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As new information carriers, antiferromagnetic magnons have great potential in the fields of spintronics and quantum information. However, the strong exchange interaction between sublattice spins in conventional antiferromagnets results in their frequencies up to the terahertz (THz) range, hindering further exploration of related applications and physics. Recently, emerging van der Waals A‐type antiferromagnets with the weak exchange interaction may bring about a change. In this study, it demonstrates two distinct tunable ultrastrong magnon–magnon couplings in the gigahertz (GHz) band using this type of antiferromagnet, CrPS4, with a maximum normalized coupling strength (η) of 0.31. It establishes orthorhombic and monoclinic models for theoretical analyses, unambiguously showing that the ultrastrong coupling strength is caused by unique magnetocrystalline anisotropy rather than exchange enhancement. Furthermore, for the first time, it observes a continuous switching process of sublattice magnon chirality arising from the orthorhombic nature of anisotropy. These findings not only deepen the understanding of antiferromagnetic spin dynamics but also offer a powerful platform for building magnonic quantum systems and chirality‐based spintronics. [ABSTRACT FROM AUTHOR]

As new information carriers, antiferromagnetic magnons have great potential in the fields of spintronics and quantum information. However, the strong exchange interaction between sublattice spins in conventional antiferromagnets results in their frequencies up to the terahertz (THz) range, hindering further exploration of related applications and physics. Recently, emerging van der Waals A‐type antiferromagnets with the weak exchange interaction may bring about a change. In this study, it demonstrates two distinct tunable ultrastrong magnon–magnon couplings in the gigahertz (GHz) band using this type of antiferromagnet, CrPS4, with a maximum normalized coupling strength (η) of 0.31. It establishes orthorhombic and monoclinic models for theoretical analyses, unambiguously showing that the ultrastrong coupling strength is caused by unique magnetocrystalline anisotropy rather than exchange enhancement. Furthermore, for the first time, it observes a continuous switching process of sublattice magnon chirality arising from the orthorhombic nature of anisotropy. These findings not only deepen the understanding of antiferromagnetic spin dynamics but also offer a powerful platform for building magnonic quantum systems and chirality‐based spintronics. [ABSTRACT FROM AUTHOR]

Prenatal alcohol exposure can result in varying degrees of neurodevelopmental deficits, growth retardation, and facial dysmorphology. Variation in these adverse outcomes not only depends on the dose and pattern of alcohol exposure but also on less well understood interactions among environmental, genetic, and maternal factors. The current study tested the hypothesis that fetal genotype is an important determinant of ethanol teratogenesis by evaluating effects of ethanol exposure via embryo culture in 3 inbred strains of mice known to differ in the vulnerability of prenatal alcohol exposure in vivo. Three strains of mice, C57BL/6N (B6), DBA/2 (D2), and 129S6/SvEvTac (129S6) were assessed in a whole embryo culture beginning on embryonic day 8.25, with or without alcohol administration at 88 mM for 6 hours followed by 42 hours culture in ethanol-free media. Contrasting strain differences in susceptibility were observed for the brain, the face, and other organ systems using the Maele-Fabry and Picard scoring system. The forebrain, midbrain, hindbrain, heart, optic vesicle, caudal neural tube, and hindlimbs of the B6 mice were severely delayed in growth, whereas compared to the respective controls, only the forebrain and optic vesicle were delayed in the D2 mice, and no effects were found in the 129S6 mice. A large number of cleaved (c)-caspase 3 positive (+) cells were found in regions of the brain, optic vesicles, cranial nerve nuclei V, VII, VIII, and IX as well as the craniofacial primordial; only a few were found in corresponding regions of the B6 controls. In contrast, only a small number of c-caspase 3 immunostaining cells were found in either the alcohol treated or the controls of the D2 embryos and in 129S6 embryos. The independent apoptotic markers TUNEL and Nile blue staining further confirmed the strain differences in apoptotic responses in both the neural tube and craniofacial primordia. Under embryo culture conditions, in which alcohol exposure factors and fetal developmental staging were controlled, and maternal and intrauterine factors were eliminated, the degree of growth retardation and the extent and type of neurodevelopmental teratogenesis varied significantly across strains. Notably, the 129S6 strain was remarkably resistant to alcohol-induced growth deficits, confirming a previous in vivo study, and the D2 strain was also significantly less affected than the B6 strain. These findings demonstrate that fetal genotype is an important factor that can contribute to the variation in fetal alcohol spectrum disorder. [ABSTRACT FROM AUTHOR]