429 research outputs found
Evaluation of Damage by Vertebrate Pests in California Vineyards and Control of Wild Turkeys by Bioacoustics
Complaints of agricultural damage by wild turkeys (Meleagris gallopavo), particularly from wine grape growers, have increased in California. We assessed damage by vertebrate pests in vineyards and tested a bioacoustic-aversion technique for turkeys as an alternative to other control techniques (e.g., reflective tape, trapping, bird netting). We selected 12 vineyards in the Napa Valley and Sierra Foothills American Viticultural Areas of California. We conducted damage surveys to assess percentages of missing or damaged grapes (i.e., grapes that had been stripped, pecked, and plucked) for every grape cluster on 20 randomly-selected vines before harvest in 2007 and on 40 vines in 2008. We assumed that all observed damage was caused by vertebrate pests and that most of this damage was caused by birds. Grape damage caused by wild turkeys was identified by contiguous sections of berries plucked from a cluster, which we referred to as stripped damage. We attributed pecked and plucked damage to passerines. In 2008, we randomly selected 3 vineyards in each area for treatment with broadcast calls (wild turkey alarm, domestic turkey alarm, crow distress). We used motion-activated video cameras to document evidence of damage caused by turkeys and other animals. Damage in the vineyard perimeter was greater than in the interior for all damage types in 2008, but only for plucked damage in 2007. In 2008, stripped, pecked, and plucked damage means for treated vineyards were 1.3%, 1.4%, and 1.5%, respectively; stripped, pecked, and plucked damage means for untreated vineyards were 1.3%, 0.7%, and 0.2%, respectively. There was no difference in mean stripped damage between treated and untreated vineyards in 2008, indicating that broadcast calls had no effect. Comparison between treated sites in 2008 with the same untreated sites in 2007 yielded similar results. Turkeys caused damage in several of the study vineyards, but the problem varied among vineyards and was inconsistent between years. Motion-activated video recordings suggested that raccoons (Procyon lotor), gray foxes (Urocyon cinereoargenteus), and other vertebrate pests were to blame for some of the stripped damage
Electronic excitation of carbonyl sulphide (COS) by high-resolution vacuum ultraviolet photoabsorption and electron-impact spectroscopy in the energy region from 4 to 11 eV
The electronic state spectroscopy of carbonyl sulphide, COS, has been investigated using high resolution vacuum ultraviolet photoabsorption spectroscopy and electron energy loss spectroscopy in the energy range of 4.0–10.8 eV. The spectrum reveals several new features not previously reported in the literature. Vibronic structure has been observed, notably in the low energy absorption dipole forbidden band assigned to the (4π←3π) (1Δ←1Σ+) transition, with a new weak transition assigned to (1Σ−←1Σ+) reported here for the first time. The absolute optical oscillator strengths are determined for ground state to 1Σ+ and 1Π transitions. Based on our recent measurements of differential cross sections for the optically allowed (1Σ+ and 1Π) transitions of COS by electron impact, the optical oscillator strength f0 value and integral cross sections (ICSs) are derived by applying a generalized oscillator strength analysis. Subsequently, ICSs predicted by the scaling are confirmed down to 60 eV in the intermediate energy region. The measured absolute photoabsorption cross sections have been used to calculate the photolysis lifetime of carbonyl sulphide in the upper stratosphere (20–50 km)
Isobutyl acetate: electronic state spectroscopy by high-resolution vacuum ultraviolet photoabsorption, He(I) photoelectron spectroscopy and ab initio calculations
The high-resolution vacuum ultraviolet photoabsorption spectrum of isobutyl acetate, C6H12O2, is presented here and was measured over the energy range 4.3–10.8 eV (290–115 nm). Valence and Rydberg transitions with their associated vibronic series have been observed in the photoabsorption spectrum and are assigned in accordance with new ab initio calculations of the vertical excitation energies and oscillator strengths. The measured photoabsorption cross sections have been used to calculate the photolysis lifetime of this ester in the Earth’s upper atmosphere (20–50 km). Calculations have also been carried out to determine the ionization energies and fine structure of the lowest ionic state of isobutyl acetate and are compared with a photoelectron spectrum (from 9.5 to 16.7 eV), recorded for the first time. Vibrational structure is observed in the first photoelectron band of this molecule
Electronic state spectroscopy of methyl formate probed by high resolution VUV photoabsorption, He(I) photoelectron spectroscopy and ab initio calculations
The first ab initio calculations of the vertical excitation energies and oscillator strengths are
presented for the neutral electronic transitions of methyl formate, C2H4O2. The highest resolution VUV photoabsorption spectrum of the molecule yet reported is presented over the wavelength
range 115 to 310 nm (10.8 to 4.0 eV) revealing several new spectral features. Valence and Rydberg transitions and their associated vibronic series, observed in the photoabsorption spectrum, have been assigned in accordance with new theoretical results. The calculations have
been carried out to determine the excitation energies of the lowest energy ionic states of methyl formate and are compared with a newly recorded He(I) photoelectron spectrum (10.4 to 17.0 eV). New vibrational structure is observed in the first photoelectron band. The photoabsorption
cross-sections have been used to calculate the photolysis lifetime of methyl formate in the upper
stratosphere (20-50 km)
Electronic excitation of furfural as probed by high-resolution vacuum ultraviolet spectroscopy, electron energy loss spectroscopy, and ab initio calculations
13 págs.; 7 figs.; 8 tabs.© 2015 AIP Publishing LLC. The electronic spectroscopy of isolated furfural (2-furaldehyde) in the gas phase has been investigated using high-resolution photoabsorption spectroscopy in the 3.5-10.8 eV energy-range, with absolute cross section measurements derived. Electron energy loss spectra are also measured over a range of kinematical conditions. Those energy loss spectra are used to derive differential cross sections and in turn generalised oscillator strengths. These experiments are supported by ab initio calculations in order to assign the excited states of the neutral molecule. The good agreement between the theoretical results and the measurements allows us to provide the first quantitative assignment of the electronic state spectroscopy of furfural over an extended energy range.F.F.S. and P.L.V. acknowledge the Portuguese Foundation
for Science and Technology (FCT-MEC) through Grant Nos.
SFRH/BPD/68979/2010 and SFRH/BSAB/105792/2014,
respectively, the research Grant Nos. PTDC/FIS-ATO/1832/
2012 and UID/FIS/00068/2013. P.L.V. also acknowledges
his Visiting Research Fellow position at Flinders University,
Adelaide, South Australia. The Patrimoine of the University
of Liège, the Fonds National de la Recherche Scientifique,
and the Fonds de la Recherche Fondamentale Collective of
Belgium have also supported this research. E.L. and R.F.C.N.
thank CNPq (Brazil) and the Science Without Borders
Programme for opportunities to study abroad. The authors
wish to acknowledge the beam time at the ISA synchrotron
at Aarhus University, Denmark. The research leading to these
results has received funding from the European Community’s
Seventh Framework Programme (Grant No. FP7/2007-2013)
CALIPSO under Grant Agreement No. 312284. D.B.J.
thanks the Australian Research Council for financial support
provided through a Discovery Early Career Research Award.
M.J.B. also thanks the Australian Research Council for some
financial support, while M.J.B. and M.C.A.L. acknowledge the
Brazilian agencies CNPq and FAPEMIG for financial support.
F.B. and G.G. acknowledge partial financial support from the
Spanish Ministry MINECO (Project No. FIS2012-31230) and
the EU COST Action No. CM1301 (CELINA). Finally, R.F.C.,
M.T.do N.V., M.H.F.B., and M.A.P.L. acknowledge support
from the Brazilian agency CNPq.Peer Reviewe
The Right Place at the Right Time: Creative Spaces in Libraries
Purpose
This essay explores the recent trend in libraries: that of the establishment of spaces specifically set aside for creative work. The rise of these dedicated creative spaces is owed to a confluence of factors that happen to be finding their expression together in recent years. This essay examines the history of these spaces and explores the factors that gave rise to them and will fuel them moving forward.
Design/Methodology/Approach
A viewpoint piece, this essay combines historical research and historical/comparative analyses to examine the ways by which libraries have supported creative work in the past and how they may continue to do so into the 21st century.
Findings
The key threads brought together include a societal recognition of the value of creativity and related skills and attributes; the philosophies, values, and missions of libraries in both their longstanding forms and in recent evolutions; the rise of participatory culture as a result of inexpensive technologies; improved means to build community and share results of efforts; and library experience and historical practice in matters related to creativity. The chapter concludes with advice for those interested in the establishment of such spaces, grounding those reflections in the author’s experiences in developing a new creative space at Virginia Commonwealth University.
Originality/value
While a number of pieces have been written that discuss the practicalities of developing certain kinds of creative spaces, very little has been written that situates these spaces in larger social and library professional contexts; this essay begins to fill that gap
Measurement of Single Soybean Seed Attributes by Near-Infrared Technologies. A Comparative Study
Four near-infrared spectrophotometers, and their associated spectral collection methods, were tested and compared for measuring three soybean single-seed attributes: weight (g), protein (%), and oil (%). Using partial least-squares (PLS) and four preprocessing methods, the attribute that was significantly most easily predicted was seed weight (RPD > 3 on average) and protein the least. The performance of all instruments differed from each other. Performances for oil and protein predictions were correlated with the instrument sampling system, with the best predictions using spectra taken from more than one seed angle. This was facilitated by the seed spinning or tumbling during spectral collection as opposed to static sampling methods. From the preprocessing methods utilized, no single one gave the best overall performances but weight measurements were often more successful with raw spectra, whereas protein and oil predictions were often enhanced by SNV and SNV + detrending.Posted with permission from Journal of Agricultural and Food Chemistry 60 (2012): 8314–8322, doi:10.1021/jf3012807. Copyright 2012 American Chemical Society.</p
COVID-19 publications: Database coverage, citations, readers, tweets, news, Facebook walls, Reddit posts
© 2020 The Authors. Published by MIT Press. This is an open access article available under a Creative Commons licence.
The published version can be accessed at the following link on the publisher’s website: https://doi.org/10.1162/qss_a_00066The COVID-19 pandemic requires a fast response from researchers to help address biological,
medical and public health issues to minimize its impact. In this rapidly evolving context,
scholars, professionals and the public may need to quickly identify important new studies. In
response, this paper assesses the coverage of scholarly databases and impact indicators
during 21 March to 18 April 2020. The rapidly increasing volume of research, is particularly
accessible through Dimensions, and less through Scopus, the Web of Science, and PubMed.
Google Scholar’s results included many false matches. A few COVID-19 papers from the
21,395 in Dimensions were already highly cited, with substantial news and social media
attention. For this topic, in contrast to previous studies, there seems to be a high degree of
convergence between articles shared in the social web and citation counts, at least in the
short term. In particular, articles that are extensively tweeted on the day first indexed are
likely to be highly read and relatively highly cited three weeks later. Researchers needing wide
scope literature searches (rather than health focused PubMed or medRxiv searches) should
start with Dimensions (or Google Scholar) and can use tweet and Mendeley reader counts as
indicators of likely importance
Valence and ionic lowest-lying electronic states of ethyl formate as studied by high-resolution vacuum ultraviolet photoabsorption, He(I) photoelectron spectroscopy, and ab initio calculations
The highest resolution vacuum ultraviolet photoabsorption spectrum of ethyl formate, C2H5OCHO, yet reported is presented over the wavelength range 115.0-275.5 nm (10.75-4.5 eV) revealing several new spectral features. Valence and Rydberg transitions and their associated vibronic series, observed in the photoabsorption spectrum, have been assigned in accordance with new ab initio calculations of the vertical excitation energies and oscillator strengths. Calculations have also been carried out to determine the ionization energies and fine structure of the lowest ionic state of ethyl formate and are compared with a newly recorded He(I) photoelectron spectrum (from 10.1 to 16.1 eV). New vibrational structure is observed in the first photoelectron band. The photoabsorption cross sections have been used to calculate the photolysis lifetime of ethyl formate in the upper stratosphere (20-50 km)
The effect of zinc on human taste perception
Zinc salts are added as a nutritional or functional ingredient in food and oral care products. The 1st experiment in this study investigated the taste and somatosensory effect of zinc salts (chloride, iodide, sulfate, bromide, acetate). The zinc salts had very little taste (bitter, salty, savory, sour, sweet), and the taste that was present was easily washed away with water rinses. The major oral quality of zinc was astringency, and the astringency lingered beyond expectoration. The 2nd experiment combined zinc salts with prototypical stimuli eliciting basic tastes. Zinc was a potent inhibitor of sweetness and bitterness (>70% reduction in taste) but did not affect salt, savory, or sour taste.<br /
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