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  • 1
    Publikationsdatum: 2013-11-01
    Beschreibung: The biogeochemical cycles of carbon (C), nitrogen (N) and phosphorus (P) are interlinked by primary production, respiration and decomposition in terrestrial ecosystems. It has been suggested that the C, N and P cycles could become uncoupled under rapid climate change because of the different degrees of control exerted on the supply of these elements by biological and geochemical processes. Climatic controls on biogeochemical cycles are particularly relevant in arid, semi-arid and dry sub-humid ecosystems (drylands) because their biological activity is mainly driven by water availability. The increase in aridity predicted for the twenty-first century in many drylands worldwide may therefore threaten the balance between these cycles, differentially affecting the availability of essential nutrients. Here we evaluate how aridity affects the balance between C, N and P in soils collected from 224 dryland sites from all continents except Antarctica. We find a negative effect of aridity on the concentration of soil organic C and total N, but a positive effect on the concentration of inorganic P. Aridity is negatively related to plant cover, which may favour the dominance of physical processes such as rock weathering, a major source of P to ecosystems, over biological processes that provide more C and N, such as litter decomposition. Our findings suggest that any predicted increase in aridity with climate change will probably reduce the concentrations of N and C in global drylands, but increase that of P. These changes would uncouple the C, N and P cycles in drylands and could negatively affect the provision of key services provided by these ecosystems.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Delgado-Baquerizo, Manuel -- Maestre, Fernando T -- Gallardo, Antonio -- Bowker, Matthew A -- Wallenstein, Matthew D -- Quero, Jose Luis -- Ochoa, Victoria -- Gozalo, Beatriz -- Garcia-Gomez, Miguel -- Soliveres, Santiago -- Garcia-Palacios, Pablo -- Berdugo, Miguel -- Valencia, Enrique -- Escolar, Cristina -- Arredondo, Tulio -- Barraza-Zepeda, Claudia -- Bran, Donaldo -- Carreira, Jose Antonio -- Chaieb, Mohamed -- Conceicao, Abel A -- Derak, Mchich -- Eldridge, David J -- Escudero, Adrian -- Espinosa, Carlos I -- Gaitan, Juan -- Gatica, M Gabriel -- Gomez-Gonzalez, Susana -- Guzman, Elizabeth -- Gutierrez, Julio R -- Florentino, Adriana -- Hepper, Estela -- Hernandez, Rosa M -- Huber-Sannwald, Elisabeth -- Jankju, Mohammad -- Liu, Jushan -- Mau, Rebecca L -- Miriti, Maria -- Monerris, Jorge -- Naseri, Kamal -- Noumi, Zouhaier -- Polo, Vicente -- Prina, Anibal -- Pucheta, Eduardo -- Ramirez, Elizabeth -- Ramirez-Collantes, David A -- Romao, Roberto -- Tighe, Matthew -- Torres, Duilio -- Torres-Diaz, Cristian -- Ungar, Eugene D -- Val, James -- Wamiti, Wanyoike -- Wang, Deli -- Zaady, Eli -- England -- Nature. 2013 Oct 31;502(7473):672-6. doi: 10.1038/nature12670.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉1] Departamento de Sistemas Fisicos, Quimicos y Naturales, Universidad Pablo de Olavide, Carretera de Utrera, kilometro 1, 41013 Sevilla, Spain [2] Area de Biodiversidad y Conservacion, Departamento de Biologia y Geologia, Escuela Superior de Ciencias Experimentales y Tecnologia, Universidad Rey Juan Carlos, Calle Tulipan Sin Numero, 28933 Mostoles, Spain.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/24172979" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Aluminum Silicates/analysis ; Biomass ; Carbon/analysis/metabolism ; Carbon Cycle ; Climate Change ; *Desert Climate ; *Desiccation ; *Ecosystem ; *Geography ; Models, Theoretical ; Nitrogen/analysis/metabolism ; Nitrogen Cycle ; Phosphoric Monoester Hydrolases/analysis/metabolism ; Phosphorus/analysis/metabolism ; Plants/metabolism ; Soil/*chemistry
    Print ISSN: 0028-0836
    Digitale ISSN: 1476-4687
    Thema: Biologie , Chemie und Pharmazie , Medizin , Allgemeine Naturwissenschaft , Physik
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 179 (1978), S. 2653-2661 
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The formation of a charge-transfer complex (CTC) between maleic anhydride and tetrahydrofuran both in bulk and in chloroform solution is proved by electronic absorption spectroscopy, and its association constant at 35°C is determined by this technique and by 1H NMR. The effect of irradiation with monochromatic 350 nm light upon the fluorescence spectrum of the CTC excited with this same radiation is studied. Significant changes are noted in the bulk system, but the changes are much smaller in the presence of methyl methacrylate which is simultaneously polymerized. The effect of oxygen on the polymerization is discussed.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 3
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Hydrosilylation reactions of 1-allyloxy-3-phenoxy-2-propanol (3) as model compound were carried out with α-dimethylsilyl-ω-hydrooligosiloxane (7; M̄n = 1200) in the presence of hexachloroplatinic acid. It was found that under stoichiometric conditions only 75--80% of the allyl groups were hydrosilylated, due to some isomerization of the allyl groups into vinyl groups, which do not undergo hydrosilylation. This isomerization could be shown to be sensitive to the type of the allyloxy structure. Thus, for example, allyloxybenzene does not undergo isomerization.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 190 (1989), S. 2789-2803 
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: All the side-reactions of a hydrosilylating model system (1-allyloxy-3-phenoxy-2-propanol/. . .-Si(CH3)2H in the presence of hexachloroplatinic acid (CPA); R = [CPA]/[SiH] 〉 10-4) are identified by 13C and 1H NMR. In such conditions the vinyl ether isomers and the residual silanes, formed when R 〈 10-4, are changed into several new species. The most important side-reaction consists in a silane-alcohol condensation (secondary alcohol of the model and, to a much lower extent, tertiary alcohol(tert-butyl alcohol) used as solvent of CPA), which leads to silyloxygrafted moieities. Hydrogen formed in this condensation can partially saturate the vinyl ether isomers the remaining fraction of which is cyclized into a 2-ethyl-1,3-dioxolane derivative. All the side-reactions observed in the case of the model system take place when α,β-diallyloligosulfones are polycondensated with α-dimethylsilyl-ω-hydrooligosiloxanes.
    Zusätzliches Material: 9 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 5
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 33 (1995), S. 1691-1703 
    ISSN: 0887-624X
    Schlagwort(e): 3-alkoxy-5,7-diiodo-6-fluorones ; visible photoinitiators ; acrylate photopolymerization ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Several 3-alkoxy-5, 7-diiodo-6-fluorones (λmax ≈ 470 nm) have been synthesized and evaluated as initiators for photopolymerization triggered with the 515.5 nm line of an Ar+ laser. 2-Acyl- and 2-alkyl-4,5,7-triiodo-3-hydroxy-6-fluorones were also tested at 515.5 nm. 9-Cyano-2-Acyl- and 9-cyano-2-alkyl-4,5,7-triiodo-3-hydroxy-6-fluorones were studied and could be excited with the 632 nm line of a He-Ne laser. Dyes with long linear carbon chain alkoxy groups at C-6 showed larger molar extinction coefficients and formed polymers with better mechanical properties than did compounds with shorter carbon chains, or did the corresponding C-6 phenols. The optimum side chain length of the C-6 ether alkyl group is between 4-7 carbon atoms. With longer carbon chain alkoxy groups at C-8, e.g., octyl, the mechanical properties of the formed polymers are inferior to systems formed with the butyl isomer as photoinitiator. In the case of alkoxy groups with branched alkyl groups (e.g., 2-ethylbutyl), the relationship between dye structure and the properties of the polymers formed is less straightforward. Though the dyes react from their triplet state, the fluorescence quantum yields of the dyes and the performance of the dyes as photoinitiators appear directly related. © 1995 John Wiley & Sons, Inc.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 6
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 1579-1592 
    ISSN: 0887-624X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Differential scanning calorimetry (DSC) has been utilized in several studies on polymerization kinetics, at different heating rates. However, there are several factors affecting the precision of kinetic parameters. In this work, the activation energy of urethane-bond formation between 2,6-tolylene diisocyanate and diethylene glycol is reported, the latter being in excess in order to minimize problems such as thermal transitions and incomplete reaction in the final step. The DSC technique was applied at different heating rates. Both the equal conversion and equal conversion rate options of the method are discussed. The latter appears to be a more adequate option for the system studied here. The results obtained show a good agreement with the model used.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 7
    ISSN: 0935-9648
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 8
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 31 (1993), S. 959-970 
    ISSN: 0887-6266
    Schlagwort(e): laser-induced processes in conducting polymer precursors ; interaction of dyes with polyelectrolytes ; lithography ; microelectronics ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The elimination reaction of polyelectrolyte films of poly(phenylene vinylene) precursor polymers into the fully conjugated chain was induced by irradiation with an Ar+ laser emitting at 514.5 nm. The experiments were conducted using as cast precursor polyelec-trolyte films of both the unsubstituted poly(phenylene vinylene), H-PPV, and its 2,5-dimethoxyphenylene derivative, DMEO-PPV. Precursor polymer films impregnated with an azosulfonic dye, which had a strong absorption at the laser emission wavelength, were also irradiated. The elimination reaction was followed by comparing the elemental analysis and the infrared and visibleultraviolet spectra of the irradiated and nonirradiated areas. With the unsubstituted PPV film no elimination was detected even at power fluence levels up to approximately 350 W/cm-2, but elimination and conversion to the conjugated polymer could be observed at 10 W/cm-2 when the dye was present. For DMEO-PPV the elimination reaction occurred with or without dye impregnation, and similar marking threshold values were measured in both cases. The molecular mechanism used to explain such observations and the possible application in the area of microelectronics are also discussed. © 1993 John Wiley & Sons, Inc.
    Zusätzliches Material: 9 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 9
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 50 (1993), S. 777-792 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Binary blends of poly(vinyl alcohol) (PVA) with poly(acrylic acid) (PAA) and polyacrylamide (PAAm) were characterized by differential scanning calorimetry (DSC), thermal gravimetric analysis (TGA), and infrared spectroscopy (IR). Molecular weight, blend composition, and heating time at 150°C were the variables used. Results obtained by DSC indicated that PAA/PVA blends are miscible in the full range of composition. Similarly, TGA traces showed that thermal stability was higher for blends than for pure polymers. Blends of PVA with high molecular weight PAA exhibited a hydrogel behavior after drying at relatively low temperature (100°C), whereas blends containing low molecular weight PAA behaved as hydrogels only after they were heated at 150°C. Hydrogel character was increased for these two PVA/PAA blends with the heating time at higher temperature (150°C). IR spectra revealed that esterification took place in these blends after thermally treated at this temperature. In contrast, addition of glyoxal in combination with heating was necessary to produce hydrogels from PAAm/PVA blends. Furthermore, the crosslinking degree of these hydrogels was estimated from their absorbency values by applying the Flory-Rehner equation. © 1993 John Wiley & Sons, Inc.
    Zusätzliches Material: 15 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 10
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 47 (1993), S. 53-59 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Graft starch-polyacrylonitrile copolymers have been obtained from cassava starch (yucca starch or tapioca), which was pre-heated at 65 and 95°C for different lengths of time. The copolymerization was carried out by using ceric ion as initiator at different concentrations (2.0 to 8.0 mmol/L) and also varying both the length of time of copolymerization and the ratio of monomer to starch. The composition, or grafting parameters, of all the obtained copolymers was determined by weight difference after they were extracted with dimethylformamide and hydrolyzed with an acidic solution. Samples of these copolymers were also hydrolyzed with an aqueous solution of potasium bydroxide to produce the corresponding hydrogels, and its absorbency in water was determined. © 1993 John Wiley & Sons, Inc.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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