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1.
Phys Rev Lett ; 128(9): 091803, 2022 Mar 04.
Article in English | MEDLINE | ID: mdl-35302807

ABSTRACT

We report the measurement of sub-MeV solar neutrinos through the use of their associated Cherenkov radiation, performed with the Borexino detector at the Laboratori Nazionali del Gran Sasso. The measurement is achieved using a novel technique that correlates individual photon hits of events to the known position of the Sun. In an energy window between 0.54 to 0.74 MeV, selected using the dominant scintillation light, we have measured 10 887_{-2103}^{+2386}(stat)±947(syst) (68% confidence interval) solar neutrinos out of 19 904 total events. This corresponds to a ^{7}Be neutrino interaction rate of 51.6_{-12.5}^{+13.9} counts/(day·100 ton), which is in agreement with the standard solar model predictions and the previous spectroscopic results of Borexino. The no-neutrino hypothesis can be excluded with >5σ confidence level. For the first time, we have demonstrated the possibility of utilizing the directional Cherenkov information for sub-MeV solar neutrinos, in a large-scale, high light yield liquid scintillator detector. This measurement provides an experimental proof of principle for future hybrid event reconstruction using both Cherenkov and scintillation signatures simultaneously.

2.
Phys Rev Lett ; 129(25): 252701, 2022 Dec 16.
Article in English | MEDLINE | ID: mdl-36608219

ABSTRACT

We present an improved measurement of the carbon-nitrogen-oxygen (CNO) solar neutrino interaction rate at Earth obtained with the complete Borexino Phase-III dataset. The measured rate, R_{CNO}=6.7_{-0.8}^{+2.0} counts/(day×100 tonnes), allows us to exclude the absence of the CNO signal with about 7σ C.L. The correspondent CNO neutrino flux is 6.6_{-0.9}^{+2.0}×10^{8} cm^{-2} s^{-1}, taking into account the neutrino flavor conversion. We use the new CNO measurement to evaluate the C and N abundances in the Sun with respect to the H abundance for the first time with solar neutrinos. Our result of N_{CN}=(5.78_{-1.00}^{+1.86})×10^{-4} displays a ∼2σ tension with the "low-metallicity" spectroscopic photospheric measurements. Furthermore, our result used together with the ^{7}Be and ^{8}B solar neutrino fluxes, also measured by Borexino, permits us to disfavor at 3.1σ C.L. the "low-metallicity" standard solar model B16-AGSS09met as an alternative to the "high-metallicity" standard solar model B16-GS98.

3.
Water Sci Technol ; 69(4): 896-902, 2014.
Article in English | MEDLINE | ID: mdl-24569293

ABSTRACT

The paper reports the results of an experiment to assess the feasibility of including a photobioreactor within the design of a wastewater treatment plant, growing microalgae on the centrate from anaerobic sludge dewatering. The growth of algal biomass would take advantage of the available nitrogen and provide a substrate for biogas production by anaerobic digestion. Tests were carried out by semi-continuously feeding a photobioreactor with a centrate-effluent blend and by increasing the fraction of centrate. The experimental results show that the centrate does not induce any toxicity and, on the contrary, can be well utilized by microalgae, whose average specific growth rate (µ), on centrate as such, was between 0.04 and 0.06 d(-1). The maximum biomass concentration in the photobioreactor effluent was 1.6 gSS/L at 10 days HRT (hydraulic retention time). Methane production tests led to biochemical methane production values of 335 ± 39, and 284 ± 68 mL 0°C, 1 atm CH4/g VS for the two tested samples, in agreement with literature values. Settling tests show that the settling capacity of microalgae, although satisfactory, could be effectively improved after mixing with activated sludge, confirming the potential to use the existing primary settler for microalgae thickening in order to feed microalgae for anaerobic digestion with primary/secondary sludge.


Subject(s)
Microalgae/growth & development , Waste Disposal, Fluid/methods , Water/chemistry , Animals , Biomass , Cyanobacteria/physiology , Methane , Rotifera/physiology
4.
Neuropsychologia ; 37(4): 395-402, 1999 Apr.
Article in English | MEDLINE | ID: mdl-10215086

ABSTRACT

Are concepts expressed in language also represented spatially? To pursue this question we investigated the structure of events. Events are defined as actions with spatial trajectories that can be perceived by our senses and described in language. Events are expressed linguistically in sentences containing verbs which determine the thematic roles of the arguments (e.g., who is doing what to whom, where). Because of previous observations we focused on whether events are represented spatially by location of thematic roles and direction of actions. Location and direction were dissociated by contrasting different kinds of verbs: 'push' vs 'pull' in which actions move toward or away from the agent. To control for spatial effects produced by the surface structure of a left to right written language, we kept the structure of sentences constant and sought for spatial biases produced by differences in the meaning of these sentences. From three experiments using drawing and sentence-picture matching reaction time tasks, we found that normal subjects located agents to the left of patients and represented actions with a left to right directionality. These results are not easily explained by features of the surface structure of language or properties of propositional representations. We suggest that events have spatial representations in addition to their propositional counterparts of verbs and thematic roles. The specific spatial properties observed may relate to functional properties of the left hemisphere.


Subject(s)
Dominance, Cerebral , Language Development , Space Perception , Adolescent , Adult , Female , Functional Laterality , Humans , Male , Nerve Net , Psychomotor Performance/physiology
5.
Blood ; 76(9): 1771-82, 1990 Nov 01.
Article in English | MEDLINE | ID: mdl-2224127

ABSTRACT

Investigations linking human megakaryocyte development and cell biology have been hindered by an inability to obtain large, relatively pure megakaryocyte cell preparations from in vitro stem cell cultures. We report here that such preparations can be generated from liquid cultures of normal human peripheral blood mononuclear cells stimulated by a serum source of megakaryocyte colony stimulating activity (Meg-CSA, the 0% to 60% ammonium sulfate protein fraction of aplastic canine serum). Adherent-depleted peripheral blood mononuclear cells are suspended at 5 x 10(5) to 10(6) cells/mL in supplemented liquid culture medium, platelet-poor human plasma 20% (vol/vol) and 1 to 2 mg/mL serum Meg-CSA protein. After 12 to 14 days of incubation, megakaryocytes constitute 3.0 +/- 2.9% (mean +/- SD, n = 8) of the unseparated cultured cell population. Megakaryocytes can be enriched by counterflow centrifugal elutriation to a purity of 58 +/- 14% (+/- SD) with a recovery of 13 +/- 7% and a viability of 67 +/- 19%. This algorithm results in the average isolation of approximately 3 x 10(5) enriched megakaryocytes from a 100-mL starting volume of peripheral blood. Cultured megakaryocytes exhibit normal light and ultrastructural morphology by Wright-Giemsa staining and electron microscopic analysis. After a 12-day culture interval, enriched megakaryocyte preparations exhibit morphologic stage distributions that are similar to normal human marrow. Stage distributions move rightward with culture duration indicating partial synchrony of megakaryocyte maturation. On cytospin preparations, megakaryocyte diameter averages 30.2 +/- 1.5 microns and increases with maturation stage. Flow cytometric analyses demonstrate the expression of platelet glycoproteins (GP) Ib and IIb/IIIa by the cultured megakaryocytes. The modal ploidy of the enriched cells at day 12 of culture is 16N and most remaining megakaryocytes are 8N or 32N. Liquid culture of serum Meg-CSA-stimulated human peripheral blood mononuclear cells represents a valuable investigative tool that should permit studies of human megakaryocyte biology that have not been possible in the past.


Subject(s)
Hematopoietic Stem Cells/cytology , Megakaryocytes/cytology , Algorithms , Cell Separation/methods , Cells, Cultured , Culture Media/analysis , DNA/analysis , DNA/genetics , Flow Cytometry , GPI-Linked Proteins , Hematopoiesis , Hematopoietic Stem Cells/chemistry , Hematopoietic Stem Cells/drug effects , Humans , Megakaryocytes/chemistry , Megakaryocytes/ultrastructure , Membrane Glycoproteins , Mesothelin , Microscopy, Electron , Ploidies , Proteins/analysis , Proteins/pharmacology
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