6,671 research outputs found
A predictive model with flavour symmetry
We propose a predictive model based on the gauge group supplemented by the discrete group, which successfully describes
the SM fermion mass and mixing pattern. The small active neutrino masses are
generated via inverse seesaw mechanism with three very light Majorana
neutrinos. The observed charged fermion mass hierarchy and quark mixing pattern
are originated from the breaking of the
discrete group at very high scale. The obtained values for the physical
observables for both quark and lepton sectors are in excellent agreement with
the experimental data. The model predicts a vanishing leptonic Dirac CP
violating phase as well as an effective Majorana neutrino mass parameter of
neutrinoless double beta decay, with values 2 and 48 meV
for the normal and the inverted neutrino mass hierarchies, respectively.Comment: 20 pages. Final version published in Nuclear Physics
Fermion mass and mixing pattern in a minimal T7 flavor 331 model
We present a model based on the
gauge symmetry having an extra
flavor group, which successfully describes the observed SM fermion mass and
mixing pattern. In this framework, the light active neutrino masses arise via
double seesaw mechanism and the observed charged fermion mass and quark mixing
hierarchy is a consequence of the symmetry
breaking at very high energy. In our minimal flavor 331 model, the
spectrum of neutrinos includes very light active neutrinos as well as heavy and
very heavy sterile neutrinos. The model has in total 16 effective free
parameters, which are fitted to reproduce the experimental values of the 18
physical observables in the quark and lepton sectors. The obtained physical
observables for both quark and lepton sectors are compatible with their
experimental values. The model predicts the effective Majorana neutrino mass
parameter of neutrinoless double beta decay to be 3 and
40 meV for the normal and the inverted neutrino spectrum, respectively.
Furthermore, our model features a vanishing leptonic Dirac CP violating phase.Comment: 18 pages. Final version. To be published in Journal of Physics G.
arXiv admin note: substantial text overlap with arXiv:1309.656
discrete group as a source of the quark mass and mixing pattern in models
We propose a model based on the
gauge symmetry with an extra
discrete group, which successfully accounts for the SM quark mass and mixing
pattern. The observed hierarchy of the SM quark masses and quark mixing matrix
elements arises from the and symmetries, which are broken at
very high scale by the scalar singlets (,) and , charged under these symmetries, respectively. The Cabbibo mixing arises from
the down type quark sector whereas the up quark sector generates the remaining
quark mixing angles. The obtained magnitudes of the CKM matrix elements, the CP
violating phase and the Jarlskog invariant are in agreement with the
experimental data.Comment: 12 pages. Version published in European Physical Journal
Introduction to cross LAK 2016: Learning analytics across spaces
For the LAK (Learning Analytics and Knowledge) community, it is highly important to pay attention to the development and deployment of learning analytics solutions for blended learning scenarios where students work at diverse digital and physical learning spaces and interact in different modalities. This workshop has been a first attempt in gathering the sub-community of LAK researchers, learning scientists and researchers from other communities, interested in ubiquitous, mobile and/or face-to-face learning analytics. It was clear for all the attendees that a key concern that has not been deeply explored yet is associated with the mechanisms to integrate and coordinate learning analytics to provide continued support to learning across digital and physical spaces. The two main goals of the workshop were to share perspectives and identify a set of guidelines that could be offered to teachers, researchers or designers to create and connect Learning Analytics solutions according to the pedagogical needs and contextual constraints to provide support across digital and physical learning spaces
The ISW-tSZ cross correlation: ISW extraction out of pure CMB data
If Dark Energy introduces an acceleration in the universal expansion then
large scale gravitational potential wells should be shrinking, causing a
blueshift in the CMB photons that cross such structures (Integrated Sachs-Wolfe
effect, [ISW]). Galaxy clusters are known to probe those potential wells. In
these objects, CMB photons also experience inverse Compton scattering off the
hot electrons of the intra-cluster medium, and this results in a distortion
with a characteristic spectral signature of the CMB spectrum (the so-called
thermal Sunyaev-Zel'dovich effect, [tSZ]). Since both the ISW and the tSZ
effects take place in the same potential wells, they must be spatially
correlated. We present how this cross ISW-tSZ signal can be detected in a
CMB-data contained way by using the frequency dependence of the tSZ effect in
multi frequency CMB experiments like {\it Planck}, {\em without} requiring the
use of external large scale structure tracers data. We find that by masking low
redshift clusters, the shot noise level decreases significantly, boosting the
signal to noise ratio of the ISW--tSZ cross correlation. We also find that
galactic and extragalactic dust residuals must be kept at or below the level of
~0.04 muK^2 at l=10, a limit that is a factor of a few below {\it Planck}'s
expectations for foreground subtraction. If this is achieved, CMB observations
of the ISW-tSZ cross correlation should also provide an independent probe for
the existence of Dark Energy and the amplitude of density perturbations.Comment: submitted to MNRA
Impact of carbonate saturation on large Caribbean benthic foraminifera assemblages
Increasing atmospheric carbon dioxide and its dissolution in seawater have
reduced ocean pH and carbonate ion concentrations, with potential implications
on calcifying organisms. To assess the response of large Caribbean benthic
foraminifera to low carbonate saturation conditions, we analyzed benthic
foraminifers' abundance and relative distribution in surface sediments in
proximity to low-carbonate-saturation submarine springs and at adjacent
control sites. Our results show that the total abundance of large benthic
foraminifera was significantly lower at the low-pH submarine springs than at
control sites, although responses were species specific. The relative
abundance of high-magnesium, porcelaneous foraminifera was higher than that
of hyaline foraminifera at the low-pH springs due to the abundant
Archaias angulatus, a chlorophyte-bearing foraminifer, which secretes
a large and robust test that is more resilient to dissolution at low-calcite
saturation. The different assemblages found at the submarine springs indicate
that calcareous symbiont-barren foraminifera are more sensitive to the
effects of ocean acidification than agglutinated and symbiont-bearing
foraminifera, suggesting that future ocean acidification will likely impact
natural benthic foraminifera populations.</p
The development of the radicular and vegetative systems of almond trees with different rootstocks following the application of biostimulants
[EN] Aim of study: Recently, the development of almond crops on a global scale has increased their area under cultivation. The demand for both plants and products that stimulate the growth of almond trees has therefore become increasingly necessary. Accordingly, in this project we have studied the response in the vegetative and root systems of almond trees with different rootstocks to varying inputs of several root stimulants.
Area of study: Valencia (Spain)
Material and methods: Several different organic biostimulants were studied in isolation, i.e. not combined with synthetic chemical fertilizers, in order to ascertain if chemical fertilizers could be at least partially replaced.
Main results: Good results were obtained by applying a biostimulant composed of organic matter rich in saccharides and carboxylates. Using an approach that enabled a distinguishing between them, plant radicular systems were shown to respond differently according to the biostimulant applied and the rootstock tested. The best results were obtained with a biostimulant composed of organic matter from corn hydrolysis and containing free amino acids and extracts from algae, as well as 0.07% zeaxanthins.
Research highlights: Although biostimulants are promoters of young almond tree growth, they should be applied to only partially replace chemical fertilizers. The present paper shows the importance of using an organic-origin biostimulant, as a complement to chemical nutritionMondragón-Valero, A.; Malheiro, R.; Salazar Hernández, DM.; Martinez-Tome, J.; Pereira, JA.; López- Cortés, I. (2020). The development of the radicular and vegetative systems of almond trees with different rootstocks following the application of biostimulants. Spanish Journal of Agricultural Research (Online). 18(4):1-11. https://doi.org/10.5424/sjar/2020184-14787S111184Apone F, Tito A, Carola A, Arciello S, Tortora A, Filippini L, 2010. A mixture of peptides and sugars derived from plant cell walls increases plant defense responses to stress and attenuates ageing-associated molecular changes in cultured skin cells. J Biotech 145: 367-376.Basak A, 2008. Effect of preharvest treatment with seaweed products, Kelpak® and Goëmar BM 86®, on fruit quality in apple. Inter J Fruit Sci 8: 1-14.Battacharyya D, Babgohari MZ, Rathor P, Prithiviraj B, 2015. Seaweed extracts as biostimulants in horticulture. Sci Hortic 196: 39-48.Bernhard R, Grasselly C, 1981. Les pêchers x amandiers. Arb Fruit 328: 37-42.Bi G, Scagel C, Cheng L, Dong S, Fuchigami L, 2003. Spring growth of almond nursery trees depends upon nitrogen from both plant reserves and spring fertilizer application. J Hortic Sci Biotech 78: 853-858.Burns AM, Zitt MA, Rowe CC, Langkamp-Henken B, Mai V, Nieves C, et al., 2016. Diet quality improves for parents and children when almonds are incorporated into their daily diet: a randomized, crossover study. Nutr Res 36: 80-89.Bussi C, Huguet J, Besset J, Girard T, 1995. Rootstock effects on the growth and fruit yield of peach. Eur J Agron 4: 387-393.Chen SK, Edwards CA, Subler S, 2003. The influence of two agricultural biostimulants on nitrogen transformations, microbial activity, and plant growth in soil microcosms. Soil Biol Biochem 35: 9-19.Chouliaras V, Tasioula M, Chatzissavvidis C, Therios I, Tsabolatidou E, 2009. The effects of a seaweed extract in addition to nitrogen and boron fertilization on productivity, fruit maturation, leaf nutritional status and oil quality of the olive (Olea europaea L.) cultivar Koroneiki. J Sci Food Agric 89: 984-988.Deliopoulos T, Kettlewell P, Hare M, 2010. Fungal disease suppression by inorganic salts. A review. Crop Prot 29: 1059-1075.Enz M, Dachler CH, 1997. Compendium of growth stage identification keys for mono- and dicotyledonous plants. Extended BBCH scale. A joint publication of BBA, BSA, IGZ, IVA, AgrEvo, BASF, Bayer, Novartis. 94 pp.Ertani A, Cavani L, Pizzeghello D, Brandellero E, Altissimo A, Ciavatta C, Nardi S, 2009. Biostimulant activity of two protein hydrolyzates in the growth and nitrogen metabolism of maize seedlings. J Plant Nutr Soil Sci 172: 237-244.Espada J, Romero J, Cmuñas F, Alonso J, 2013. Nuevos patrones para el melocotonero: mejora de la eficiencia y calidad del fruto. Gobierno de Aragón, Zaragoza, Spain.European Biostimulants Industry Council, 2018. Economic overview of biostimulants sector in Europe. http://www.biostimulants.eu/.Felipe A, 2009. Felinem, Garnem and Monegro almond x peach hybrid rootstocks. HortScience 44: 196-197.Forcada C, Gogorcena Y, Moreno M, 2012. Agronomical and fruit quality traits of two peach cultivars on peach-almond hybrid rootstocks growing on Mediterranean conditions. Sci Hortic 140: 157-163.Gómez-Aparisi J, Carrera M, Felipe A, Socias I Company R, 2001. Garnem, Monegro y Felinem: Nuevos patrones híbridos almendro x melocotonero, resistentes a nematodos y de hoja roja para frutales de hueso. Inf Téc Econ Agrar 97: 282-288.Goss M, Miller M, Bailey L, Grant C, 1993. Root growth and distribution in relation to nutrient availability and uptake. Eur J Agron 2: 57-67.INC, 2019. Global statistical review 2017-2018. International Nut and Dried Fruit Council, Reus, Spain.Khan W, Rayirath UP, Subramanian S, Jithesh MN, Rayorath P, Hodges DM, et al., 2009. Seaweed extracts as biostimulants of plant growth and development. J Plant Growth Reg 28: 386-399.Lopus SE, Santibañez MP, Beede RH, Duncan RA, Edstrom J, Niederholzer FJA, et al., 2010. Survey examines the adoption of perceived best management practices for almond nutrition. Calif Agric 64: 149-154.Mondragón-Valero A, Lopéz-Cortés I, Salazar DM, Córdova PF, 2017. Physical mechanisms produced in the development of nursery almond trees (Prunus dulcis Miller) as a response to the plant adaptation to different substrates. Rhizosphere 3: 44-49.Moreno M, Gogorcena Y, Pinochet J, 2008. Mejora y selección de patrones de prunus tolerantes a estreses abióticos. In: La adaptación al ambiente y los estreses abióticos en la mejora vegetal, pp. 451-475. Junta de Andalucía, Dirección General de Planificación y Análisis de Mercados, Servicio de Publicaciones y Divulgación, Sevilla.Muhammad S, Luedeling E, Brown P, 2009. A nutrient budget approach to nutrient management in almond. XVI Proc Int Plant Nutr Col, California (USA), pp: 1-9.Nardi S, Pizzeghello D, Schiavon M, Ertani A, 2016. Plant biostimulants: physiological responses induced by protein hydrolyzed-based products and humic substances in plant metabolism. Sci Agric 73: 18-23.Olivares FL, Busato JG, Paula AM, Lima LS, Aguiar NO, Canellas LP, 2017. Plant growth promoting bacteria and humic substances: crop promotion and mechanisms of action. Chem Biol Tech Agric 4: 30.Pinochet J, 2010. 'Replantpac' (Rootpac R), a plum-almond hybrid rootstock for replant situations. HortScience 45: 299-301.Pinochet J, Bordas M, Torrents J, 2011. ROOTPAC R: un nuevo portainjerto de Prunus para situaciones de replante. Revista de Fruticultura 15: 4-10.Pizzeghello D, Francioso O, Ertani A, Muscolo A, Nardi S, 2013. Isopentenyladenosine and cytokinin-like activity of different humic substances. J Geochem Expl 129: 70-75.Rayorath P, Jithesh M. Farid A, Khan W, Palanisamy R, 2008. Rapid bioassays to evaluate the plant growth promoting activity of Ascophyllum nodosum (L.) Le Jol. using a model plant, Arabidopsis thaliana (L.) Heynh. J Appl Phycol 20: 423-429.Rouphael Y, Cardarelli M, Bonini P, Colla G, 2017. Synergistic action of a microbial-based biostimulant and a plant derived-protein hydrolysate enhances lettuce tolerance to alkalinity and salinity. Front Plant Sci 8: 131.Salazar D, Melgarejo P, 2002. El cultivo del almendro. Mundi-Prensa, Madrid, Spain. 307 pp.Scaglia B, Pognani M, Adani F, 2017. The anaerobic digestion process capability to produce biostimulant: the case study of the dissolved organic matter (DOM) vs. auxin-like property. Sci Total Environ 589: 36-45.Sotomayor C, Castro J, Bustos E, 2008. Nuevos portainjertos para Chile. Rev Agron For UC 35: 22-26.Vargas F, Romero M, Altea N, 1985. Porte-greffe d'amandier: Aspects importants des programmes de Centre Agropecuari Mas Bové. GREMPA, colloque 1985. CIHEAM, Paris. Opt Mediterr Sér Etudes 1985-I: 61-68. http://om.ciheam.org/om/pdf/s09/CI010822.pdfVernieri P, Borghesi E, Ferrante A, Magnani G, 2005. Application of biostimulants in floating system for improving rocket quality. J Food Agric Environ 3: 86-88.Wells C, Labranche A, Mccarty L, Skipper H, 2003. Biostimulants encourage strong root growth. Turfgrass Trend 59: 56-59.Williams L, Smith R, 1991. The effect of rootstocck on the partitioning of dry weight, nitrogen and potassium and root distribution of cabernet sauvignon grapevines. Am J Enol Vitic 42: 118-112.Zhang X, Ervin E, 2004. Cytokinin-containing seaweed and humic acid extracts associated with creeping bentgrass leaf cytokinins and drought resistance. J Appl Phycol 44: 1737-1745
The HADES RV Programme with HARPS-N at TNG XI. GJ 685 b: a warm super-Earth around an active M dwarf
Small rocky planets seem to be very abundant around low-mass M-type stars.
Their actual planetary population is however not yet precisely understood.
Currently several surveys aim to expand the statistics with intensive detection
campaigns, both photometric and spectroscopic. We analyse 106 spectroscopic
HARPS-N observations of the active M0-type star GJ 685 taken over the past five
years. We combine these data with photometric measurements from different
observatories to accurately model the stellar rotation and disentangle its
signals from genuine Doppler planetary signals in the RV data. We run an MCMC
analysis on the RV and activity indexes time series to model the planetary and
stellar signals present in the data, applying Gaussian Process regression
technique to deal with the stellar activity signals. We identify three periodic
signals in the RV time series, with periods of 9, 24, and 18 d. Combining the
analyses of the photometry of the star with the activity indexes derived from
the HARPS-N spectra, we identify the 18 d and 9 d signals as activity-related,
corresponding to the stellar rotation period and its first harmonic
respectively. The 24 d signals shows no relations with any activity proxy, so
we identify it as a genuine planetary signal. We find the best-fit model
describing the Doppler signal of the newly-found planet, GJ 685\,b,
corresponding to an orbital period d and a
minimum mass M. We also study a
sample of 70 RV-detected M-dwarf planets, and present new statistical evidence
of a difference in mass distribution between the populations of single- and
multi-planet systems, which can shed new light on the formation mechanisms of
low-mass planets around late-type stars.Comment: 18 pages, 13 figures, accepted for publication in A&
Income variability and agricultural policy
In Mexico, the policies of Guarantee Prices (PG) and direct support for the income of the producer, known as procampo (PC), have been applied in an alternative way. Such policies have a different effect on the variability of producers' incomes. Variance was used as a measure of variability of producer income. Information was used from 1980 to 1994 for PG and from 1995 to 2018 for PC. Agricultural income was taken as the product of price by yield, and then the cyclical effect of the trend was decomposed. The selected crops were maize and wheat. For corn, the states used were: Sinaloa, Jalisco, Edo. Mexico, Michoacán and Chiapas; while for wheat the states were: Sonora, Baja California Norte, Guanajuato, Sinaloa and Michoacán. Agricultural income was found to be more volatile in the period of the guarantee price policy than in the period of direct payments.Objective: To compare producer income volatility under two types of policies (support prices and direct payments).
Design/Methodology/Approach: Producer income is understood as the result of multiplying price by yield; therefore, income is the product of two random variables modeled with a lognormal distribution, accounting for the covariance. After the subtracting trend, the cyclical component is subjected to a volatile analysis under each policy studied.
Results: Income volatility is systematically higher for support price programs than for the direct payment policy.
Study Limitations/Implications: Government programs have recently taken up support prices again; therefore, income variability should be reviewed.
Findings/Conclusions: Government programs aim to increase producer income by different means. However, they overlook possible volatility implications. By taking up support price programs again, producer income may be at risk of rebounding
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