2,011 research outputs found
Root exudate carbon mitigates nitrogen loss in a semi-arid soil
AbstractThe need for increased food production to support the growing global population requires more efficient nutrient management and prevention of nitrogen (N) losses from both applied fertiliser and organic matter (OM) decomposition. This is particularly important in semi-arid rainfed cropping soils, where soil water and temperature are the dominant drivers of N cycling rather than agricultural management. Here we used 14C and 15N techniques to examine how peptide/amino acid turnover, gross and net N transformation rates and nitrous oxide (N2O) emissions responded to long-term plant residue additions and/or short-term root exudate additions. Soil was collected from a semi-arid rainfed field trial with one winter crop per year followed by a summer fallow period, where additional inputs of straw/chaff over 10 years had increased total soil organic C (SOC) by 76% compared to no extra additions (control). These field soils were incubated in the laboratory with or without a synthetic root exudate mixture at a range of temperatures reflecting regional field conditions (5–50 °C). Long-term plant residue additions (to build up total soil OM) did not decrease the risk of N loss as defined by the nitrification:immobilisation (N:I) ratio at most temperatures, so was not an effective management tool to control N losses. In comparison, short-term root exudate additions decreased the risk of N loss at all temperatures in both the control and plant residue treatment field soils. Increased net N mineralisation and decreased microbial C use efficiency at temperatures greater than 30 °C resulted in significant ammonium (NH4+) accumulation. Microbial decomposers appeared to use amino acid-C for growth but peptide-C for energy production. Findings indicate that the greatest risk of N loss in these semi-arid soils will occur during rains at the start of the growing season, due to inorganic N accumulation over summer fallow when there are high soil temperatures, occasional significant rainfall events and no growing plants to release root exudates. While most attempts to manipulate the soil N cycle have occurred during the winter cropping period, our findings highlight the need to manage N supply during summer fallow if we are to minimise losses to the environment from semi-arid soils
Dilepton Production in Nucleon-Nucleon Interactions
Starting from a realistic one--boson--exchange--model fitted to the
amplitudes of elastic nucleon--nucleon scattering and the process
we perform a fully relativistic and gauge invariant
calculation for the dilepton production in nucleon--nucleon collisions,
including the important effect of propagating the --resonance. We
compare the results of our calculations with the latest experimental data on
dilepton production. We also show how to implement various electromagnetic
formfactors for the hadrons in our calculations without loosing
gauge--invariance and discuss their influence on dilepton spectra.Comment: 24 pages, figures will be sent on reques
Simple model for scanning tunneling spectroscopy of noble metal surfaces with adsorbed Kondo impurities
A simple model is introduced to describe conductance measurements between a
scanning tunneling microscope (STM) tip and a noble metal surface with adsorbed
transition metal atoms which display the Kondo effect. The model assumes a
realistic parameterization of the potential created by the surface and a
d3z2-r2 orbital for the description of the adsorbate. Fano lineshapes
associated with the Kondo resonance are found to be sensitive to details of the
adsorbate-substrate interaction. For instance, bringing the adsorbate closer to
the surface leads to more asymmetric lineshapes while their dependence on the
tip distance is weak. We find that it is important to use a realistic surface
potential, to properly include the tunnelling matrix elements to the tip and to
use substrate states which are orthogonal to the adsorbate and tip states. An
application of our model to Co adsorbed on Cu explains the difference in the
lineshapes observed between Cu(100) and Cu(111) surfaces.Comment: 11 pages, 8 eps figure
Determining patterns in the composition of dissolved organic matter in fresh waters according to land use and management
In fresh waters, the origins of dissolved organic matter (DOM) have been found to exert a fundamental control on its reactivity, and ultimately, its ecosystem functional role. A detailed understanding of landscape scale factors that control the export of DOM to aquatic ecosystems is, therefore, pivotal if the effects of DOM flux to fresh waters are to be fully understood. In this study we present data from a national sampling campaign across the United Kingdom in which we explore the variability in DOM composition in three broad landscape types defined by similar precipitation, geology, land use and management, hydrology, and nutrient enrichment status. We characterised samples from fifty-one sites, grouping them into one of three major underlying classifications: circumneutral streams underlain by clay and mudstone (referred to as ‘clay’), alkaline streams underlain by Cretaceous Chalk or by Carboniferous or Jurassic Limestone (‘limestone’), and acidic streams in peatland catchments underlain by a range of low permeability lithologies (‘peat’). DOM composition was assessed through organic matter stoichiometry (organic carbon: organic nitrogen; organic carbon: organic phosphorus; C/N(P)DOM) and metrics derived from ultra-violet (UV)/visible spectroscopic analysis of DOM such as specific UV absorption (a254 nm; SUVA254). We found similar SUVA254, C/NDOM and DOM/a254 relationships within classifications, demonstrating that despite a large degree of heterogeneity within environments, catchments with shared environmental character and anthropogenic disturbance export DOM with a similar composition and character. Improving our understanding of DOM characterisation is important to help predict shifts in stream ecosystem function, and ecological responses to enrichment or mitigation efforts and how these may result in species composition shifts and biodiversity loss in freshwater ecosystems
Nonlinear r-Modes in Neutron Stars: Instability of an unstable mode
We study the dynamical evolution of a large amplitude r-mode by numerical
simulations. R-modes in neutron stars are unstable growing modes, driven by
gravitational radiation reaction. In these simulations, r-modes of amplitude
unity or above are destroyed by a catastrophic decay: A large amplitude r-mode
gradually leaks energy into other fluid modes, which in turn act nonlinearly
with the r-mode, leading to the onset of the rapid decay. As a result the
r-mode suddenly breaks down into a differentially rotating configuration. The
catastrophic decay does not appear to be related to shock waves at the star's
surface. The limit it imposes on the r-mode amplitude is significantly smaller
than that suggested by previous fully nonlinear numerical simulations.Comment: Published in Phys. Rev. D Rapid Comm. 66, 041303(R) (2002
Characterisation of riverine dissolved organic matter using a complementary suite of chromatographic and mass spectrometric methods
Dissolved organic matter (DOM) plays a fundamental role in nutrient cycling dynamics in riverine systems. Recent research has confirmed that the concentration of riverine DOM is not the only factor regulating its functional significance; the need to define the chemical composition of DOM is a priority. Past studies of riverine DOM rested on bulk quantification, however technological advancements have meant there has been a shift towards analytical methods which allow the characterisation of DOM either at compound class or more recently molecular level. However, it is important to consider that all analytical methods only consider a defined analytical window. Thus, herein, we explore the use of a hierarchy of methods which can be used in combination for the investigation of a wide range of DOM chemistries. By using these methods to investigate the DOM composition of a range of streams draining catchments of contrasting environmental character, a wide range of compounds were identified across a range of polarities and molecular weight, thereby extending the analytical window. Through the elucidation of the DOM character in stream samples, information can be collected about likely the sources of DOM. The identification of individual key compounds within the DOM pool is a key step in the design of robust and informative bioassay experiments, used to understand in-stream ecosystem responses. This is critical if we are to assess the role of DOM as a bioavailable nutrient resource and/or ecotoxicological factor in freshwater
Transverse Fresnel-Fizeau drag effects in strongly dispersive media
A light beam normally incident upon an uniformly moving dielectric medium is
in general subject to bendings due to a transverse Fresnel-Fizeau light drag
effect. In conventional dielectrics, the magnitude of this bending effect is
very small and hard to detect. Yet, it can be dramatically enhanced in strongly
dispersive media where slow group velocities in the m/s range have been
recently observed taking advantage of the electromagnetically induced
transparency (EIT) effect. In addition to the usual downstream drag that takes
place for positive group velocities, we predict a significant anomalous
upstream drag to occur for small and negative group velocities. Furthermore,
for sufficiently fast speeds of the medium, higher order dispersion terms are
found to play an important role and to be responsible for peculiar effects such
as light propagation along curved paths and the restoration of the spatial
coherence of an incident noisy beam. The physics underlying this new class of
slow-light effects is thoroughly discussed
Separable potential model for interactions at low energies
The effective separable meson-baryon potentials are constructed to match the
equivalent chiral amplitudes up to the second order in external meson momenta.
We fit the model parameters (low energy constants) to the threshold and low
energy data. In the process, the -proton bound state problem is
solved exactly in the momentum space and the 1s level characteristics of the
kaonic hydrogen are computed simultaneously with the available low energy
cross sections. The model is also used to describe the
mass spectrum and the energy dependence of the amplitude.Comment: 31 pages, v2 - added corrections to make it compatible with the
published versio
Characterisation of riverine dissolved organic matter using a complementary suite of chromatographic and mass spectrometric methods
Dissolved organic matter (DOM) plays a fundamental role in nutrient cycling dynamics in riverine systems. Recent research has confirmed that the concentration of riverine DOM is not the only factor regulating its functional significance; the need to define the chemical composition of DOM is a priority. Past studies of riverine DOM rested on bulk quantification, however technological advancements have meant there has been a shift towards analytical methods which allow the characterisation of DOM either at compound class or more recently molecular level. However, it is important to consider that all analytical methods only consider a defined analytical window. Thus, herein, we explore the use of a hierarchy of methods which can be used in combination for the investigation of a wide range of DOM chemistries. By using these methods to investigate the DOM composition of a range of streams draining catchments of contrasting environmental character, a wide range of compounds were identified across a range of polarities and molecular weight, thereby extending the analytical window. Through the elucidation of the DOM character in stream samples, information can be collected about likely the sources of DOM. The identification of individual key compounds within the DOM pool is a key step in the design of robust and informative bioassay experiments, used to understand in-stream ecosystem responses. This is critical if we are to assess the role of DOM as a bioavailable nutrient resource and/or ecotoxicological factor in freshwater
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