Quantum dot-based multiphoton fluorescent pipettes for targeted neuronal electrophysiology

Targeting visually identified neurons for electrophysiological recording is a fundamental neuroscience technique; however, its potential is hampered by poor visualization of pipette tips in deep brain tissue. We describe quantum dot-coated glass pipettes that provide strong two-photon contrast at deeper penetration depths than those achievable with current methods. We demonstrated the pipettes' utility in targeted patch-clamp recording experiments and single-cell electroporation of identified rat and mouse neurons in vitro and in vivo

Non-resonant direct p- and d-wave neutron capture by 12C

Discrete gamma-rays from the neutron capture state of 13C to its low-lying bound states have been measured using pulsed neutrons at En = 550 keV. The partial capture cross sections have been determined to be 1.7+/-0.5, 24.2+/-1.0, 2.0+/-0.4 and 1.0+/-0.4 microb for the ground (1/2-), first (1/2+), second (3/2-) and third (5/2+) excited states, respectively. From a comparison with theoretical predictions based on the non-resonant direct radiative capture mechanism, we could determine the spectroscopic factor for the 1/2+ state to be 0.80 +/- 0.04, free from neutron-nucleus interaction ambiguities in the continuum. In addition we have detected the contribution of the non-resonant d-wave capture component in the partial cross sections for transitions leading to the 1/2- and 3/2- states. While the s-wave capture dominates at En < 100 keV, the d-wave component turns out to be very important at higher energies. From the present investigation the 12C(n,gamma)13C reaction rate is obtained for temperatures in the range 10E+7 - 10E+10 K.Comment: Accepted for publication in Phys. Rev. C. - 16 pages + 8 figure

Incidence of Pathogenic Variants in Those With a Family History of Pancreatic Cancer

Discovery of a hereditary cancer syndrome can be one of the factors that determine whether a healthy individual completes pancreas cancer screening or whether an individual with cancer receives certain chemotherapies. Retrospective review was completed to determine the likelihood of detection of a pathogenic variant causing a hereditary cancer syndrome based on personal and family history. Study was completed through the hereditary cancer clinic at Mayo Clinic Florida over a 6 year period, 1/2012 through 1/2018. All participants were referred based on suspicion for a hereditary cancer syndrome based on personal and/or family history. Patients' personal oncologic history at time of consultation was recorded, as well as, cancer diagnoses in the family history and the number of family members with a history of pancreas cancer. Test result and gene name, if variant was pathogenic or likely pathogenic, were noted as well. A total of 2,019 patients completed genetic testing during study period. Personal history of cancer included a variety of primaries, including breast (N = 986), ovarian (N = 119), colon (N = 106), prostate (N = 65), and pancreas (N = 59). A positive result was discovered in 11% of the total group. Two hundred and eighty five reported a family history of pancreas cancer. The incidence of pathogenic variants was 13% (37/285) in those with any family history and 23% (13/56) in those with two or more relatives with pancreatic cancer. Those with multiple relatives with pancreatic cancer were significantly more likely to carry a pathogenic variant than those with a personal history of breast cancer under the age of 45 (23.2 vs. 11.9%, p = 0.02). Presence of multiple family members with a reported history of pancreatic cancer significantly increased the likelihood that a pathogenic variant would be identified in the patient even over other significant risk factors, like personal history of early onset breast cancer

Making better use of local data in flood frequency estimation

Flood frequency estimates are an essential part of flood risk management. They are an important ingredient of many important decisions, informing the cost-effectiveness, design and operation of flood defences, flood mapping and planning decisions in flood risk areas. They also inform the National Flood Risk Assessment, the setting of insurance premiums and long-term investment planning. Methods described in the Flood Estimation Handbook (FEH) published in 1999, and many subsequent updates, are considered the industry standard for flood estimation in the UK. They are used extensively by hydrologists from both the public and private sectors. Flood frequency estimates – also known as design flood estimates – are associated with many sources of uncertainty. These hydrological uncertainties often constitute the most uncertain component in any flood study. Uncertainty can lead to difficulty in having confidence in the outputs of studies, whether these are for investment planning, insurance, asset design, development planning or other purposes. As a result, there is considerable benefit to be gained from any reduction in the uncertainty of flood frequency estimation. There are many supplementary sources of information that can help to refine estimates of design floods and potentially reduce uncertainty. Examples include long-term flood history, river level records, photographs of floods and information obtained from field visits. These and similar types of information are defined as ‘local data’. The FEH Local research project aimed to: quantify the uncertainty of design floods estimated from FEH methods develop procedures and guidance for incorporating local and historical data into flood estimation to reduce uncertainties The primary objective of this report is to describe the reviews and research carried out during the FEH Local project. Another output from the project was a document giving guidance to practitioners on how to estimate uncertainty in flood frequency and how to find and incorporate local data. The practitioner guidance, ‘Using Local Data to Reduce Uncertainty in Flood Frequency Estimation’, will be disseminated early in 2017. This report aims to avoid duplication with the practitioner guidance and so is intended mainly for those with an interest in the background to the methods presented in the guidance

Homeostatic competition drives tumor growth and metastasis nucleation

We propose a mechanism for tumor growth emphasizing the role of homeostatic regulation and tissue stability. We show that competition between surface and bulk effects leads to the existence of a critical size that must be overcome by metastases to reach macroscopic sizes. This property can qualitatively explain the observed size distributions of metastases, while size-independent growth rates cannot account for clinical and experimental data. In addition, it potentially explains the observed preferential growth of metastases on tissue surfaces and membranes such as the pleural and peritoneal layers, suggests a mechanism underlying the seed and soil hypothesis introduced by Stephen Paget in 1889 and yields realistic values for metastatic inefficiency. We propose a number of key experiments to test these concepts. The homeostatic pressure as introduced in this work could constitute a quantitative, experimentally accessible measure for the metastatic potential of early malignant growths.Comment: 13 pages, 11 figures, to be published in the HFSP Journa

Dependence of direct neutron capture on nuclear-structure models

The prediction of cross sections for nuclei far off stability is crucial in the field of nuclear astrophysics. We calculate direct neutron capture on the even-even isotopes $^{124-145}$Sn and $^{208-238}$Pb with energy levels, masses, and nuclear density distributions taken from different nuclear-structure models. The utilized structure models are a Hartree-Fock-Bogoliubov model, a relativistic mean field theory, and a macroscopic-microscopic model based on the finite-range droplet model and a folded-Yukawa single-particle potential. Due to the differences in the resulting neutron separation and level energies, the investigated models yield capture cross sections sometimes differing by orders of magnitude. This may also lead to differences in the predicted astrophysical r-process paths. Astrophysical implications are discussed.Comment: 25 pages including 12 figures, RevTeX, to appear in Phys. Rev.