly, most of the dissolved phosphate must have been released by microbially catalyzed reductive dissolution of iron (oxhydroxides. However, rates of release and association of P and iron, respectively, are not directly represented in profiles of element specific sediment compositions. Results from steady-state based transport-reaction modelling suggest that particle mixing due to active bioturbation, or rather a physical net downward transport of P associated to iron (oxyhydroxides, is an essential process for the balance of the inspected benthic cycles. This study emphasizes the importance of balancing analytical data for a comprehensive understanding of all processes involved in biogeochemical cycles.

  10. Identification of Iron-Bearing Minerals in Solid Residues from Industrial Kaolin Processing

    International Nuclear Information System (INIS)

    During the industrial processing of kaolin, the ore material is submitted to bleaching treatments with sulfuric and phosphoric acids and metallic zinc, in order to remove colored iron-rich minerals. The effluent waste is initially strongly acidic, and is chemically neutralized with calcium oxide and left to dry in open pits dug out in the terrain surrounding the industrial plant. The dried residue is then accumulated in deposits so as to produce the 'solid reject'. The Fe in these reject deposits precipitates as poorly crystalline iron-bearing compounds, which are difficult to identify by conventional X-ray diffraction techniques, and must be further characterized by complementary 57Fe Moessbauer analysis. 298 and 80 K Moessbauer spectra of the whole sample collected from the solid reject deposit of the Caolim Azzi industrial plant, in the city of Mar de Espanha, MG, Brazil, revealed that Fe3+ is mainly in octahedral sites of silicates. After treating this whole sample with NaOH, the Moessbauer parameters at 298 and 80 K indicated mainly the presence of iron oxide (hematite; ideal formula, αFe2O3) and oxyhydroxides, such as lepidocrocite (γFeOOH), goethite (αFeOOH) and iron hydroxysulphate, as jarosite (MFe3(SO4)2(OH)6; M = mono or divalent cation).

  11. Sedimentary and tectonic history of the Holowilena Ironstone, a Neoproterozoic iron formation in South Australia

    Science.gov (United States)

    Lechte, Maxwell Alexander; Wallace, Malcolm William

    2015-11-01

    The Holowilena Ironstone is a Neoproterozoic iron formation in South Australia associated with glacial deposits of the Sturtian glaciation. Through a comprehensive field study coupled with optical and scanning electron microscopy, X-ray fluorescence, and X-ray diffraction, a detailed description of the stratigraphy, sedimentology, mineralogy, and structure of the Holowilena Ironstone was obtained. The Holowilena Ironstone comprises ferruginous shales, siltstones, diamictites, and is largely made up of hematite and jasper, early diagenetic replacement minerals of precursor iron oxyhydroxides, and silica. These chemical precipitates are variably influenced by turbidites and debris flows contributing clastic detritus to the depositional system. Structural and stratigraphic evidence suggests deposition within a synsedimentary half-graben. A model for the Holowilena Ironstone is proposed, in which dense oxic fluids expelled during sea ice formation in the Cryogenian pool in the depression of the half-graben, allowing for long-lived mixing with the ferruginous seawater and the deposition of iron oxides. This combination of glacial dynamics, tectonism, and ocean chemistry may explain the return of iron formations in the Neoproterozoic.

  12. Iron deficiency in Europe.

    Science.gov (United States)

    Hercberg, S; Preziosi, P; Galan, P

    2001-04-01

    In Europe, iron deficiency is considered to be one of the main nutritional deficiency disorders affecting large fractions of the population, particularly such physiological groups as children, menstruating women and pregnant women. Some factors such as type of contraception in women, blood donation or minor pathological blood loss (haemorrhoids, gynaecological bleeding...) considerably increase the difficulty of covering iron needs. Moreover, women, especially adolescents consuming low-energy diets, vegetarians and vegans are at high risk of iron deficiency. Although there is no evidence that an absence of iron stores has any adverse consequences, it does indicate that iron nutrition is borderline, since any further reduction in body iron is associated with a decrease in the level of functional compounds such as haemoglobin. The prevalence of iron-deficient anaemia has slightly decreased in infants and menstruating women. Some positive factors may have contributed to reducing the prevalence of iron-deficiency anaemia in some groups of population: the use of iron-fortified formulas and iron-fortified cereals; the use of oral contraceptives and increased enrichment of iron in several countries; and the use of iron supplements during pregnancy in some European countries. It is possible to prevent and control iron deficiency by counseling individuals and families about sound iron nutrition during infancy and beyond, and about iron supplementation during pregnancy, by screening persons on the basis of their risk for iron deficiency, and by treating and following up persons with presumptive iron deficiency. This may help to reduce manifestations of iron deficiency and thus improve public health. Evidence linking iron status with risk of cardiovascular disease or cancer is unconvincing and does not justify changes in food fortification or medical practice, particularly because the benefits of assuring adequate iron intake during growth and development are well established

  13. Operation of Marine Diesel Engines on Biogenic Fuels: Modification of Emissions and Resulting Climate Effects

    OpenAIRE

    Petzold, A.; Lauer, P.; Fritsche, U.; Hasselbach, J.; M. Lichtenstern; Schlager, H.; Fleischer, F.

    2011-01-01

    The modification of emissions of climate-sensitive exhaust compounds such as CO2, NOx, hydrocarbons, and particulate matter from medium-speed marine diesel engines was studied for a set of fossil and biogenic fuels. Applied fossil fuels were the reference heavy fuel oil (HFO) and the low-sulfur marine gas oil (MGO); biogenic fuels were palm oil, soybean oil, sunflower oil, and animal fat. Greenhouse gas (GHG) emissions related to the production of biogenic fuels were treated by means of a fue...

  14. The Impact of Iron on Soil N2O Production Depends on Oxygen Availability

    Science.gov (United States)

    Zhu, X.; Doane, T. A.; Burger, M.; Horwath, W. R.

    2014-12-01

    The continuous increase of nitrous oxide (N2O) abundance in the atmosphere is a global concern. Soils are both an important source and sink of N2O, which is produced and consumed through biological processes including ammonia oxidation, heterotrophic denitrification, codenitrification, and through abiotic processes such as chemodenitrification. Iron is the most abundant element in the earth and is also the most prevalent redox-active metal in the biosphere. Its role in both chemical and biochemical reactions in N biogeochemistry cycling is well recognized. However, iron's significance to N2O production is poorly understood, especially under varying O2 concentration. We examined N2O production under different O2 concentrations following amorphous iron (III) oxyhydroxide and ammonical N fertilizer additions in four soil slurries and two static soils (soil moisture was 50% of water holding capacity). Under 21% O2, the addition of iron (III) significantly decreased N2O production in all the soil slurries and static soils, while the opposite phenomenon was observed once the O2 concentration became limited (≤3% in the soil slurry and ≤0.5% in the static soil). Our results show that the influence of iron on soil N2O production depends on O2 availability, which is the dominant controller of N2O production pathways. We hypothesize that under ambient O2 conditions, iron can react with nitrite produced during ammonia oxidation, thus reducing the probability of NO2- being used by nitrifiers as electron acceptor in nitrifier denitrification. In contrast, under anaerobic conditions (O2release of N2O.These findings imply that management practices which focus on mitigating N2O emission should avoid the application of iron-rich materials such as biosolids when anaerobic conditions might develop. In contrast, use of such materials could be a beneficial component of strategies to minimize N2O emission in well-aerated systems.

  15. Iron-Deficiency Anemia

    Medline Plus

    Full Text Available ... Deficiency Anemia Explore Iron-Deficiency Anemia What Is... CAUSES WHO IS AT RISK SIGNS & SYMPTOMS DIAGNOSIS TREATMENTS ... less hemoglobin than normal. Iron-deficiency anemia can cause fatigue (tiredness), shortness of breath, chest pain, and ...

  16. Total iron binding capacity

    Science.gov (United States)

    ... page: //medlineplus.gov/ency/article/003489.htm Total iron binding capacity To use the sharing features on this page, please enable JavaScript. Total iron binding capacity (TIBC) is a blood test to ...

  17. Iron in diet

    Science.gov (United States)

    Diet - iron; Ferric acid; Ferrous acid; Ferritin ... The human body needs iron to make the oxygen-carrying proteins hemoglobin and myoglobin. Hemoglobin is found in red blood cells and myoglobin is found ...

  18. Iron supplements (image)

    Science.gov (United States)

    The mineral iron is an essential nutrient for humans because it is part of blood cells, which carry oxygen to all body cells. There is no conclusive evidence that iron supplements contribute to heart attacks.

  19. Iron-Deficiency Anemia

    Medline Plus

    Full Text Available ... and women are the two groups at highest risk for iron-deficiency anemia. Outlook Doctors usually can successfully ... With and Managing Iron-Deficiency Anemia 05/18/2011 This video— ...

  20. Iron-Deficiency Anemia

    Medline Plus

    Full Text Available ... levels usually are due to blood loss, poor diet, or an inability to absorb enough iron from ... iron levels. Susan also made changes to her diet, such as focusing more on green leafy vegetables, ...

  1. Iron-Deficiency Anemia

    Medline Plus

    Full Text Available ... This Content: NEXT >> Featured Video Living With and Managing Iron-Deficiency Anemia 05/18/2011 This video— ... treatment. For more information about living with and managing iron-deficiency anemia, go to the Health Topics ...

  2. Iron-Deficiency Anemia

    Medline Plus

    Full Text Available ... iron-rich protein that carries oxygen from the lungs to the rest of the body. Iron-deficiency ... 2011 This video—presented by the National Heart, Lung, and Blood Institute, part of the National Institutes ...

  3. Iron-Deficiency Anemia

    Medline Plus

    Full Text Available ... intravenous iron therapy. Rate This Content: NEXT >> Featured Video Living With and Managing Iron-Deficiency Anemia 05/18/2011 This video—presented by the National Heart, Lung, and Blood ...

  4. Iron Therapy for Preterm Infants

    OpenAIRE

    Rao, Raghavendra; Georgieff, Michael K.

    2009-01-01

    Preterm infants are at risk for both iron deficiency and iron overload. The role of iron in multiple organ functions suggests that iron supplementation is essential for the preterm infant. Conversely, the potential for iron overload and the poorly developed anti-oxidant measures in the preterm infant argues against indiscriminate iron supplementation in this population. The purpose of this article is to review the predisposing factors and consequences of iron deficiency and iron overload in t...

  5. Moessbauer and XRD Comparative Study of Host Rock and Iron Rich Mineral Samples from Paz del Rio Iron Ore Mineral Mine in Colombia

    Energy Technology Data Exchange (ETDEWEB)

    Fajardo, M.; Perez Alcazar, G. A. [Universidad del Valle, Departamento de Fisica (Colombia); Moreira, A. M.; Speziali, N. L. [Universidade Federal de Minas Gerais, Departamento de Fisica (Brazil)

    2004-12-15

    A comparative study between the host rock and the iron rich mineral samples from the Paz del Rio iron ore mineral mine in Colombia was performed using X-ray diffraction and Moessbauer spectroscopy. Diffraction results of the iron rich mineral sample show that goethite, hematite, quartz, kaolinite and siderite are the main phases, and that a small amount of illite is also present. By Moessbauer spectroscopy at room temperature (RT) the presence of all the above mentioned phases was detected except quartz as well as an additional presence of small amount of biotite. The goethite, which appears as four sextets with hyperfine fields of 33.5, 30.5, 27.5 and 18.5 T, respectively, is the majority phase. This result shows the different grades of formation of this oxyhydroxide. The Moessbauer spectrum of this sample at 80 K presents the same phases obtained at RT without any superparamagnetic effect. In this case the goethite appears as two sextets. Diffraction results of the host rock sample show a large amount of quartz and kaolinite and small amounts of illite and biotite, whereas by Moessbauer spectroscopy illite, kaolinite and biotite were detected.

  6. Special thermite cast irons

    Directory of Open Access Journals (Sweden)

    Yu. Zhiguts

    2008-07-01

    Full Text Available The given paper deals with the problems of the synthesis of cast iron by metallothermy synthesis. On the basis of investigated method of calculations structures of charges have been arranged and cast iron has been synthesized further. Peculiarities metallothermic smelting were found, mechanical properties and structure of received cast iron were investigated and different technologies for cast iron receiving were worked out.

  7. Alternative iron making routes

    Energy Technology Data Exchange (ETDEWEB)

    Kaushik, P.; Sharma, T. [Indian School of Mines, Dhanbad (India)

    2002-07-01

    The versatile route of iron production 'blast furnace' technique is being replaced by widely accepted Corex technology, Midrex process using Fastmelt ironmaking, eco-friendly Romelt process, more innovative Ausmelt & Hismelt technology, TATA KORF Mini blast furnace improvement, 'quickest iron through Orbiting Plasma', Direct iron ore smelting process, Conred, AISI-Hyl, Inred processes, Direct iron ore reduction methods, their comparison and proposed modifications. 18 refs., 11 figs., 14 tabs.

  8. Iron deficiency and cognition

    OpenAIRE

    Hulthén, Lena

    2003-01-01

    Iron deficiency is the most prevalent nutritional disorder in the world. One of the most worrying consequences of iron deficiency in children is the alteration of behaviour and cognitive performance. In iron-deficient children, striking behavioural changes are observed, such as reduced attention span, reduced emotional responsiveness and low scores on tests of intelligence. Animal studies on nutritional iron deficiency show effects on learning ability that parallel the human studies. Despite ...

  9. Synthesis of Derivatives of Biogenic Amines Labelled with Radioactive Tracers for Brain Imaging

    OpenAIRE

    Arturo A. Vitale

    2000-01-01

    Endogenous derivatives of biogenic amines, such as phenethylamines, indolalkylamines and harmines, have been extensively studied as usual constituents of body fluids. Methylated derivatives of indolalkylamines have been also related to mental disorders, e.g. schizophrenia and hallucination.

  10. Iron-Deficiency Anemia

    Medline Plus

    Full Text Available ... the body. Iron-deficiency anemia usually develops over time if your body doesn't have enough iron ... Institutes of Health—shows how Susan, a full-time worker and student, has coped with having iron- ...

  11. Iron-Deficiency Anemia

    Medline Plus

    Full Text Available ... body. Low iron levels usually are due to blood loss, poor diet, or an inability to absorb enough iron from food. Overview Iron-deficiency anemia is a common type of anemia . The term "anemia" usually refers to ...

  12. Iron-Deficiency Anemia

    Medline Plus

    Full Text Available ... the NHLBI on Twitter. What Is Iron-Deficiency Anemia? Español Iron-deficiency anemia is a common, easily ... Featured Video Living With and Managing Iron-Deficiency Anemia 05/18/2011 This video—presented by the ...

  13. Iron-Deficiency Anemia

    Science.gov (United States)

    ... the NHLBI on Twitter. What Is Iron-Deficiency Anemia? Español Iron-deficiency anemia is a common, easily ... Featured Video Living With and Managing Iron-Deficiency Anemia 05/18/2011 This video—presented by the ...

  14. Iron-Deficiency Anemia

    Medline Plus

    Full Text Available ... page from the NHLBI on Twitter. What Is Iron-Deficiency Anemia? Español Iron-deficiency anemia is a ... Content: NEXT >> Featured Video Living With and Managing Iron-Deficiency Anemia 05/18/2011 This video—presented ...

  15. Synthesis of Nano sized Zinc-Doped Cobalt Oxyhydroxide Parties by a Dropping Method and Their Carbon Monoxide Gas Sensing Properties

    International Nuclear Information System (INIS)

    Two nano structures of cobalt oxyhydroxide (CoOOH) and Zinc-(Zn-) doped CoOOH (1–4% Zn) are prepared from Co(NO3)2 solution via microtitration with NaOH and oxidation in air. The X-ray diffraction (XRD) analysis results show that a pure state of nano-CoOOH can be obtained at an alkalinity (OH−/Co+) of 5 with 40°C heat treatment after 6 h. The Zn ions preferentially substitute Co ions in the CoOOH structure, resulting in a decrease of its crystallinity. The disc-like CoOOH nano structure exhibits good sensitivity to carbon monoxide (CO) in a temperature range of 40–110°C with maximum sensitivity to CO at around 70–80°C. When CoOOH nano structure is doped with 1% Zn, its sensitivity and selectivity for CO gas are improved at 70–80°C; further Zn doping to 2% degraded the CO sensing properties of nano-CoOOH. The results of a cross-sensitivity investigation of the sensor to various gases coexisting at early stages of a fire show that the sensitivity of Zn-doped nano-CoOOH is the highest toward CO. Zn-doped nano-CoOOH film exhibits a high sensitivity to CO at room temperature, making it a promising sensor for early-stage fire detection.

  16. Effects of pH and surface metal oxyhydroxides on deposition and transport of carboxyl-functionalized graphene in saturated porous media

    International Nuclear Information System (INIS)

    This work investigated the effects of solution pH and surface metal oxyhydroxides on the transport behaviors of carboxyl-functionalized graphene (GR) in saturated porous media. Column experiments were conducted to elucidate the transport behavior of functionalized GR in acid-cleaned and natural sand under different solution pH conditions (i.e., 5.6 and 8.3). The results showed that the functionalized GR was highly mobile in the acid-cleaned sand columns at both pH 5.6 and 8.3 with recovery rates close to 100 %. The deposition of the functionalized GR was higher in the natural sand columns, and the recovery rates were 88.4 and 96.5 % for pH 5.6 and 8.3, respectively. The reductions of the mobility of the functionalized GR in the natural sand columns could be caused by the interaction between carboxyl functional groups of the GR and the surface metal hydroxides on the sand grains, which is pH dependent. An advection–dispersion-reaction model was applied to the data and successfully simulated the transport of the functionalized GR through the acid-cleaned and natural sand columns

  17. Assessing the Role of Iron Sulfides in the Long Term Sequestration of U by Sulfate Reducing Bacteria

    Energy Technology Data Exchange (ETDEWEB)

    Rittman, Bruce; Zhou, Chen; Vannela, Raveender

    2013-12-31

    This four-year project’s overarching aim was to identify the role of biogenic and synthetic iron-sulfide minerals in the long-term sequestration of reduced U(IV) formed under sulfate-reducing conditions when subjected to re-oxidizing conditions. As stated in this final report, significant progress was achieved through the collaborative research effort conducted at Arizona State University (ASU) and the University of Michigan (UM).

  18. Applications of Satellite Remote Sensing Data for Biogenic Emission Estimates in Southeastern Texas

    Science.gov (United States)

    Feldman, M. S.; Howard, T.; Mullins, G.; McDonald-Buller, E.; Allen, D. T.

    2007-12-01

    Biogenic hydrocarbons, including isoprene, monoterpenes, and oxygenated compounds, are emitted in substantial quantities by vegetation and dominate the overall volatile organic compound emission inventory in Southeastern Texas. Spatial distributions of biogenic emissions in Texas are heterogeneous, and biogenic emission processes are affected by the characterization of land cover, leaf area index, drought stress, and surface temperatures. On a regional scale, biogenic emissions, particularly isoprene, in the presence of high levels of nitrogen oxides (NOx), will produce elevated ground-level ozone concentrations. The sensitivity of biogenic emission estimates and air quality model predictions to the characterization of land use/land cover (LULC) in southeastern Texas is examined. A LULC database has been developed for the region based on source imagery collected by the Landsat 7 Enhanced Thematic Mapper-Plus sensor between 1999 and 2003, and data from field studies used for species identification and quantification of biomass densities. This database and the LULC database currently used in regulatory air quality models by the State of Texas are compared. Effects of the LULC data on biogenic emission estimates and modeled ozone concentrations are examined using the Global Biosphere Emissions and Interactions System and the Comprehensive Air Quality Model with extensions during an August 22-September 6, 2000 episode developed for the Houston/Galveston area. These results are also compared to biogenic emission estimates from the recently created Model of Emissions of Gases and Aerosols from Nature (MEGAN), which includes a global vegetation map compiled from recent satellite data and ecosystem inventories. Biogenic emissions estimated from the new LULC dataset showed good general spatial agreement with those from the currently used LULC dataset but significantly lower emissions (~40% less hourly emissions across the modeling domain), primarily due to differences in

  19. Validation of an HPLC Analytical Method for Determination of Biogenic Amines in Agricultural Products and Monitoring of Biogenic Amines in Korean Fermented Agricultural Products.

    Science.gov (United States)

    Yoon, Hyeock; Park, Jung Hyuck; Choi, Ari; Hwang, Han-Joon; Mah, Jae-Hyung

    2015-09-01

    An HPLC analytical method was validated for the quantitative determination of biogenic amines in agricultural products. Four agricultural foods, including apple juice, Juk, corn oil and peanut butter, were selected as food matrices based on their water and fat contents (i.e., non-fatty liquid, non-fatty solid, fatty liquid and fatty solid, respectively). The precision, accuracy, recovery, limit of detection (LOD) and quantification (LOQ) were determined to test the validity of an HPLC procedure for the determination of biogenic amines, including tryptamine, β-phenylethylamine, putrescine, cadaverine, histamine, tyramine, spermidine and spermine, in each matrix. The LODs and LOQs for the biogenic amines were within the range of 0.01~0.10 mg/kg and 0.02~0.31 mg/kg, respectively. The relative standard deviation (RSD) of intraday for biogenic amine concentrations ranged from 1.86 to 5.95%, whereas the RSD of interday ranged from 2.08 to 5.96%. Of the matrices spiked with biogenic amines, corn oil with tyramine and Juk with putrescine exhibited the least accuracy of 84.85% and recovery rate of 89.63%, respectively, at the lowest concentration (10 mg/kg). Therefore, the validation results fulfilled AOAC criteria and recommendations. Subsequently, the method was applied to the analysis of biogenic amines in fermented agricultural products for a total dietary survey in Korea. Although the results revealed that Korean traditional soy sauce and Doenjang contained relatively high levels of histamine, the amounts are of no concern if these fermented agricultural products serve as condiments. PMID:26483889

  20. Investigation of Cl corrosion products of iron archaeological artefacts using micro-focused synchrotron X-ray absorption spectroscopy

    International Nuclear Information System (INIS)

    Synchrotron-based micro-X-ray absorption spectroscopy is used in the present study to obtain chemical information at the microscopic scale such as coordination and oxidation state of Fe atoms in phases constituting corrosion products within archaeological iron artefacts buried in soil. This technique is required in order to answer questions about the iron corrosion process related to the presence of chloride, particularly for restoration and conservation of metallic artefacts of the cultural heritage. The samples available for X-ray microprobe analyses are cross sections from corroded iron archaeological objects. Previously, complementary techniques have been used such as μXRD and μRaman. This specific study applies micro-X-ray absorption spectroscopy to determine the spatial variation of the predominant Fe oxidation state and to identify the corresponding crystallographic phase. The analyses performed at Fe and Cl K-edges (μXANES) reveal the correlation between the valence distribution in the corrosion products and the evolution of the chloride concentration. In addition to the presence of the well-known iron oxyhydroxide β-FeOOH: akaganeite, we highlight the presence of another important phase, the β-Fe2(OH)3Clhydroxychloride. These important findings help to gain new insights concerning the influence of such phases in the iron corrosion mechanism within their precise characterization. (orig.)

  1. Evolution of cyclonic eddies and biogenic fluxes in the northern Bay of Bengal

    OpenAIRE

    M. Nuncio; Prasanna Kumar, S.

    2013-01-01

    The Bay of Bengal has been traditionally known for its low primary productivity and varied reasons were attributed to it. The data analysis from the sediment traps deployed in the northern Bay of Bengal during the 5 yr from 1994 show episodic events of enhanced downward biogenic flux every year which was not related to monsoon-driven seasonal cycle. Satellite-derived sea level anomaly suggests that the episodic increase in the biogenic flu...

  2. Cocaine affects foraging behaviour and biogenic amine modulated behavioural reflexes in honey bees

    OpenAIRE

    Eirik Søvik; Naïla Even; Radford, Catherine W.; Barron, Andrew B.

    2014-01-01

    In humans and other mammals, drugs of abuse alter the function of biogenic amine pathways in the brain leading to the subjective experience of reward and euphoria. Biogenic amine pathways are involved in reward processing across diverse animal phyla, however whether cocaine acts on these neurochemical pathways to cause similar rewarding behavioural effects in animal phyla other than mammals is unclear. Previously, it has been shown that bees are more likely to dance (a signal of perceived rew...

  3. Administration of biogenic amines to Saanen kids: effects on growth performance and meat quality

    OpenAIRE

    E. Fusi; R. Rebucci; C. Pecorini; Rossi, L.; F. Cheli

    2011-01-01

    Biogenic amines are low molecular weight organic bases present in all organisms. The most common are putrescine, cadaverine, spermine, spermidine, histamine, tryptamine and β- phenylethylamine. In low concentrations they are essential for the normal growth and differentiation of cells (Bardócz et al., 1995), but in larger quantities are harmful to humans and livestock. Biogenic amines are naturally present in silage; however their presence in high concentrations may be a sign of u...

  4. Managing your wine fermentation to reduce the risk of biogenic amine formation

    OpenAIRE

    MaretDu Toit

    2012-01-01

    Biogenic amines are nitrogenous organic compounds produced in wine from amino acid precursors mainly by microbial decarboxylation. The concentration of biogenic amines that can potentially be produced is dependent on the amount of amino acid precursors in the medium, the presence of decarboxylase positive microorganisms and conditions that enable microbial or biochemical activity such as the addition of nutrients to support the alcoholic and malolactic fermentation (MLF) inoculated starter cu...

  5. A Review: Microbiological, Physicochemical and Health Impact of High Level of Biogenic Amines in Fish Sauce

    OpenAIRE

    Muhammad Z. Zaman; A. S. Abdulamir; Fatimah A. Bakar; Jinap Selamat; Jamilah Bakar

    2009-01-01

    Problem statement: Biogenic amines are basic nitrogenous compounds present in a wide variety of foods and beverages. Their formations were mainly due to the amino acids decarboxylase activity of certain microorganisms. Excessive intake of biogenic amines could induce many undesirable physiological effects determined by their psychoactive and vasoactive action. Fish sauce which is considered as a good source of dietary protein, amino acids, vitamins and minerals was a popular condiment in Sout...

  6. Analysis of Biogenic Amines by GC/FID and GC/MS

    OpenAIRE

    Nakovich, Laura

    2003-01-01

    Low levels of biogenic amines occur naturally, but high levels (FDA sets 50 ppm of histamine in fish as the maximum allowable level) can lead to scombroid poisoning. Amines in general are difficult to analyze by Gas Chromatography (GC) due to their lack of volatility and their interaction with the GC column, often leading to significant tailing and poor reproducibility. Biogenic amines need to be derivatized before both GC and HPLC analyses. The objective of this research was to devel...

  7. Changes of the content of biogenic amines during winemaking of Sauvignon wines

    OpenAIRE

    Kovačević Ganić, Karin; Gracin, L.; Komes, Draženka; Ćurko, Natka; Lovrić, T.

    2009-01-01

    The aim of the present work was to study the changes of the content of biogenic amines during winemaking and maturation processes of wines made from Vitis vinifera cv Sauvignon grapes from Slavonia region (vintage 2008). Biogenic amines were quantified using a reversed-phase high performance liquid chromatography (HPLC) with fluorescence detection after pre-column derivatization with o-phthalaldehyde (OPA). Samples used in this study were obtained during production of Sauvignon wines in three...

  8. Control of Biogenic Amines in Food—Existing and Emerging Approaches

    OpenAIRE

    Naila, Aishath; Flint, Steve; Fletcher, Graham; Bremer, Phil; Meerdink, Gerrit

    2010-01-01

    Biogenic amines have been reported in a variety of foods, such as fish, meat, cheese, vegetables, and wines. They are described as low molecular weight organic bases with aliphatic, aromatic, and heterocyclic structures. The most common biogenic amines found in foods are histamine, tyramine, cadaverine, 2-phenylethylamine, spermine, spermidine, putrescine, tryptamine, and agmatine. In addition octopamine and dopamine have been found in meat and meat products and fish. The formation of biogeni...

  9. Managing Your Wine Fermentation to Reduce the Risk of Biogenic Amine Formation

    OpenAIRE

    Smit, Anita Yolandi; Engelbrecht, Lynn; du Toit, Maret

    2012-01-01

    Biogenic amines are nitrogenous organic compounds produced in wine from amino acid precursors mainly by microbial decarboxylation. The concentration of biogenic amines that can potentially be produced is dependent on the amount of amino acid precursors in the medium, the presence of decarboxylase positive microorganisms and conditions that enable microbial or biochemical activity such as the addition of nutrients to support the inoculated starter cultures for alcoholic and malolactic fermenta...

  10. Levels of histamine and other biogenic amines in high quality red wines.

    OpenAIRE

    Konakovsky, Viktor; Focke, Margarete; Hoffmann-Sommergruber, Karin; Schmid, Rainer,; Scheiner, Otto; Moser, Peter; Jarisch, Reinhart; Hemmer, Wolfgang

    2011-01-01

    Abstract Biogenic amines in wine may impair sensory wine quality and cause adverse health effects in susceptible individuals. In this study, histamine and other biogenic amines were determined by HPLC after amine derivatization to dansyl chloride conjugates in 100 selected high quality red wines made from seven different cultivars. Amine levels varied considerably between different wines. The most abundant amines were putrescine (median 19.4 mg/L, range 2.9-122), histamine (7.2, 0....

  11. Metabolism of biogenic amines in acute cerebral ischemia: Influence of systemic hyperglycemia

    Directory of Open Access Journals (Sweden)

    Milovanović Aleksandar

    2012-01-01

    Full Text Available Dopamine, norepinephrine and serotonin are biogenic amines which are transmitters of the central nervous system. The effects of ischemia on the brain parenchyma depends on many factors, such is the mechanism of blood flow interruption, velocity of the occurring blood flow interruption, duration of an ischemic episode, organization of anatomical structures of the brain blood vessels etc., which all influence the final outcome. During interruption of the brain circulation in experimental or clinical conditions, neurotransmitter metabolism, primarily of biogenic amines, is disturbed. Many researches with various experimental models of complete ischemia reported a decrease in the content of norepinephrine, dopamine and serotonin in the CNS tissue. It was proven that hyperglycemia can drastically increase cerebral injury followed by short-term cerebral ischemia. Considering the fact that biogenic amines (dopamine, norepinephrine and serotonin influence the size of neurologic damage, as well as the fact that in hyperglycemic conditions infarct size (from the morphological aspect is larger relative to normoglycemic status, the intention was to evaluate the role of biogenic amines in occurrence of damage in conditions of hyperglycemia, i.e. in the case of brain apoplexia in diabetics. Analysis of biogenic amines metabolism in states of acute hyperglycemia, as well as analysis of the effects of reversible and irreversible brain ischemia on metabolism of serotonin, dopamine and norepinephrine, showed that acute hyperglycemia slows down serotonin, dopamine and norepinephrine metabolism in the cerebral cortex and n. caudatus. Brain ischemia in normoglycemic animals by itself has no influence on biogenic amines metabolism, but the effect of ischemia becomes apparent during reperfusion. In recirculation, which corresponds to the occurrences in penumbra, release of biogenic amines is uncontrolled and increased. Brain ischemia in acute hyperglycemic animals

  12. Relationship Between Biogenic Amines and Free Amino Acid Contents of Winesand Musts from Alentejo (Portugal)

    OpenAIRE

    Herbert, Paulo; Cabrita, Maria Joao; Ratola, Nuno; Laureano, Olga; Alves, Arminda

    2006-01-01

    The concentration of biogenic amines and free amino acids was studied in 102 Portuguese wines and 18 musts from Alentejo demarcated (D.O.C.) regions. Most wines were commercial, except for 38 monovarietals obtained by micro vinification. Musts from the varieties used to produce the latter wines were also studied. Both biogenic amines and free amino acids were analyzed by HPLC using fluorescence detection for their o-phthalaldehyde/fluorenylmethyl chloroformate (OPA/FMOC) deriva...

  13. Ligand-gated chloride channels are receptors for biogenic amines in C. elegans

    OpenAIRE

    Ringstad, Niels; Abe, Namiko; Horvitz, H. Robert

    2009-01-01

    Biogenic amines such as serotonin and dopamine are intercellular signaling molecules that function widely as neurotransmitters and neuromodulators. We have identified in the nematode Caenorhabditis elegans three ligand-gated chloride channels that are receptors for biogenic amines: LGC-53 is a high-affinity dopamine receptor, LGC-55 is a high-affinity tyramine receptor, and LGC-40 is a low-affinity serotonin receptor that is also gated by choline and acetylcholine. lgc-55 mutants are defectiv...

  14. PCR methods for the detection of biogenic amine-producing bacteria on wine

    OpenAIRE

    Landete, José María; Rivas, Blanca de las; Marcobal, Ángela; Muñoz, Rosario

    2011-01-01

    Biogenic amines are low molecular weight organic bases frequently found in wine. Several toxicological problems resulting from the ingestion of wine containing biogenic amines have been described. In wine, histamine, tyramine, and putrescine are mainly produced by the decarboxylation of the amino acid histidine, tyrosine, and ornithine, respectively, by lactic acid bacteria action. The bacterial ability to decarboxylate amino acids is highly variable, and therefore the...

  15. Studio della formazione di ammine biogene e di altri composti azotati negli alimenti

    OpenAIRE

    Congiu, Francesca

    2014-01-01

    The aim of this thesis was the qualitative and quantitative determination of biogenic amines (BA) and amino acids (AA), in particular the essential AA, in different food matrices typical of Sardinia (Italy). The study was focused on wines and table olives, which are potential source of biogenic amines due to their fermentation processes involved in their production. The decision to follow this research field is based on the importance of having updated information to assess the actual r...

  16. Screening of biogenic amine production by lactic acid bacteria isolated from grape musts and wine

    OpenAIRE

    Moreno-Arribas, M. Victoria; Polo, María Carmen; Jorganes, Felisa; Muñoz, Rosario

    2003-01-01

    The potential to produce the biogenic amines tyramine, histamine and putrescine, was investigated for lactic acid bacteria (LAB) of various origin, including commercial malolactic starter cultures, type strains and 78 strains isolated from Spanish grape must and wine. The presence of biogenic amines in a decarboxylase synthetic broth was determined by reverse-phase high performance liquid chromatography (RP-HPLC). Tyramine was the main amine formed by the LAB strains investigated. ...

  17. Biogenic caliches in Texas: The role of organisms and effect of climate

    Science.gov (United States)

    Zhou, Jie; Chafetz, Henry S.

    2009-12-01

    Biogenic constituents are ubiquitous and abundant in the caliches of Texas. Investigation of 51 caliche profiles on various host strata (alluvium, limestone, igneous rocks, etc.) across approximately 900 km of Texas from subhumid east to arid west has shown that 43 of these profiles exhibit prominent biogenic constituents. These profiles exhibit significant differences in thickness (varying from centimeters to meters) and maturity (varying from I to VI). All of the different caliche facies are composed of low-Mg calcite. Biogenic features generally occur in the upper part of the profiles, including the uppermost portion of massive caliche horizons, platy horizons, laminar crusts, and pisoids. The main biogenic caliche facies include rhizoliths (calcified root structures), stromatolite-like laminar crusts, and coated grains. Compared to the abiogenic massive micritic to microsparitic calcite groundmass, biogenic constituents are morphologically distinct. These biogenic constituents are composed of several microscopic mineral components, including calcified filaments, needle fiber calcite (e.g., single crystalline needles and needle pairs, triangular crystals, and polycrystalline chains of rhombohedrons), spherulites, micro-rods, and nano-spheres. A large number of calcified root cellular structures and micro-organisms, e.g., fungal filaments, actinomycetes, and rod-like bacteria, are also present. Plant roots as well as soil biota produce distinctive structures and also enhance lithification by inducing calcite precipitation in the caliches, i.e., biologically controlled or influenced processes. Host strata did not significantly influence the abundance nor type of biogenic features in the caliches. In contrast, climate had an evident effect on the development of biogenic constituents in these caliches in terms of the amount as well as type. The thickness of laminar crusts and grain coatings and the abundance of biotic constituents within those facies decrease as the

  18. Über den Einfluss biogener Amine auf unkonditionierten und konditionierten Stimulus

    OpenAIRE

    Buckemüller, Christina

    2014-01-01

    Biogenic amines play an important role in the modulation of behavior in vertebrates and invertebrates. Octopamine, a biogenic amine, exclusively for invertebrates is an important neurotransmitter and neuromodulator and has a considerable role as stress hormone. Octopamine plays a central role in learning and behavior in insects. The precise role in such behavior has been discussed over the last years. The signaling pathways of octopamine, tyramine and dopamine interact. Therefore, it is di...

  19. Diclofenac and 2‐anilinophenylacetate degradation by combined activity of biogenic manganese oxides and silver

    OpenAIRE

    Meerburg, Francis; Hennebel, Tom; Vanhaecke, Lynn; Verstraete, Willy; Boon, Nico

    2012-01-01

    Summary The occurrence of a range of recalcitrant organic micropollutants in our aquatic environment has led to the development of various tertiary wastewater treatment methods. In this study, biogenic manganese oxides (Bio‐MnOx), biogenic silver nanoparticles (Bio‐Ag0) and ionic silver were used for the oxidative removal of the frequently encountered drug diclofenac and its dechlorinated form, 2‐anilinophenylacetate (APA). Diclofenac was rapidly degraded during ongoing manganese oxidation by...

  20. Biogenic hardparts: Difficult archives of the geological past (Invited)

    Science.gov (United States)

    Immenhauser, A.; Schone, B. R.; Hoffmann, R.; Niedermayr, A.

    2013-12-01

    Biomineralized exo- or endoskeletons of fossil marine invertebrates are widespread and diverse components of the Phanerozoic rock record of Earth's past and present oceans. Exoskeletons serve as protection against environmental pressure or predators, whilst endoskeletons can act as support or serve as an attachment for muscles and ligaments and hence as a mechanism for transmitting muscular forces. Biogenic hard parts represent sophisticated products resulting from the hierarchical interaction of inorganic minerals (95%) and macromolecular organic matrices, forming commonly less than 5%. The significance of many biogenic carbonate archives lies in the time-resolved growth patterns and their ability to record ambient environmental conditions in the form of multiple geochemical properties (multi-proxy archives) that have been widely used to assess past oceanic seawater properties. Here, we compile and review published work dealing with crystallization pathways of skeletal hard parts secreted by mollusks (i.e., bivalves and cephalopods) as well as brachiopods as widely used archives of ancient neritic epeiric settings. Bivalves and cephalopods (e.g., extinct ammonoids and belemnites and extant Sepia, Nautilus and Spirula) all form accretionary calcitic, aragonitic or vateritic skeletal hard parts. Despite the fact that mollusks and brachiopods form part of very different branches of the animal phylogenetic tree, their biomineralization strategies are surprisingly similar. Our main focus lies in a critical assessment of the complex pathways of ions and aquo-complexes from their source (seawater) to the final product (biomineral). We do this as an attempt to critically test the commonly held hypothesis that many fossil hard parts precipitated (under favorable conditions and pending subsequent diagenetic alteration) in equilibrium with seawater. Two main observations stand out: (1) the present knowledge on pathways and mechanisms (e.g., ion channel trans-membrane or

  1. Sub-Antarctic marine aerosol: significant contributions from biogenic sources

    Directory of Open Access Journals (Sweden)

    J. Schmale

    2013-03-01

    Full Text Available Biogenic influences on the composition and characteristics of aerosol were investigated on Bird Island (54°00' S, 38°03' W in the South Atlantic during November and December 2010. This remote marine environment is characterised by large seabird and seal colonies. The chemical composition of the submicron particles, measured by an aerosol mass spectrometer (AMS, was 21% non-sea salt sulfate 2% nitrate, 7% ammonium, 22% organics and 47% sea salt including sea salt sulfate. A new method to isolate the sea salt signature from the high-resolution AMS data was applied. Generally, the aerosol was found to be less acidic than in other marine environments due to the high availability of ammonia, from local fauna emissions. By positive matrix factorisation five different organic aerosol (OA profiles could be isolated: an amino acids/amine factor (AA-OA, 18% of OA mass, a methanesulfonic acid OA factor (MSA-OA, 25%, a marine oxygenated OA factor (M-OOA, 40%, a sea salt OA fraction (SS-OA, 7% and locally produced hydrocarbon-like OA (HOA, 9%. The AA-OA was dominant during the first two weeks of November and found to be related with the hatching of penguins in a nearby colony. This factor, rich in nitrogen (C : N ratio = 0.13, has implications for the biogeochemical cycling of nitrogen in the area as particulate matter is often transported over longer distances than gaseous N-rich compounds. The MSA-OA was mainly transported from more southerly latitudes where phytoplankton bloomed. The bloom was identified as one of three sources for particulate sulfate on Bird Island, next to sea salt sulfate and sulfate transported from South America. M-OOA was the dominant organic factor and found to be similar to marine OA observed at Mace Head, Ireland. An additional OA factor highly correlated with sea salt aerosol was identified (SS-OA. However, based on the available data the type of mixture, internal or external, could not be determined. Potassium was not

  2. Sub-Antarctic marine aerosol: dominant contributions from biogenic sources

    Directory of Open Access Journals (Sweden)

    J. Schmale

    2013-09-01

    Full Text Available Biogenic influences on the composition and characteristics of aerosol were investigated on Bird Island (54°00' S, 38°03' W in the South Atlantic during November and December 2010. This remote marine environment is characterised by large seabird and seal colonies. The chemical composition of the submicron particles, measured by an aerosol mass spectrometer (AMS, was 21% non-sea-salt sulfate, 2% nitrate, 8% ammonium, 22% organics and 47% sea salt including sea salt sulfate. A new method to isolate the sea spray signature from the high-resolution AMS data was applied. Generally, the aerosol was found to be less acidic than in other marine environments due to the high availability of ammonia, from local fauna emissions. By positive matrix factorisation five different organic aerosol (OA profiles could be isolated: an amino acid/amine factor (AA-OA, 18% of OA mass, a methanesulfonic acid OA factor (MSA-OA, 25%, a marine oxygenated OA factor (M-OOA, 41%, a sea spray OA fraction (SS-OA, 7% and locally produced hydrocarbon-like OA (HOA, 9%. The AA-OA was dominant during the first two weeks of November and found to be related with the hatching of penguins in a nearby colony. This factor, rich in nitrogen (N : C ratio = 0.13, has implications for the biogeochemical cycling of nitrogen in the area as particulate matter is often transported over longer distances than gaseous N-rich compounds. The MSA-OA was mainly transported from more southerly latitudes where phytoplankton bloomed. The bloom was identified as one of three sources for particulate sulfate on Bird Island, next to sea salt sulfate and sulfate transported from South America. M-OOA was the dominant organic factor and found to be similar to marine OA observed at Mace Head, Ireland. An additional OA factor highly correlated with sea spray aerosol was identified (SS-OA. However, based on the available data the type of mixture, internal or external, could not be determined. Potassium was not

  3. Sub-Antarctic marine aerosol: significant contributions from biogenic sources

    Science.gov (United States)

    Schmale, J.; Schneider, J.; Nemitz, E.; Tang, Y. S.; Dragosits, U.; Blackall, T. D.; Trathan, P. N.; Phillips, G. J.; Sutton, M.; Braban, C. F.

    2013-03-01

    Biogenic influences on the composition and characteristics of aerosol were investigated on Bird Island (54°00' S, 38°03' W) in the South Atlantic during November and December 2010. This remote marine environment is characterised by large seabird and seal colonies. The chemical composition of the submicron particles, measured by an aerosol mass spectrometer (AMS), was 21% non-sea salt sulfate 2% nitrate, 7% ammonium, 22% organics and 47% sea salt including sea salt sulfate. A new method to isolate the sea salt signature from the high-resolution AMS data was applied. Generally, the aerosol was found to be less acidic than in other marine environments due to the high availability of ammonia, from local fauna emissions. By positive matrix factorisation five different organic aerosol (OA) profiles could be isolated: an amino acids/amine factor (AA-OA, 18% of OA mass), a methanesulfonic acid OA factor (MSA-OA, 25%), a marine oxygenated OA factor (M-OOA, 40%), a sea salt OA fraction (SS-OA, 7%) and locally produced hydrocarbon-like OA (HOA, 9%). The AA-OA was dominant during the first two weeks of November and found to be related with the hatching of penguins in a nearby colony. This factor, rich in nitrogen (C : N ratio = 0.13), has implications for the biogeochemical cycling of nitrogen in the area as particulate matter is often transported over longer distances than gaseous N-rich compounds. The MSA-OA was mainly transported from more southerly latitudes where phytoplankton bloomed. The bloom was identified as one of three sources for particulate sulfate on Bird Island, next to sea salt sulfate and sulfate transported from South America. M-OOA was the dominant organic factor and found to be similar to marine OA observed at Mace Head, Ireland. An additional OA factor highly correlated with sea salt aerosol was identified (SS-OA). However, based on the available data the type of mixture, internal or external, could not be determined. Potassium was not associated to sea

  4. Sub-Antarctic marine aerosol: dominant contributions from biogenic sources

    Science.gov (United States)

    Schmale, J.; Schneider, J.; Nemitz, E.; Tang, Y. S.; Dragosits, U.; Blackall, T. D.; Trathan, P. N.; Phillips, G. J.; Sutton, M.; Braban, C. F.

    2013-09-01

    Biogenic influences on the composition and characteristics of aerosol were investigated on Bird Island (54°00' S, 38°03' W) in the South Atlantic during November and December 2010. This remote marine environment is characterised by large seabird and seal colonies. The chemical composition of the submicron particles, measured by an aerosol mass spectrometer (AMS), was 21% non-sea-salt sulfate, 2% nitrate, 8% ammonium, 22% organics and 47% sea salt including sea salt sulfate. A new method to isolate the sea spray signature from the high-resolution AMS data was applied. Generally, the aerosol was found to be less acidic than in other marine environments due to the high availability of ammonia, from local fauna emissions. By positive matrix factorisation five different organic aerosol (OA) profiles could be isolated: an amino acid/amine factor (AA-OA, 18% of OA mass), a methanesulfonic acid OA factor (MSA-OA, 25%), a marine oxygenated OA factor (M-OOA, 41%), a sea spray OA fraction (SS-OA, 7%) and locally produced hydrocarbon-like OA (HOA, 9%). The AA-OA was dominant during the first two weeks of November and found to be related with the hatching of penguins in a nearby colony. This factor, rich in nitrogen (N : C ratio = 0.13), has implications for the biogeochemical cycling of nitrogen in the area as particulate matter is often transported over longer distances than gaseous N-rich compounds. The MSA-OA was mainly transported from more southerly latitudes where phytoplankton bloomed. The bloom was identified as one of three sources for particulate sulfate on Bird Island, next to sea salt sulfate and sulfate transported from South America. M-OOA was the dominant organic factor and found to be similar to marine OA observed at Mace Head, Ireland. An additional OA factor highly correlated with sea spray aerosol was identified (SS-OA). However, based on the available data the type of mixture, internal or external, could not be determined. Potassium was not associated

  5. Magnesium stable isotope fractionation in marine biogenic calcite and aragonite

    Science.gov (United States)

    Wombacher, F.; Eisenhauer, A.; Böhm, F.; Gussone, N.; Regenberg, M.; Dullo, W.-Chr.; Rüggeberg, A.

    2011-10-01

    This survey of magnesium stable isotope compositions in marine biogenic aragonite and calcite includes samples from corals, sclerosponges, benthic porcelaneous and planktonic perforate foraminifera, coccolith oozes, red algae, and an echinoid and brachiopod test. The analyses were carried out using MC-ICP-MS with an external repeatability of ±0.22‰ (2SD for δ 26Mg; n = 37), obtained from a coral reference sample (JCp-1). Magnesium isotope fractionation in calcitic corals and sclerosponges agrees with published data for calcitic speleothems with an average Δ 26Mg calcite-seawater = -2.6 ± 0.3‰ that appears to be weakly related to temperature. With one exception ( Vaceletia spp.), aragonitic corals and sclerosponges also display uniform Mg isotope fractionations relative to seawater with Δ 26Mg biogenic aragonite-seawater = -0.9 ± 0.2. Magnesium isotopes in high-Mg calcites from red algae, echinoids and perhaps some porcelaneous foraminifera as well as in all low-Mg calcites (perforate foraminifera, coccoliths and brachiopods) display significant biological influences. For planktonic foraminifera, the Mg isotope data is consistent with the fixation of Mg by organic material under equilibrium conditions, but appears to be inconsistent with Mg removal from vacuoles. Our preferred model, however, suggests that planktonic foraminifera synthesize biomolecules that increase the energetic barrier for Mg incorporation. In this model, the need to remove large quantities of Mg from vacuole solutions is avoided. For the high-Mg calcites from echinoids, the precipitation of amorphous calcium carbonate may be responsible for their weaker Mg isotope fractionation. Disregarding superimposed biological effects, it appears that cation light isotope enrichments in CaCO 3 principally result from a chemical kinetic isotope effect, related to the incorporation of cations at kink sites. In this model, the systematics of cation isotope fractionations in CaCO 3 relate to the

  6. Characteristics of aerosolized ice forming marine biogenic particles

    Science.gov (United States)

    Alpert, Peter A.

    atomus and Emiliania huxleyi, cells and cell fragments efficiently nucleate ice in the deposition mode, however, only T. pseudonana and N. atomus form ice in the immersion mode, presumably due to different cell wall compositions. This further corroborates the role of phytoplanktonic species for aerosolization of marine biogenic cloud active particles. Experimental data are used to parameterize marine biogenic particle fluxes and heterogeneous ice nucleation as a function of biological activity. The atmospheric implications of the results and their implementation into cloud and climate models are discussed.

  7. Anthropogenic impact on biogenic Si pools in temperate soils

    Directory of Open Access Journals (Sweden)

    W. Clymans

    2011-05-01

    Full Text Available Human land use changes directly affect silica (Si mobilisation and Si storage in terrestrial ecosystems and influence Si export from the continents, although the magnitudes of the impact are unknown. Yet biogenic silica (BSi in soils is an understudied aspect. We have quantified and compared total biogenic (PSia and easily soluble (PSie Si pools at four sites along a gradient of disturbance in southern Sweden. An estimate of the magnitude of change in temperate continental BSi pools due to human disturbance is provided. Land use clearly affects BSi pools and their distribution. Total PSia and PSie for a continuous forested site at Siggaboda Nature Reserve (66 900 ± 22 800 kg SiO2 ha−1 and 952 ± 16 kg SiO2 ha−1 are significantly higher than disturbed land use types from the Råshult Culture Reserve including arable land (28 800 ± 7200 kg SiO2 ha−1 and 239 ± 91 kg SiO2 ha−1, pasture sites (27 300 ± 5980 kg SiO2 ha−1 and 370 ± 129 kg SiO2 ha−1 and grazed forest (23 600 ± 6370 kg SiO2 ha−1 and 346 ± 123 kg SiO2 ha−1. Vertical PSia and PSie profiles show significant (p<0.05 variation among the sites. These differences in size and distribution are interpreted as the long-term effect of reduced BSi replenishment and increased mobilisation of the PSia in disturbed soils. In temperate regions, total PSia showed a 10 % decline since agricultural development (3000BCE. Recent agricultural expansion (after 1700CE has resulted in an average export of 1.1 ± 0.8 Tmol Si yr−1, leading to an annual contribution of ca. 20 % to the global land-ocean Si flux carried by rivers. Human activities clearly exert a long-term influence on Si cycling in soils and

  8. Study on biogenic amines in various dry salted fish consumed in China

    Science.gov (United States)

    Wu, Yanyan; Chen, Yufeng; Li, Laihao; Yang, Xianqing; Yang, Shaoling; Lin, Wanling; Zhao, Yongqiang; Deng, Jianchao

    2016-05-01

    This study was carried out to investigate the biogenic amines (BAs), physicochemical property and microorganisms in dry salted fish, a traditional aquatic food consumed in China. Forty three samples of dry salted fish were gathered from retail and wholesale markets and manufacturers, which had been produced in various regions in China. Cadaverine (CAD) and putrescine (PUT) were quantitatively the most common biogenic amines. About 14% of the samples exceeded the histamine content standards established by the FDA and/or EU. The highest histamine content was found in Silver pomfret (Pampus argenteus) (347.79 mg kg-1). Five of forty three samples exceeded the acceptable content of TYR (100 mg kg-1), and 23.26% of dried-salted fish contained high contents of biogenic amines (above 600 mg kg-1). In addition, species, regions, pickling processes and drying methods made the physicochemical property, microorganisms and biogenic amines in dry salted fish to be different to some extents. The total plate count (TPC) was much higher than that of total halophilic bacteria in all samples. The biogenic amines, physicochemical property and microbiological counts exhibited large variations among samples. Furthermore, no significant correlation between biogenic amines and physicochemical property and TPC was observed. This study indicated that dry salted fish may still present healthy risk for BAs, depending on the processing methods, storage conditions among others.

  9. Study on biogenic amines in various dry salted fish consumed in China

    Science.gov (United States)

    Wu, Yanyan; Chen, Yufeng; Li, Laihao; Yang, Xianqing; Yang, Shaoling; Lin, Wanling; Zhao, Yongqiang; Deng, Jianchao

    2016-08-01

    This study was carried out to investigate the biogenic amines (BAs), physicochemical property and microorganisms in dry salted fish, a traditional aquatic food consumed in China. Forty three samples of dry salted fish were gathered from retail and wholesale markets and manufacturers, which had been produced in various regions in China. Cadaverine (CAD) and putrescine (PUT) were quantitatively the most common biogenic amines. About 14% of the samples exceeded the histamine content standards established by the FDA and/or EU. The highest histamine content was found in Silver pomfret ( Pampus argenteus) (347.79 mg kg-1). Five of forty three samples exceeded the acceptable content of TYR (100 mg kg-1), and 23.26% of dried-salted fish contained high contents of biogenic amines (above 600 mg kg-1). In addition, species, regions, pickling processes and drying methods made the physicochemical property, microorganisms and biogenic amines in dry salted fish to be different to some extents. The total plate count (TPC) was much higher than that of total halophilic bacteria in all samples. The biogenic amines, physicochemical property and microbiological counts exhibited large variations among samples. Furthermore, no significant correlation between biogenic amines and physicochemical property and TPC was observed. This study indicated that dry salted fish may still present healthy risk for BAs, depending on the processing methods, storage conditions among others.

  10. Operation of marine diesel engines on biogenic fuels: modification of emissions and resulting climate effects.

    Science.gov (United States)

    Petzold, Andreas; Lauer, Peter; Fritsche, Uwe; Hasselbach, Jan; Lichtenstern, Michael; Schlager, Hans; Fleischer, Fritz

    2011-12-15

    The modification of emissions of climate-sensitive exhaust compounds such as CO(2), NO(x), hydrocarbons, and particulate matter from medium-speed marine diesel engines was studied for a set of fossil and biogenic fuels. Applied fossil fuels were the reference heavy fuel oil (HFO) and the low-sulfur marine gas oil (MGO); biogenic fuels were palm oil, soybean oil, sunflower oil, and animal fat. Greenhouse gas (GHG) emissions related to the production of biogenic fuels were treated by means of a fuel life cycle analysis which included land use changes associated with the growth of energy plants. Emissions of CO(2) and NO(x) per kWh were found to be similar for fossil fuels and biogenic fuels. PM mass emission was reduced to 10-15% of HFO emissions for all low-sulfur fuels including MGO as a fossil fuel. Black carbon emissions were reduced significantly to 13-30% of HFO. Changes in emissions were predominantly related to particulate sulfate, while differences between low-sulfur fossil fuels and low-sulfur biogenic fuels were of minor significance. GHG emissions from the biogenic fuel life cycle (FLC) depend crucially on energy plant production conditions and have the potential of shifting the overall GHG budget from positive to negative compared to fossil fuels. PMID:22044020

  11. Emission and role of biogenic volatile organic compounds in biosphere

    International Nuclear Information System (INIS)

    Plants are an essential part of the biosphere. Under the influence of climate change, plants respond in multiple ways within the ecosystem. One such way is the release of assimilated carbon back to the atmosphere in form of biogenic volatile organic compounds (BVOCs), which are produced by plants and are involved in plant growth, reproduction, defense and other . These compounds are emitted from vegetation into the atmosphere under different environmental situations. Plants produce an extensive range of BVOCs, including isoprenoids, sequisterpenes, aldehydes, alcohols and terpenes in different tissues above and below the ground. The emission rates vary with various environmental conditions and the plant growth stage in its life span.BVOCs are released under biotic and abiotic stress changes, like heat, drought, land-use changes, higher atmospheric CO concentrations, increased UV radiation and insect or disease attack. Plants emit BVOCs in atmosphere in order to avoid stress, and adapt to harsh circumstances. These compounds also have a significant role in plant-plant interaction, communication and competition. BVOCs have the ability to alter atmospheric chemistry; they readily react with atmospheric pollutant gases under high temperature and form tropospheric ozone, which is a potent air pollutant for global warming and disease occurrence. BVOCs may be a cause of photochemical smog and increase the stay of other GHGs in the atmosphere. Therefore, further study is required to assess the behavior of BVOCs in the biosphere as well as the atmosphere. (author)

  12. Analysis of Some Biogenic Amines by Micellar Liquid Chromatography

    Directory of Open Access Journals (Sweden)

    Irena Malinowska

    2012-01-01

    Full Text Available Micellar liquid chromatography (MLC with the use of high performance liquid chromatography (HPLC was used to determine some physicochemical parameters of six biogenic amines: adrenaline, dopamine, octopamine, histamine, 2-phenylethylamine, and tyramine. In this paper, an influence of surfactant’s concentration and pH of the micellar mobile phase on the retention of the tested substances was examined. To determine the influence of surfactant’s concentration on the retention of the tested amines, buffered solutions (at pH 7.4 of ionic surfactant—sodium dodecyl sulfate SDS (at different concentrations with acetonitrile as an organic modifier (0.8/0.2 v/v were used as the micellar mobile phases. To determine the influence of pH of the micellar mobile phase on the retention, mobile phases contained buffered solutions (at different pH values of sodium dodecyl sulfate SDS (at 0.1 M with acetonitrile (0.8/0.2 v/v. The inverse of value of retention factor (1/ versus concentration of micelles ( relationships were examined. Other physicochemical parameters of solutes such as an association constant analyte—micelle (ma—and partition coefficient of analyte between stationary phase and water (hydrophobicity descriptor (swΦ were determined by the use of Foley’s equation.

  13. Biogenic Emissions of Volatile Organic Compounds by Urban Forests

    Institute of Scientific and Technical Information of China (English)

    CENTRITTOMauro; LIUShirong; LORETOFrancesco

    2005-01-01

    All plants emit a wide range of volatile compounds, the so-called biogenic volatile organic compounds (BVOC). BVOC emissions have received increased scientific attention in the last two decades because they may profoundly influence the chemical and physical properties of the atmosphere, and may modulate plant tolerance to heat, pollutants, oxidative stress and abiotic stresses, and affect plant-plant and plant-insect interactions. Urban forestry may have a high impact on atmospheric composition, air quality, environment,and quality of life in urban areas. However, few studies have been carried out where the emission of BVOC could have important consequence for the quality of air and contribute to pollution episodes. A screening of BVOC emission by the mixed stand constituting urban forests is therefore required if emissions are to be reliably predicted. Monitoring the emission rates simultaneously with measurements of air quality, plant physiology and micrometeorology on selected urban forests, will allow detailed quantitative information on the inventory of BVOC emissions by urban vegetation to be compiled. This information will make it possible to propose an innovative management of urban vegetation in cities characterised by heavy emissions of anthropogenic pollutants, aiming at the abatement of BVOC emissions through the introduction or selection of non-BVOC emitting species in urban areas subjected to pollution episodes and in the new afforestation areas covering peri-urban parks, green belts and green corridors between peri-urban rural areas and the conurbations.

  14. A marine biogenic source of atmospheric ice-nucleating particles

    Energy Technology Data Exchange (ETDEWEB)

    Wilson, T. W.; Ladino, L. A.; Alpert, Peter A.; Breckels, M. N.; Brooks, I. M.; Browse, J.; Burrows, Susannah M.; Carslaw, K. S.; Huffman, J. A.; Judd, C.; Kilthau, W. P.; Mason, R. H.; McFiggans, Gordon; Miller, L. A.; Najera, J.; Polishchuk, E. A.; Rae, S.; Schiller, C. L.; Si, M.; Vergara Temprado, J.; Whale, Thomas; Wong, J P S; Wurl, O.; Yakobi-Hancock, J. D.; Abbatt, JPD; Aller, Josephine Y.; Bertram, Allan K.; Knopf, Daniel A.; Murray, Benjamin J.

    2015-09-09

    The formation of ice in clouds is facilitated by the presence of airborne ice nucleating particles1,2. Sea spray is one of the major global sources of atmospheric particles, but it is unclear to what extent these particles are capable of nucleating ice3–11. Here we show that material in the sea surface microlayer, which is enriched in surface active organic material representative of that found in sub-micron sea- spray aerosol12–21, nucleates ice under conditions that occur in mixed-phase clouds and high-altitude ice clouds. The ice active material is likely biogenic and is less than ~0.2 ?m in size. We also show that organic material (exudate) released by a common marine diatom nucleates ice when separated from cells and propose that organic material associated with phytoplankton cell exudates are a candidate for the observed ice nucleating ability of the microlayer samples. By combining our measurements with global model simulations of marine organic aerosol, we show that ice nucleating particles of marine origin are dominant in remote marine environments, such as the Southern Ocean, the North Pacific and the North Atlantic.

  15. Biogenic aldehyde determination by reactive paper spray ionization mass spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Bag, Soumabha; Hendricks, P.I. [Aston Labs, Department of Chemistry, Purdue University, West Lafayette, IN 47907 (United States); Reynolds, J.C. [Centre for Analytical Science, Loughborough University, Loughborough, Leicestershire (United Kingdom); Cooks, R.G., E-mail: cooks@purdue.edu [Aston Labs, Department of Chemistry, Purdue University, West Lafayette, IN 47907 (United States)

    2015-02-20

    Highlights: • In-situ derivatization and simultaneous ionization used to detect aldehydes. • Biogenic aliphatic and aromatic aldehydes reacted with 4-aminophenol. • Derivatized products yield structurally characteristic fragment ions. • This measurement demonstrated using a miniaturized portable mass spectrometer. - Abstract: Ionization of aliphatic and aromatic aldehydes is improved by performing simultaneous chemical derivatization using 4-aminophenol to produce charged iminium ions during paper spray ionization. Accelerated reactions occur in the microdroplets generated during the paper spray ionization event for the tested aldehydes (formaldehyde, n-pentanaldehyde, n-nonanaldehyde, n-decanaldehyde, n-dodecanaldehyde, benzaldehyde, m-anisaldehyde, and p-hydroxybenzaldehyde). Tandem mass spectrometric analysis of the iminium ions using collision-induced dissociation demonstrated that straight chain aldehydes give a characteristic fragment at m/z 122 (shown to correspond to protonated 4-(methyleneamino)phenol), while the aromatic aldehyde iminium ions fragment to give a characteristic product ion at m/z 120. These features allow straightforward identification of linear and aromatic aldehydes. Quantitative analysis of n-nonaldehyde using a benchtop mass spectrometer demonstrated a linear response over 3 orders of magnitude from 2.5 ng to 5 μg of aldehyde loaded on the filter paper emitter. The limit of detection was determined to be 2.2 ng for this aldehyde. The method had a precision of 22%, relative standard deviation. The experiment was also implemented using a portable ion trap mass spectrometer.

  16. Biogenic aldehyde determination by reactive paper spray ionization mass spectrometry

    International Nuclear Information System (INIS)

    Highlights: • In-situ derivatization and simultaneous ionization used to detect aldehydes. • Biogenic aliphatic and aromatic aldehydes reacted with 4-aminophenol. • Derivatized products yield structurally characteristic fragment ions. • This measurement demonstrated using a miniaturized portable mass spectrometer. - Abstract: Ionization of aliphatic and aromatic aldehydes is improved by performing simultaneous chemical derivatization using 4-aminophenol to produce charged iminium ions during paper spray ionization. Accelerated reactions occur in the microdroplets generated during the paper spray ionization event for the tested aldehydes (formaldehyde, n-pentanaldehyde, n-nonanaldehyde, n-decanaldehyde, n-dodecanaldehyde, benzaldehyde, m-anisaldehyde, and p-hydroxybenzaldehyde). Tandem mass spectrometric analysis of the iminium ions using collision-induced dissociation demonstrated that straight chain aldehydes give a characteristic fragment at m/z 122 (shown to correspond to protonated 4-(methyleneamino)phenol), while the aromatic aldehyde iminium ions fragment to give a characteristic product ion at m/z 120. These features allow straightforward identification of linear and aromatic aldehydes. Quantitative analysis of n-nonaldehyde using a benchtop mass spectrometer demonstrated a linear response over 3 orders of magnitude from 2.5 ng to 5 μg of aldehyde loaded on the filter paper emitter. The limit of detection was determined to be 2.2 ng for this aldehyde. The method had a precision of 22%, relative standard deviation. The experiment was also implemented using a portable ion trap mass spectrometer

  17. Technological Factors Affecting Biogenic Amine Content in Foods: A Review.

    Science.gov (United States)

    Gardini, Fausto; Özogul, Yesim; Suzzi, Giovanna; Tabanelli, Giulia; Özogul, Fatih

    2016-01-01

    Biogenic amines (BAs) are molecules, which can be present in foods and, due to their toxicity, can cause adverse effects on the consumers. BAs are generally produced by microbial decarboxylation of amino acids in food products. The most significant BAs occurring in foods are histamine, tyramine, putrescine, cadaverine, tryptamine, 2-phenylethylamine, spermine, spermidine, and agmatine. The importance of preventing the excessive accumulation of BAs in foods is related to their impact on human health and food quality. Quality criteria in connection with the presence of BAs in food and food products are necessary from a toxicological point of view. This is particularly important in fermented foods in which the massive microbial proliferation required for obtaining specific products is often relater with BAs accumulation. In this review, up-to-date information and recent discoveries about technological factors affecting BA content in foods are reviewed. Specifically, BA forming-microorganism and decarboxylation activity, genetic and metabolic organization of decarboxylases, risk associated to BAs (histamine, tyramine toxicity, and other BAs), environmental factors influencing BA formation (temperature, salt concentration, and pH). In addition, the technological factors for controlling BA production (use of starter culture, technological additives, effects of packaging, other non-thermal treatments, metabolizing BA by microorganisms, effects of pressure treatments on BA formation and antimicrobial substances) are addressed. PMID:27570519

  18. Analysis of irradiated biogenic amines by computational chemistry and spectroscopy

    International Nuclear Information System (INIS)

    Biogenic Amines (B A) are nitrogenous compounds able to cause food poisoning. In this work, we studied the tyramine, one of the most common BA present in foods by combining experimental measured IR (Infrared) and GC/MS (Gas Chromatograph / Mass Spectrometry) spectra and computational quantum chemistry. Density Functional Theory (DFT) and the Deformed Atoms in Molecules (DMA) method was used to compute the partition the electronic densities in a chemically-intuitive way and electrostatic potentials of molecule to identify the acid and basic sites. Trading pattern was irradiated using a Cs 137 radiator, and each sample was identified by IR and GC/MS. Calculated and experimental IR spectra were compared. We observed that ionizing gamma irradiation was very effective in decreasing the population of standard amine, resulting in fragments that could be rationalized through the quantum chemistry calculations. In particular, we could locate the acid and basic sites of both molecules and identify possible sites of structural weaknesses, which allowed to propose mechanistic schemes for the breaking of chemical bonds by the irradiation. Moreover, from this work we hope it will be also possible to properly choose the dose of gamma irradiation which should be provided to eliminate each type of contamination. (author)

  19. Ion-induced nucleation of pure biogenic particles

    Science.gov (United States)

    Kirkby, Jasper; Duplissy, Jonathan; Sengupta, Kamalika; Frege, Carla; Gordon, Hamish; Williamson, Christina; Heinritzi, Martin; Simon, Mario; Yan, Chao; Almeida, João; Tröstl, Jasmin; Nieminen, Tuomo; Ortega, Ismael K.; Wagner, Robert; Adamov, Alexey; Amorim, Antonio; Bernhammer, Anne-Kathrin; Bianchi, Federico; Breitenlechner, Martin; Brilke, Sophia; Chen, Xuemeng; Craven, Jill; Dias, Antonio; Ehrhart, Sebastian; Flagan, Richard C.; Franchin, Alessandro; Fuchs, Claudia; Guida, Roberto; Hakala, Jani; Hoyle, Christopher R.; Jokinen, Tuija; Junninen, Heikki; Kangasluoma, Juha; Kim, Jaeseok; Krapf, Manuel; Kürten, Andreas; Laaksonen, Ari; Lehtipalo, Katrianne; Makhmutov, Vladimir; Mathot, Serge; Molteni, Ugo; Onnela, Antti; Peräkylä, Otso; Piel, Felix; Petäjä, Tuukka; Praplan, Arnaud P.; Pringle, Kirsty; Rap, Alexandru; Richards, Nigel A. D.; Riipinen, Ilona; Rissanen, Matti P.; Rondo, Linda; Sarnela, Nina; Schobesberger, Siegfried; Scott, Catherine E.; Seinfeld, John H.; Sipilä, Mikko; Steiner, Gerhard; Stozhkov, Yuri; Stratmann, Frank; Tomé, Antonio; Virtanen, Annele; Vogel, Alexander L.; Wagner, Andrea C.; Wagner, Paul E.; Weingartner, Ernest; Wimmer, Daniela; Winkler, Paul M.; Ye, Penglin; Zhang, Xuan; Hansel, Armin; Dommen, Josef; Donahue, Neil M.; Worsnop, Douglas R.; Baltensperger, Urs; Kulmala, Markku; Carslaw, Kenneth S.; Curtius, Joachim

    2016-05-01

    Atmospheric aerosols and their effect on clouds are thought to be important for anthropogenic radiative forcing of the climate, yet remain poorly understood. Globally, around half of cloud condensation nuclei originate from nucleation of atmospheric vapours. It is thought that sulfuric acid is essential to initiate most particle formation in the atmosphere, and that ions have a relatively minor role. Some laboratory studies, however, have reported organic particle formation without the intentional addition of sulfuric acid, although contamination could not be excluded. Here we present evidence for the formation of aerosol particles from highly oxidized biogenic vapours in the absence of sulfuric acid in a large chamber under atmospheric conditions. The highly oxygenated molecules (HOMs) are produced by ozonolysis of α-pinene. We find that ions from Galactic cosmic rays increase the nucleation rate by one to two orders of magnitude compared with neutral nucleation. Our experimental findings are supported by quantum chemical calculations of the cluster binding energies of representative HOMs. Ion-induced nucleation of pure organic particles constitutes a potentially widespread source of aerosol particles in terrestrial environments with low sulfuric acid pollution.

  20. Ion-induced nucleation of pure biogenic particles.

    Science.gov (United States)

    Kirkby, Jasper; Duplissy, Jonathan; Sengupta, Kamalika; Frege, Carla; Gordon, Hamish; Williamson, Christina; Heinritzi, Martin; Simon, Mario; Yan, Chao; Almeida, João; Tröstl, Jasmin; Nieminen, Tuomo; Ortega, Ismael K; Wagner, Robert; Adamov, Alexey; Amorim, Antonio; Bernhammer, Anne-Kathrin; Bianchi, Federico; Breitenlechner, Martin; Brilke, Sophia; Chen, Xuemeng; Craven, Jill; Dias, Antonio; Ehrhart, Sebastian; Flagan, Richard C; Franchin, Alessandro; Fuchs, Claudia; Guida, Roberto; Hakala, Jani; Hoyle, Christopher R; Jokinen, Tuija; Junninen, Heikki; Kangasluoma, Juha; Kim, Jaeseok; Krapf, Manuel; Kürten, Andreas; Laaksonen, Ari; Lehtipalo, Katrianne; Makhmutov, Vladimir; Mathot, Serge; Molteni, Ugo; Onnela, Antti; Peräkylä, Otso; Piel, Felix; Petäjä, Tuukka; Praplan, Arnaud P; Pringle, Kirsty; Rap, Alexandru; Richards, Nigel A D; Riipinen, Ilona; Rissanen, Matti P; Rondo, Linda; Sarnela, Nina; Schobesberger, Siegfried; Scott, Catherine E; Seinfeld, John H; Sipilä, Mikko; Steiner, Gerhard; Stozhkov, Yuri; Stratmann, Frank; Tomé, Antonio; Virtanen, Annele; Vogel, Alexander L; Wagner, Andrea C; Wagner, Paul E; Weingartner, Ernest; Wimmer, Daniela; Winkler, Paul M; Ye, Penglin; Zhang, Xuan; Hansel, Armin; Dommen, Josef; Donahue, Neil M; Worsnop, Douglas R; Baltensperger, Urs; Kulmala, Markku; Carslaw, Kenneth S; Curtius, Joachim

    2016-05-26

    Atmospheric aerosols and their effect on clouds are thought to be important for anthropogenic radiative forcing of the climate, yet remain poorly understood. Globally, around half of cloud condensation nuclei originate from nucleation of atmospheric vapours. It is thought that sulfuric acid is essential to initiate most particle formation in the atmosphere, and that ions have a relatively minor role. Some laboratory studies, however, have reported organic particle formation without the intentional addition of sulfuric acid, although contamination could not be excluded. Here we present evidence for the formation of aerosol particles from highly oxidized biogenic vapours in the absence of sulfuric acid in a large chamber under atmospheric conditions. The highly oxygenated molecules (HOMs) are produced by ozonolysis of α-pinene. We find that ions from Galactic cosmic rays increase the nucleation rate by one to two orders of magnitude compared with neutral nucleation. Our experimental findings are supported by quantum chemical calculations of the cluster binding energies of representative HOMs. Ion-induced nucleation of pure organic particles constitutes a potentially widespread source of aerosol particles in terrestrial environments with low sulfuric acid pollution. PMID:27225125

  1. Mechanisms of iron-silica aqueous interaction and the genesis of Precambrian iron formation

    Science.gov (United States)

    Chemtob, S. M.; Catalano, J. G.; Moynier, F.; Pringle, E. A.

    2015-12-01

    Iron formations (IFs), Fe- and Si-rich chemical sediments common in Precambrian successions, preserve key information about the compositional, biological, and oxidative evolution of the Precambrian ocean. Stable Si isotopes (δ30Si) of IF have been used to infer paleo-oceanic composition, and secular variations in δ30Si may reflect ancient biogeochemical cycles. The δ30Si of primary Fe-Si precipitates that formed IF depends not only on the δ30Si of aqueous silica but also on the precipitation mechanism. Multiple formation mechanisms for these primary precipitates are plausible. Aqueous Si may have adsorbed on newly precipitated iron oxyhydroxide surfaces; alternatively, Fe and Si may have coprecipitated as a single phase. Here we explore variations in the Si isotope fractionation factor (ɛ) with Fe-Si aqueous interaction mechanism (adsorption vs. coprecipitation). In adsorption experiments, sodium silicate solutions (pH 8.1, 125-2000 µM Si) were reacted with iron oxide particles (hematite, ferrihydrite, goethite, and magnetite) for 24 to 72 hours. Resultant solutions had δ30Si between 0 and +6‰. Calculated ɛ varied significantly with oxide mineralogy and morphology. For ferrihydrite, ɛ = -1.7‰; for hematite, ɛ = -2 to -5‰, depending on particle morphology. Apparent ɛ decreased upon surface site saturation, implying a smaller isotope effect for polymeric Si adsorption than monomeric adsorption. In coprecipitation experiments, solutions of Na-silicate and Fe(II) chloride (0.4-10 mM) were prepared anaerobically, then air-oxidized for 3 days to induce precipitation. At low Si concentrations, magnetite formed; near silica saturation, lepidocrocite and ferrihydrite formed. The Si isotope fractionation factor for coprecipitation was within the range of ɛ observed for adsorption (ɛ = -2.3 ± 1.0‰). These results indicate that the mechanism of Fe-Si interaction affects ɛ, presumably due to varying silicate coordination environments. These isotopic

  2. Iron toxicity in yeast.

    Science.gov (United States)

    Wiśnicka, R; Krzepiłko, A; Wawryn, J; Biliński, T

    1997-01-01

    It has been found that yeast cells are sensitive to iron overload only when grown on glucose as a carbon source. Effective concentration of ferrous iron is much higher than that found in natural environments. Effects of ferrous iron are strictly oxygen dependent, what suggest that the formation of hydroxyl radicals in the Fenton reaction is a cause of the toxicity. Respiratory deficiency and pretreatment of cells with antimycin A prevent toxic effects in the late exponential phase of growth, whereas uncouplers and 2mM magnesium salts completely protect even the most vulnerable exponential cells. Generally, toxic effects correlate with the ability of cells to take up this metal. The results presented suggest that during ferrous iron overload iron is transported through the unspecific divalent cation uptake system which is known in fungi. The data suggest that recently described high and low affinity systems of iron uptake in yeast are the only source of iron in natural environments. PMID:9516981

  3. Application of Moessbauer spectroscopy to the study of tannins inhibition of iron and steel corrosion

    Energy Technology Data Exchange (ETDEWEB)

    Jaen, Juan A., E-mail: jjaen@ancon.up.ac.pa [Universidad de Panama, CITEN, Depto. de Quimica Fisica (Panama); Obaldia, J. De; Rodriguez, M. V. [Universidad de Panama, Escuela de Quimica, Facultad de Ciencias Naturales, Exactas y Tecnologia (Panama)

    2011-11-15

    The inhibitory effect of tannins was investigated using, among others, potentiodynamic polarizations and Moessbauer spectroscopy. These techniques confirmed that the nature, pH and concentration of tannic solution are of upmost importance in the inhibitory properties of the solutions. It is observed that at low tannin concentration or pH, both, hydrolizable and condensed tannins, effectively inhibit iron corrosion, due to the redox properties of tannins. At pH Almost-Equal-To 0, Moessbauer spectra of the frozen aqueous solutions of iron(III) with the tannin solutions showed that iron is in the form of a monomeric species [Fe(H{sub 2}O){sub 6}]{sup 3 + }, without coordination with the functional hydroxyl groups of the tannins. The suspended material consisted of amorphous ferric oxide and oxyhydroxides, though with quebracho tannin partly resulted in complex formation and in an iron (II) species from a redox process. Other tannins, such as chestnut hydrolysable tannins, do not complex iron at this low pH. Tannins react at high concentrations or pH (3 and 5) to form insoluble blue-black amorphous complexes of mono-and bis-type tannate complexes, with a relative amount of the bis-ferric tannate generally increasing with pH. Some Fe{sup 2 + } in the form of hydrated polymeric ferrous tannate could be obtained. At pH 7, a partially hydrolyzed ferric tannate complex was also formed. The latter two phases do not provide corrosion protection. Tannin solutions at natural pH react with electrodeposited iron films (approx. 6 {mu}m) to obtain products consisting only on the catecholate mono-complex of ferric tannate. Some aspects of the mechanism of tannins protection against corrosion are discussed.

  4. Characterisation by Moessbauer Spectroscopy of the Forms of Iron in Sulfide-Rich Fulvic Acid Solutions

    International Nuclear Information System (INIS)

    Variations in the nature of the bonding between iron and fulvic acid as a function of pH in sulfide-rich solutions have been investigated by 57Fe Moessbauer spectroscopy. In all solutions iron was enriched to 95% in the 57Fe isotope and ratios of Fe : fulvic acid were maintained at 1 : 100 on a weight basis for all measurements. When the pH was decreased below 5.0, there was a progressive change in the composition of the spectra, which contained three distinct components that were similar to those seen in the absence of sulfide; i.e., a sextet from magnetically-dilute Fe(III) and doublets from Fe(II) and Fe(III). There was, however, a higher proportion of the iron as Fe(II) in the sulfide-containing solutions and this represented the only form of iron at very low pH. Establishment of equilibria was slow as evidenced by considerable hysteresis between the compositions of the solutions with decreasing and increasing pHs. On increasing the pH, sulfide prevented the formation of magnetically dilute Fe(III) species and instead, in the range 3.5-6.0, compounds were generated with parameters consistent with sulfur being coordinated to the iron. One had parameters similar to those of pyrite and hence probably contains disulfide (S22-) units, whilst a second, with poorly defined magnetic hyperfine splitting, may contain monosulfide (S2-) units, with structures related to either pyrrhotite (Fe1-xS) or greigite (Fe3S4). A third component probably corresponds to a mononuclear low spin Fe(II) complex, involving sulfur and fulvic acid in the iron coordination sphere. These species were oxygen-sensitive and decomposed to yield magnetically dilute Fe(III) complexes and Fe(III) oxyhydroxides on aeration of the solutions.

  5. Characterisation by Moessbauer Spectroscopy of the Forms of Iron in Sulfide-Rich Fulvic Acid Solutions

    Energy Technology Data Exchange (ETDEWEB)

    Goodman, B. A., E-mail: bgoodm@scri.sari.ac.uk [Scottish Crop Research Institute, Invergowrie (United Kingdom); Cheshire, M. V. [Macaulay Land Use Research Institute, Craigiebuckler (United Kingdom)

    2002-09-15

    Variations in the nature of the bonding between iron and fulvic acid as a function of pH in sulfide-rich solutions have been investigated by {sup 57}Fe Moessbauer spectroscopy. In all solutions iron was enriched to 95% in the {sup 57}Fe isotope and ratios of Fe : fulvic acid were maintained at 1 : 100 on a weight basis for all measurements. When the pH was decreased below 5.0, there was a progressive change in the composition of the spectra, which contained three distinct components that were similar to those seen in the absence of sulfide; i.e., a sextet from magnetically-dilute Fe(III) and doublets from Fe(II) and Fe(III). There was, however, a higher proportion of the iron as Fe(II) in the sulfide-containing solutions and this represented the only form of iron at very low pH. Establishment of equilibria was slow as evidenced by considerable hysteresis between the compositions of the solutions with decreasing and increasing pHs. On increasing the pH, sulfide prevented the formation of magnetically dilute Fe(III) species and instead, in the range 3.5-6.0, compounds were generated with parameters consistent with sulfur being coordinated to the iron. One had parameters similar to those of pyrite and hence probably contains disulfide (S{sub 2}{sup 2-}) units, whilst a second, with poorly defined magnetic hyperfine splitting, may contain monosulfide (S{sup 2-}) units, with structures related to either pyrrhotite (Fe{sub 1-x}S) or greigite (Fe{sub 3}S{sub 4}). A third component probably corresponds to a mononuclear low spin Fe(II) complex, involving sulfur and fulvic acid in the iron coordination sphere. These species were oxygen-sensitive and decomposed to yield magnetically dilute Fe(III) complexes and Fe(III) oxyhydroxides on aeration of the solutions.

  6. A Holocene record of endogenic iron and manganese precipitation, isotopic composition of endogenic carbonate, and vegetation history in a lake-fen complex in northwestern Minnesota

    Science.gov (United States)

    Dean, Walter E.; Doner, Lisa A.

    2011-01-01

    Little Shingobee Lake and Fen are part of an extensive network of lakes and wetlands in the Shingobee River headwaters area of northwestern Minnesota. Prior to about 9800 radiocarbon years, most of the lakes in the Shingobee watershed area were interconnected to form glacial Lake Willobee. From 9800 to 7700 radiocarbon years, the level of Lake Willobee fell as a result of breaching of a dam, leaving small separated basins containing the existing lakes and wetlands. The dominant components in the sediments in a 9-meter core from Little Shingobee Lake (LSL-B), and lacustrine sediments under 3.3 meters of peat in a 17-meter core from Little Shingobee Fen (LSF-10) are detrital clastic material, endogenic CaCO3, and organic matter. The detrital fraction in the Holocene section in core LSL-B varies considerably from 7 weight percent to 82 weight percent and closely parallels the concentration of detrital quartz measured by X-ray diffraction. The CaCO3 concentration, which also varies considerably from 10 weight percent to 70 weight percent, is generally antithetic to the detrital concentration owing to the dilution of detrital material by CaCO3, particularly during the early to middle Holocene (about 9000-6500 calendar years). The organic-matter content varies from 5 weight percent to 25 weight percent and, together with CaCO3, serves to dilute the allogenic detrital fraction. In both cores almost all of the iron (Fe) and manganese (Mn) is in endogenic minerals, presumed to be oxyhydroxide minerals, that are important components throughout the core; little Fe and Mn are contributed by detrital aluminosilicate minerals. The endogenic Fe mineral, calculated as Fe(OH)3, forms a larger percentage of the sediment than endogenic organic material throughout most of the Holocene section in the LSL-B core and in the lacustrine sediments below the peat in the LSF-10 core. Biogenic silica as opal (biopal; diatom debris) was not measured, but the average calculated biopal is 5

  7. Characterization of lacustrine iron sulfide particles with proton-induced X-ray emission

    International Nuclear Information System (INIS)

    Black particles, collected by filtration (1.2-μ pore size) from the anoxic waters of a soft-water lake, were examined by a scanning proton microprobe which permitted quantitative elemental analysis by proton-induced X-ray emission (PIXE) and Rutherford backscattering (RBS). There was a uniform distribution of sulfur across the filter, but Fe, and to a lesser extent, Mn, was localized in ∼5-μm diameter clusters. Elemental analysis with 1-μm-diameter beams revealed that the Fe clusters were mainly comprised of iron oxides. Iron sulfide material not in the Fe clusters had stoichiometric proportions of Fe1.0S0.60P0.60Ca0.24K0.14. Although a purely biogenic origin for P, Ca, and K cannot be ruled out, the composition is consistent with the particles originating as authigenic iron oxides which react with sulfide as they sink through the water column. The iron sulfide particles are richer in Cu (4,000 ppm) and Zn (6,000 ppm) than the iron oxides, suggesting that these elements are also concentrated as their insoluble sulfides. The coexistence of iron oxides and sulfides indicates that either the supply of sulfide is limiting or that some iron oxide particles are unreactive. 20 refs., 2 figs., 1 tab

  8. Effects of iron on arsenic speciation and redox chemistry in acid mine water

    Science.gov (United States)

    Bednar, A.J.; Garbarino, J.R.; Ranville, J.F.; Wildeman, T.R.

    2005-01-01

    Concern about arsenic is increasing throughout the world, including areas of the United States. Elevated levels of arsenic above current drinking-water regulations in ground and surface water can be the result of purely natural phenomena, but often are due to anthropogenic activities, such as mining and agriculture. The current study correlates arsenic speciation in acid mine drainage and mining-influenced water with the important water-chemistry properties Eh, pH, and iron(III) concentration. The results show that arsenic speciation is generally in equilibrium with iron chemistry in low pH AMD, which is often not the case in other natural-water matrices. High pH mine waters and groundwater do not always hold to the redox predictions as well as low pH AMD samples. The oxidation and precipitation of oxyhydroxides deplete iron from some systems, and also affect arsenite and arsenate concentrations through sorption processes. ?? 2004 Elsevier B.V. All rights reserved.

  9. Surface Interrogation Scanning Electrochemical Microscopy of Ni(1-x)Fe(x)OOH (0 < x < 0.27) Oxygen Evolving Catalyst: Kinetics of the "fast" Iron Sites.

    Science.gov (United States)

    Ahn, Hyun S; Bard, Allen J

    2016-01-13

    Nickel-iron mixed metal oxyhydroxides have attracted significant attention as an oxygen evolution reaction (OER) catalyst for solar fuel renewable energy applications. Here, we performed surface-selective and time-dependent redox titrations to directly measure the surface OER kinetics of Ni(IV) and Fe(IV) in NiOOH, FeOOH, and Ni(1-x)Fe(x)OOH (0 electrodes. Most importantly, two types of surface sites exhibiting "fast" and "slow" kinetics were found, where the fraction of "fast" sites in Ni(1-x)Fe(x)OOH matched the iron atom content in the film. This finding provides experimental support to the theory-proposed model of active sites in Ni(1-x)Fe(x)OOH. The OER rate constant of the "fast" site was 1.70 s(-1) per atom. PMID:26645678

  10. Distinguishing and understanding thermogenic and biogenic sources of methane using multiply substituted isotopologues

    Science.gov (United States)

    Stolper, D. A.; Martini, A. M.; Clog, M.; Douglas, P. M.; Shusta, S. S.; Valentine, D. L.; Sessions, A. L.; Eiler, J. M.

    2015-07-01

    Sources of methane to sedimentary environments are commonly identified and quantified using the stable isotopic compositions of methane. The methane "clumped-isotope geothermometer", based on the measurement of multiply substituted methane isotopologues (13CH3D and 12CH2D2), shows promise in adding new constraints to the sources and formational environments of both biogenic and thermogenic methane. However, questions remain about how this geothermometer behaves in systems with mixtures of biogenic and thermogenic gases and different biogenic environments. We have applied the methane clumped-isotope thermometer to a mixed biogenic-thermogenic system (Antrim Shale, USA) and to biogenic gas from gas seeps (Santa Barbara and Santa Monica Basin, USA), a pond on the Caltech campus, and methanogens grown in pure culture. We demonstrate that clumped-isotope based temperatures add new quantitative constraints to the relative amounts of biogenic vs. thermogenic gases in the Antrim Shale indicating a larger proportion (∼50%) of thermogenic gas in the system than previously thought. Additionally, we find that the clumped-isotope temperature of biogenic methane appears related to the environmental settings in which the gas forms. In systems where methane generation rates appear to be slow (e.g., the Antrim Shale and gas seeps), microbial methane forms in or near both internal isotopic equilibrium and hydrogen-isotope equilibrium with environmental waters. In systems where methane forms rapidly, microbial methane is neither in internal isotopic equilibrium nor hydrogen-isotope equilibrium with environmental waters. A quantitative model of microbial methanogenesis that incorporates isotopes is proposed to explain these results.

  11. An approach for verifying biogenic greenhouse gas emissions inventories with atmospheric CO2 concentration data

    International Nuclear Information System (INIS)

    Verifying national greenhouse gas (GHG) emissions inventories is a critical step to ensure that reported emissions data to the United Nations Framework Convention on Climate Change (UNFCCC) are accurate and representative of a country’s contribution to GHG concentrations in the atmosphere. Furthermore, verifying biogenic fluxes provides a check on estimated emissions associated with managing lands for carbon sequestration and other activities, which often have large uncertainties. We report here on the challenges and results associated with a case study using atmospheric measurements of CO2 concentrations and inverse modeling to verify nationally-reported biogenic CO2 emissions. The biogenic CO2 emissions inventory was compiled for the Mid-Continent region of United States based on methods and data used by the US government for reporting to the UNFCCC, along with additional sources and sinks to produce a full carbon balance. The biogenic emissions inventory produced an estimated flux of −408 ± 136 Tg CO2 for the entire study region, which was not statistically different from the biogenic flux of −478 ± 146 Tg CO2 that was estimated using the atmospheric CO2 concentration data. At sub-regional scales, the spatial density of atmospheric observations did not appear sufficient to verify emissions in general. However, a difference between the inventory and inversion results was found in one isolated area of West-central Wisconsin. This part of the region is dominated by forestlands, suggesting that further investigation may be warranted into the forest C stock or harvested wood product data from this portion of the study area. The results suggest that observations of atmospheric CO2 concentration data and inverse modeling could be used to verify biogenic emissions, and provide more confidence in biogenic GHG emissions reporting to the UNFCCC. (letter)

  12. Corrosion of iron: A study for radioactive waste canisters

    Science.gov (United States)

    Lagha, S. Ben; Crusset, D.; Mabille, I.; Tran, M.; Bernard, M. C.; Sutter, E.

    2007-05-01

    The purpose of this study is to examine the risks of atmospheric corrosion of steel waste canisters following their deep geological disposal in the temperature range from 303 to 363 K. The work was performed using iron samples deposited as thin films on a quartz crystal microbalance (QCM) and disposed in a climatic chamber. The experiments showed that, in the temperature under study (298-363 K), the mass increase due to the formation of oxide/hydroxide rose sharply above 70% RH, as is commonly observed at room temperatures, indicating that the phenomenon remains electrochemical in nature. Ex situ Raman spectrometric analyses indicate the formation of magnetite, maghemite and oxyhydroxides species in the 298-363 K temperature range, and for oxygen contents above 1 vol.%, whereas only Fe3O4 and γ-Fe2O3 are detected at 363 K. In this work, the kinetics of the rust growth is discussed, on the bases of the rate of mass increase and of the composition of the rust, as a function of the climatic parameters and the oxygen content of the atmosphere.

  13. Microbial iron cycling in acidic geothermal springs of Yellowstone National Park: Integrating molecular surveys, geochemical processes and isolation of novel Fe-active microorganisms

    Directory of Open Access Journals (Sweden)

    Mark A Kozubal

    2012-03-01

    Full Text Available Geochemical, molecular, and physiological analyses of microbial isolates were combined to study the geomicrobiology of acidic iron oxide mats in Yellowstone National Park (YNP. Nineteen sampling locations from 11 geothermal springs were studied ranging in temperature from 53 to 84 °C and pH 2.4 to 3.6. All iron-oxide mats exhibited high diversity of crenarchaeal sequences from the Sulfolobales, Thermoproteales, and Desulfurococcales. The predominant Sulfolobales sequences were highly similar to Metallosphaera yellowstonensis str. MK1, previously isolated from one of these sites. Other groups of archaea were consistently associated with different types of iron oxide mats, including undescribed members of the phyla Thaumarchaeota and Euryarchaeota. Bacterial sequences were dominated by relatives of Hydrogenobaculum spp. above 65-70 °C, but increased in diversity below 60 °C. Cultivation of relevant iron-oxidizing and iron-reducing microbial isolates included Sulfolobus str. MK3, Sulfobacillus str. MK2, Acidicaldus str. MK6, and a new candidate genus in the Sulfolobales referred to as Sulfolobales str. MK5. Strains MK3 and MK5 are capable of oxidizing ferrous iron autotrophically, while strain MK2 oxidizes iron mixotrophically. Similar rates of iron oxidation were observed for M. yellowstonensis str. MK1 and Sulfolobales str. MK5 cultures, and these rates are close to those measured in situ. Biomineralized phases of ferric iron varied among cultures and field sites, and included ferric oxyhydroxides, K-jarosite, goethite, hematite, and scorodite depending on geochemical conditions. Strains MK5 and MK6 are capable of reducing ferric iron under anaerobic conditions with complex carbon sources. The combination of geochemical and molecular data as well as physiological observations of isolates suggests that the community structure of acidic Fe mats is linked with Fe cycling across temperatures ranging from 53 to 88 oC.

  14. Biogenic carbon fluxes from global agricultural production and consumption

    Energy Technology Data Exchange (ETDEWEB)

    Wolf, Julie; West, Tristram O.; Le Page, Yannick LB; Kyle, G. Page; Zhang, Xuesong; Collatz, George; Imhoff, Marc L.

    2015-10-01

    Quantification of biogenic carbon fluxes from agricultural lands is needed to generate comprehensive bottom-up estimates of net carbon exchange for global and regional carbon monitoring. We estimated global agricultural carbon fluxes associated with annual crop net primary production (NPP), harvested biomass, and consumption of biomass by humans and livestock. These estimates were combined for a single estimate of net carbon exchange (NCE) and spatially distributed to 0.05 degree resolution using MODIS satellite land cover data. Global crop NPP in 2011 was estimated at 5.25 ± 0.46 Pg C yr-1, of which 2.05 ± 0.05 Pg C yr-1 was harvested and 0.54 Pg C yr-1 was collected from crop residues for livestock fodder. Total livestock feed intake in 2011 was 2.42 ± 0.21 Pg C yr-1, of which 2.31 ± 0.21 Pg C yr-1 was emitted as CO2, 0.07 ± 0.01 Pg C yr-1 was emitted as CH4, and 0.04 Pg C yr-1 was contained within milk and egg production. Livestock grazed an estimated 1.27 Pg C yr-1 in 2011, which constituted 52.4% of total feed intake. Global human food intake was 0.57 ± 0.03 Pg C yr-1 in 2011, the majority of which is respired as CO2. Completed global cropland carbon budgets accounted for the ultimate use of ca. 80% of harvested biomass. The spatial distribution of these fluxes may be used for global carbon monitoring, estimation of regional uncertainty, and for use as input to Earth system models.

  15. Historical anthropogenic radiative forcing of changes in biogenic secondary aerosol

    Science.gov (United States)

    Acosta Navarro, Juan; D'Andrea, Stephen; Pierce, Jeffrey; Ekman, Annica; Struthers, Hamish; Zorita, Eduardo; Guenther, Alex; Arneth, Almut; Smolander, Sampo; Kaplan, Jed; Farina, Salvatore; Scott, Catherine; Rap, Alexandru; Farmer, Delphine; Spracklen, Domink; Riipinen, Ilona

    2016-04-01

    Human activities have lead to changes in the energy balance of the Earth and the global climate. Changes in atmospheric aerosols are the second largest contributor to climate change after greenhouse gases since 1750 A.D. Land-use practices and other environmental drivers have caused changes in the emission of biogenic volatile organic compounds (BVOCs) and secondary organic aerosol (SOA) well before 1750 A.D, possibly causing climate effects through aerosol-radiation and aerosol-cloud interactions. Two numerical emission models LPJ-GUESS and MEGAN were used to quantify the changes in aerosol forming BVOC emissions in the past millennium. A chemical transport model of the atmosphere (GEOS-Chem-TOMAS) was driven with those BVOC emissions to quantify the effects on radiation caused by millennial changes in SOA. We found that global isoprene emissions decreased after 1800 A.D. by about 12% - 15%. This decrease was dominated by losses of natural vegetation, whereas monoterpene and sesquiterpene emissions increased by about 2% - 10%, driven mostly by rising surface air temperatures. From 1000 A.D. to 1800 A.D, isoprene, monoterpene and sesquiterpene emissions decline by 3% - 8% driven by both, natural vegetation losses, and the moderate global cooling between the medieval climate anomaly and the little ice age. The millennial reduction in BVOC emissions lead to a 0.5% to 2% reduction in climatically relevant aerosol particles (> 80 nm) and cause a direct radiative forcing between +0.02 W/m² and +0.07 W/m², and an indirect radiative forcing between -0.02 W/m² and +0.02 W/m².

  16. Biogenic Carbon on Mars: A Subsurface Chauvinistic Viewpoint

    Science.gov (United States)

    Onstott, T. C.; Lau, C. Y. M.; Magnabosco, C.; Harris, R.; Chen, Y.; Slater, G.; Sherwood Lollar, B.; Kieft, T. L.; van Heerden, E.; Borgonie, G.; Dong, H.

    2015-12-01

    A review of 150 publications on the subsurface microbiology of the continental subsurface provides ~1,400 measurements of cellular abundances down to 4,800 meter depth. These data suggest that the continental subsurface biomass is comprised of ~1016-17 grams of carbon, which is higher than the most recent estimates of ~1015 grams of carbon (1 Gt) for the marine deep biosphere. If life developed early in Martian history and Mars sustained an active hydrological cycle during its first 500 million years, then is it possible that Mars could have developed a subsurface biomass of comparable size to that of Earth? Such a biomass would comprise a much larger fraction of the total known Martian carbon budget than does the subsurface biomass on Earth. More importantly could a remnant of this subsurface biosphere survive to the present day? To determine how sustainable subsurface life could be in isolation from the surface we have been studying subsurface fracture fluids from the Precambrian Shields in South Africa and Canada. In these environments the energetically efficient and deeply rooted acetyl-CoA pathway for carbon fixation plays a central role for chemolithoautotrophic primary producers that form the base of the biomass pyramid. These primary producers appear to be sustained indefinitely by H2 generated through serpentinization and radiolytic reactions. Carbon isotope data suggest that in some subsurface locations a much larger population of secondary consumers are sustained by the primary production of biogenic CH4 from a much smaller population of methanogens. These inverted biomass and energy pyramids sustained by the cycling of CH4 could have been and could still be active on Mars. The C and H isotopic signatures of Martian CH4 remain key tools in identifying potential signatures of an extant Martian biosphere. Based upon our results to date cavity ring-down spectroscopic technologies provide an option for making these measurements on future rover missions.

  17. Biogenic silver nanoparticles: efficient and effective antifungal agents

    Science.gov (United States)

    Netala, Vasudeva Reddy; Kotakadi, Venkata Subbaiah; Domdi, Latha; Gaddam, Susmila Aparna; Bobbu, Pushpalatha; Venkata, Sucharitha K.; Ghosh, Sukhendu Bikash; Tartte, Vijaya

    2016-04-01

    Biogenic synthesis of silver nanoparticles (AgNPs) by exploiting various plant materials is an emerging field and considered green nanotechnology as it involves simple, cost effective and ecofriendly procedure. In the present study AgNPs were successfully synthesized using aqueous callus extract of Gymnema sylvestre. The aqueous callus extract treated with 1nM silver nitrate solution resulted in the formation of AgNPs and the surface plasmon resonance (SPR) of the formed AgNPs showed a peak at 437 nm in the UV Visible spectrum. The synthesized AgNPs were characterized using Fourier transform infrared spectroscopy (FTIR), Transmission electron microscopy (TEM), and X-ray diffraction spectroscopy (XRD). FTIR spectra showed the peaks at 3333, 2928, 2361, 1600, 1357 and 1028 cm-1 which revealed the role of different functional groups possibly involved in the synthesis and stabilization of AgNPs. TEM micrograph clearly revealed the size of the AgNPs to be in the range of 3-30 nm with spherical shape and poly-dispersed nature; it is further confirmed by Particle size analysis that the stability of AgNPs is due its high negative Zeta potential (-36.1 mV). XRD pattern revealed the crystal nature of the AgNPs by showing the braggs peaks corresponding to (111), (200), (220) and (311) planes of face-centered cubic crystal phase of silver. Selected area electron diffraction pattern showed diffraction rings and confirmed the crystalline nature of synthesized AgNPs. The synthesized AgNPs exhibited effective antifungal activity against Candida albicans, Candida nonalbicans and Candida tropicalis.

  18. Emissions of biogenic volatile organic compounds & their photochemical transformation

    Science.gov (United States)

    Yu, Zhujun; Hohaus, Thorsten; Tillmann, Ralf; Andres, Stefanie; Kuhn, Uwe; Rohrer, Franz; Wahner, Andreas; Kiendler-Scharr, Astrid

    2015-04-01

    Natural and anthropogenic activities emit volatile organic compounds (VOC) into the atmosphere. While it is known that land vegetation accounts for 90% of the global VOC emissions, only a few molecules' emission factors are understood. Through VOCs atmospheric oxidation intermediate products are formed. The detailed chemical mechanisms involved are insufficiently known to date and need to be understood for air quality management and climate change predictions. In an experiment using a PTR-ToF-MS with the new-built plant chamber SAPHIR-PLUS in Forschungszentrum Juelich, biogenic emissions of volatile organic compounds (BVOC) from Quercus ilex trees were measured. The BVOC emissions were dominated by monoterpenes, minor emissions of isoprene and methanol were also observed with the overall emission pattern typical for Quercus ilex trees in the growing season. Monoterpenes and isoprene emissions showed to be triggered by light. Additionally, their emissions showed clear exponential temperature dependence under constant light condition as reported in literature. As a tracer for leaf growth, methanol emission showed an abrupt increase at the beginning of light exposure. This is explained as instantaneous release of methanol produced during the night once stomata of leaves open upon light exposure. Emission of methanol showed a near linear increase with temperature in the range of 10 to 35 °C. BVOC were transferred from the plant chamber PLUS to the atmospheric simulation chamber SAPHIR, where their oxidation products from O3 oxidation were measured with PTR-ToF-MS. Gas phase oxidation products such as acetone and acetaldehyde were detected. A quantitative analysis of the data will be presented, including comparison of observations to the Master Chemical Mechanism model.

  19. Iron ochre – a pre-catalyst for the cracking of methane

    Science.gov (United States)

    Alharthi, Abdulrahman; Blackley, Ross A; Flowers, T Hugh; Hargreaves, Justin S J; Pulford, Ian D; Wigzell, James; Zhou, Wuzong

    2014-01-01

    BACKGROUND Iron ochres are gelatinous sludges that can cause problems in terms of water management. In this work, the application of iron ochre obtained from a river has been applied to catalytically crack methane – another potential waste product – into two useful products, hydrogen and a magnetic carbon-containing composite. RESULTS The powder X-ray diffraction (XRD) pattern of the iron ochre was found to be consistent with the expected 2-line ferrihydrite, and energy dispersive X-ray (EDX) analysis showed Fe to be a major component although some Si and Ca were present. The sample was observed to contain a fraction with a tubular morphology consistent with the presence of extra-cellular biogenic iron oxide formed by leptothrix. Upon exposure to methane at elevated temperatures, the material was found to transform into an active catalyst for hydrogen production yielding a magnetic carbon-containing composite material comprising filamentous carbon and encapsulating graphite. CONCLUSION The application of two waste products – iron ochre and methane – to generate two useful products – hydrogen and a magnetic carbon-containing composite – has been demonstrated. Furthermore, the ochre has been shown to comprise tubular morphology extra-cellular biogenic iron oxide which may be of interest in terms of other applications. © 2014 The Authors. Journal of Chemical Technology & Biotechnology published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry. PMID:25558121

  20. Colour Metallography of Cast Iron

    Institute of Scientific and Technical Information of China (English)

    Zhou Jiyang; Liu Jincheng

    2010-01-01

    @@ Chapter 3 Spheroidal Graphite Cast Iron(I) Spheroidal Graphite Cast Iron, SG iron in short, refers to the cast iron in which graphite precipitates as spheroidal shape during solidification of liquid iron. The graphite in common commercial cast iron can only be changed from flake to spheroidal shape by spheroidising treatment. Since spheroidal graphite reduces the cutting effect of stress concentration, the metal matrix strength of SG iron can be applied around 70%-90%, thus the mechanical property of SG iron is significantly superior to other cast irons;even the tensile strength of SG iron is higher than that carbon steel.

  1. Colour Metallography of Cast Iron

    Institute of Scientific and Technical Information of China (English)

    Zhou Jiyang; Liu Jincheng

    2010-01-01

    @@ Spheroidal Graphite Cast Iron(Ⅳ) 3.7 Segregation of SG iron The non-uniform distribution of solute elements during solidification results in the micro segregation of SG iron.As for the redistribution of elements in the phases of the solidification structure,there is no intrinsic difference between SG iron and grey iron[132].

  2. Iron regulation by hepcidin

    OpenAIRE

    Zhao, Ningning; Zhang, An-Sheng; Enns, Caroline A

    2013-01-01

    Hepcidin is a key hormone that is involved in the control of iron homeostasis in the body. Physiologically, hepcidin is controlled by iron stores, inflammation, hypoxia, and erythropoiesis. The regulation of hepcidin expression by iron is a complex process that requires the coordination of multiple proteins, including hemojuvelin, bone morphogenetic protein 6 (BMP6), hereditary hemochromatosis protein, transferrin receptor 2, matriptase-2, neogenin, BMP receptors, and transferrin. Misregulati...

  3. Iron deficiency anemia Review

    OpenAIRE

    Yıldız, İnci

    2009-01-01

    Iron deficiency anemia is the most frequent and widespread anemia around the world Its prevalence is increased in infants and adolescent girls The etiologic factors may vary but anemia is essentially related to iron deficient nutrition blood loss and malabsorption Children may have paleness cardiovascular and neurologic impacts of anemia pica epithelial changes as koilonychia glossitis angular stomatitis Treatment is by oral or parenteral supplementation of iron Turk Arch Ped 2009; 44 Suppl: ...

  4. Temperature-dependent accumulation mode particle and cloud nuclei concentrations from biogenic sources during WACS 2010

    Directory of Open Access Journals (Sweden)

    L. Ahlm

    2012-10-01

    Full Text Available Submicron aerosol particles collected simultaneously at the mountain peak (2182 m a.s.l. and at a forested mid-mountain site (1300 m a.s.l. on Whistler Mountain, British Columbia, Canada, during June and July 2010 were analyzed by Fourier transform infrared (FTIR spectroscopy for quantification of organic functional groups. Positive matrix factorization (PMF was applied to the FTIR spectra. Three PMF factors associated with (1 combustion, (2 biogenics, and (3 vegetative detritus, were identified at both sites. The biogenic factor was correlated with both temperature and several volatile organic compounds (VOCs. The combustion factor dominated the submicron particle mass during the beginning of the campaign when the temperature was lower and advection was from the Vancouver area, but as the temperature started to rise in early July the biogenic factor came to dominate as a result of increased emissions of biogenic VOCs and thereby increased formation of secondary organic aerosol (SOA. On average, the biogenic factor represented 69% and 49% of the submicron organic particle mass at Whistler Peak and at the mid-mountain site, respectively. The lower fraction at the mid-mountain site was a result of more vegetative detritus there, and also higher influence from local combustion sources.

    The biogenic factor was strongly correlated (r ~ 0.9 to number concentration of particles with diameter (Dp> 100 nm, whereas the combustion factor was better correlated to number concentration of particles with Dp < 100 nm (r~ 0.4. The number concentration of cloud condensation nuclei (CCN was correlated (r ~ 0.7 to the biogenic factor for supersaturations (S of 0.2% or higher, which indicates that particle condensational growth from biogenic vapors was an important factor in controlling the CCN concentration for clouds where S≥0.2%. Both the number concentration of particles with

  5. Temperature-dependent accumulation mode particle and cloud nuclei concentrations from biogenic sources during WACS 2010

    Directory of Open Access Journals (Sweden)

    L. Ahlm

    2013-03-01

    Full Text Available Submicron aerosol particles collected simultaneously at the mountain peak (2182 m a.s.l. and at a forested mid-mountain site (1300 m a.s.l. on Whistler Mountain, British Columbia, Canada, during June and July 2010 were analyzed by Fourier transform infrared (FTIR spectroscopy for quantification of organic functional groups. Positive matrix factorization (PMF was applied to the FTIR spectra. Three PMF factors associated with (1 combustion, (2 biogenics, and (3 vegetative detritus were identified at both sites. The biogenic factor was correlated with both temperature and several volatile organic compounds (VOCs. The combustion factor dominated the submicron particle mass during the beginning of the campaign, when the temperature was lower and advection was from the Vancouver area, but as the temperature started to rise in early July, the biogenic factor came to dominate as a result of increased emissions of biogenic VOCs, and thereby increased formation of secondary organic aerosol (SOA. On average, the biogenic factor represented 69% and 49% of the submicron organic particle mass at Whistler Peak and at the mid-mountain site, respectively. The lower fraction at the mid-mountain site was a result of more vegetative detritus there, and also higher influence from local combustion sources. The biogenic factor was strongly correlated (r~0.9 to number concentration of particles with diameter (Dp> 100 nm, whereas the combustion factor was better correlated to number concentration of particles with Dpr~0.4. The number concentration of cloud condensation nuclei (CCN was correlated (r~0.7 to the biogenic factor for supersaturations (S of 0.2% or higher, which indicates that particle condensational growth from biogenic vapors was an important factor in controlling the CCN concentration for clouds where S≥0.2%. Both the number concentration of particles with Dp>100 nm and numbers of CCN for S≥0.2% were correlated to temperature. Considering the biogenic

  6. Iron overload and immunity

    Institute of Scientific and Technical Information of China (English)

    Gra(c)a Porto; Maria De Sousa

    2007-01-01

    Progress in the characterization of genes involved in the control of iron homeostasis in humans and in mice has improved the definition of iron overload and of the cells affected by it. The cell involved in iron overload with the greatest effect on immunity is the macrophage.Intriguing evidence has emerged, however, in the last 12 years indicating that parenchymal iron overload is linked to genes classically associated with the immune system. This review offers an update of the genes and proteins relevant to iron metabolism expressed in cells of the innate immune system, and addresses the question of how this system is affected in clinical situations of iron overload. The relationship between iron and the major cells of adaptive immunity, the T lymphocytes,will also be reviewed. Most studies addressing this last question in humans were performed in the clinical model of Hereditary Hemochromatosis. Data will also be reviewed demonstrating how the disruption of molecules essentially involved in adaptive immune responses result in the spontaneous development of iron overload and how they act as modifiers of iron overload.

  7. Recalling the Iron Girls

    Institute of Scientific and Technical Information of China (English)

    1998-01-01

    The phrase "iron girl" is symbolic of an era. Widely used in the 1960s and the early 1970s, it was a term that described women who, in the spirit of sexual equality, found in themselves a physical strength that surpassed their psychologi cal expectations. With their might and power, they proved to society that women could do everything that men could. The title of "iron girl" was their pride.The well-known writer Fan Xiaoqing, was one such iron girl. She says the "iron girls" were nothing less than a quest for perfection.

  8. Iron metabolism and iron supplementation in cancer patients.

    Science.gov (United States)

    Ludwig, Heinz; Evstatiev, Rayko; Kornek, Gabriela; Aapro, Matti; Bauernhofer, Thomas; Buxhofer-Ausch, Veronika; Fridrik, Michael; Geissler, Dietmar; Geissler, Klaus; Gisslinger, Heinz; Koller, Elisabeth; Kopetzky, Gerhard; Lang, Alois; Rumpold, Holger; Steurer, Michael; Kamali, Houman; Link, Hartmut

    2015-12-01

    Iron deficiency and iron deficiency-associated anemia are common complications in cancer patients. Most iron deficient cancer patients present with functional iron deficiency (FID), a status with adequate storage iron, but insufficient iron supply for erythroblasts and other iron dependent tissues. FID is the consequence of the cancer-associated cytokine release, while in absolute iron deficiency iron stores are depleted resulting in similar but often more severe symptoms of insufficient iron supply. Here we present a short review on the epidemiology, pathophysiology, diagnosis, clinical symptoms, and treatment of iron deficiency in cancer patients. Special emphasis is given to intravenous iron supplementation and on the benefits and limitations of different formulations. Based on these considerations and recommendations from current international guidelines we developed recommendations for clinical practice and classified the level of evidence and grade of recommendation according to the principles of evidence-based medicine. PMID:26373748

  9. Characterization of Highly Oxidized Molecules in Fresh and Aged Biogenic Secondary Organic Aerosol.

    Science.gov (United States)

    Tu, Peijun; Hall, Wiley A; Johnston, Murray V

    2016-04-19

    In this work, highly oxidized multifunctional molecules (HOMs) in fresh and aged secondary organic aerosol (SOA) derived from biogenic precursors are characterized with high-resolution mass spectrometry. Fresh SOA was generated by mixing ozone with a biogenic precursor (β-pinene, limonene, α-pinene) in a flow tube reactor. Aging was performed by passing the fresh SOA through a photochemical reactor where it reacted with hydroxyl radicals. Although these aerosols were as a whole not highly oxidized, molecular analysis identified a significant number of HOMs embedded within it. HOMs in fresh SOA consisted mostly of monomers and dimers, which is consistent with condensation of extremely low-volatility organic compounds (ELVOCs) that have been detected in the gas phase in previous studies and linked to SOA particle formation. Aging caused an increase in the average number of carbon atoms per molecule of the HOMs, which is consistent with particle phase oxidation of (less oxidized) oligomers already existing in fresh SOA. HOMs having different combinations of oxygen-to-carbon ratio, hydrogen-to-carbon ratio and average carbon oxidation state are discussed and compared to low volatility oxygenated organic aerosol (LVOOA), which has been identified in ambient aerosol based on average elemental composition but not fully understood at a molecular level. For the biogenic precursors and experimental conditions studied, HOMs in fresh biogenic SOA have molecular formulas more closely resembling LVOOA than HOMs in aged SOA, suggesting that aging of biogenic SOA is not a good surrogate for ambient LVOOA. PMID:27000653

  10. Evolution of cyclonic eddies and biogenic fluxes in the northern Bay of Bengal

    Directory of Open Access Journals (Sweden)

    M. Nuncio

    2013-10-01

    Full Text Available The Bay of Bengal has been traditionally known for its low primary productivity and varied reasons were attributed to it. The data analysis from the sediment traps deployed in the northern Bay of Bengal during the 5 yr from 1994 show episodic events of enhanced downward biogenic flux every year which was not related to monsoon-driven seasonal cycle. Satellite-derived sea level anomaly suggests that the episodic increase in the biogenic flux was associated with the presence of cyclonic eddies in the sediment trap location. Cyclonic eddy-induced down ward biogenic flux in the sediment trap location was larger than the amplitude, ∼40 mg m−2 d−1, of the seasonal cycle. The magnitude of the peak episodic fluxes were one-and-half to two-and-half times the annual mean flux, while the anomaly of peak episodic fluxes was at least equal to or greater than the magnitude of the seasonal flux value. Cyclonic eddies responsible for high biogenic flux during 1994 and 1996 were formed in the northern Bay of Bengal during February–March of respective years due to the interaction of northward flowing western boundary current and coastally trapped Kelvin wave. In contrast, cyclonic eddies during 1997 and 1998 were formed from the breaking of westward propagating Rossby waves. The sediment trap data provided the observational evidence that eddy-induced biological productivity is an important mechanism in the Bay of Bengal that contributes significantly to the mid-depth biogenic flux.

  11. Cocaine affects foraging behaviour and biogenic amine modulated behavioural reflexes in honey bees

    Directory of Open Access Journals (Sweden)

    Eirik Søvik

    2014-11-01

    Full Text Available In humans and other mammals, drugs of abuse alter the function of biogenic amine pathways in the brain leading to the subjective experience of reward and euphoria. Biogenic amine pathways are involved in reward processing across diverse animal phyla, however whether cocaine acts on these neurochemical pathways to cause similar rewarding behavioural effects in animal phyla other than mammals is unclear. Previously, it has been shown that bees are more likely to dance (a signal of perceived reward when returning from a sucrose feeder after cocaine treatment. Here we examined more broadly whether cocaine altered reward-related behaviour, and biogenic amine modulated behavioural responses in bees. Bees developed a preference for locations at which they received cocaine, and when foraging at low quality sucrose feeders increase their foraging rate in response to cocaine treatment. Cocaine also increased reflexive proboscis extension to sucrose, and sting extension to electric shock. Both of these simple reflexes are modulated by biogenic amines. This shows that systemic cocaine treatment alters behavioural responses that are modulated by biogenic amines in insects. Since insect reward responses involve both octopamine and dopamine signalling, we conclude that cocaine treatment altered diverse reward-related aspects of behaviour in bees. We discuss the implications of these results for understanding the ecology of cocaine as a plant defence compound. Our findings further validate the honey bee as a model system for understanding the behavioural impacts of cocaine, and potentially other drugs of abuse.

  12. Managing your wine fermentation to reduce the risk of biogenic amine formation

    Directory of Open Access Journals (Sweden)

    Anita Yolandi Smit

    2012-03-01

    Full Text Available Biogenic amines are nitrogenous organic compounds produced in wine from amino acid precursors mainly by microbial decarboxylation. The concentration of biogenic amines that can potentially be produced is dependent on the amount of amino acid precursors in the medium, the presence of decarboxylase positive microorganisms and conditions that enable microbial or biochemical activity such as the addition of nutrients to support the alcoholic and malolactic fermentation (MLF inoculated starter cultures. MLF can be conducted using co-inoculation or inoculated after the completion of alcoholic fermentation (AF that may also affect the level of biogenic amine in the wine. This study focussed on the impact the addition of complex commercial yeast and bacterial nutrients and the use of different MLF inoculation scenarios could have on the production of biogenic amine in the wine. Results obtained with wine showed that in this study the amine that was influenced by nutrient addition was histamine. In the synthetic winemaking using 12 different treatments no clear tendencies were observed. It was shown that in certain conditions co-inoculation could reduce the amount of biogenic amines produced.

  13. Safety assessment of the biogenic amines in fermented soya beans and fermented bean curd.

    Science.gov (United States)

    Yang, Juan; Ding, Xiaowen; Qin, Yingrui; Zeng, Yitao

    2014-08-01

    To evaluate the safety of biogenic amines, high performance liquid chromatography (HPLC) was used to evaluate the levels of biogenic amines in fermented soya beans and fermented bean curd. In fermented soya beans, the total biogenic amines content was in a relatively safe range in many samples, although the concentration of histamine, tyramine, and β-phenethylamine was high enough in some samples to cause a possible safety threat, and 8 of the 30 samples were deemed unsafe. In fermented bean curd, the total biogenic amines content was more than 900 mg/kg in 19 white sufu amples, a level that has been determined to pose a safety hazard; putrescine was the only one detected in all samples and also had the highest concentration, which made samples a safety hazard; the content of tryptamine, β-phenethylamine, tyramine, and histamine had reached the level of threat to human health in some white and green sufu samples, and that may imply another potential safety risk; and 25 of the 33 samples were unsafe. In conclusion, the content of biogenic amines in all fermented soya bean products should be studied and appropriate limits determined to ensure the safety of eating these foods. PMID:25029555

  14. Characterization of biogenic secondary organic aerosols using statistical methods; Charakterisierung Biogener Sekundaerer Organischer Aerosole mit Statistischen Methoden

    Energy Technology Data Exchange (ETDEWEB)

    Spindler, Christian

    2010-07-01

    Atmospheric aerosols have important influence on the radiation balance of the Earth, on visibility and human health. Secondary organic aerosol is formed from gas-to-particle conversion of oxidized volatile organic compounds. A dominant fraction of the gases originates from plant emissions, making biogenic secondary organic aerosol (BSOA) an especially important constituent of the atmosphere. Knowing the chemical composition of BSOA particles is crucial for a thorough understanding of aerosol processes in the environment. In this work, the chemical composition of BSOA particles was measured with aerosol mass spectrometry and analyzed with statistical methods. The experimental part of the work comprises process studies of the formation and aging of biogenic aerosols in simulation chambers. Using a plant chamber, real tree emissions were used to produce particles in a way close to conditions in forest environments. In the outdoor chamber SAPHIR, OH-radicals were produced from the photooxidation of ozone under illumination with natural sunlight. Here, BSOA was produced from defined mixtures of mono- and sesquiterpenes that represent boreal forest emissions. A third kind of experiments was performed in the indoor chamber AIDA. Here, particles were produced from ozonolysis of single monoterpenes and aged by condensing OH-oxidation products. Two aerosol mass spectrometers (AMS) were used to measure the chemical composition of the particles. One of the instruments is equipped with a quadrupole mass spectrometer providing unit mass resolution. The second instrument contains a time-of-flight mass spectrometer and provides mass resolution sufficient to distinguish different fragments with the same nominal mass. Aerosol mass spectra obtained with these instruments are strongly fragmented due to electron impact ionization of the evaporated molecules. In addition, typical BSOA mass spectra are very similar to each other. In order to get a more detailed knowledge about the mass

  15. Molecular control of vertebrate iron homeostasis by iron regulatory proteins

    OpenAIRE

    Wallander, Michelle L.; Leibold, Elizabeth A.; Eisenstein, Richard S.

    2006-01-01

    Both deficiencies and excesses of iron represent major public health problems throughout the world. Understanding the cellular and organismal processes controlling iron homeostasis is critical for identifying iron-related diseases and in advancing the clinical treatments for such disorders of iron metabolism. Iron regulatory proteins (IRPs) 1 and 2 are key regulators of vertebrate iron metabolism. These RNA binding proteins post-transcriptionally control the stability or translation of mRNAs ...

  16. Biogenic nanoparticles: production, characterization, and application of bacterial magnetosomes

    International Nuclear Information System (INIS)

    The ability of magnetotactic bacteria (MTB) to navigate along magnetic field lines is based on unique nanosized organelles (magnetosomes), which are membrane-enclosed intracellular crystals of a magnetic iron mineral that assemble into highly ordered chain-like structures. The biomineralization of magnetosomes is a process with genetic control over the accumulation of iron, the deposition of the magnetic crystal within a specific compartment, as well as the assembly, alignment and intracellular organization of particle chains. Magnetite crystals produced by MTB have uniform species-specific morphologies and sizes, which are mostly unknown from inorganic systems. The unusual characteristics of magnetosome particles have attracted a great interdisciplinary interest and inspired numerous ideas for their biotechnological application. In this article, we summarize the current knowledge of magnetosome biomineralization in bacteria. In addition, we will present results on the mass production, as well as the biochemical and physico-chemical analysis and functionalization of bacterial magnetosomes, with emphasis on their characterization as a novel class of magnetic nanoparticles. Finally, we describe the potential of magnetosomes in various biomedical and technological applications

  17. Biogenic carbon in combustible waste: Waste composition, variability and measurement uncertainty

    DEFF Research Database (Denmark)

    Larsen, Anna Warberg; Fuglsang, Karsten; Pedersen, Niels H.;

    2013-01-01

    described in the literature. This study addressed the variability of biogenic and fossil carbon in combustible waste received at a municipal solid waste incinerator. Two approaches were compared: (1) radiocarbon dating (14C analysis) of carbon dioxide sampled from the flue gas, and (2) mass and energy......Obtaining accurate data for the contents of biogenic and fossil carbon in thermally-treated waste is essential for determination of the environmental profile of waste technologies. Relations between the variability of waste chemistry and the biogenic and fossil carbon emissions are not well...... balance calculations using the balance method. The ability of the two approaches to accurately describe short-term day-to-day variations in carbon emissions, and to which extent these short-term variations could be explained by controlled changes in waste input composition, was evaluated. Finally, the...

  18. Effect of gamma irradiation on the activity of some microorganisms producing biogenic amines in some foods

    International Nuclear Information System (INIS)

    The effect of gamma irradiation on the proximate chemical composition ( moisture content , protein , fat, ash) chemical freshness tests (TBA, TVB-N, TMA, FAN, ph) and microbiological changes (total bacterial count, proteolytic bacteria, Enterobacteriaceae, moulds and yeasts counts) occurred in sardine fish and pastirma during cold storage at (4 ± 1 degree C) were fully investigated. Furthermore, the bacterial activity causing the formation of biogenic amines were also studied. In addition, the determination of biogenic amines in sardine fish and pastirma produced by these bacteria were explored. The effects of irradiation doses (1, 3 and 5 kGy) which were applied as a trial to reduce biogenic amines formation in sardine fish and pastirma were also investigated. In addition, the effect of the tested irradiation doses (1, 3 and 5 kGy) on organoleptic properties of the treated sardine fish and pastirma were determined.

  19. Simultaneous determination of selected biogenic amines in alcoholic beverage samples by isotachophoretic and chromatographic methods.

    Science.gov (United States)

    Jastrzębska, Aneta; Piasta, Anna; Szłyk, Edward

    2014-01-01

    A simple and useful method for the determination of biogenic amines in beverage samples based on isotachophoretic separation is described. The proposed procedure permitted simultaneous analysis of histamine, tyramine, cadaverine, putrescine, tryptamine, 2-phenylethylamine, spermine and spermidine. The data presented demonstrate the utility, simplicity, flexibility, sensitivity and environmentally friendly character of the proposed method. The precision of the method expressed as coefficient of variations varied from 0.1% to 5.9% for beverage samples, whereas recoveries varied from 91% to 101%. The results for the determination of biogenic amines were compared with an HPLC procedure based on a pre-column derivatisation reaction of biogenic amines with dansyl chloride. Furthermore, the derivatisation procedure was optimised by verification of concentration and pH of the buffer, the addition of organic solvents, reaction time and temperature. PMID:24350674

  20. The Li isotope composition of modern biogenic carbonates

    Science.gov (United States)

    Dellinger, M.; West, A. J.; Adkins, J. F.; Paris, G.; Eagle, R.; Freitas, P. S.; Bagard, M. L.; Ries, J. B.; Corsetti, F. A.; Pogge von Strandmann, P.; Ullmann, C. V.

    2015-12-01

    The lithium stable isotope composition (δ7Li) of sedimentary carbonates has great potential to unravel weathering rates and intensity in the past, with implications for understanding the carbon cycle over geologic time. However, so far very little is known about the potential influence of fractionation of the stable Li isotope composition of biogenic carbonates. Here, we investigate the δ7Li of various organisms (particularly mollusks, echinoderms and brachiopods) abundant in the Phanerozoic record, in order to understand which geologic archives might provide the best targets for reconstructing past seawater composition. The range of measured samples includes (i) modern calcite and aragonite shells from variable natural environments, (ii) shells from organisms grown under controlled conditions (temperature, salinity, pCO2), and (iii) fossil shells from a range of species collected from Miocene deposits. When possible, both the inner and outer layers of bivalves were micro-sampled to assess the intra-shell heterogeneity. For calcitic shells, the measured δ7Li of bivalve species range from +32 to +41‰ and is systematically enriched in the heavy isotope relative to seawater (31 ‰) and to inorganic calcite, which is characterized by Δ7Licalcite-seawater = -2 to -5‰ [1]. The Li isotope composition of aragonitic bivalves, ranging from +16 to +22‰, is slightly fractionated to both high and low δ7Li relative to inorganic aragonite. The largest intra-shell Li isotope variability is observed for mixed calcite-aragonite shells (more than 20‰) whereas in single mineralogy shells, intra-shell δ7Li variability is generally less than 3‰. Overall, these results suggest a strong influence of vital effects on Li isotopes during bio-calcification of bivalve shells. On the contrary, measured brachiopods systematically exhibit fractionation that is very similar to inorganic calcite, with a mean δ7Li of 27.0±1.5‰, suggesting that brachiopods may provide good

  1. Triple oxygen isotopes in biogenic and sedimentary carbonates

    Science.gov (United States)

    Passey, Benjamin H.; Hu, Huanting; Ji, Haoyuan; Montanari, Shaena; Li, Shuning; Henkes, Gregory A.; Levin, Naomi E.

    2014-09-01

    The 17O anomaly (Δ17O) of natural waters has been shown to be sensitive to evaporation in a way analogous to deuterium excess, with evaporated bodies of water (e.g., leaf waters, lake waters, animal body waters) tending to have lower Δ17O than primary meteoric waters. In animal body water, Δ17O relates to the intake of evaporated waters, evaporative effluxes of water, and the Δ17O value of atmospheric O2, which itself carries signatures of global carbon cycling and photochemical reactions in the stratosphere. Carbonates have the potential to record the triple oxygen isotope compositions of parent waters, allowing reconstruction of past water compositions, but such investigations have awaited development of methods for high-precision measurement of Δ17O of carbonate. We describe optimized methods based on a sequential acid digestion/reduction/fluorination approach that yield Δ17O data with the high precision (∼0.010‰, 1σ) needed to resolve subtle environmental signals. We report the first high-precision Δ17O dataset for terrestrial carbonates, focusing on vertebrate biogenic carbonates and soil carbonates, but also including marine invertebrates and high-temperature carbonates. We determine apparent three-isotope fractionation factors between the O2 analyte derived from carbonate and the parent waters of the carbonate. These in combination with appropriate temperature estimates (from clumped isotope thermometry, or known or estimated body temperatures) are used to calculate the δ18O and Δ17O of parent waters. The clearest pattern to emerge is the strong 17O-depletion in avian, dinosaurian, and mammalian body water (from analyses of eggshell and tooth enamel) relative to meteoric waters, following expected influences of evaporated water (e.g., leaf water) and atmospheric O2 on vertebrate body water. Parent waters of the soil carbonates studied here have Δ17O values that are similar to or slightly lower than global precipitation. Our results suggest

  2. Hepcidin in iron overload disorders

    OpenAIRE

    Papanikolaou, George; Tzilianos, Michalis; Christakis, John I.; Bogdanos, Dionisios; Tsimirika, Konstantina; MacFarlane, Julie; Goldberg, Y. Paul; Sakellaropoulos, Nikos; Ganz, Tomas; Nemeth, Elizabeta

    2005-01-01

    Hepcidin is the principal regulator of iron absorption in humans. The peptide inhibits cellular iron efflux by binding to the iron export channel ferroportin and inducing its internalization and degradation. Either hepcidin deficiency or alterations in its target, ferroportin, would be expected to result in dysregulated iron absorption, tissue maldistribution of iron, and iron overload. Indeed, hepcidin deficiency has been reported in hereditary hemochromatosis and attributed to mutations in ...

  3. Thin Wall Iron Castings

    Energy Technology Data Exchange (ETDEWEB)

    J.F. Cuttino; D.M. Stefanescu; T.S. Piwonka

    2001-10-31

    Results of an investigation made to develop methods of making iron castings having wall thicknesses as small as 2.5 mm in green sand molds are presented. It was found that thin wall ductile and compacted graphite iron castings can be made and have properties consistent with heavier castings. Green sand molding variables that affect casting dimensions were also identified.

  4. Iron-Deficiency Anemia

    Medline Plus

    Full Text Available ... Susan got counseling on how to improve her health and well-being. She began taking iron supplements and multivitamins to improve her iron levels. Susan also made changes to her diet, such as focusing more on green leafy vegetables, red meats, nuts, dried fruits, and beans. Other ...

  5. Iron-Deficiency Anemia

    Medline Plus

    Full Text Available ... Blood Tests Blood Transfusion Restless Legs Syndrome Send a link to NHLBI to someone by E-MAIL | ... Iron-Deficiency Anemia? Español Iron-deficiency anemia is a common, easily treated condition that occurs if you ...

  6. Insights into Methane Formation Temperatures, Biogenic Methanogenesis, and Natural Methane Emissions from Clumped Isotopes

    Science.gov (United States)

    Douglas, P. M.; Stolper, D. A.; Walter Anthony, K. M.; Dallimore, S.; Paull, C. K.; Wik, M.; Crill, P. M.; Winterdahl, M.; Smith, D. A.; Luhmann, A. J.; Ding, K.; Seyfried, W. E., Jr.; Eiler, J. M.; Ponton, C.; Sessions, A. L.

    2015-12-01

    Multiply substituted isotopologues of methane are a valuable new tool for characterizing and understanding the source of methane in different Earth environments. Here we present methane clumped isotope results from natural gas wells, hydrothermal vents, marine and lacustrine methane seeps, and culture experiments. We observe a wide range of formation temperatures for thermogenic methane. Methane samples from low-maturity reservoirs indicate formation temperatures between 102-144° C, high-maturity conventional and shale gasses indicate temperatures between 158-246 °C, and thermogenic coal gases indicate temperatures between 174-267 °C. Methane formation temperatures generally correlate positively with δ13C, and negatively with gas wetness indices. Methane samples from a set of marine hydrothermal vents indicate a formation temperature of 290-350 °C. Methane sampled from subsurface and marine biogenic sources typically indicate temperatures consistent with the formation environment (0-64° C). In contrast, freshwater biogenic methane samples, and cultures of hydrogenotrophic and methylotrophic methanogens, express low levels of isotopic clumping inconsistent with their formation temperature. These data and complementary models suggest that kinetic isotope effects, likely modulated by rates and pathways of methanogenesis, affect biogenic methane in cultures and freshwater environments. Alternatively, non-equilibrium signatures may result from mixing of methane with widely differing δD and δ13C values. Analyses of biogenic methane emissions from lakes indicate a correlation between methane flux and non-equilibrium clumped isotope fractionations in a given lake. Results from large methane seeps in Alaskan lakes confirm that some seeps emit thermogenic methane, but also indicate that other seeps emit subsurface biogenic methane or variable mixtures of biogenic and thermogenic methane. These results point to diverse sources for large Arctic methane seeps.

  7. Biogenic contribution to PM-2.5 ambient aerosol from radiocarbon measurements

    Science.gov (United States)

    Lewis, C.; Klouda, G.; Ellenson, W.

    2003-04-01

    Knowledge of the relative contributions of biogenic versus anthropogenic sources to ambient aerosol is of great interest in the formulation of strategies to achieve nationally mandated air quality standards. Radiocarbon (14C) measurements provide a means to quantify the biogenic fraction of any carbon-containing sample of ambient aerosol. In the absence of an impact from biomass burning (e.g., during summertime) such measurements can provide an estimate of the contribution of biogenic secondary organic aerosol, from biogenic volatile organic compound precursors. Radiocarbon results for 11.5-h PM-2.5 samples collected near Nashville, Tennessee, USA, during summer 1999 will be presented. On average the measured biogenic fraction was surprisingly large (more than half), with the average biogenic fraction for night samples being only slightly smaller than for day samples. Discussion will include (a) description of the radiocarbon methodology, (b) use of radiocarbon measurements on local vegetation and fuel samples as calibration data, (c) concurrent measurements of organic carbon and elemental carbon ambient concentrations, (d) assessment of organic aerosol sampling artifact through use of organic vapor denuders, variable face velocities, and filter extraction, and (e) comparison with published radiocarbon results obtained in Houston, Texas in a similar study. Disclaimer: This work has been funded wholly or in part by the United States Environmental Protection Agency under Interagency Agreement No. 13937923 to the National Institute of Standards and Technology, and Contract No. 68-D5-0049 to ManTech Environmental Tecnology, Inc. It has been subjected to Agency review and approved for publication.

  8. Environmental and biogeochemical process of accumulation of iron-phosphorus in marine sediments

    Institute of Scientific and Technical Information of China (English)

    WENG Huanxin; ZHANG Xingmao; WU Nengyou; CHEN Lihong; CHEN Jingfeng; WANG Ying; QIN Yachao; TIAN Rongxiang

    2004-01-01

    This paper discusses the environmental and biogeochemical process of accumulation of iron-phosphorus in marine sediments for the north aktian of the South China Sea and analyzes the relationships between the contents of iron, phosphorus and calcium carbonate as well as their existent characteristics. The results show that the variances of phosphorus and calcium carbonate contents with depths are opposite and those of iron and calcium carbonate contents are almost accordant. It is not only related to the biogeochemical process of accumulation of biogenous calcium carbonate in sediments, which resulted from the fact that the marine primary productivity was stimulated by part of terrigenous phosphorus dissolved into seawater due to decline of superficial water temperature and increase of carbon dioxide content in the glacial period, but also related to iron impelled oxidation and accelerated deposit by the dissolved oxygen from the atmosphere and the photosynthesis of hydrophytes in seawater. The variance of soluble iron-phos- phorus species (Fe-P) in sediment columns can sensitively reflect the changes of climate and environment, which suggests that the accumulative characteristics and existent states of iron-phosphorus species (Fe-P) in marine sediments have the significance as an indicator of the changes of paleoclimate and paleoenvironment.

  9. Sedimentary and mineral dust sources of dissolved iron to the World Ocean

    Directory of Open Access Journals (Sweden)

    J. K. Moore

    2007-04-01

    Full Text Available A worldwide database of dissolved iron observations is used to improve simulations of the marine iron cycle within a global-scale, Biogeochemical Elemental Cycling (BEC ocean model. Modifications to the model include: 1 an improved particle scavenging parameterization based on the sinking mass flux of particulate organic material, biogenic silica, calcium carbonate, and mineral dust particles; 2 desorption of dissolved iron from sinking particles; and 3 an improved sedimentary source for dissolved iron. Most scavenged iron (90% is put on sinking particles to remineralize deeper in the water column. The model-observation mismatches are greatly reduced both in surface waters and in the deeper ocean. Inclusion of desorption has little effect on surface water iron concentrations where adsorption/scavenging is strongly dominant, but significantly increases simulated iron concentrations in the deep ocean. Our results suggest that there must be substantial removal of dissolved iron from subsurface waters (where iron concentrations are <0.6 nM in most regions to match observed distributions. Aggregation and removal on sinking particles of Fe bound to organic colloids is a likely mechanism.

    The improved BEC model is used to address the relative contributions of mineral dust and marine sediments in driving ocean productivity and observed dissolved iron distributions. The sedimentary iron source from the continental margins has a strong impact on open ocean iron concentrations, particularly in the North Pacific. Plumes of elevated dissolved iron concentrations develop at depth in the Southern Ocean, extending from source regions in the SW Atlantic and around New Zealand. The lower particle flux and weaker scavenging in this region allows the continental iron source to be advected far from source areas. Both the margin sediment and mineral dust Fe sources significantly impact global scale primary production, export production, and nitrogen fixation

  10. Iron budgets for three distinct biogeochemical sites around the Kerguelen archipelago (Southern Ocean during the natural fertilisation experiment KEOPS-2

    Directory of Open Access Journals (Sweden)

    A. R. Bowie

    2014-12-01

    Full Text Available Iron availability in the Southern Ocean controls phytoplankton growth, community composition and the uptake of atmospheric CO2 by the biological pump. The KEOPS-2 experiment took place around the Kerguelen plateau in the Indian sector of the Southern Ocean, a region naturally fertilised with iron at the scale of hundreds to thousands of square kilometres, producing a mosaic of spring blooms which showed distinct biological and biogeochemical responses to fertilisation. This paper presents biogeochemical iron budgets (incorporating vertical and lateral supply, internal cycling, and sinks for three contrasting sites: an upstream high-nutrient low-chlorophyll reference, over the plateau, and in the offshore plume east of Kerguelen Island. These budgets show that distinct regional environments driven by complex circulation and transport pathways are responsible for differences in the mode and strength of iron supply, with vertical supply dominant on the plateau and lateral supply dominant in the plume. Iron supply from "new" sources to surface waters of the plume was double that above the plateau and 20 times greater than at the reference site, whilst iron demand (measured by cellular uptake in the plume was similar to the plateau but 40 times greater than the reference. "Recycled" iron supply by bacterial regeneration and zooplankton grazing was a relative minor component at all sites (<8% of "new" supply, in contrast to earlier findings from other biogeochemical iron budgets in the Southern Ocean. Over the plateau, a particulate iron dissolution term of 2.5% was invoked to balance the budget; this approximately doubled the standing stock of dissolved iron in the mixed layer. The exchange of iron between dissolved, biogenic and lithogenic particulate pools was highly dynamic in time and space, resulting in a decoupling of iron supply and carbon export and, importantly, controlling the efficiency of fertilisation.

  11. Iron budgets for three distinct biogeochemical sites around the Kerguelen archipelago (Southern Ocean) during the natural fertilisation experiment KEOPS-2

    Science.gov (United States)

    Bowie, A. R.; van der Merwe, P.; Quéroué, F.; Trull, T.; Fourquez, M.; Planchon, F.; Sarthou, G.; Chever, F.; Townsend, A. T.; Obernosterer, I.; Sallée, J.-B.; Blain, S.

    2014-12-01

    Iron availability in the Southern Ocean controls phytoplankton growth, community composition and the uptake of atmospheric CO2 by the biological pump. The KEOPS-2 experiment took place around the Kerguelen plateau in the Indian sector of the Southern Ocean, a region naturally fertilised with iron at the scale of hundreds to thousands of square kilometres, producing a mosaic of spring blooms which showed distinct biological and biogeochemical responses to fertilisation. This paper presents biogeochemical iron budgets (incorporating vertical and lateral supply, internal cycling, and sinks) for three contrasting sites: an upstream high-nutrient low-chlorophyll reference, over the plateau, and in the offshore plume east of Kerguelen Island. These budgets show that distinct regional environments driven by complex circulation and transport pathways are responsible for differences in the mode and strength of iron supply, with vertical supply dominant on the plateau and lateral supply dominant in the plume. Iron supply from "new" sources to surface waters of the plume was double that above the plateau and 20 times greater than at the reference site, whilst iron demand (measured by cellular uptake) in the plume was similar to the plateau but 40 times greater than the reference. "Recycled" iron supply by bacterial regeneration and zooplankton grazing was a relative minor component at all sites (<8% of "new" supply), in contrast to earlier findings from other biogeochemical iron budgets in the Southern Ocean. Over the plateau, a particulate iron dissolution term of 2.5% was invoked to balance the budget; this approximately doubled the standing stock of dissolved iron in the mixed layer. The exchange of iron between dissolved, biogenic and lithogenic particulate pools was highly dynamic in time and space, resulting in a decoupling of iron supply and carbon export and, importantly, controlling the efficiency of fertilisation.

  12. Iron budgets for three distinct biogeochemical sites around the Kerguelen Archipelago (Southern Ocean) during the natural fertilisation study, KEOPS-2

    Science.gov (United States)

    Bowie, A. R.; van der Merwe, P.; Quéroué, F.; Trull, T.; Fourquez, M.; Planchon, F.; Sarthou, G.; Chever, F.; Townsend, A. T.; Obernosterer, I.; Sallée, J.-B.; Blain, S.

    2015-07-01

    Iron availability in the Southern Ocean controls phytoplankton growth, community composition and the uptake of atmospheric CO2 by the biological pump. The KEOPS-2 (KErguelen Ocean and Plateau compared Study 2) "process study", took place around the Kerguelen Plateau in the Indian sector of the Southern Ocean. This is a region naturally fertilised with iron on the scale of hundreds to thousands of square kilometres, producing a mosaic of spring blooms which show distinct biological and biogeochemical responses to fertilisation. This paper presents biogeochemical iron budgets (incorporating vertical and lateral supply, internal cycling, and sinks) for three contrasting sites: an upstream high-nutrient low-chlorophyll reference, over the plateau and in the offshore plume east of the Kerguelen Islands. These budgets show that distinct regional environments driven by complex circulation and transport pathways are responsible for differences in the mode and strength of iron supply, with vertical supply dominant on the plateau and lateral supply dominant in the plume. Iron supply from "new" sources (diffusion, upwelling, entrainment, lateral advection, atmospheric dust) to the surface waters of the plume was double that above the plateau and 20 times greater than at the reference site, whilst iron demand (measured by cellular uptake) in the plume was similar to that above the plateau but 40 times greater than at the reference site. "Recycled" iron supply by bacterial regeneration and zooplankton grazing was a relatively minor component at all sites (< 8 % of new supply), in contrast to earlier findings from other biogeochemical iron budgets in the Southern Ocean. Over the plateau, a particulate iron dissolution term of 2.5 % was invoked to balance the budget; this approximately doubled the standing stock of dissolved iron in the mixed layer. The exchange of iron between dissolved, biogenic particulate and lithogenic particulate pools was highly dynamic in time and space

  13. Colour Metallography of Cast Iron

    Institute of Scientific and Technical Information of China (English)

    Zhou Jiyang; Liu Jincheng

    2011-01-01

    White Cast Iron (Ⅰ) White cast iron or ‘white iron' refers to the type of cast iron in which all of the carbon exists as carbide;there is no graphite in the as-cast structure and the fractured surface shows a white colour.White cast iron can be divided in three classes:· Normal white cast iron — this iron contains only C,Si,Mn,P and S,with no other alloying elements.· Low-alloy white cast iron — the total mass fraction of alloying elements is less than 5%.

  14. Iron replacement therapy

    DEFF Research Database (Denmark)

    Nielsen, Ole Haagen; Coskun, Mehmet; Weiss, Günter

    2016-01-01

    PURPOSE OF REVIEW: Approximately, one-third of the world's population suffers from anemia, and at least half of these cases are because of iron deficiency. With the introduction of new intravenous iron preparations over the last decade, uncertainty has arisen when these compounds should be...... administered and under which circumstances oral therapy is still an appropriate and effective treatment. RECENT FINDINGS: Numerous guidelines are available, but none go into detail about therapeutic start and end points or how iron-deficiency anemia should be best treated depending on the underlying cause of...... iron deficiency or in regard to concomitant underlying or additional diseases. SUMMARY: The study points to major issues to be considered in revisions of future guidelines for the true optimal iron replacement therapy, including how to assess the need for treatment, when to start and when to stop...

  15. Microbes: mini iron factories.

    Science.gov (United States)

    Joshi, Kumar Batuk

    2014-12-01

    Microbes have flourished in extreme habitats since beginning of the Earth and have played an important role in geological processes like weathering, mineralization, diagenesis, mineral formation and destruction. Biotic mineralization is one of the most fascinating examples of how microbes have been influencing geological processes. Iron oxidizing and reducing bacteria are capable of precipitating wide varieties of iron oxides (magnetite), carbonates (siderite) and sulphides (greigite) via controlled or induced mineralization processes. Microbes have also been considered to play an important role in the history of evolution of sedimentary rocks on Earth from the formation of banded iron formations during the Archean to modern biotic bog iron and ochre deposits. Here, we discuss the role that microbes have been playing in precipitation of iron and the role and importance of interdisciplinary studies in the field of geology and biology in solving some of the major geological mysteries. PMID:25320452

  16. Formation and destruction of biogenic amines in Chunjang (a black soybean paste) and Jajang (a black soybean sauce).

    Science.gov (United States)

    Bai, Xuezhi; Byun, Bo Young; Mah, Jae-Hyung

    2013-11-15

    Chunjang and Jajang samples were analysed for biogenic amine contents by using HPLC equipped with a UV-Vis detector. Chunjang samples contained relatively large amounts of histamine (up to 273mg/kg) and tyramine (up to 131mg/kg), whereas Jajang samples had relatively small amounts of biogenic amines (mostly less than 40mg/kg). There appeared to be a strong relationship between biogenic amine contents in Chunjang and Jajang, and the biogenic amines in Chunjang were found to be pyrolysed during frying thereof to prepare Jajang. Meanwhile, the total plate counts of Chunjang samples ranged from 5 to 8logcfu/g, and most strains that were isolated from Chunjang samples were identified to be Bacillus subtilis (91.0%). The strains isolated from a sample in which relatively small amounts of biogenic amines were detected showed significantly weak abilities to produce biogenic amines. This indicates that biogenic amine contents in Chunjang are primarily attributed to bacterial abilities to produce biogenic amines. PMID:23790882

  17. BIOGENIC AMINES CONTENT IN SELECTED COMMERCIAL FERMENTED PRODUCTS OF ANIMAL ORIGIN

    OpenAIRE

    Vendula Pachlová; Radka Flasarová; Ludmila Zálešáková; František Buňka; Pavel Budinský; Leona Buňková

    2012-01-01

    The aim of this study was to monitor of biogenic amines contents in commercial fermented products, especially various type of ripening cheeses and fermented meat products (15 cheese samples and nine dry fermented meat products obtained from Czech Republic, Slovak Republic, Poland, and Germany). Furthermore, the changes in samples during storage were also observed. The samples were stored at 6±1°C. The samples were taken the first day of storage and the last day of shelf-life. The biogenic ami...

  18. Evaluation of N-nitrosopiperidine formation from biogenic amines during the production of dry fermented sausages

    OpenAIRE

    De Mey, Eveline; De Maere, Hannelore; Goemaere, Olivier; Steen, Liselot; Peeters, Christine; Derdelinckx, Guy; Paelinck, Hubert; Fraeye, Ilse

    2014-01-01

    The aim of this study was to determine the role of the precursors cadaverine and piperidine in the N-nitrosopiperidine (NPIP) formation during the production of dry fermented sausages. The influences of pH (4.9 and 5.3), sodium nitrite (0 and 150 mg/kg) and ascorbate (0 and 500 mg/kg) were investigated by the use of a dry fermented sausage model. The biogenic amines and volatile N-nitrosamines were analyzed by HPLC-UV and GC-TEA. The major biogenic amines were tyramine (TYR), putrescine (PUT)...

  19. Biogenic amine content, histamine-forming bacteria, and adulteration of pork in tuna sausage products.

    Science.gov (United States)

    Kung, Hsien-Feng; Tsai, Yung-Hsiang; Chang, Shih-Chih; Hong, Tang-Yao

    2012-10-01

    Twenty-five tuna sausage products were purchased from retail markets in Taiwan. The rates of occurrence of biogenic amines, histamine-forming bacteria, and adulteration by pork and poultry were determined. The average content of various biogenic amines in all tested samples was less than 2.0 mg/100 g (Thunnus albacares for 22 samples (88%), Thunnus alalunga for 1 sample (4%), and Thunnus thynnus for 1 sample (4%), whereas the remaining sample was identified as Makaira nigricans (blue marlin). PMID:23043830

  20. Fractionation of fulvic acid by iron and aluminum oxides: influence on copper toxicity to Ceriodaphnia dubia

    Science.gov (United States)

    Smith, Kathleen S.; James F. Ranville; Emily K. Lesher; Daniel J. Diedrich; Diane M. McKnight; Ruth M. Sofield

    2014-01-01

    This study examines the effect on aquatic copper toxicity of the chemical fractionation of fulvic acid (FA) that results from its association with iron and aluminum oxyhydroxide precipitates. Fractionated and unfractionated FAs obtained from streamwater and suspended sediment were utilized in acute Cu toxicity tests on ,i>Ceriodaphnia dubia. Toxicity test results with equal FA concentrations (6 mg FA/L) show that the fractionated dissolved FA was 3 times less effective at reducing Cu toxicity (EC50 13 ± 0.6 μg Cu/L) than were the unfractionated dissolved FAs (EC50 39 ± 0.4 and 41 ± 1.2 μg Cu/L). The fractionation is a consequence of preferential sorption of molecules having strong metal-binding (more aromatic) moieties to precipitating Fe- and Al-rich oxyhydroxides, causing the remaining dissolved FA to be depleted in these functional groups. As a result, there is more bioavailable dissolved Cu in the water and hence greater potential for Cu toxicity to aquatic organisms. In predicting Cu toxicity, biotic ligand models (BLMs) take into account dissolved organic carbon (DOC) concentration; however, unless DOC characteristics are accounted for, model predictions can underestimate acute Cu toxicity for water containing fractionated dissolved FA. This may have implications for water-quality criteria in systems containing Fe- and Al-rich sediment, and in mined and mineralized areas in particular. Optical measurements, such as specific ultraviolet absorbance at 254 nm (SUVA254), show promise for use as spectral indicators of DOC chemical fractionation and inferred increased Cu toxicity.

  1. Biogenic amines content in Spanish and French natural ciders: Application of qPCR for quantitative detection of biogenic amine-producers

    OpenAIRE

    Ladero Losada, Víctor Manuel; Coton, M.; Fernández García, María; Burón, Nicolás; Martín, M. Cruz; Guichard, Hugues; Coton, E.; Álvarez González, Miguel Ángel

    2011-01-01

    Biogenic amines (BA) are low molecular weight nitrogenous bases commonly found in fermented foods and beverages and their consumption can induce undesirable reactions. In this work, the BA content in natural cider from Spain and France was determined. Samples from commercially available cider or obtained during the elaboration process were analyzed. A different profile and BA concentration was observed depending on cider origin. qPCR tools developed for the quantitative detection of BA produc...

  2. Validation of an HPLC Analytical Method for Determination of Biogenic Amines in Agricultural Products and Monitoring of Biogenic Amines in Korean Fermented Agricultural Products

    OpenAIRE

    Yoon, Hyeock; Park, Jung Hyuck; Choi, Ari; Hwang, Han-Joon; Mah, Jae-Hyung

    2015-01-01

    An HPLC analytical method was validated for the quantitative determination of biogenic amines in agricultural products. Four agricultural foods, including apple juice, Juk, corn oil and peanut butter, were selected as food matrices based on their water and fat contents (i.e., non-fatty liquid, non-fatty solid, fatty liquid and fatty solid, respectively). The precision, accuracy, recovery, limit of detection (LOD) and quantification (LOQ) were determined to test the validity of an HPLC procedu...

  3. Natural biogenic solid fuels - environmentally relevant characteristics and possible influences. Final report; Naturbelassene biogene Festbrennstoffe - umweltrelevante Eigenschaften und Einflussmoeglichkeiten. Abschlussbericht

    Energy Technology Data Exchange (ETDEWEB)

    Hartmann, H.; Boehm, T.; Maier, L. [Bayerische Landesanstalt fuer Landtechnik, Friesing-Weihenstephan (Germany). Arbeitsgruppe Festbrennstoffe

    2000-09-01

    , Weizenstroh und Weizenganzpflanzen. Eine Datenbank fuer naturbelassene biogene Festbrennstoffe wurde errichtet. Hierfuer wurde ein relationales Datenbankmodell gewaehlt. Dessen Struktur wurde so angelegt, dass neben den eigentlichen Messgroessen auch eine Vielzahl weiterer Eigenschaften und Informationen zum Brennstoff sowie seine Herkunftsmerkmale und die verwendeten Analyseverfahren festgehalten werden konnten. Die in den eigenen Versuchsserien zustande gekommenen Analyseergebnisse wurden durch weitere Daten aus einer umfangreichen Recherche (Befragung) sowie aus Literaturangaben ergaenzt, so dass insgesamt ca. 1.238 Datensaetze (Stand April 1999) zusammengetragen werden konnten. (orig.)

  4. Iron economy in Chlamydomonas reinhardtii

    Science.gov (United States)

    Glaesener, Anne G.; Merchant, Sabeeha S.; Blaby-Haas, Crysten E.

    2013-01-01

    While research on iron nutrition in plants has largely focused on iron-uptake pathways, photosynthetic microbes such as the unicellular green alga Chlamydomonas reinhardtii provide excellent experimental systems for understanding iron metabolism at the subcellular level. Several paradigms in iron homeostasis have been established in this alga, including photosystem remodeling in the chloroplast and preferential retention of some pathways and key iron-dependent proteins in response to suboptimal iron supply. This review presents our current understanding of iron homeostasis in Chlamydomonas, with specific attention on characterized responses to changes in iron supply, like iron-deficiency. An overview of frequently used methods for the investigation of iron-responsive gene expression, physiology and metabolism is also provided, including preparation of media, the effect of cell size, cell density and strain choice on quantitative measurements and methods for the determination of metal content and assessing the effect of iron supply on photosynthetic performance. PMID:24032036

  5. From Iron Bowl to Iron Stomach

    Institute of Scientific and Technical Information of China (English)

    MICHAEL; L.; O’NEAL

    2009-01-01

    A few decades ago, "Iron Bowl" referred to not having to go hungry in China if you were employed by the Agovernment. The government gave you a job that secured the filling of one’s rice bowl. This concept and practice did create loyalty, as the times were hard. China has moved far past those times to become the

  6. A cytosolic iron chaperone that delivers iron to ferritin

    OpenAIRE

    Shi, Haifeng; Bencze, Krisztina Z.; Stemmler, Timothy L.; Philpott, Caroline C.

    2008-01-01

    Ferritins are the main iron storage proteins found in animals, plants, and bacteria. The capacity to store iron in ferritin is essential for life in mammals, but the mechanism by which cytosolic iron is delivered to ferritin is unknown. Human ferritins expressed in yeast contain little iron. Human Poly r(C)-Binding Protein 1 (PCBP1) increased the amount of iron loaded into ferritin when expressed in yeast. PCBP1 bound to ferritin in vivo, and bound iron and facilitated iron loading into ferri...

  7. Biogenic arsenic volatilisation from an acidic wetland soil

    Science.gov (United States)

    Ilgen, Gunter; Huang, Jen-How; Lu, Shipeng; Tian, Liyan; Alewell, Christine

    2014-05-01

    Biogenic arsenic (As) volatilisation was budgeted at 26000 t yr-1as the largest input of the global As release into the atmosphere, thereby playing an important role in the biogeochemical cycle of As in the surface environment. In order to quantify As volatilisation from wetland soils and to elucidate the geochemical and microbiological factors governing As volatilisation, a series of incubations with an acidic wetland soil collected in NE-Bavaria in Germany were performed at 15oC for 4 months with addition of NaN3, arsenite (As(III)), FeCl3, NaSO4 and NaOAc with N2 and air in the headspace. Speciation of gaseous As in the headspace using GC-ICP-MS/ ESI-MS coupling showed the predominance of either arsine (AsH3) or trimethylarsine ((CH3)3As) in all treatments during the time course of incubation. Monomethylarsine ((CH3)AsH2) and dimethylarsine ((CH3)2AsH) could be only detected in trace amounts. Arsenic speciation in porewater with HPLC-ICP-MS revealed the predominance of As(III) and methylated As was never detectable. Arsenic volatilisation summed to 2.3 ng As (88% as AsH3) in the control incubations, which accounted for ~0.25 % of the total As storage in the wetland soil. Treatments with 10 mM NaN3 resulted in emission of only 0.03 ng As. In contrast, addition of 10 mM NaOAc stimulated microbial activities in wetland soils and subsequently rose As volatilisation to 8.5 ng As. It could be therefore concluded that As volatilisation from the wetland soils was mainly biological. Spiking 67 μM As(III) increased 10 times of As volatilisation and the proportion of methylated arsines increased to 66%, which is supposed to be caused by the largely enhanced As availability in porewater for microbes (480 ppb, ~65 times higher than those in the controls). Adding 10 mM FeCl3 stimulated microbial Fe(III) reducing activities but suppressed other microbial activities by lowering soil pH from 5 to 3.6, decreasing consequently As volatilisation to 0.3 ng As. The much lower redox

  8. 21 CFR 310.518 - Drug products containing iron or iron salts.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 5 2010-04-01 2010-04-01 false Drug products containing iron or iron salts. 310... Drug products containing iron or iron salts. Drug products containing elemental iron or iron salts as...) that contains iron or iron salts for use as an iron source shall bear the following statement:...

  9. Effects of iron availability on pigment signature and biogenic silica production in the coastal diatom Chaetoceros gracilis

    Digital Repository Service at National Institute of Oceanography (India)

    Biswas, H.; Bandyopadhyay, D.

    activated a strong photoprotection mechanism by maximising the conversion of diadinoxanthin to diatoxanthin and by increasing overall amount of photoprotective pigments relative to light harvesting pigments. The xanthophyll cycle comprising of diadinoxanthin...

  10. Biogenic inorganic crystalline phase formation as a result of biogeochemical interactions in between the chemolithotrophic archaeon Metallosphaera sedula and meteorite: implications for potential microbial biosignatures

    Science.gov (United States)

    Milojevic, Tetyana; Blazevic, Amir; Kutlucinar, Kaan Georg

    2016-04-01

    Chemolithotrophy has been indicated as the most primordial form of microbial metabolism on the early Earth and proposed as a possible metabolic form for other iron-mineral-rich planets like Mars. Rock-eating extremophiles represent an exciting field of research for the study of microbe-mineral interactions in order to find the unique biosignatures of life in the extreme conditions. Metallosphaera sedula is the chemolithotrophic archaeon, which thrives at 73°C and pH 2, using energy derived from metal oxidation at the edge of living limits. When given an access to extraterrestrial material (a stony meteorite H5 ordinary chondrite NWA1172), M. sedula releases soluble metal ions into the solution from NWA1172 due to its metal oxidizing metabolic activity. Here we report the formation of inorganic crystalline phase as a result of biogeochemical interactions in between M. sedula and extraterrestrial material. Inorganic ions released from meteorite as a result of M. sedula mediated leaching were trapped into crystalline material by solvent evaporation technique. Scanning Electron Microscopy observations and EDX analysis revealed that this crystalline phase is mainly composed of Ni, S, Mg and O elements. Biogenicity of this inorganic crystalline material was evaluated by comparing to abiotic conditions. Biological nature of Ni-, S-, Mg- and O -containing crystalline phase was established, since it was not mimicked in abiotic experimental conditions, allowing clearly to exclude abiogenic origin. Further investigations of exact mineralogical nature of biogenic of Ni-, S-, Mg- and O -crystalline material and its implication as a biosignature for detection of life are going to be investigated.

  11. Application of Mössbauer spectroscopy to the study of tannins inhibition of iron and steel corrosion

    Science.gov (United States)

    Jaén, Juan A.; de Obaldía, J.; Rodríguez, M. V.

    2011-11-01

    The inhibitory effect of tannins was investigated using, among others, potentiodynamic polarizations and Mössbauer spectroscopy. These techniques confirmed that the nature, pH and concentration of tannic solution are of upmost importance in the inhibitory properties of the solutions. It is observed that at low tannin concentration or pH, both, hydrolizable and condensed tannins, effectively inhibit iron corrosion, due to the redox properties of tannins. At pH ≈ 0, Mössbauer spectra of the frozen aqueous solutions of iron(III) with the tannin solutions showed that iron is in the form of a monomeric species [Fe(H2O)6]3 + , without coordination with the functional hydroxyl groups of the tannins. The suspended material consisted of amorphous ferric oxide and oxyhydroxides, though with quebracho tannin partly resulted in complex formation and in an iron (II) species from a redox process. Other tannins, such as chestnut hydrolysable tannins, do not complex iron at this low pH. Tannins react at high concentrations or pH (3 and 5) to form insoluble blue-black amorphous complexes of mono-and bis-type tannate complexes, with a relative amount of the bis-ferric tannate generally increasing with pH. Some Fe2 + in the form of hydrated polymeric ferrous tannate could be obtained. At pH 7, a partially hydrolyzed ferric tannate complex was also formed. The latter two phases do not provide corrosion protection. Tannin solutions at natural pH react with electrodeposited iron films (approx. 6 μm) to obtain products consisting only on the catecholate mono-complex of ferric tannate. Some aspects of the mechanism of tannins protection against corrosion are discussed.

  12. Application of Mössbauer spectroscopy to the study of tannins inhibition of iron and steel corrosion

    International Nuclear Information System (INIS)

    The inhibitory effect of tannins was investigated using, among others, potentiodynamic polarizations and Mössbauer spectroscopy. These techniques confirmed that the nature, pH and concentration of tannic solution are of upmost importance in the inhibitory properties of the solutions. It is observed that at low tannin concentration or pH, both, hydrolizable and condensed tannins, effectively inhibit iron corrosion, due to the redox properties of tannins. At pH ≈ 0, Mössbauer spectra of the frozen aqueous solutions of iron(III) with the tannin solutions showed that iron is in the form of a monomeric species [Fe(H2O)6]3 + , without coordination with the functional hydroxyl groups of the tannins. The suspended material consisted of amorphous ferric oxide and oxyhydroxides, though with quebracho tannin partly resulted in complex formation and in an iron (II) species from a redox process. Other tannins, such as chestnut hydrolysable tannins, do not complex iron at this low pH. Tannins react at high concentrations or pH (3 and 5) to form insoluble blue–black amorphous complexes of mono-and bis-type tannate complexes, with a relative amount of the bis-ferric tannate generally increasing with pH. Some Fe2 +  in the form of hydrated polymeric ferrous tannate could be obtained. At pH 7, a partially hydrolyzed ferric tannate complex was also formed. The latter two phases do not provide corrosion protection. Tannin solutions at natural pH react with electrodeposited iron films (approx. 6 μm) to obtain products consisting only on the catecholate mono-complex of ferric tannate. Some aspects of the mechanism of tannins protection against corrosion are discussed.

  13. Colour Metallography of Cast Iron

    Institute of Scientific and Technical Information of China (English)

    Zhou Jiyang; Ph.D Liu Jincheng

    2010-01-01

    @@ Note: This book consists of five sections: Chapter 1 Introduction, Chapter 2 Grey Iron, Chapter 3 Spheroidal Graphite Cast Iron, Chapter 4 Vermicular Cast Iron, and Chapter 5 White Cast Iron. CHINA FOUNDRY publishes this book in several parts serially, starting from the first issue of 2009.

  14. Colour Metallography of Cast Iron

    Institute of Scientific and Technical Information of China (English)

    Zhou Jiyang; Liu Jincheng

    2009-01-01

    @@ This book consists of five sections:Chapter 1 Introduction,Chapter 2 Grey Iron,Chapter 3 Ductile Iron,Chapter 4Vermicular Cast Iron,and Chapter 5 White Cast Iron. CHINA FOUNDRY publishs this book in several parts serially,starting from the first issue of 2009.

  15. Observations of continental biogenic impacts on marine aerosol and clouds off the coast of California

    Science.gov (United States)

    Coggon, M. M.; Sorooshian, A.; Wang, Z.; Craven, J. S.; Metcalf, A. R.; Lin, J. J.; Nenes, A.; Jonsson, H. H.; Flagan, R. C.; Seinfeld, J. H.

    2014-06-01

    During the 2011 Eastern Pacific Emitted Aerosol Cloud Experiment (E-PEACE) and 2013 Nucleation in California Experiment (NiCE) field campaigns, a predominantly organic aerosol (> 85% by mass) was observed in the free troposphere over marine stratocumulus off the coast of California. These particles originated from a densely forested region in the Northwestern United States. The organic mass spectrum resolved by positive matrix factorization is consistent with the mass spectra of previously measured biogenic organic aerosol. Particulate organic mass exhibits a latitudinal gradient that corresponds to the geographical distribution of vegetation density and composition, with the highest concentration over regions impacted by densely populated monoterpene sources. Due to meteorological conditions during summer months, cloud-clearing events transport aerosol from the Northwestern United States into the free troposphere above marine stratocumulus. Based on the variation of meteorological variables with altitude, dry air containing enhanced biogenic organic aerosol is shown to entrain into the marine boundary layer. Fresh impacts on cloud water composition are observed north of San Francisco, CA which is consistent with fresh continental impacts on the marine atmosphere at higher latitudes. Continental aerosol size distributions are bimodal. Particles in the 100 nm mode are impacted by biogenic sources, while particles in the ˜ 30 nm mode may originate from fresh biogenic emissions. Continental aerosol in the 100 nm mode is cloud condensation nuclei active and may play a role in modulating marine stratocumulus microphysics.

  16. Sediment waves with a biogenic twist in Pleistocene cool water carbonates, Great Australian Bight

    DEFF Research Database (Denmark)

    Anderskouv, Kresten; Surlyk, Finn; Huuse, Mads;

    2010-01-01

    contours immediately off the shelf–slope break. They are asymmetrical, showing up-slope migration, and mainly occur in trains. The sediment waves were drilled during ODP leg 182 in 1998, and were interpreted as biogenic reef mounds. New high-quality seismic and multibeam bathymetry data were acquired on...

  17. Discrimination of biogenic and detrital magnetite through a double Verwey transition temperature

    Science.gov (United States)

    Chang, Liao; Heslop, David; Roberts, Andrew P.; Rey, Daniel; Mohamed, Kais J.

    2016-01-01

    Magnetite occurs widely in natural environments in both inorganic and biogenic forms. Discrimination of the origin of magnetite has important implications, from searching for past microbial activity to interpreting paleomagnetic and environmental magnetic records in a wide range of settings. In this study, we present rock magnetic and electron microscopic analyses of marine sediments from the continental margin of Oman. Low-temperature magnetic data reveal two distinct Verwey transition (Tv) temperatures that are associated with the presence of biogenic and inorganic magnetite. This interpretation is consistent with room temperature magnetic properties and is confirmed by electron microscopic analyses. Our study justifies the use of two distinct Tv temperatures as a diagnostic signature for discriminating inorganic and biogenic magnetite. Simple low-temperature magnetic measurements, therefore, provide a tool to recognize rapidly the origin of magnetite within natural samples. In addition, our analyses reveal progressive down-core dissolution of detrital and biogenic magnetite, but with preservation of significant amounts of fine-grained magnetite within sediments that have been subjected to severe diagenetic alteration. We demonstrate that preservation of magnetite in such environments is due to protection of fine-grained magnetite inclusions within silicate hosts. Our results, therefore, also provide new insights into diagenetic processes in marine sediments.

  18. Enhancement of Biogenic Coalbed Methane Production and Back Injection of Coalbed Methane Co-Produced Water

    Energy Technology Data Exchange (ETDEWEB)

    Song Jin

    2007-05-31

    Biogenic methane is a common constituent in deep subsurface environments such as coalbeds and oil shale beds. Coalbed methane (CBM) makes significant contributions to world natural gas industry and CBM production continues to increase. With increasing CBM production, the production of CBM co-produced water increases, which is an environmental concern. This study investigated the feasibility in re-using CBM co-produced water and other high sodic/saline water to enhance biogenic methane production from coal and other unconventional sources, such as oil shale. Microcosms were established with the selected carbon sources which included coal, oil shale, lignite, peat, and diesel-contaminated soil. Each microcosm contained either CBM coproduced water or groundwater with various enhancement and inhibitor combinations. Results indicated that the addition of nutrients and nutrients with additional carbon can enhance biogenic methane production from coal and oil shale. Methane production from oil shale was much greater than that from coal, which is possibly due to the greater amount of available Dissolved Organic Carbon (DOC) from oil shale. Inconclusive results were observed from the other sources since the incubation period was too low. WRI is continuing studies with biogenic methane production from oil shale.

  19. Crystal and fine structural transformation of Heat-treated biogenic manganese oxide

    Czech Academy of Sciences Publication Activity Database

    Kimura, N.; Hashimoto, H.; Miyata, N.; Nishina, Y.; Kusano, Y.; Ikeda, Y.; Nakanishi, Y.; Fujii, T.; Šafařík, Ivo; Šafaříková, Miroslava; Takada, J.

    2013-01-01

    Roč. 60, č. 3 (2013), s. 92-98. ISSN 0532-8799 R&D Projects: GA MŠk(CZ) LH11111 Institutional support: RVO:67179843 Keywords : microorganisms * biogenic manganese oxides * phase transitions * nano -sheets * microstructures Subject RIV: EH - Ecology, Behaviour

  20. Molecular- and Nano-Scale Structure and Reactivity of Biogenic Uranium(IV) Oxide

    Science.gov (United States)

    Schofield, E. J.; Bargar, J. R.; Veeramani, H.; Sharp, J. O.; Bernier-Latmani, R.; Survova, E.; Giammar, D. E.; Ulrich, K.; Mehta, A.; Webb, S. M.; Conradson, S. D.; Clark, D. L.; Ilton, E. S.

    2008-12-01

    Bioremediation has been proposed and extensively researched as an in-situ immobilization strategy for uranium contamination in the subsurface with nanoparticulate uraninite (UO2) being the commonly reported product. Little detail is known about the structure and reactivity of this material, but based on comparison to its closest abiotic analog, UO2+x (0 powder diffraction and TEM. The lattice parameter of the nanoparticulate phase is seen to be consistent with bulk UO2. There is no evidence for hyperstoichiometry or strain of the UO2 particles, the latter indicating that surface energy is relatively modest. Similar results were obtained for biogenic UO2 particles produced by other metal reducing bacteria indicating that biological variability may play a minimal role in structure. In agreement with the structural analysis, the surface area-normalized dissolution rate of the biogenic UO2 was found to be comparable to that of coarser, synthetic UO2.00. Mn2+ was found to attenuate the particle size of biogenic UO2+xand to be structurally incorporated. This finding suggests that groundwater composition can have a pronounced impact on the structure and properties of biogenic uraninite.

  1. Inhibitory Effects of Spices on Biogenic Amine Accumulation during Fish Sauce Fermentation.

    Science.gov (United States)

    Zhou, Xuxia; Qiu, Mengting; Zhao, Dandan; Lu, Fei; Ding, Yuting

    2016-04-01

    The presence of high levels of biogenic amines is detrimental to the quality and safety of fish sauce. This study investigated the effects of ethanol extracts of spices, including garlic, ginger, cinnamon, and star anise extracts, in reducing the accumulation of biogenic amines during fish sauce fermentation. The concentrations of biogenic amines, which include histamine, putrescine, tyramine, and spermidine, all increased during fish sauce fermentation. When compared with the samples without spices, the garlic and star anise extracts significantly reduced these increases. The greatest inhibitory effect was observed for the garlic ethanolic extracts. When compared with controls, the histamine, putrescine, tyramine, and spermidine contents and the overall biogenic amine levels of the garlic extract-treated samples were reduced by 30.49%, 17.65%, 26.03%, 37.20%, and 27.17%, respectively. The garlic, cinnamon, and star anise extracts showed significant inhibitory effects on aerobic bacteria counts. Furthermore, the garlic and star anise extracts showed antimicrobial activity against amine producers. These findings may be helpful for enhancing the safety of fish sauce. PMID:26953496

  2. Methyl chavicol: characterization of its biogenic emission rate, abundance, and oxidation products in the atmosphere

    Science.gov (United States)

    Bouvier-Brown, N. C.; Goldstein, A. H.; Worton, D. R.; Matross, D. M.; Gilman, J. B.; Kuster, W. C.; Welsh-Bon, D.; Warneke, C.; de Gouw, J. A.; Cahill, T. M.; Holzinger, R.

    2009-03-01

    We report measurements of ambient atmospheric mixing ratios for methyl chavicol and determine its biogenic emission rate. Methyl chavicol, a biogenic oxygenated aromatic compound, is abundant within and above Blodgett Forest, a ponderosa pine forest in the Sierra Nevada Mountains of California. Methyl chavicol was detected simultaneously by three in-situ instruments - a gas chromatograph with mass spectrometer detector (GC-MS), a proton transfer reaction mass spectrometer (PTR-MS), and a thermal desorption aerosol GC-MS (TAG) - and found to be abundant within and above Blodgett Forest. Methyl chavicol atmospheric mixing ratios are strongly correlated with 2-methyl-3-buten-2-ol (MBO), a light- and temperature-dependent biogenic emission from the ponderosa pine trees at Blodgett Forest. Scaling from this correlation, methyl chavicol emissions account for 4-68% of the carbon mass emitted as MBO in the daytime, depending on the season. From this relationship, we estimate a daytime basal emission rate of 0.72-10.2 μgCg-1 h-1, depending on needle age and seasonality. We also present the first observations of its oxidation products (4-methoxybenzaldehyde and 4-methyoxy benzene acetaldehyde) in the ambient atmosphere. Methyl chavicol is a major essential oil component of many plant species. This work suggests that methyl chavicol plays a significant role in the atmospheric chemistry of Blodgett Forest, and potentially other sites, and should be included explicitly in both biogenic volatile organic carbon emission and atmospheric chemistry models.

  3. Biogenic silica in tidal freshwater marsh sediments and vegetation (Schelde estuary, Belgium)

    NARCIS (Netherlands)

    Struyf, E.; van Damme, S.; Gribsholt, B.; Middelburg, J.J.; Meire, P.

    2005-01-01

    To date, estuarine ecosystem research has mostly neglected silica cycling in freshwater intertidal marshes. However, tidal marshes can store large amounts of biogenic silica (BSi) in vegetation and sediment. BSi content of the typical freshwater marsh plants Phragmites australis, Impatiens glandulif

  4. Biogenic silica in space and time in sediments of Central Indian Ocean

    Digital Repository Service at National Institute of Oceanography (India)

    Pattan, J.N.; Gupta, S.M.; Mudholkar, A.V.; Parthiban, G.

    silica (30-35%) in the surface sediments from 11 degrees to 13 degrees S, may be due to higher productivity and better preservation of siliceous tests. The lowest biogenic silica at approximately 100 to 140 x 10 sup(3) y BP is suppressed with higher...

  5. Distinguishing black carbon from biogenic humic substances in soil clay fractions

    Science.gov (United States)

    Laird, D.A.; Chappell, M.A.; Martens, D.A.; Wershaw, R. L.; Thompson, M.

    2008-01-01

    Most models of soil humic substances include a substantial component of aromatic C either as the backbone of humic heteropolymers or as a significant component of supramolecular aggregates of degraded biopolymers. We physically separated coarse (0.2-2.0????m e.s.d.), medium (0.02-0.2????m e.s.d.), and fine (> 0.02????m e.s.d.) clay subfractions from three Midwestern soils and characterized the organic material associated with these subfractions using 13C-CPMAS-NMR, DTG, SEM-EDX, incubations, and radiocarbon age. Most of the C in the coarse clay subfraction was present as discrete particles (0.2-5????m as seen in SEM images) of black carbon (BC) and consisted of approximately 60% aromatic C, with the remainder being a mixture of aliphatic, anomeric and carboxylic C. We hypothesize that BC particles were originally charcoal formed during prairie fires. As the BC particles aged in soil their surfaces were oxidized to form carboxylic groups and anomeric and aliphatic C accumulated in the BC particles either by adsorption of dissolved biogenic compounds from the soil solution or by direct deposition of biogenic materials from microbes living within the BC particles. The biogenic soil organic matter was physically separated with the medium and fine clay subfractions and was dominated by aliphatic, anomeric, and carboxylic C. The results indicate that the biogenic humic materials in our soils have little aromatic C, which is inconsistent with the traditional heteropolymer model of humic substances.

  6. Biogenic amines determination in some traditional cheeses in West Azerbaijan province of Iran.

    Science.gov (United States)

    Razavi Rohani, Seyed Mehdi; Aliakbarlu, Javad; Ehsani, Ali; Hassanzadazar, Hassan

    2013-01-01

    Biogenic amines (BA) are nitrogenous compounds that possess biological activity. The source of production is the microbial decarboxylation of amino acids. This compounds are found in various types of cheese. The aim of this work was to evaluate the BA content of some traditional cheeses in West Azerbaijan province Iran. For this purpose, 70 samples of Koopeh, 10 samples of Lighvan and 5 samples of Red Salmas cheeses were obtained from local supermarkets of different cities of West Azerbaijan province. After preparation of samples, biogenic amines content was evaluated by modified HPLC method. The presence of histamine, cadaverine, putrescine and tyramine in tested cheeses were observed. Total amount of biogenic amines was highest in Red Salmas cheese with 1426.91 ppm. It followed by Lighvan cheese and Koopeh cheese with 1008.98 and 517.71 ppm, respectively. Putrescine, cadaverine, histamine and tyramine were detected in Koopeh cheese at levels up to 156.09, 282.34, 70.80, 8.48 ppm respectively. These amines were detected also in Lighvan cheese at levels up to 277.53, 342.74, 37.58, 351.12 ppm and in Red Salmas cheese samples at levels up to 438.03, 701.05, 105.21, 182.62 ppm, respectively. Large amounts of biogenic amines can indicate non hygienic conditions and contamination of used milk for cheese production. PMID:25653782

  7. Age and Gender-Related Changes in Biogenic Amine Metabolites in Cerebrospinal Fluid in Children.

    Science.gov (United States)

    Kuśmierska, Katarzyna; Szymańska, Krystyna; Rokicki, Dariusz; Kotulska, Katarzyna; Jóźwiak, Sergiusz; Sykut-Cegielska, Jolanta; Mierzewska, Hanna; Szczepanik, Elzbieta; Pronicka, Ewa; Demkow, Urszula

    2016-01-01

    Metabolites of cerebrospinal biogenic amines (dopamine and serotonin)are an important tool in clinical research and diagnosis of children with neurotransmitter disorders. In this article we focused on finding relationships between the concentration of biogenic amine metabolites, age, and gender. We analyzed 148 samples from children with drug resistant seizures of unknown etiology and children with mild stable encephalopathy aged 0-18 years. A normal profile of biogenic amineswas found in 107 children and those children were enrolled to the study group. The CSF samples were analyzed by HPLC with an electrochemical detector. The concentrations of the dopamine and serotonin metabolites homovanillic acid (HVA) and 5-hydroxyindoleacetic acid (5-HIAA), respectively, were high at birth, gradually decreasing afterward until the 18 years of age. Nevertheless, the HVA/5-HIAA ratio did not vary with age, except in the children below 1 year of age. In the youngest group we observed a strong relationship between the HVA/5-HIAA ratio and age (r = 0.69, p biogenic amine metabolites is age and sex dependent. PMID:26453071

  8. Differential behavioral responses of two plant-parasitic nematodes to biogenic amines

    Science.gov (United States)

    Hatching and infective juvenile (J2) behavior in two species of plant-parasitic nematodes, Heterodera glycines and Meloidogyne incognita, were affected by in vitro treatment with the biogenic amines dopamine, octopamine, and serotonin. While the overall responses of each species to amine exposures w...

  9. Synthesis of Derivatives of Biogenic Amines Labelled with Radioactive Tracers for Brain Imaging

    Directory of Open Access Journals (Sweden)

    Arturo A. Vitale

    2000-03-01

    Full Text Available Endogenous derivatives of biogenic amines, such as phenethylamines, indolalkylamines and harmines, have been extensively studied as usual constituents of body fluids. Methylated derivatives of indolalkylamines have been also related to mental disorders, e.g. schizophrenia and hallucination.

  10. Effect of biogenic amines on the mating and egg-laying behaviors in the stable fly

    Science.gov (United States)

    The stable fly Stomoxys calcitrans (L.) (Diptera: Muscidae), is one of the most significant biting fly pests affecting livestock.The annual economic damage to the U.S. cattle industry is estimated at over one billion US dollars. Biogenic amines are known to play critical roles in feeding and reprodu...

  11. A ratiometric fluorescent probe for detection of biogenic primary amines with nanomolar sensitivity.

    Science.gov (United States)

    Mallick, Suman; Chandra, Falguni; Koner, Apurba L

    2016-02-01

    An ultrasensitive ratiometric fluorescent sensor made of an N,N-dimethylaminonaphthalene anhydride moiety for detection of aliphatic primary amines is reported. Biogenic amines at nanomolar concentration is detected with the additional ability to discriminate between primary, secondary and tertiary amines by using both UV-Visible and fluorescence spectroscopy. PMID:26734688

  12. Biogenic amines determination in some traditional cheeses in West Azerbaijan province of Iran

    Directory of Open Access Journals (Sweden)

    Seyed Mehdi Razavi Rohani

    2013-06-01

    Full Text Available Biogenic amines (BA are nitrogenous compounds that possess biological activity. The source of production is the microbial decarboxylation of amino acids. This compounds are found in various types of cheese. The aim of this work was to evaluate the BA content of some traditional cheeses in West Azerbaijan province Iran. For this purpose, 70 samples of Koopeh, 10 samples of Lighvan and 5 samples of Red Salmas cheeses were obtained from local supermarkets of different cities of West Azerbaijan province. After preparation of samples, biogenic amines content was evaluated by modified HPLC method. The presence of histamine, cadaverine, putrescine and tyramine in tested cheeses were observed. Total amount of biogenic amines was highest in Red Salmas cheese with 1426.91 ppm. It followed by Lighvan cheese and Koopeh cheese with 1008.98 and 517.71 ppm, respectively. Putrescine, cadaverine, histamine and tyramine were detected in Koopeh cheese at levels up to 156.09, 282.34, 70.80, 8.48 ppm respectively. These amines were detected also in Lighvan cheese at levels up to 277.53, 342.74, 37.58, 351.12 ppm and in Red Salmas cheese samples at levels up to 438.03, 701.05, 105.21, 182.62 ppm, respectively. Large amounts of biogenic amines can indicate non hygienic conditions and contamination of used milk for cheese production.

  13. Importance of particle formation to reconstructed water column biogenic silica fluxes

    NARCIS (Netherlands)

    Moriceau, B.; Gallinari, M.; Soetaert, K.E.R.; Ragueneau, O.

    2007-01-01

    The particles sinking out of the ocean's surface layer are made up of a mixture of living and dead algal cells, fecal pellets, and aggregates, while the parameters used to describe the behavior of biogenic silica (bSiO2) in today's models are experimentally determined on freely suspended diatoms (FC

  14. 77 FR 21772 - Notification of Two Public Teleconferences of the Science Advisory Board Biogenic Carbon...

    Science.gov (United States)

    2012-04-11

    ... of Air and Radiation requested SAB review of EPA's draft accounting framework. As noticed in 76 FR... Stationary Sources (September 2011). As noticed in 76 FR 80368-80369, the Panel discussed its draft reports... AGENCY Notification of Two Public Teleconferences of the Science Advisory Board Biogenic Carbon...

  15. Radiocarbon AMS determination of the biogenic component in CO{sub 2} emitted from waste incineration

    Energy Technology Data Exchange (ETDEWEB)

    Calcagnile, L., E-mail: lucio.calcagnile@unisalento.it [CEDAD-Department of Innovation Engineering, University of Salento, via per Monteroni, 73100 Lecce (Italy); Quarta, G., E-mail: gianluca.quarta@unisalento.it [CEDAD-Department of Innovation Engineering, University of Salento, via per Monteroni, 73100 Lecce (Italy); D' Elia, M., E-mail: marisa.delia@unisalento.it [CEDAD-Department of Innovation Engineering, University of Salento, via per Monteroni, 73100 Lecce (Italy); Ciceri, G., E-mail: giovanni.ciceri@erse-web.it [Ricerca sul Sistema Energetico-RSE spa, Dipartimento Ambiente e Sviluppo Sostenibile, Via R. Rubattino, 54, 20134 Milano (Italy); Martinotti, V., E-mail: valter.Martinotti@erse-web.it [Ricerca sul Sistema Energetico-RSE spa, Dipartimento Ambiente e Sviluppo Sostenibile, Via R. Rubattino, 54, 20134 Milano (Italy)

    2011-12-15

    The thermal utilization of waste for energy production is gaining importance in European countries. Nevertheless, the combustion of waste leads to significant CO{sub 2} emissions in the atmosphere which, depending on the fraction of biogenic and fossil materials, have to be only partially accounted for the national greenhouse gas inventory. For this reason the development of proper methodologies for the measurement of the biogenic fraction in the combusted waste is an active research field. In fact the determination of the radiocarbon concentration in the carbon dioxide stack emissions allows to have a direct indication of the biogenic component in the burned fuel. We present the results of the AMS radiocarbon analyses carried out on carbon dioxide sampled at the stack of three power plants located in Northern Italy burning natural gas, landfill biogas and SRF (Solid Recovered Fuel) derived from MSW (Municipal Solid Waste). The sampling apparatus and the applied processing protocols are described together with the calculation procedures used to determine, from the measured radiocarbon concentrations, the proportion of biogenic and fossil component in the flue gas and in the combusted fuel. The results confirm the high potentialities of this approach in the analysis of industrial CO{sub 2} emissions.

  16. Radiocarbon AMS determination of the biogenic component in CO 2 emitted from waste incineration

    Science.gov (United States)

    Calcagnile, L.; Quarta, G.; D'Elia, M.; Ciceri, G.; Martinotti, V.

    2011-12-01

    The thermal utilization of waste for energy production is gaining importance in European countries. Nevertheless, the combustion of waste leads to significant CO 2 emissions in the atmosphere which, depending on the fraction of biogenic and fossil materials, have to be only partially accounted for the national greenhouse gas inventory. For this reason the development of proper methodologies for the measurement of the biogenic fraction in the combusted waste is an active research field. In fact the determination of the radiocarbon concentration in the carbon dioxide stack emissions allows to have a direct indication of the biogenic component in the burned fuel. We present the results of the AMS radiocarbon analyses carried out on carbon dioxide sampled at the stack of three power plants located in Northern Italy burning natural gas, landfill biogas and SRF (Solid Recovered Fuel) derived from MSW (Municipal Solid Waste). The sampling apparatus and the applied processing protocols are described together with the calculation procedures used to determine, from the measured radiocarbon concentrations, the proportion of biogenic and fossil component in the flue gas and in the combusted fuel. The results confirm the high potentialities of this approach in the analysis of industrial CO 2 emissions.

  17. Carbon-14 based determination of the biogenic fraction of industrial CO2 emissions : Application and validation

    NARCIS (Netherlands)

    Palstra, S. W. L.; Meijer, H. A. J.

    2010-01-01

    The C-14 method is a very reliable and sensitive method for industrial plants, emission authorities and emission inventories to verify data estimations of biogenic fractions of CO2 emissions. The applicability of the method is shown for flue gas CO2 samples that have been sampled in I-h intervals at

  18. Biocompatibility assessment of rice husk-derived biogenic silica nanoparticles for biomedical applications.

    Science.gov (United States)

    Alshatwi, Ali A; Athinarayanan, Jegan; Periasamy, Vaiyapuri Subbarayan

    2015-02-01

    Synthetic forms of silica have low biocompatibility, whereas biogenic forms have myriad beneficial effects in current toxicological applications. Among the various sources of biogenic silica, rice husk is considered a valuable agricultural biomass material and a cost-effective resource that can provide biogenic silica for biomedical applications. In the present study, highly pure biogenic silica nanoparticles (bSNPs) were successfully harvested from rice husks using acid digestion under pressurized conditions at 120°C followed by a calcination process. The obtained bSNPs were subjected to phase identification analysis using X-ray diffraction, which revealed the amorphous nature of the bSNPs. The morphologies of the bSNPs were observed using transmission electron microscopy (TEM), which revealed spherical particles 10 to 30 nm in diameter. Furthermore, the biocompatibility of the bSNPs with human lung fibroblast cells (hLFCs) was investigated using a viability assay and assessing cellular morphological changes, intracellular ROS generation, mitochondrial transmembrane potential and oxidative stress-related gene expression. Our results revealed that the bSNPs did not have any significant incompatibility in these in vitro cell-based approaches. These preliminary findings suggest that bSNPs are biocompatible, could be the best alternative to synthetic forms of silica and are applicable to food additive and biomedical applications. PMID:25492167

  19. Biogenic acids produced on epoxy linings installed in sewer crown and tidal zones.

    Science.gov (United States)

    Valix, M; Shanmugarajah, K

    2015-09-01

    In this study the biogenic acids generated by microbes on the surface of Bisphenol A epoxy mortar coupons were investigated for up to 30 months. The epoxy coupons were installed in six sewers in three city locations, Sydney, Melbourne and Perth. Coupons were installed in both the crown and the tidal zones of the sewers to capture the effect of location within the pipe on acid production. The coupons were retrieved approximately every 6 months to provide a dynamic analysis of the biogenic acid production. Our results reveal the colonisation of epoxy mortar by the more aggressive acidophilic bacteria occurred within six months to two years of their installation in the sewer pipes. Biogenic acid generation appear to occur homogeneously from the tidal zone to the crown of the sewer pipes. The reduction in the surface pH of the epoxy lining was supported by the successive growth of microbes beginning with fungi followed be neutrophilic and heterotrophic bacteria and finally by the acidophilic bacteria and the corresponding accumulation of organic and sulphuric acids attributed to these organisms. This study also revealed the potential inhibiting effects on the microbes induced by the accumulation of metabolic products on the epoxy surface. The accumulation of organic acids and H2S coincided with the growth and metabolism inhibition of fungi and acidophilic bacteria. These results provide insights into the microbial interaction and biogenic acids production that contribute to lining degradation and corrosion of concrete in sewer pipes. PMID:26005783

  20. Buried iron archaeological artefacts: Corrosion mechanisms related to the presence of Cl-containing phases

    International Nuclear Information System (INIS)

    Deterioration after excavation of archaeological iron artefacts buried in soil is often associated with the presence of Cl-containing phases in corrosion products, leading to serious problems for conservation of metallic objects of cultural heritage. Thus, in order to better understand the corrosion process related to the presence of chlorine, some high-resolution techniques of materials characterisation are implemented. Particularly this paper shows the great utility of the combination of micro-X-ray diffraction, micro-Raman spectroscopy and micro-X-ray absorption spectroscopy. The analyses are realised on the cross sections of iron corroded objects excavated on archaeological sites dated from the 12th to the 16th century AD. In addition to the common oxyhydroxide containing chloride, akaganeite (β-FeOOH) often mentioned in the literature, a ferrous hydroxychloride β-Fe2(OH)3Cl was also found in the corrosion layers. In order to explain the corrosion system formed during burial, a corrosion mechanism including the presence of chlorine, is proposed

  1. Production and Early Preservation of Lipid Biomarkers in Iron Hot Springs

    Energy Technology Data Exchange (ETDEWEB)

    Parenteau, Mary N.; Jahnke, Linda L.; Farmer, Jack D.; Cady, Sherry L.

    2014-06-01

    The bicarbonate-buffered anoxic vent waters at Chocolate Pots hot springs in Yellowstone National Park are 51–54°C, pH 5.5–6.0, and are very high in dissolved Fe(II) at 5.8–5.9 mg/L. The aqueous Fe(II) is oxidized by a combination of biotic and abiotic mechanisms and precipitated as primary siliceous nanophase iron oxyhydroxides (ferrihydrite). Four distinct prokaryotic photosynthetic microbial mat types grow on top of these iron deposits. Lipids were used to characterize the community composition of the microbial mats, link source organisms to geologically significant biomarkers, and investigate how iron mineralization degrades the lipid signature of the community. The phospholipid and glycolipid fatty acid profiles of the highest-temperature mats indicate that they are dominated by cyanobacteria and green nonsulfur filamentous anoxygenic phototrophs (FAPs). Diagnostic lipid biomarkers of the cyanobacteria include midchain branched mono- and dimethylalkanes and, most notably, 2-methylbacteriohopanepolyol. Diagnostic lipid biomarkers of the FAPs (Chloroflexus and Roseiflexus spp.) include wax esters and a long-chain tri-unsaturated alkene. Surprisingly, the lipid biomarkers resisted the earliest stages of microbial degradation and diagenesis to survive in the iron oxides beneath the mats. Understanding the potential of particular sedimentary environments to capture and preserve fossil biosignatures is of vital importance in the selection of the best landing sites for future astrobiological missions to Mars. Finally, this study explores the nature of organic degradation processes in moderately thermal Fe(II)-rich groundwater springs—environmental conditions that have been previously identified as highly relevant for Mars exploration.

  2. Production and early preservation of lipid biomarkers in iron hot springs.

    Science.gov (United States)

    Parenteau, Mary N; Jahnke, Linda L; Farmer, Jack D; Cady, Sherry L

    2014-06-01

    The bicarbonate-buffered anoxic vent waters at Chocolate Pots hot springs in Yellowstone National Park are 51-54°C, pH 5.5-6.0, and are very high in dissolved Fe(II) at 5.8-5.9 mg/L. The aqueous Fe(II) is oxidized by a combination of biotic and abiotic mechanisms and precipitated as primary siliceous nanophase iron oxyhydroxides (ferrihydrite). Four distinct prokaryotic photosynthetic microbial mat types grow on top of these iron deposits. Lipids were used to characterize the community composition of the microbial mats, link source organisms to geologically significant biomarkers, and investigate how iron mineralization degrades the lipid signature of the community. The phospholipid and glycolipid fatty acid profiles of the highest-temperature mats indicate that they are dominated by cyanobacteria and green nonsulfur filamentous anoxygenic phototrophs (FAPs). Diagnostic lipid biomarkers of the cyanobacteria include midchain branched mono- and dimethylalkanes and, most notably, 2-methylbacteriohopanepolyol. Diagnostic lipid biomarkers of the FAPs (Chloroflexus and Roseiflexus spp.) include wax esters and a long-chain tri-unsaturated alkene. Surprisingly, the lipid biomarkers resisted the earliest stages of microbial degradation and diagenesis to survive in the iron oxides beneath the mats. Understanding the potential of particular sedimentary environments to capture and preserve fossil biosignatures is of vital importance in the selection of the best landing sites for future astrobiological missions to Mars. This study explores the nature of organic degradation processes in moderately thermal Fe(II)-rich groundwater springs--environmental conditions that have been previously identified as highly relevant for Mars exploration. PMID:24886100

  3. Iron-Deficiency Anemia

    Medline Plus

    Full Text Available ... symptoms. Severe iron-deficiency anemia can lead to heart problems, infections, problems with growth and development in ... 18/2011 This video—presented by the National Heart, Lung, and Blood Institute, part of the National ...

  4. Study of iron fluorination

    International Nuclear Information System (INIS)

    This report deals with the action of fluorine on iron. Comprehensive descriptions are given of the particular technological methods and of the preparation of the reactants. This fluorination reaction has been investigated over a very broad range of temperature and pressure. A nucleation and growth phenomenon is described. The influence of a pollution of the gas phase by oxygen on the fluorination process is reported. The solid-state reaction between ferric fluoride and iron has been studied by calorimetry and hydrated fluorides βFeF3, 3 H2O and FeF3, H2O have been studied by Moessbauer effect. A special study has been made of the growth of iron deposits by thermal decomposition of gaseous iron fluorides. (author)

  5. Iron-Deficiency Anemia

    Medline Plus

    Full Text Available ... Entire Site Health Topics News & Resources Intramural Research Public Health Topics Education & Awareness Resources Contact The Health ... Severe iron-deficiency anemia can lead to heart problems, infections, problems with growth and development in children, ...

  6. Iron-Deficiency Anemia

    Medline Plus

    Full Text Available ... of red blood cells. Red blood cells carry oxygen and remove carbon dioxide (a waste product) from ... Hemoglobin is an iron-rich protein that carries oxygen from the lungs to the rest of the ...

  7. Iron-Deficiency Anemia

    Medline Plus

    Full Text Available ... Digg. Share this page from the NHLBI on Facebook. Add this link to the NHLBI to my ... such as tiredness, poor skin tone, dizziness, and depression. After her doctor diagnosed her with iron-deficiency ...

  8. Iron-Deficiency Anemia

    Medline Plus

    Full Text Available ... Deficiency Anemia What Is... CAUSES WHO IS AT RISK SIGNS & SYMPTOMS DIAGNOSIS TREATMENTS PREVENTION LIVING WITH CLINICAL ... and women are the two groups at highest risk for iron-deficiency anemia. Outlook Doctors usually can ...

  9. Ocean iron fertilization

    Digital Repository Service at National Institute of Oceanography (India)

    Naqvi, S.W.A.; Smetacek, V.

    In 2009 and 2010, an Indo-German scientific expedition dusted the ocean with iron to stimulate the biological pump that captures atmosphereic carbon dioxide. Two onboard scientists tell the story of this controversial project. Besides raising...

  10. Iron-Deficiency Anemia

    Medline Plus

    Full Text Available ... Topics Anemia Blood Tests Blood Transfusion Restless Legs Syndrome Send a link to NHLBI to someone by ... symptoms. Severe iron-deficiency anemia can lead to heart problems, infections, problems with growth and development in ...

  11. Iron-Deficiency Anemia

    Medline Plus

    Full Text Available ... CAUSES WHO IS AT RISK SIGNS & SYMPTOMS DIAGNOSIS TREATMENTS PREVENTION LIVING WITH CLINICAL TRIALS LINKS Related Topics ... Doctors usually can successfully treat iron-deficiency anemia. Treatment will depend on the cause and severity of ...

  12. Iron-Deficiency Anemia

    Medline Plus

    Full Text Available ... Events Spokespeople Email Alerts E-Newsletters About NHLBI Organization NHLBI Director Budget, Planning, & Legislative Advisory Committees Contact ... counseling on how to improve her health and well-being. She began taking iron supplements and multivitamins ...

  13. Iron-Deficiency Anemia

    Medline Plus

    Full Text Available ... Health Topics Education & Awareness Resources Contact The Health Information Center Health Professionals Systematic Evidence Reviews & Clinical Practice ... and see the benefits of treatment. For more information about living with and managing iron-deficiency anemia, ...

  14. Iron in diet

    Science.gov (United States)

    ... Soybeans Dried beans and peas Kidney beans Seeds: Almonds Brazil nuts Vegetables: Broccoli Spinach Kale Collards Asparagus ... infant's additional iron needs are met by breast milk. Infants that are not breastfed should be given ...

  15. Iron-Deficiency Anemia

    Medline Plus

    Full Text Available ... Alerts E-Newsletters About NHLBI Organization NHLBI Director Budget, Planning, & Legislative Advisory Committees Contact Us FAQs Home » ... severity of the condition. Treatments may include dietary changes, medicines, and surgery. Severe iron-deficiency anemia may ...

  16. Photocatalytic oxidation of chloroform using immobilized-biogenic TiO2 nanoparticles

    Science.gov (United States)

    Kim, Y.; Cho, Y.; Yoo, H.

    2011-12-01

    Although commercial titanium dioxide (TiO2) nanoparticles as a suspension in water are one of the most popular photocatalysts for treatment of chlorinated organic compounds, the reuse and recovery of the nanoscale phtocatalyst is a practical challenge for application in water and groundwater treatment system. As part of efforts to overcome this practical limitation, development of immobilized TiO2 is needed. Diatom Pinnularia sp. were found to be capable of producing nanoscale TiO2 in their microscale silica shells. In order to obtain biogenic TiO2 nanoparticles from Pinnularia sp., soluble Ti was fed to the silicon-starved cells, resulting in deposition of titanium on the microscale features of the silica shells. After thermal treatment at 720 oC for 2 hr, the titanium was eventually converted to nanoscale TiO2. In order to determine the physical and chemical properties of the immobilized TiO2, material characterization such as TEM, STEM-EDS, BET and XRD analysis was carried out. In this study, a novel type of immobilized photocatalytic nanoparticles, biogenic TiO2 on silica shells was used for the mineralization of chloroform in water. Batch tests were conducted to evaluate the chloroform removal efficiency of biogenic and commercial TiO2 nanoparticles. Also, the amount of Cl- ions in water during the mineralization was measured to check mineralization of chloroform by biogenic TiO2 nanoparticles. Kinetic models were used to determine the rate of chloroform mineralization. In addition, the effect of UVA (ultraviolet-A) intensity on chloroform mineralization was investigated. The results obtained from this study could provide useful information for practical application of biogenic TiO2 in the groundwater treatment contaminated with some chlorinated organic compounds.

  17. Biocompatibility assessment of rice husk-derived biogenic silica nanoparticles for biomedical applications

    Energy Technology Data Exchange (ETDEWEB)

    Alshatwi, Ali A., E-mail: alshatwi@ksu.edu.sa; Athinarayanan, Jegan; Periasamy, Vaiyapuri Subbarayan

    2015-02-01

    Synthetic forms of silica have low biocompatibility, whereas biogenic forms have myriad beneficial effects in current toxicological applications. Among the various sources of biogenic silica, rice husk is considered a valuable agricultural biomass material and a cost-effective resource that can provide biogenic silica for biomedical applications. In the present study, highly pure biogenic silica nanoparticles (bSNPs) were successfully harvested from rice husks using acid digestion under pressurized conditions at 120 °C followed by a calcination process. The obtained bSNPs were subjected to phase identification analysis using X-ray diffraction, which revealed the amorphous nature of the bSNPs. The morphologies of the bSNPs were observed using transmission electron microscopy (TEM), which revealed spherical particles 10 to 30 nm in diameter. Furthermore, the biocompatibility of the bSNPs with human lung fibroblast cells (hLFCs) was investigated using a viability assay and assessing cellular morphological changes, intracellular ROS generation, mitochondrial transmembrane potential and oxidative stress-related gene expression. Our results revealed that the bSNPs did not have any significant incompatibility in these in vitro cell-based approaches. These preliminary findings suggest that bSNPs are biocompatible, could be the best alternative to synthetic forms of silica and are applicable to food additive and biomedical applications. - Highlights: • Simple, rapid and convenient process • Amorphous and spherical with 10–30 nm size SiO{sub 2} nanoparticles were fabricated. • Biogenic silica nanoparticles showed biocompatibility. • bSNPs are an alternative to synthetic forms of silica.

  18. New procedure of selected biogenic amines determination in wine samples by HPLC

    Energy Technology Data Exchange (ETDEWEB)

    Piasta, Anna M.; Jastrzębska, Aneta, E-mail: aj@chem.uni.torun.pl; Krzemiński, Marek P.; Muzioł, Tadeusz M.; Szłyk, Edward

    2014-06-27

    Highlights: • We proposed new procedure for derivatization of biogenic amines. • The NMR and XRD analysis confirmed the purity and uniqueness of derivatives. • Concentration of biogenic amines in wine samples were analyzed by RP-HPLC. • Sample contamination and derivatization reactions interferences were minimized. - Abstract: A new procedure for determination of biogenic amines (BA): histamine, phenethylamine, tyramine and tryptamine, based on the derivatization reaction with 2-chloro-1,3-dinitro-5-(trifluoromethyl)-benzene (CNBF), is proposed. The amines derivatives with CNBF were isolated and characterized by X-ray crystallography and {sup 1}H, {sup 13}C, {sup 19}F NMR spectroscopy in solution. The novelty of the procedure is based on the pure and well-characterized products of the amines derivatization reaction. The method was applied for the simultaneous analysis of the above mentioned biogenic amines in wine samples by the reversed phase-high performance liquid chromatography. The procedure revealed correlation coefficients (R{sup 2}) between 0.9997 and 0.9999, and linear range: 0.10–9.00 mg L{sup −1} (histamine); 0.10–9.36 mg L{sup -1} (tyramine); 0.09–8.64 mg L{sup −1} (tryptamine) and 0.10–8.64 mg L{sup −1} (phenethylamine), whereas accuracy was 97%–102% (recovery test). Detection limit of biogenic amines in wine samples was 0.02–0.03 mg L{sup −1}, whereas quantification limit ranged 0.05–0.10 mg L{sup −1}. The variation coefficients for the analyzed amines ranged between 0.49% and 3.92%. Obtained BA derivatives enhanced separation the analytes on chromatograms due to the inhibition of hydrolysis reaction and the reduction of by-products formation.

  19. Arsenite Removal from Simulated Groundwater by Biogenic Schwertmannite: A Column Trial

    Institute of Scientific and Technical Information of China (English)

    XIE Yue; ZHOU Li-Xiang

    2013-01-01

    To assess the feasibility of biogenic schwertmannite to act as a sorbent for removing arsenite from groundwater,a series of biogenic schwertmannite-packed column adsorption experiments were conducted on simulated As(Ⅲ)-containing groundwater.Empty bed contact time (EBCT),As(Ⅲ) concentration in effluent,and the removal efficiency of As(Ⅲ) through the column were investigated at pH 8.0 and temperature 25 ± 0.5 ℃.The results showed that the breakthrough curves were mainly dependent on EBCT values when the influent As(Ⅲ) concentration was 500 μg L-1 and the optimum EBCT was 4.0 min.When the effluent As(Ⅲ) concentration reached 10 and 50 μg L-1,the breakthrough volumes for the schwertmannite adsorption column were 4200 and 5600 bed volume (BV),with As(Ⅲ) adsorption capacity of 2.1 and 2.8 mg g-1,respectively.Biogenic schwertmannite could be regenerated by 1.0 mol L-1 NaOH solution,and more than 80% of As(Ⅲ) adsorbed on the surface of schwertmannite could be released after 3 successive regenerations.The breakthrough volume for the regenerated schwertmannite-packed column still maintained 4 000-4 200 BV when the As(Ⅲ) concentration in effluent was below 10 μg L-1.Compared with other sorbents for As(Ⅲ) removal,the biogenic schwertmannitepacked column had a higher breakthrough volume and a much higher adsorption capacity,implying that biogenic schwertmannite was a highly efficient and potential sorbent to purify As(Ⅲ)-contaminated groundwater.

  20. Biocompatibility assessment of rice husk-derived biogenic silica nanoparticles for biomedical applications

    International Nuclear Information System (INIS)

    Synthetic forms of silica have low biocompatibility, whereas biogenic forms have myriad beneficial effects in current toxicological applications. Among the various sources of biogenic silica, rice husk is considered a valuable agricultural biomass material and a cost-effective resource that can provide biogenic silica for biomedical applications. In the present study, highly pure biogenic silica nanoparticles (bSNPs) were successfully harvested from rice husks using acid digestion under pressurized conditions at 120 °C followed by a calcination process. The obtained bSNPs were subjected to phase identification analysis using X-ray diffraction, which revealed the amorphous nature of the bSNPs. The morphologies of the bSNPs were observed using transmission electron microscopy (TEM), which revealed spherical particles 10 to 30 nm in diameter. Furthermore, the biocompatibility of the bSNPs with human lung fibroblast cells (hLFCs) was investigated using a viability assay and assessing cellular morphological changes, intracellular ROS generation, mitochondrial transmembrane potential and oxidative stress-related gene expression. Our results revealed that the bSNPs did not have any significant incompatibility in these in vitro cell-based approaches. These preliminary findings suggest that bSNPs are biocompatible, could be the best alternative to synthetic forms of silica and are applicable to food additive and biomedical applications. - Highlights: • Simple, rapid and convenient process • Amorphous and spherical with 10–30 nm size SiO2 nanoparticles were fabricated. • Biogenic silica nanoparticles showed biocompatibility. • bSNPs are an alternative to synthetic forms of silica