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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Environmental science & technology 29 (1995), S. 751-761 
    ISSN: 1520-5851
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    [s.l.] : Macmillan Magazines Ltd.
    Nature 400 (1999), S. 858-861 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Dissolved-iron availability plays a critical role in controlling phytoplankton growth in the oceans,. The dissolved iron is overwhelmingly (∼99%) bound to organic ligands with a very high affinity for iron, but the origin, chemical identity and biological availability of this ...
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1573-1421
    Keywords: Metals ; pentasulfide ; metal-pentasulfide complexes ; stability constants ; voltammetry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract A series of stable pentasulfide complexes of the common base metals, Mn, Fe, Co, Ni, Cu and Zn exist in aqueous solutions at ambient temperatures. Pure sodium pentasulfide was prepared and reacted with the divalent cations of Mn, Fe, Co, Ni, Cu and Zn in aqueous solution at ambient temperature. The S52- complexes were found to exist as determined by voltammetric methods. Pentasulfide complexes with compositions assigned as [M(η1-S5)] and [M2(μ- S5)]2+ occur for Mn, Fe, Co and Ni where only one terminal S atom in the S52- binds to one metal (η1 = mono-dentate ligand or M-S-S-S-S-S, μ = ligand bridging two metal centers or M-S-S-S-S-S-M). Conditional stability constants are similar for all four metals with log β1 between 5.3 and 5.7 and log β2 between 11.0 and 11.6. The constants for these pentasulfide complexes are similar to the tetrasulfide complexes and are approximately 0.4–0.8 log units higher than for comparable bisulfide complexes [M(SH)]+ as expected based on the higher nucleophilicity of S52- compared to HS-. Voltammetric results indicate that these are labile complexes. As with the bisulfide and tetrasulfide complexes, Zn(II) and Cu(II) are chemically distinct from the other metals. Zn(II) reacts with pentasulfide to form a stable monomeric pentasulfide chelate, [Zn(η1-S5)] with log β = 8.7. Cu(II) reacts with pentasulfide to form a complex with the probable stoichiometry [Cu(S5)]2 with log β estimated to be 20.2. As with the other four metals, these complexes are comparable with the tetrasulfide complexes. Discrete voltammetric peaks are observed for these complexes and indicate they are electrochemically inert to dissociation. Reactions of Zn(II) and Cu(II) also lead to significant breakup of the polysulfide. The relative strength of the complexes is Cu 〉 Zn 〉 Mn, Fe, Co, Ni. Cu displaces Zn from [Zn(η1- S5)] and both Cu and Zn displace Mn, Fe, Co and Ni from their pentasulfide complexes.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Biogeochemistry 29 (1995), S. 159-181 
    ISSN: 1573-515X
    Keywords: iron ; microbial mat ; porewater ; pyrite ; sedimentary geochemistry ; Spartina alterniflora ; sulfur
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract This study combines an analysis of porewater chemistry with new, solid phase wet chemical extractions to examine the seasonal cycling of Fe in vegetated and unvegetated (cyanobacterial mat) saltmarsh sediments. Saltmarsh sediments are shown to contain more solid phase reactive Fe than other marine sediments studied so far. From the partitioning and speciation of solid Fe, and solid/soluble reduced S analysis in 10 sediment cores, we have observed that a majority of solid Fe in these sediments is cycled rapidly and completely between oxidized reactive Fe and reduced Fe as pyrite. Vegetated porewaters showed a lower pH and much higher Fe(II) concentrations on average than unvegetated porewaters in the top 10 cm, whereas sulfate, alkalinity, and sulfide concentrations were similar in the two environments. The amorphous Fe(III) oxide fraction showed a high negative correlation to solid and soluble reduced S (r 2 = −0.86 and −0.71, respectively) in surface vegetated sediments whereas the crystalline Fe(III) oxide fraction showed a high negative correlation (r 2 = −0.96) to sulfide only at depth. Though reactive Fe was observed in unvegetated sediments, no seasonal trend was apparent and the speciation of solid Fe revealed that most of it was reduced. Solid phase and porewater chemistry support the dominant role of the biota (Spartina alterniflora and bacteria) in controlling the reactivity of Fe and suggest that the current definition of solid phase, reactive Fe should be expanded to include crystalline Fe(III) minerals which are available for pyrite formation in saltmarsh sediments. In support of previous saltmarsh studies, we present evidence that the redox cycle of solid Fe is controlled by sulfate reduction and sediment oxidation which respond to both annual cycles (light, temperature) and to short-term, episodic effects such as weather and tides.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Aquatic geochemistry 1 (1995), S. 89-104 
    ISSN: 1573-1421
    Keywords: Molecular iodine ; iodination kinetics ; iodine speciation ; organic iodine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract The reactivity of 2 µM molecular iodine in seawater toward various organic compounds containing aromatic, α-keto, amino, olefinic and sugar functional groups was investigated. More detailed studies have been made of the reduction kinetics with salicylic acid, α-ketoglutaric acid and the polypeptide oxidized glutathione, particularly to establish whether variation over the pH range 4–9 would provide a similar reduction reactivity or “fingerprint” to that of molecular iodine added to natural seawater. The data indicates that compounds with only one functional group react with first order kinetics whereas compounds with multiple functional groups show more complex behaviour. Kinetic and thermodynamic modelling indicates that HOI is the main iodine species reacting with organic matter at seawater pH of 8.2. Based on the pH “fingerprints”, peptides and compounds containing carbonyl or α-keto groups are the key reductants of molecular iodine added to seawater. These compounds form C-I and N-I bonds which can allow for a rich organic iodine chemistry in seawater. The model compound results are discussed in relation to oceanic processes.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Aquatic geochemistry 1 (1995), S. 175-188 
    ISSN: 1573-1421
    Keywords: alkylation ; groundwater ; mold ; ocean ; polonium ; volatilization
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract Polonium, like other elements in the Group VI Oxygen series (S, Se, Te), has the potential to form volatile alkyl derivatives. This may be evident in its pervasive radioactive excesses in the atmosphere and coastal waters, and its deficiency in surface open ocean waters. We present evidence for the formation of volatile polonium species. The first evidence comes from duplicating experiments that proved the existence of volatile tellurium, its Group VI congener. Cultures of bread mold at room temperature spiked with polonium tracers showed a significant and reproducible loss of about 0.5% per day of volatile polonium species. In another set of experiments, between 30–50% loss of210Po was observed from Floridan groundwater when nitrogen was bubbled through it over durations of 5–30 minutes. Polonium volatility is highly relevant for biogeochemical studies because it may provide a natural radiochemical tracer for recycling of similar volatile sulfur and other Group VI metal species between the geosphere, atmosphere, and hydrosphere.
    Type of Medium: Electronic Resource
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