ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Oecologia 25 (1976), S. 229-241 
    ISSN: 1432-1939
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Epiphytic lichen growth is abundant on the boles and branches of balsam fir trees at high elevations in New Hampshire. These lichens absorb elements needed for growth from solutions flowing over their surfaces and from direct impaction of water droplets. This study describes how epiphytic lichens and fir needles altered the chemistry of simulated rain water solutions under laboratory conditions. Experiments showed: 1) lichens absorbed ammonium and nitrate from solution; the rate of uptake increased with increasing temperature of the solution, 2) lichens lost calcium, magnesium, and hydrogen to the solution, 3) lichen thalli also initially lost potassium, but in time, net movement was reversed back into the thallus, 4) cation movement increased with increasing temperature, and 5) fir needles responded in a manner similar to that of the lichens, but the amount of change was much less. From these results it seems that epiphytic lichens have potential ecological importance in altering the chemistry of throughfall and stemflow.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 2
    ISSN: 1573-515X
    Keywords: carbon dioxide ; carbon mineralization ; fermentation ; methane ; sulfate reduction ; West Virginia ; wetland
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract The mineralization of organic carbon to CH4 and CO2 inSphagnum-derived peat from Big Run Bog, West Virginia, was measured at 4 times in the year (February, May, September, and November) using anaerobic, peat-slurry incubations. Rates of both CH4 production and CO2 production changed seasonally in surface peat (0–25 cm depth), but were the same on each collection date in deep peat (30–45 cm depth). Methane production in surface peat ranged from 0.2 to 18.8 μmol mol(C)−1 hr−1 (or 0.07 to 10.4 μg(CH4) g−1 hr−1) between the February and September collections, respectively, and was approximately 1 μmol mol(C)−1 hr−1 in deep peat. Carbon dioxide production in surface peat ranged from 3.2 to 20 μmol mol(C)−1 hr−1 (or 4.8 to 30.3 μg(CO2) g−1 hr−1) between the February and September collections, respectively, and was about 4 μmol mol(C)−1 hr−1 in deep peat. In surface peat, temperature the master variable controlling the seasonal pattern in CO2 production, but the rate of CH4 production still had the lowest values in the February collection even when the peat was incubated at 19°C. The addition of glucose, acetate, and H2 to the peat-slurry did not stimulate CH4 production in surface peat, indicating that CH4 production in the winter was limited by factors other than glucose degradation products. The low rate of carbon mineralization in deep peat was due, in part, to poor chemical quality of the peat, because adding glucose and hydrogen directly stimulated CH4 production, and CO2 production to a lesser extent. Acetate was utilized in the peat by methanogens, but became a toxin at low pH values. The addition of SO4 2− to the peat-slurry inhibited CH4 production in surface peat, as expected, but surprisingly increased carbon mineralization through CH4 production in deep peat. Carbon mineralization under anaerobic conditions is of sufficient magnitude to have a major influence on peat accumulation and helps to explain the thin (〈 2 m deep), old (〉 13,000 yr) peat deposit found in Big Run Bog.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Biogeochemistry 5 (1988), S. 221-242 
    ISSN: 1573-515X
    Keywords: carbon bonded S ; ester sulfate S ; sulfate reduction ; sulfide oxidation ; sulfur cycling ; West Virginia ; wetland
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract Total S concentration in the top 35 cm of Big Run Bog peat averaged 9.7 μmol·g — wet mass−1 (123 μmol·g dry mass−1). Of that total, an average of 80.8% was carbon bonded S, 10.4% was ester sulfate S, 4.5% was FeS2­S, 2.7% was FeS­S, 1.2% was elemental S, and 0.4% was SO4 2−­S. In peat collected in March 1986, injected with35S­SO4 2− and incubated at 4 °C, mean rates of dissimilatory sulfate reduction (formation of H2S + S0 + FeS + FeS2), carbon bonded S formation, and ester sulfate S formation averaged 3.22, 0.53, and 0.36 nmol·g wet mass−1·h−1, respectively. Measured rates of sulfide oxidation were comparable to rates of sulfate reduction. Although dissolved SO4 2− concentrations in Big Run Bog interstitial water (〈 200 µM) are low enough to theoretically limit sulfate reducing bacteria, rates of sulfate reduction integrated throughout the top 30–35 cm of peat of 9 and 34 mmol·m−2·d−1 (at 4 °C are greater than or comparable to rates in coastal marine sediments. We suggest that sulfate reduction was supported by a rapid turnover of the dissolved SO4 2− pool (average turnover time of 1.1 days). Although over 90% of the total S in Big Run Bog peat was organic S, cycling of S was dominated by fluxes through the inorganic S pools.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Biogeochemistry 10 (1990), S. 81-104 
    ISSN: 1573-515X
    Keywords: Appalachian Mountains ; bogs ; carbon dioxide ; methane ; peat ; sulfate reduction
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract Anaerobic carbon mineralization was evaluated over a 1-year period in two Sphagnum-dominated peatlands, Big Run Bog, West Virginia, and Buckle's Bog, Maryland. In the top 35 cm of peat, mean rates of methane production, anaerobic carbon dioxide production, and sulfate reduction at Big Run Bog were 63,406 and 146 μmol L-1 d-1, respectively, and at Buckle's Bog were 18, 486 and 104 μmol L-1 d-1. Annual anaerobic carbon mineralization to methane and carbon dioxide at Big Run Bog and Buckle's Bog was 52.8 and 57.2 mol m-2, respectively. Rates of methane production were similar to rates reported for other freshwater peatlands, but methane production accounted for only 11.7 and 2.8%, respectively, of the total anaerobic carbon mineralization at these two sites. Carbon dioxide production, resulting substantially from sulfate reduction, dominated anaerobic carbon mineralization. Considerable sulfate reduction despite low instantaneous dissolved sulfate concentrations (typically 〈 300 μmol L-1 of substrate) was apparently fueled by oxidation and rapid turnover of the reduced inorganic sulfur pool. The coincidence of high sulfate inputs to the Big Run Bog and Buckle's Bog watersheds through acid precipitation with the unexpected importance of sulfate reduction leads us to suggest a new hypothesis: peatlands not receiving high sulfate loading should exhibit low rates of anaerobic decomposition, and a predominance of methane production over sulfate reduction; however, if such peatlands become subjected to high rates of sulfur deposition, sulfate reduction may be enhanced as an anaerobic mineralization pathway with attendant effects on carbon balance and peat accumulation.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Water, air & soil pollution 23 (1984), S. 381-396 
    ISSN: 1573-2932
    Source: Springer Online Journal Archives 1860-2000
    Topics: Energy, Environment Protection, Nuclear Power Engineering
    Notes: Abstract Comparisons of stream water chemistry over a 2 yr period in East Fork, which drains an entirely forested watershed, and Big Run, which drains a forested watershed 8 % of which is occupied by Big Run Bog, indicated that Big Run Bog had no effect on stream water H+ or Cl− concentrations, but with increasing stream discharge the wetland was a source of Ca++ Mg++, K+, Na+, NO3 −, and SO4 −, and a sink for Fe+ +. Further comparisons with Tub Run, which drains a forested watershed, 13 and 12% of which is occupied by Tub Run Bog and an abandoned, unreclaimed coal surface mine, respectively, suggested that Tub Run Bog removes H+, Ca ++, Mg++, Fe++, and 504 − from inputs of acid mine drainage. Wetland areas on the landscape contribute to the regulation of stream water chemistry in ways that are different from upland areas, and wetlands may have considerable applied potential for minimizing the impact of the mine drainage on stream water quality.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Water, air & soil pollution 29 (1986), S. 309-320 
    ISSN: 1573-2932
    Source: Springer Online Journal Archives 1860-2000
    Topics: Energy, Environment Protection, Nuclear Power Engineering
    Notes: Abstract Comparisons among 4 peatland sites representing a gradient of increasing Fe, Al, Mn, and S loading revealed significant accumulation of total Fe, Al, and S, but not Mn, in surface (0 to 20 cm deep) peat along the gradient. Iron and Al accumulation were contributed mainly by organically bound fractions, with oxides contributing to a lesser extent. Although SO4 2− and Fe sulfides showed significant increases in concentration along the gradient, most of the accumulation of total S was contributed by organic, rather than inorganic S. Laboratory studies of Fe2+ adsorption by peat indicated that increasing the pH of added Fe2+ solutions (pH values of 3, 4, 5, and 6) did not significantly affect Langmuir equation estimates of either maximum Fe2+ adsorption capacity or the affinity of peat for Fe2+. Regardless of the pH of the added Fe2+ solutions, final solution pH values were relatively uniform, averaging about 3.4, reflecting a considerable bufferring capacity of Sphagnum peat. Factors affecting the accumulation of metals and S in peat remain topics for further investigation.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Water, air & soil pollution 37 (1988), S. 177-191 
    ISSN: 1573-2932
    Source: Springer Online Journal Archives 1860-2000
    Topics: Energy, Environment Protection, Nuclear Power Engineering
    Notes: Abstract Runoff from a highway interchange in western Maryland had Al concentrations averaging about 50 mg L−1, with a maximum of 206 mg L−1. As an alternative to expensive chemical treatment of this Al-rich water, in August 1984, the drainage was diverted through a 500 m2 man-made wetland, constructed from organic peat. For a 10 week period, Al concentrations in water leaving the wetland averaged 1.5 mg L−1. as compared to Al concentrations at the two major inflows to the wetland of 35.3 and 6.6 mg L−1. However, effective treatment of the drainage by the wetland was not observed over the entire 27 mo sampling period. Peat chemical analysis indicated that over the 27 mo, total Al concentration in the peat increased from 2375 μg g−1 to 13 634 μg g−1. Of this increase 5.5 % was contributed by exchangeable Al, 4.3% by adsorbed Al, 39.8% by organically bound Al, 33.1% by oxide bound Al, and 17.2% by precipitated and residual Al. Changes in Fe, Mn, Ca, Mg, K, and Na chemistry in the peat associated with Al retention are discussed.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 109 (1976), S. 2691-2697 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Kinetics of the Acid Hydrolysis of Tris(salicylaldehydato)chromium(III)The kinetics of the acid hydrolysis of tris(salicylaldehydato)chromium(III) were studied spectro-photometrically in mixtures of 1 N H2SO4, 1 N HClO4, and 6 N HClO4 With ethanol, and in the temperature range 30-50°C. The aquation proceeds via a sequence of three consecutive steps of first order and finally leads to hydrated chromium(III) cation. Two intermediates are observed, the absorption spectra of which were calculated.  -  At 40°C the following ratio of rate constants for the three steps of aquation was obtained (ethanol : 1 N H2SO4 = 1 : 1) k1 : k2 : k3 = 61 : 6.5 : 1. The activation parameters were determined. k3 is strongly dependent on the type of acid applied.
    Notes: Die Kinetik der Säurehydrolyse von Tris(salicylaldehydato)chrom(III) Wurde in Gemischen von 1 N H2SO4, 1 N HClO4 bzw. 6 N HClO4 und Äthanol im Temperaturbereich 30-50° spektro-photometrisch untersucht. Die Aquotisierung verläuft über eine Folge von drei Reaktionen 1. Ordnung und führt schließlich zum hydratisierten Chrom(III)-Kation. Dabei werden zwei Zwischenprodukte beobachtet, deren Absorptionsspektren berechnet wurden.  -  Für die Geschwindig-keitskonstanten der drei Teilschritte gilt bei 40° (Äthanol : 1 N H2SO4 = 1 : 1) k1 : k2 : k3 = 61 : 6.5 : 1. Die Aktivierungsparameter wurden bestimmt. k3 ist stark abhängig von der Art der eingesetzten Säure.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 9
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Separation of the Intermediates of the Acid Hydrolysis of Tris(salicylaldehydato)chromium(III) and Kinetics of the Acid Hydrolysis of the Cation Tetraaquamono(salicylaldehydato)chromium(III)The intermediates of the acid hydrolysis of tris(salicylaldehydato)chromium(III) were separated and identified by ion exchange and electrophoresis to be the cations diaquabis(salicylaldehydato)chromium(III) and tetraaquamono(salicylaldehydato)chromium(III) (= [Cr(SA)(H2O)4]2+). The hydrolysis of the cation [Cr(SA)(H2O)4]2+ with perchloric acid is of pseudo-first order and leads to the cation [Cr(H2O)6]3+. For constant ionic strength (I = 3) and [HCIO4] = 0.1-3 N kexp = k′ + k″[H+] is deduced. The mechanism is discussed on the basis of the ΔH≠-and ΔS≠ values obtained.
    Notes: Als Zwischenprodukte der Säurehydrolyse von Tris(salicylaldehydato)chrom(III) wurden durch Ionenaustausch und Elektrophorese die Kationen Diaquabis(salicylaldehydato)chrom(III) und Tetraaquamono(salicylaldehydato)chrom(III) (= [Cr(SA)(H2O)4](2+) identifiziert. Die Hydrolyse des [Cr(SA)(H2O)4]2+-Kations mit Perchlorsäure führt in einer Reaktion pseudo-erster Ordnung zum [Cr(H2O)6]3+-Kation. Für konstante Ionenstärke (I = 3) und [HCIO4] = 0.1-3 N gilt: kexp = k′ + k″[H+]. Der Mechanismus wird anhand der ermittelten ΔH≠- und ΔS≠-Werte diskutiert.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 111 (1978), S. 1315-1322 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Influence of Various Anions on the Kinetics of the Acid Hydrolysis of the Cation Tetraaquamono(salicylaldehydato)chromium(III)The kinetics of the acid hydrolysis of the cation tetraaquamono(salicylaldehydato)chromium(III) in perchloric acid were studied at 70°C at constant ionic strength as a function of various anions added to the system. The hydrolysis is strongly accelerated by oxyanions like sulfate and nitrate, while halide anions like chloride and bromide affect the rate only slightly. The findings are explained on the basis of the „cis-effect“ of the oxyanions. The reaction is interpreted by an associative interchange mechanism (Ia).
    Notes: Die Kinetik der Säurehydrolyse des Tetraaquamono(salicylaldehydato)chrom(III)-Kations in perchlorsaurer Lösung wurde in Abhängigkeit vom Zusatz verschiedener Anionen bei 70°C und konstanter Ionenstärke untersucht. Die Hydrolyse wird durch die Oxyanionen Sulfat und Nitrat stark beschleunigt, während die Halogenid-Ionen Chlorid und Bromid die Reaktionsgeschwindigkeit nur geringfügig erhöhen. Dieses Ergebnis wird mit dem „cis-Effekt“ der Oxyanionen erklärt. Der Reaktionsablauf wird mit einem assoziativen Interchange-Mechanismus (Ia) interpretiert.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...