Living roots magnify the response of soil organic carbon decomposition to temperature in temperate grassland.

Increasing atmospheric carbon dioxide (CO2) concentration is both a strong driver of primary productivity and widely believed to be the principal cause of recent increases in global temperature. Soils are the largest store of the world's terrestrial C. Consequently, many investigations have attempted to mechanistically understand how microbial mineralisation of soil organic carbon (SOC) to CO2 will be affected by projected increases in temperature. Most have attempted this in the absence of plants as the flux of CO2 from root and rhizomicrobial respiration in intact plant-soil systems confounds interpretation of measurements. We compared the effect of a small increase in temperature on respiration from soils without recent plant C with the effect on intact grass swards. We found that for 48 weeks, before acclimation occurred, an experimental 3 °C increase in sward temperature gave rise to a 50% increase in below ground respiration (ca.0.4 kg C m−2; Q10=3.5), whereas mineralisation of older SOC without plants increased with a Q10 of only 1.7 when subject to increases in ambient soil temperature. Subsequent 14C dating of respired CO2 indicated that the presence of plants in swards more than doubled the effect of warming on the rate of mineralisation of SOC with an estimated mean C age of ca.8 y or older relative to incubated soils without recent plant inputs. These results not only illustrate the formidable complexity of mechanisms controlling C fluxes in soils, but also suggest that the dual biological and physical effects of CO2 on primary productivity and global temperature have the potential to synergistically increase the mineralisation of existing soil C

The effects of the maintenance of children act on Akan and Ewe notions of paternal responsibility

Domestic rights & duties in Southern Ghan

Child welfare

Aspects of family welfare and plannin

Annona muricata (graviola): toxic or therapeutic

This paper examines annona muricata (graviola): toxic or therapeutic

Reflectionless measures and the Mattila-Melnikov-Verdera uniform rectifiability theorem

A new proof is given of the Mattila-Melnikov-Verdera theorem on the uniform rectifiability of an Ahlfors-David regular measure whose associated Cauchy transform operator is bounded.Comment: 31 pages, 5 figure

Activation of pluripotency genes in human fibroblast cells by a novel mRNA based approach

Background: Several methods have been used to induce somatic cells to re-enter the pluripotent state. Viral transduction of reprogramming genes yields higher efficiency but involves random insertions of viral sequences into the human genome. Although induced pluripotent stem (iPS) cells can be obtained with the removable PiggyBac transposon system or an episomal system, both approaches still use DNA constructs so that resulting cell lines need to be thoroughly analyzed to confirm they are free of harmful genetic modification. Thus a method to change cell fate without using DNA will be very useful in regenerative medicine. Methodology/Principal Findings: In this study, we synthesized mRNAs encoding OCT4, SOX2, cMYC, KLF4 and SV40 large T (LT) and electroporated them into human fibroblast cells. Upon transfection, fibroblasts expressed these factors at levels comparable to, or higher than those in human embryonic stem (ES) cells. Ectopically expressed OCT4 localized to the cell nucleus within 4 hours after mRNA introduction. Transfecting fibroblasts with a mixture of mRNAs encoding all five factors significantly increased the expression of endogenous OCT4, NANOG, DNMT3 beta, REX1 and SALL4. When such transfected fibroblasts were also exposed to several small molecules (valproic acid, BIX01294 and 5'-aza-2'-deoxycytidine) and cultured in human embryonic stem cell (ES) medium they formed small aggregates positive for alkaline phosphatase activity and OCT4 protein within 30 days. Conclusion/Significance: Our results demonstrate that mRNA transfection can be a useful approach to precisely control the protein expression level and short-term expression of reprogramming factors is sufficient to activate pluripotency genes in differentiated cells

Priming of the decomposition of ageing soil organic matter: concentration dependence and microbial control

The amount of carbon (C) stored in soil is an important regulator for the global climate and soil fertility and is the balance between formation and decomposition of soil organic matter (SOM). Decomposition of SOM can be powerfully affected by labile carbon (C) supplements in, for example, the rhizosphere. A stimulation of SOM mineralisation induced by labile C additions is termed priming', and the mechanisms for this phenomenon remain elusive. The most widely held explanation assigns priming to successional dynamics in r- and K-selected groups within the microbial community; groups which have also been connected with fungal (K-selected) and bacterial (r-selected) decomposers. New evidence has also suggested that recently formed SOM is particularly sensitive to priming. We investigated (i) the labile C concentration dependence of SOM mineralisation, (ii) the susceptibility of differently aged SOM to priming and (iii) if priming is due to bacterial or fungal growth dynamics. To create an age gradient of traceable SOM, we spiked a pasture soil using C-14 glucose, and subsampled plots 1day, 2months, 5months and 13months after application (i.e. SOM aged 1day - 13months). Glucose (0-4000g C g(-1)) was added in subsequent laboratory experiments, and respiration, SOM mineralisation ((CO2)-C-14 evolution), bacterial growth rates (leucine incorporation) and fungal biomass (ergosterol) were tracked during ca. 1week. Mineralisation of SOM aged 2-13months showed similar labile C concentration dependencies, and priming increased mineralisation of SOM systematically by up to 350%. The glucose treatments induced variable microbial growth responses for differently aged SOM, which were unrelated to the priming effect. That successional dynamics in microbial r- and K-selected groups, or bacterial and fungal decomposers, respectively, underpinned priming was incompatible with the results obtained. An alternative explanation could be that SOM transformation by extracellular enzymes, for subsequent respiration, could be triggered by labile C. In conclusion, labile C primed the mineralisation of 2-13months aged SOM, and the mechanism for this priming was unrelated to microbial growth dynamics

Superfluid Spin-down, with Random Unpinning of the Vortices

The so-called ``creeping'' motion of the pinned vortices in a rotating superfluid involves ``random unpinning'' and ``vortex motion'' as two physically separate processes. We argue that such a creeping motion of the vortices need not be (biased) in the direction of an existing radial Magnus force, nor should a constant microscopic radial velocity be assigned to the vortex motion, in contradiction with the basic assumptions of the ``vortex creep'' model. We point out internal inconsistencies in the predictions of this model which arise due to this unjustified foundation that ignores the role of the actual torque on the superfluid. The proper spin-down rate of a pinned superfluid is then calculated and turns out to be much less than that suggested in the vortex creep model, hence being of even less observational significance for its possible application in explaining the post-glitch relaxations of the radio pulsars.Comment: To be published in J. Low Temp. Phys., Vol. 139, May 2005 [Eqs 11, 15-17 here, have been revised and, may be substituted for the corresponding ones in that paper

STELLA Facilitates Differentiation of Germ Cell and Endodermal Lineages of Human Embryonic Stem Cells

Stella is a developmentally regulated gene highly expressed in mouse embryonic stem (ES) cells and in primordial germ cells (PGCs). In human, the gene encoding the STELLA homologue lies on chromosome 12p, which is frequently amplified in long-term cultured human ES cells. However, the role played by STELLA in human ES cells has not been reported. In the present study, we show that during retinoic acid (RA)-induced differentiation of human ES cells, expression of STELLA follows that of VASA, a marker of germline differentiation. By contrast, human embryonal carcinoma cells express STELLA at a higher level compared with both karyotypically normal and abnormal human ES cell lines. We found that over-expression of STELLA does not interfere with maintenance of the stem cell state of human ES cells, but following retinoic acid induction it leads to up-regulation of germline- and endodermal-associated genes, whereas neural markers PAX6 and NEUROD1 are down-regulated. Further, STELLA over-expression facilitates the differentiation of human ES cells into BE12-positive cells, in which the expression of germline- and endodermal-associated genes is enriched, and suppresses differentiation of the neural lineage. Taken together, this finding suggests a role for STELLA in facilitating germline and endodermal differentiation of human ES cells

Tackling Systematic Errors in Quantum Logic Gates with Composite Rotations

We describe the use of composite rotations to combat systematic errors in single qubit quantum logic gates and discuss three families of composite rotations which can be used to correct off-resonance and pulse length errors. Although developed and described within the context of NMR quantum computing these sequences should be applicable to any implementation of quantum computation.Comment: 6 pages RevTex4 including 4 figures. Will submit to Phys. Rev.