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1.
Phys Rev Lett ; 132(16): 162502, 2024 Apr 19.
Article in English | MEDLINE | ID: mdl-38701465

ABSTRACT

The nuclear charge radius of ^{32}Si was determined using collinear laser spectroscopy. The experimental result was confronted with ab initio nuclear lattice effective field theory, valence-space in-medium similarity renormalization group, and mean field calculations, highlighting important achievements and challenges of modern many-body methods. The charge radius of ^{32}Si completes the radii of the mirror pair ^{32}Ar-^{32}Si, whose difference was correlated to the slope L of the symmetry energy in the nuclear equation of state. Our result suggests L≤60 MeV, which agrees with complementary observables.

2.
Phys Rev Lett ; 131(10): 102501, 2023 Sep 08.
Article in English | MEDLINE | ID: mdl-37739365

ABSTRACT

Charge radii of neutron deficient ^{40}Sc and ^{41}Sc nuclei were determined using collinear laser spectroscopy. With the new data, the chain of Sc charge radii extends below the neutron magic number N=20 and shows a pronounced kink, generally taken as a signature of a shell closure, but one notably absent in the neighboring Ca, K, and Ar isotopic chains. Theoretical models that explain the trend at N=20 for the Ca isotopes cannot reproduce this puzzling behavior.

3.
Phys Rev Lett ; 129(13): 132501, 2022 Sep 23.
Article in English | MEDLINE | ID: mdl-36206412

ABSTRACT

Nuclear charge radii of ^{55,56}Ni were measured by collinear laser spectroscopy. The obtained information completes the behavior of the charge radii at the shell closure of the doubly magic nucleus ^{56}Ni. The trend of charge radii across the shell closures in calcium and nickel is surprisingly similar despite the fact that the ^{56}Ni core is supposed to be much softer than the ^{48}Ca core. The very low magnetic moment µ(^{55}Ni)=-1.108(20) µ_{N} indicates the impact of M1 excitations between spin-orbit partners across the N,Z=28 shell gaps. Our charge-radii results are compared to ab initio and nuclear density functional theory calculations, showing good agreement within theoretical uncertainties.

4.
Phys Rev Lett ; 127(18): 182503, 2021 Oct 29.
Article in English | MEDLINE | ID: mdl-34767412

ABSTRACT

The nuclear root-mean-square charge radius of ^{54}Ni was determined with collinear laser spectroscopy to be R(^{54}Ni)=3.737(3) fm. In conjunction with the known radius of the mirror nucleus ^{54}Fe, the difference of the charge radii was extracted as ΔR_{ch}=0.049(4) fm. Based on the correlation between ΔR_{ch} and the slope of the symmetry energy at nuclear saturation density (L), we deduced 21≤L≤88 MeV. The present result is consistent with the L from the binary neutron star merger GW170817, favoring a soft neutron matter EOS, and barely consistent with the PREX-2 result within 1σ error bands. Our result indicates the neutron-skin thickness of ^{48}Ca as 0.15-0.21 fm.

5.
Ethology ; 125(8): 565-574, 2019 Aug.
Article in English | MEDLINE | ID: mdl-33688110

ABSTRACT

Mating displays often contain multiple signals. Different combinations of these signals may be equally successful at attracting a mate, as environment and signal combination may influence relative signal weighting by choosy individuals. This variation in signal weighting among choosy individuals may facilitate the maintenance of polymorphic displays and signalling behaviour. One group of animals known for their polymorphic patterning are Batesian mimetic butterflies, where the interaction of sexual selection and predation pressures are hypothesized to influence the maintenance of polymorphic wing patterning and behaviour. Males in the female-limited polymorphic Batesian mimetic butterfly Papilio polytes use female wing pattern and female activity levels when determining whom to court. They court stationary females with mimetic wing patterns more often than stationary females with non-mimetic, male-like wing patterns, and active females more often than inactive females. It is unclear whether females modify their behaviour to increase (or decrease) their likelihood of receiving male courtship, or whether non-mimetic females spend more time in cryptic environments than mimetic females, to compensate for their lack of mimicry-driven predation protection (at the cost of decreased visibility to males). In addition, relative signal weighting of female wing pattern and activity to male mate selection is unknown. To address these questions, we conducted a series of observational studies of a polymorphic P. polytes population in a large butterfly enclosure. We found that males exclusively courted active females, irrespective of female wing pattern. However, males did court active non-mimetic females significantly more often than expected given their relative abundance in the population. Females exhibited similar activity levels, and selected similar resting environments, irrespective of wing pattern. Our results suggest that male preference for non-mimetic females may play an active role in the maintenance of the non-mimetic female form in natural populations, where males are likely to be in the presence of active, as well as inactive, mimetic and non-mimetic females.

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