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We applied a top-down systems biology approach to understand how Chlamydomonas reinhardtii acclimates to long-term heat stress (HS) and recovers from it. For this, we shifted cells from 25 to 42 degrees C for 24 h and back to 25 degrees C for >= 8 h and monitored abundances of 1856 proteins/protein groups, 99 polar and 185 lipophilic metabolites, and cytological and photosynthesis parameters. Our data indicate that acclimation of Chlamydomonas to long-term HS consists of a temporally ordered, orchestrated implementation of response elements at various system levels. These comprise (1) cell cycle arrest; (2) catabolism of larger molecules to generate compounds with roles in stress protection; (3) accumulation of molecular chaperones to restore protein homeostasis together with compatible solutes; (4) redirection of photosynthetic energy and reducing power from the Calvin cycle to the de novo synthesis of saturated fatty acids to replace polyunsaturated ones in membrane lipids, which are deposited in lipid bodies; and (5) when sinks for photosynthetic energy and reducing power are depleted, resumption of Calvin cycle activity associated with increased photorespiration, accumulation of reactive oxygen species scavengers, and throttling of linear electron flow by antenna uncoupling. During recovery from HS, cells appear to focus on processes allowing rapid resumption of growth rather than restoring pre-HS conditions.
Leaching of dissolved C in arable hummocky ground moraine soil landscapes is characterized by a spatial continuum of more or less erosion-affected Luvisols, Calcaric Regosols at exposed positions, and Colluvic Regosols in depressions. Our objective was to estimate the fluxes of dissolved C in four differently eroded soils as affected by erosion-induced pedological and soil structural alterations. In this model study, we considered landscape position effects by adapting the water table as the bottom boundary condition and erosion effects by using pedon-specific soil hydraulic properties. The one-dimensional vertical water movement was described with the Richards equation using HYDRUS-1D. Solute fluxes were obtained by combining calculated water fluxes with concentrations of dissolved organic and inorganic C (DOC and DIC, respectively) measured from soil solution extracted by suction cups at biweekly intervals. In the 3-yr period (2010-2012), DOC fluxes in the 2-m soil depth were similar at the three non-colluvic locations with -0.8 +/- 0.1 g m(-2) yr(-1) (i.e., outflow) but were 0.4 g m(-2) yr(-1) (i.e., input) in the depression. The DIC fluxes ranged from -10.2 g m(-2) yr(-1) for the eroded Luvisol, -9.2 g m(-2) yr(-1) for the Luvisol, and -6.1 g m(-2) yr(-1) for the Calcaric Regosol to 3.2 g m(-2) yr(-1) for the Colluvic Regosol. The temporal variations in DOC and DIC fluxes were controlled by water fluxes. The spatially distributed leaching results corroborate the hypothesis that the effects of soil erosion influence fluxes through modified hydraulic and transport properties and terrain-dependent boundary conditions.
The size and dynamics of biogenic silicon (BSi) pools influence silicon (Si) fluxes from terrestrial to aquatic ecosystems. The research focus up to now was on the role of plants in Si cycling. In recent studies on old forests annual biosilicification rates of idiosomic testate amoebae (i.e. TA producing self-secreted silica shells) were shown to be of the order of Si uptake by trees. However, no comparable data exist for initial ecosystems. We analyzed the protozoic BSi pool (idiosomic TA), corresponding annual biosilicification rates and readily available and amorphous Si fractions along a 10-year chronosequence in a post-mining landscape in Brandenburg, Germany.
Idiosomic Si pools ranged from 3 to 680 g Si ha(-1) and were about 3-4 times higher at vegetated compared to uncovered spots. They increased significantly with age and were related to temporal development of soil chemical properties. The calculation of annual biosilicification resulted in maxima between 2 and 16 kg Si ha(-1) with rates always higher at vegetated spots. Our results showed that the BSi pool of idiosomic TA is built up rapidly during the initial phases of ecosystem development and is strongly linked to plant growth. Furthermore, our findings highlight the importance of TA for Si cycling in young artificial ecosystems. (C) 2014 Elsevier B.V. All rights reserved.
Background: Pavlovian processes are thought to play an important role in the development, maintenance and relapse of alcohol dependence, possibly by influencing and usurping ongoing thought and behavior. The influence of pavlovian stimuli on ongoing behavior is paradigmatically measured by pavlovian-to-instrumental transfer (PIT) tasks. These involve multiple stages and are complex. Whether increased PIT is involved in human alcohol dependence is uncertain. We therefore aimed to establish and validate a modified PIT paradigm that would be robust, consistent and tolerated by healthy controls as well as by patients suffering from alcohol dependence, and to explore whether alcohol dependence is associated with enhanced PIT. Methods: Thirty-two recently detoxified alcohol-dependent patients and 32 age- and gender-matched healthy controls performed a PIT task with instrumental go/no-go approach behaviors. The task involved both pavlovian stimuli associated with monetary rewards and losses, and images of drinks. Results: Both patients and healthy controls showed a robust and temporally stable PIT effect. Strengths of PIT effects to drug-related and monetary conditioned stimuli were highly correlated. Patients more frequently showed a PIT effect, and the effect was stronger in response to aversively conditioned CSs (conditioned suppression), but there was no group difference in response to appetitive CSs. Conclusion: The implementation of PIT has favorably robust properties in chronic alcohol-dependent patients and in healthy controls. It shows internal consistency between monetary and drug-related cues. The findings support an association of alcohol dependence with an increased propensity towards PIT.
Processing of reward is the basis of adaptive behavior of the human being. Neural correlates of reward processing seem to be influenced by developmental changes from adolescence to late adulthood. The aim of this study is to uncover these neural correlates during a slot machine gambling task across the lifespan. Therefore, we used functional magnetic resonance imaging to investigate 102 volunteers in three different age groups: 34 adolescents, 34 younger adults, and 34 older adults. We focused on the core reward areas ventral striatum (VS) and ventromedial prefrontal cortex (VMPFC), the valence processing associated areas, anterior cingulate cortex (ACC) and insula, as well as information integration associated areas, dorsolateral prefrontal cortex (DLPFC), and inferior parietal lobule (IPL). Results showed that VS and VMPFC were characterized by a hyperactivation in adolescents compared with younger adults. Furthermore, the ACC and insula were characterized by a U-shape pattern (hypoactivation in younger adults compared with adolescents and older adults), whereas the DLPFC and IPL were characterized by a J-shaped form (hyperactivation in older adults compared with younger groups). Furthermore, a functional connectivity analysis revealed an elevated negative functional coupling between the inhibition-related area rIFG and VS in younger adults compared with adolescents. Results indicate that lifespan-related changes during reward anticipation are characterized by different trajectories in different reward network modules and support the hypothesis of an imbalance in maturation of striatal and prefrontal cortex in adolescents. Furthermore, these results suggest compensatory age-specific effects in fronto-parietal regions. Hum Brain Mapp 35:5153-5165, 2014. (c) 2014 Wiley Periodicals, Inc.
We investigated the systems response of metabolism and growth after an increase in irradiance in the nonsaturating range in the algal model Chlamydomonas reinhardtii. In a three-step process, photosynthesis and the levels of metabolites increased immediately, growth increased after 10 to 15 min, and transcript and protein abundance responded by 40 and 120 to 240 min, respectively. In the first phase, starch and metabolites provided a transient buffer for carbon until growth increased. This uncouples photosynthesis from growth in a fluctuating light environment. In the first and second phases, rising metabolite levels and increased polysome loading drove an increase in fluxes. Most Calvin-Benson cycle (CBC) enzymes were substrate-limited in vivo, and strikingly, many were present at higher concentrations than their substrates, explaining how rising metabolite levels stimulate CBC flux. Rubisco, fructose-1,6-biosphosphatase, and seduheptulose-1,7-bisphosphatase were close to substrate saturation in vivo, and flux was increased by posttranslational activation. In the third phase, changes in abundance of particular proteins, including increases in plastidial ATP synthase and some CBC enzymes, relieved potential bottlenecks and readjusted protein allocation between different processes. Despite reasonable overall agreement between changes in transcript and protein abundance (R-2 = 0.24), many proteins, including those in photosynthesis, changed independently of transcript abundance.