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Selected AbstractsThe impact of an alien plant on a native plant,pollinator network: an experimental approachECOLOGY LETTERS, Issue 7 2007Martha E. Lopezaraiza, Mikel Abstract Studies of pairwise interactions have shown that an alien plant can affect the pollination of a native plant, this effect being mediated by shared pollinators. Here we use a manipulative field experiment, to investigate the impact of the alien plant Impatiens glandulifera on an entire community of coflowering native plants. Visitation and pollen transport networks were constructed to compare replicated I. glandulifera invaded and I. glandulifera removal plots. Invaded plots had significantly higher visitor species richness, visitor abundance and flower visitation. However, the pollen transport networks were dominated by alien pollen grains in the invaded plots and consequently higher visitation may not translate in facilitation for pollination. The more generalized insects were more likely to visit the alien plant, and Hymenoptera and Hemiptera were more likely to visit the alien than Coleoptera. Our data indicate that generalized native pollinators can provide a pathway of integration for alien plants into native visitation systems. [source] Thrombin potently enhances swelling-sensitive glutamate efflux from cultured astrocytesGLIA, Issue 9 2007Gerardo Ramos-Mandujano Abstract High concentrations of thrombin (Thr) have been linked to neuronal damage in cerebral ischemia and traumatic brain injury. In the present study we found that Thr markedly enhanced swelling-activated efflux of 3H -glutamate from cultured astrocytes exposed to hyposmotic medium. Thr (0.5,5 U/mL) elicited small 3H -glutamate efflux under isosmotic conditions and increased the hyposmotic glutamate efflux by 5- to 10-fold, the maximum effect being observed at 15% osmolarity reduction. These Thr effects involve its protease activity and are fully mimicked by SFFLRN, the synthetic peptide activating protease-activated receptor-1. Thr potentiation of 3H -glutamate efflux was largely dependent on a Thr-elicited increases in cytosolic Ca2+ (Ca2+i) concentration ([Ca2+]i). Preventing Ca2+i rise by treatment with EGTA-AM or with the phospholipase C blocker U73122 reduced the Thr-increased glutamate efflux by 68%. The protein kinase C blockers Go6976 or chelerythrine reduced the Thr effect by 19%,22%, while Ca/calmodulin blocker W7 caused a 63% inhibition. In addition to this Ca2+ -sensitive pathway, Thr effect on glutamate efflux also involved activation of phosphoinositide-3 kinase (PI3K), since it was reduced by the PI3K inhibitor wortmannin (51% inhibition). Treating cells with EGTA-AM plus wortmannin essentially abolished Thr-dependent glutamate efflux. Thr-activated glutamate release was potently inhibited by the blockers of the volume-sensitive anion permeability pathway, NPPB (IC50 15.8 ,M), DCPIB (IC50 4.2 ,M). These results suggest that Thr may contribute to the excitotoxic neuronal injury by elevating extracellular glutamate release from glial cells. Therefore, this work may aid in search of neuroprotective strategies for treating cerebral ischemia and brain trauma. © 2007 Wiley-Liss, Inc. [source] Patterns of mortality for each life-history stage in a population of the endangered New Zealand stitchbirdJOURNAL OF ANIMAL ECOLOGY, Issue 4 2009Matthew Low Summary 1Using data from 396 breeding attempts over an 8-year period, we investigated age- and stage-specific survival rates and their modifying factors in a closed island population of the New Zealand stitchbird (or hihi, Notiomystis cincta Du Bus). 2Survival probability generally increased over time; however, at each life-history transition, survival in the new stage started lower than at the end of the previous stage, creating a ,saw-tooth' function of age-related survival. 3The probability of an egg hatching was low (0·73 ± 0·01): most likely a consequence of genetic bottlenecks previously endured by this population. There was strong support for a positive relationship between hatching rate and the subsequent survival of the female parent, and hatching success declining for females > 4 years old. 4Nestling survival probability increased as a function of brood size and days since hatching, and decreased relative to daily maximum ambient temperature and hatching date. Support for models including ambient temperature was greater than for other covariates, with the majority of this temperature-mediated survival effect being restricted to the early nestling stage. 5Fledglings had low survival rates in the first two weeks after leaving the nest, with post-fledging survival related to the fledgling's mass. Two months after fledging, juvenile survival probability plateaued and remained relatively constant for the following autumn, winter and spring/summer breeding season. There was no effect of sex or season on adult survival probability. However, there was strong support for age-specific variation in adult survival, with survival likelihood increasing during the first four years before showing evidence of a senescence decline. 6Within-stage survival increases were likely related to stage-specific selection pressures initially weeding out individuals of poorer phenotypes for the environment specific to each life-history stage. Such a mechanism explains the initial high mortality at life-history transitions; a well-adapted phenotype for one stage may not necessarily be so well adapted for subsequent stages. These patterns are not only valuable for examining life-history theory, but also for understanding the regulation of vital rates in an endangered species and providing a basis from which better population management models and harvesting regimes can be derived. [source] Inhibition and possible induction of rat CYP2D after short- and long-term treatment with antidepressantsJOURNAL OF PHARMACY AND PHARMACOLOGY: AN INTERNATI ONAL JOURNAL OF PHARMACEUTICAL SCIENCE, Issue 11 2002Wladys, awa A. Daniel The aim of this study was to investigate the influence of tricyclic antidepressants (imipramine, amitriptyline, clomipramine, desipramine), selective serotonin reuptake inhibitors (SSRIs: fluoxetine, sertraline) and novel antidepressant drugs (mirtazapine, nefazodone) on the activity of CYP2D, measured as a rate of ethylmorphine O -deethylation. The reaction was studied in control liver microsomes in the presence of the antidepressants, as well as in microsomes of rats treated intraperitoneally for one day or two weeks (twice a day) with pharmacological doses of the drugs (imipramine, amitriptyline, clomipramine, nefazodone 10 mg kg,1 i.p.; desipramine, fluoxetine, sertraline 5 mg kg,1 i.p.; mirtazapine 3 mg kg,1 i.p.), in the absence of the antidepressants in-vitro. Antidepressants decreased the activity of the rat CYP2D by competitive inhibition of the enzyme, the potency of their inhibitory effect being as follows: clomipramine (Ki = 14 ,M) > sertraline , fluoxetine (Ki = 17 and 16 ,M, respectively) > imipramine , amitriptyline (Ki = 26 and 25 ,M, respectively) > desipramine (Ki = 44 ,M) > nefazodone (Ki = 55 ,M) > mirtazapine (Ki = 107 ,M). A one-day treatment with antidepressants caused a significant decrease in the CYP2D activity after imipramine, fluoxetine and sertraline. After prolonged administration of antidepressants, the decreased CYP2D activity produced by imipramine, fluoxetine and sertraline was still maintained. Moreover, amitriptyline and nefazodone significantly decreased, while mirtazapine increased the activity of the enzyme. Desipramine and clomipramine did not produce any effect when administered in-vivo. The obtained results indicate three different mechanisms of the antidepressants-CYP2D interaction: firstly, competitive inhibition of CYP2D shown in-vitro, the inhibitory effects of tricyclic antidepressants and SSRIs being stronger than those of novel drugs; secondly, in-vivo inhibition of CYP2D produced by both one-day and chronic treatment with tricyclic antidepressants (except for desipramine and clomipramine) and SSRIs, which suggests inactivation of the enzyme apoprotein by reactive metabolites; and thirdly, in-vivo inhibition by nefazodone and induction by mirtazapine of CYP2D produced only by chronic treatment with the drugs, which suggests their influence on the enzyme regulation. [source] Nitrogen biomarkers and their fate in soil,JOURNAL OF PLANT NUTRITION AND SOIL SCIENCE, Issue 6 2003Wulf Amelung Abstract More than 90,% of the nitrogen (N) in soils can be organically bound, but the mechanisms and rates by which it is cycled have eluded researchers. The objective of this research was to contribute to a better understanding of the origin and transformation of soil organic N (SON) by using amino sugars and the enantiomers of amino acids as markers for microbial residues and/or aging processes. Studied samples presented here comprised (1) soil transects across different climates, (2) arable soils with different duration of cropping, and (3) radiocarbon-dated soil profiles. The results suggested that increased microbial alteration of SON temporarily results in a sequestration of N in microbial residues, which are mineralized at later stages of SON decomposition. Microorganisms increasingly sequestered N within intact cell wall residues as frost periods shortened. At a mean annual temperature above 12,15,°C, these residues were mineralized, probably due to limitations in additional substrates. Breaking the grassland for cropping caused rapid SON losses. Microbial residues were decomposed in preference to total N, this effect being enhanced at higher temperatures. Hence, climate and cultivation interactively affected SON dynamics. Nevertheless, not all SON was available to soil microorganisms. In soil profiles, L-aspartic acid and L-lysine slowly converted into their D-form, for lysine even at a similar rate in soils of different microbial activity. Formation of D-aspartate with time was, therefore, induced by microorganisms while that of D-lysine was not. The racemization of the two amino acids indicates that SON not available to microorganisms ages biotically and abiotically. In native soils, the latter is conserved for centuries, despite N deficiency frequently occurring in living terrestrial environments. Climate was not found to affect the fate of old protein constituents in surface soil. When native grassland was broken for cropping, however, old SON constituents had become available to microorganisms and were degraded. Stickstoff-Biomarker und ihre Dynamik im Boden Über 90,% des Stickstoffs im Boden können organisch gebunden sein. Um zu einem besseren Verständnis der Norg -Dynamik im Boden beitragen zu können, analysierte ich Aminozucker und Aminosäure-Enantiomere als Marker für mikrobielle N-Rückstände und/oder Alterungsprozesse von Norg im Boden. Das hier vorgestellte Untersuchungsmaterial umfasste (1) Bodentransekte entlang unterschiedlicher Klimate, (2) Ackerböden mit verschiedener Nutzungsdauer und (3) 14C-datierte Bodenprofile. Die Ergebnisse zeigten, dass mit fortschreitender Umwandlung des Norg mikrobielle N-Rückstände nur vorübergehend im Boden akkumulieren, da sie in späteren Abbauphasen wieder mineralisiert werden. Mikroorganismen bauten zunehmend N in intakte Zellwandrückstände ein, wenn sich die Frostperioden verkürzten. Bei einer Jahresmitteltemperatur über 12,15,°C sank der Beitrag mikrobieller Rückstände zum N-Gehalt, vermutlich weil Mikroorganismen diese mangels anderer Substrate verstärkt mineralisierten. Umbrüche von Gras- zu Ackerland führten zu raschen N-Verlusten. Mikrobielle N-Rückstände wurden bevorzugt abgebaut, ein Effekt, den höhere Temperaturen verstärkten. Demnach steuerte das Klima die Intensität von Nutzungseffekten auf die Norg -Dynamik. Doch nicht der gesamte Norg war für Mikroorganismen zugänglich. Der D-Gehalt von Asparaginsäure und Lysin nahm mit steigendem Alter der organischen Bodensubstanz zu, Lysin racemisierte in den verschiedenen Böden sogar mit gleicher Geschwindigkeit. Anders als die Bildung von D-Asparaginsäure wurde die von Lysin also nicht durch Mikroorganismen beeinflusst. Die Racemisierung der beiden Aminosäuren deutet deshalb darauf hin, dass nicht-bioverfügbare Norg -Bestandteile biotisch und abiotisch im Boden altern. Klimaeinwirkungen auf den Verbleib alter Proteinrückstände ließen sich nicht feststellen. Mit Umbruch von Gras- zu Ackerland erhielten Mikroorganismen allerdings Zugang zu alten Norg -Verbindungen und bauten diese ab. [source] Saturated double-angle method for rapid B1+ mappingMAGNETIC RESONANCE IN MEDICINE, Issue 6 2006Charles H. Cunningham Abstract For in vivo magnetic resonance imaging at high field (,3 T) it is essential to consider the homogeneity of the active B1 field (B1+), particularly if surface coils are used for RF transmission. A new method is presented for highly rapid B1+ magnitude mapping. It combines the double angle method with a B1 -insensitive magnetization-reset sequence such that the choice of repetition time (TR) is independent of T1 and with a multislice segmented (spiral) acquisition to achieve volumetric coverage with adequate spatial resolution in a few seconds. Phantom experiments confirmed the accuracy of this technique even when TR , T1, with the side effect being lowered SNR. The speed of this method enabled B1+ mapping in the chest and abdomen within a single breath-hold. In human cardiac imaging, the method enabled whole-heart coverage within a single 16-s breath-hold. Results from phantoms and healthy volunteers at 1.5 T and 3 T are presented. Magn Reson Med, 2006. © 2006 Wiley-Liss, Inc. [source] |