4 research outputs found
Interpreting Attoclock Measurements of Tunnelling Times
Resolving in time the dynamics of light absorption by atoms and molecules,
and the electronic rearrangement this induces, is among the most challenging
goals of attosecond spectroscopy. The attoclock is an elegant approach to this
problem, which encodes ionization times in the strong-field regime. However,
the accurate reconstruction of these times from experimental data presents a
formidable theoretical challenge. Here, we solve this problem by combining
analytical theory with ab-initio numerical simulations. We apply our theory to
numerical attoclock experiments on the hydrogen atom to extract ionization time
delays and analyse their nature. Strong field ionization is often viewed as
optical tunnelling through the barrier created by the field and the core
potential. We show that, in the hydrogen atom, optical tunnelling is
instantaneous. By calibrating the attoclock using the hydrogen atom, our method
opens the way to identify possible delays associated with multielectron
dynamics during strong-field ionization.Comment: 33 pages, 10 figures, 3 appendixe
Whole genome analysis reveals aneuploidies in early pregnancy loss in the horse
The first 8 weeks of pregnancy is a critical time, with the majority of pregnancy losses occurring during this period. Abnormal chromosome number (aneuploidy) is a common finding in human miscarriage, yet is rarely reported in domestic animals. Equine early pregnancy loss (EPL) has no diagnosis in over 80% of cases. The aim of this study was to characterise aneuploidies associated with equine EPL. Genomic DNA from clinical cases of spontaneous miscarriage (EPLs; 14–65 days of gestation) and healthy control placentae (various gestational ages) were assessed using a high density genotyping array. Aneuploidy was detected in 12/55 EPLs (21.8%), and 0/15 healthy control placentae. Whole genome sequencing (30X) and digital droplet PCR (ddPCR) validated results. The majority of these aneuploidies have never been reported in live born equines, supporting their embryonic/fetal lethality. Aneuploidies were detected in both placental and fetal compartments. Rodents are currently used to study how maternal ageing impacts aneuploidy risk, however the differences in reproductive biology is a limitation of this model. We present the first evidence of aneuploidy in naturally occurring equine EPLs at a similar rate to human miscarriage. We therefore suggest the horse as an alternative to rodent models to study mechanisms resulting in aneuploid pregnancies